Canonical Allele Identifier: CA1548139502
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882205C= , CM000667.2:g.56882205C= GRCh38
NC_000005.9:g.56178032C= , CM000667.1:g.56178032C= GRCh37
NC_000005.8:g.56213789C= NCBI36
NG_031884.1:g.72133C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.3005C= MANE Select ENSP00000382423.3:p.Ser1002=
ENST00000399503.3:c.3005C= ENSP00000382423.3:p.Ser1002=
NM_005921.1:c.3005C= NP_005912.1:p.Ser1002=
XM_005248519.3:c.2627C= XP_005248576.2:p.Ser876=
XM_011543406.1:c.2750C= XP_011541708.1:p.Ser917=
XM_011543407.1:c.2726C= XP_011541709.1:p.Ser909=
XM_011543408.1:c.3005C= XP_011541710.1:p.Ser1002=
XM_017009484.1:c.2594C= XP_016864973.1:p.Ser865=
XM_017009485.1:c.2516C= XP_016864974.1:p.Ser839=
XR_001742068.2:n.3036C=
NM_005921.2:c.3005C= MANE Select NP_005912.1:p.Ser1002=