Canonical Allele Identifier: CA1548136440
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56875213C= , CM000667.2:g.56875213C= GRCh38
NC_000005.9:g.56171040C= , CM000667.1:g.56171040C= GRCh37
NC_000005.8:g.56206797C= NCBI36
NG_031884.1:g.65141C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.1868C= MANE Select ENSP00000382423.3:p.Ser623=
ENST00000399503.3:c.1868C= ENSP00000382423.3:p.Ser623=
NM_005921.1:c.1868C= NP_005912.1:p.Ser623=
XM_005248519.3:c.1490C= XP_005248576.2:p.Ser497=
XM_011543406.1:c.1613C= XP_011541708.1:p.Ser538=
XM_011543407.1:c.1686+2208C= XP_011541709.1:n.1686+2208C=
XM_011543408.1:c.1868C= XP_011541710.1:p.Ser623=
XM_017009484.1:c.1457C= XP_016864973.1:p.Ser486=
XM_017009485.1:c.1379C= XP_016864974.1:p.Ser460=
XR_001742068.2:n.1899C=
NM_005921.2:c.1868C= MANE Select NP_005912.1:p.Ser623=