Canonical Allele Identifier: CA1548139314
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56881808C= , CM000667.2:g.56881808C= GRCh38
NC_000005.9:g.56177635C= , CM000667.1:g.56177635C= GRCh37
NC_000005.8:g.56213392C= NCBI36
NG_031884.1:g.71736C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2608C= MANE Select ENSP00000382423.3:p.Gln870=
ENST00000399503.3:c.2608C= ENSP00000382423.3:p.Gln870=
NM_005921.1:c.2608C= NP_005912.1:p.Gln870=
XM_005248519.3:c.2230C= XP_005248576.2:p.Gln744=
XM_011543406.1:c.2353C= XP_011541708.1:p.Gln785=
XM_011543407.1:c.2329C= XP_011541709.1:p.Gln777=
XM_011543408.1:c.2608C= XP_011541710.1:p.Gln870=
XM_017009484.1:c.2197C= XP_016864973.1:p.Gln733=
XM_017009485.1:c.2119C= XP_016864974.1:p.Gln707=
XR_001742068.2:n.2639C=
NM_005921.2:c.2608C= MANE Select NP_005912.1:p.Gln870=