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: CA1539051343
Gene: IL7R HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.35872926T= , CM000667.2:g.35872926T= GRCh38
NC_000005.9:g.35873028T= , CM000667.1:g.35873028T= GRCh37
NC_000005.8:g.35908785T= NCBI36
NG_009567.1:g.21038T= , LRG_74:g.21038T=

Transcript Alleles

HGVS Amino-acid Change
NM_002185.5:c.538-554T= MANE Select NP_002176.2:n.538-554T=
ENST00000303115.8:c.538-554T= MANE Select ENSP00000306157.3:n.538-554T=
NM_002185.3:c.538-554T= NP_002176.2:n.538-554T=
NM_002185.4:c.538-554T= NP_002176.2:n.538-554T=
NR_120485.1:n.640+1713T=
NR_120485.2:n.666+1713T=
NR_120485.3:n.624+1713T=
ENST00000303115.7:c.538-554T= ENSP00000306157.3:n.538-554T=
ENST00000506850.5:c.538-554T= ENSP00000421207.1:n.538-554T=
ENST00000514217.5:c.537+1713T= ENSP00000427688.1:n.537+1713T=
XM_005248299.2:c.538-554T= XP_005248356.1:n.538-554T=
XM_005248299.4:c.538-554T= XP_005248356.1:n.538-554T=
XM_005248300.1:c.538-554T= XP_005248357.1:n.538-554T=
XM_011514037.1:c.538-554T= XP_011512339.1:n.538-554T=
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