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: CA9090873
Gene: MAP2K2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.4101144C>A , CM000681.2:g.4101144C>A GRCh38
NC_000019.9:g.4101142C>A , CM000681.1:g.4101142C>A GRCh37
NC_000019.8:g.4052142C>A NCBI36
NG_007996.1:g.27985G>T , LRG_750:g.27985G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000394867.9:n.1020-1G>T
ENST00000687128.1:n.1020-1G>T
ENST00000689792.1:n.521-1G>T
ENST00000262948.10:c.581-1G>T MANE Select ENSP00000262948.4:n.581-1G>T
ENST00000262948.9:c.581-1G>T ENSP00000262948.3:n.581-1G>T
ENST00000394867.8:c.290-1G>T ENSP00000378336.1:n.290-1G>T
ENST00000593364.5:n.528-1G>T
ENST00000597008.5:n.182-1G>T
ENST00000597263.5:n.45-1G>T
ENST00000599345.1:n.851-1G>T
ENST00000601786.5:n.882-1G>T
ENST00000602167.5:n.301-1G>T
NM_030662.3:c.581-1G>T , LRG_750t1:c.581-1G>T NP_109587.1:n.581-1G>T
XM_006722799.2:c.581-1G>T XP_006722862.1:n.581-1G>T
XM_011528133.1:c.11-1G>T XP_011526435.1:n.11-1G>T
XM_017026989.1:c.581-1G>T XP_016882478.1:n.581-1G>T
XM_017026990.1:c.581-1G>T XP_016882479.1:n.581-1G>T
XM_017026991.1:c.581-1G>T XP_016882480.1:n.581-1G>T
NM_030662.4:c.581-1G>T MANE Select NP_109587.1:n.581-1G>T
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