Canonical Allele Identifier: CA1548139243
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881629C= , CM000667.2:g.56881629C= GRCh38
NC_000005.9:g.56177456C= , CM000667.1:g.56177456C= GRCh37
NC_000005.8:g.56213213C= NCBI36
NG_031884.1:g.71557C=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.2429C= MANE Select ENSP00000382423.3:p.Ser810=
ENST00000399503.3:c.2429C= ENSP00000382423.3:p.Ser810=
NM_005921.1:c.2429C= NP_005912.1:p.Ser810=
XM_005248519.3:c.2051C= XP_005248576.2:p.Ser684=
XM_011543406.1:c.2174C= XP_011541708.1:p.Ser725=
XM_011543407.1:c.2150C= XP_011541709.1:p.Ser717=
XM_011543408.1:c.2429C= XP_011541710.1:p.Ser810=
XM_017009484.1:c.2018C= XP_016864973.1:p.Ser673=
XM_017009485.1:c.1940C= XP_016864974.1:p.Ser647=
XR_001742068.2:n.2460C=
NM_005921.2:c.2429C= MANE Select NP_005912.1:p.Ser810=