Canonical Allele Identifier: CA1548139279
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881738C= , CM000667.2:g.56881738C= GRCh38
NC_000005.9:g.56177565C= , CM000667.1:g.56177565C= GRCh37
NC_000005.8:g.56213322C= NCBI36
NG_031884.1:g.71666C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2538C= MANE Select ENSP00000382423.3:p.Ser846=
ENST00000399503.3:c.2538C= ENSP00000382423.3:p.Ser846=
NM_005921.1:c.2538C= NP_005912.1:p.Ser846=
XM_005248519.3:c.2160C= XP_005248576.2:p.Ser720=
XM_011543406.1:c.2283C= XP_011541708.1:p.Ser761=
XM_011543407.1:c.2259C= XP_011541709.1:p.Ser753=
XM_011543408.1:c.2538C= XP_011541710.1:p.Ser846=
XM_017009484.1:c.2127C= XP_016864973.1:p.Ser709=
XM_017009485.1:c.2049C= XP_016864974.1:p.Ser683=
XR_001742068.2:n.2569C=
NM_005921.2:c.2538C= MANE Select NP_005912.1:p.Ser846=