Canonical Allele Identifier: CA1548129255
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56859884G= , CM000667.2:g.56859884G= GRCh38
NC_000005.9:g.56155711G= , CM000667.1:g.56155711G= GRCh37
NC_000005.8:g.56191468G= NCBI36
NG_031884.1:g.49812G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.803G= MANE Select ENSP00000382423.3:p.Gly268=
ENST00000399503.3:c.803G= ENSP00000382423.3:p.Gly268=
NM_005921.1:c.803G= NP_005912.1:p.Gly268=
XM_005248519.3:c.425G= XP_005248576.2:p.Gly142=
XM_011543406.1:c.548G= XP_011541708.1:p.Gly183=
XM_011543407.1:c.803G= XP_011541709.1:p.Gly268=
XM_011543408.1:c.803G= XP_011541710.1:p.Gly268=
XM_017009484.1:c.392G= XP_016864973.1:p.Gly131=
XM_017009485.1:c.314G= XP_016864974.1:p.Gly105=
XR_001742068.2:n.834G=
NM_005921.2:c.803G= MANE Select NP_005912.1:p.Gly268=