This is a test version of the ClinGen Allele Registry and hosts obsolete or unreal identifiers. Please visit here for the production version.
Canonical Allele Identifier: CA2365766303
Gene: HNF4A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.44423882G= , CM000682.2:g.44423882G= GRCh38
NC_000020.10:g.43052522G= , CM000682.1:g.43052522G= GRCh37
NC_000020.9:g.42485936G= NCBI36
NG_009818.1:g.73082G= , LRG_483:g.73082G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000316673.9:c.827-136G= MANE Select ENSP00000315180.4:n.827-136G=
ENST00000316099.10:c.893-136G= ENSP00000312987.3:n.893-136G=
ENST00000619550.5:c.867-136G=
ENST00000316099.9:c.893-136G= ENSP00000312987.3:n.893-136G=
ENST00000316099.8:c.893-136G= ENSP00000312987.3:n.893-136G=
ENST00000316673.8:c.827-136G= ENSP00000315180.4:n.827-136G=
ENST00000372920.1:c.*660-136G= ENSP00000362011.1:n.*660-136G=
ENST00000415691.2:c.893-136G= ENSP00000412111.1:n.893-136G=
ENST00000443598.6:c.893-136G= ENSP00000410911.2:n.893-136G=
ENST00000457232.5:c.827-136G= ENSP00000396216.1:n.827-136G=
ENST00000609795.5:c.827-136G= ENSP00000476609.1:n.827-136G=
ENST00000619550.4:c.818-136G= ENSP00000481331.1:n.818-136G=
NM_000457.4:c.893-136G= , LRG_483t2:c.893-136G= NP_000448.3:n.893-136G=
NM_001030003.2:c.827-136G= NP_001025174.1:n.827-136G=
NM_001030004.2:c.827-136G= NP_001025175.1:n.827-136G=
NM_001258355.1:c.872-136G= NP_001245284.1:n.872-136G=
NM_001287182.1:c.818-136G= NP_001274111.1:n.818-136G=
NM_001287183.1:c.818-136G= , LRG_483t3:c.818-136G= NP_001274112.1:n.818-136G=
NM_001287184.1:c.818-136G= NP_001274113.1:n.818-136G=
NM_175914.4:c.827-136G= , LRG_483t1:c.827-136G= NP_787110.2:n.827-136G=
NM_178849.2:c.893-136G= NP_849180.1:n.893-136G=
NM_178850.2:c.893-136G= NP_849181.1:n.893-136G=
XM_005260407.2:c.1010-136G= XP_005260464.1:n.1010-136G=
XM_011528797.1:c.941-136G= XP_011527099.1:n.941-136G=
XM_011528798.1:c.941-136G= XP_011527100.1:n.941-136G=
XM_005260407.4:c.1010-136G= XP_005260464.1:n.1010-136G=
NM_001030003.3:c.827-136G= NP_001025174.1:n.827-136G=
NM_001030004.3:c.827-136G= NP_001025175.1:n.827-136G=
NM_001258355.2:c.872-136G= NP_001245284.1:n.872-136G=
NM_001287182.2:c.818-136G= NP_001274111.1:n.818-136G=
NM_001287184.2:c.818-136G= NP_001274113.1:n.818-136G=
NM_178849.3:c.893-136G= NP_849180.1:n.893-136G=
NM_178850.3:c.893-136G= NP_849181.1:n.893-136G=
NM_000457.5:c.893-136G= NP_000448.3:n.893-136G=
NM_000457.6:c.893-136G= NP_000448.3:n.893-136G=
NM_001287183.2:c.818-136G= NP_001274112.1:n.818-136G=
NM_175914.5:c.827-136G= MANE Select NP_787110.2:n.827-136G=
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