Canonical Allele Identifier: CA1548139451
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882105T= , CM000667.2:g.56882105T= GRCh38
NC_000005.9:g.56177932T= , CM000667.1:g.56177932T= GRCh37
NC_000005.8:g.56213689T= NCBI36
NG_031884.1:g.72033T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000399503.4:c.2905T= MANE Select ENSP00000382423.3:p.Ser969=
ENST00000399503.3:c.2905T= ENSP00000382423.3:p.Ser969=
NM_005921.1:c.2905T= NP_005912.1:p.Ser969=
XM_005248519.3:c.2527T= XP_005248576.2:p.Ser843=
XM_011543406.1:c.2650T= XP_011541708.1:p.Ser884=
XM_011543407.1:c.2626T= XP_011541709.1:p.Ser876=
XM_011543408.1:c.2905T= XP_011541710.1:p.Ser969=
XM_017009484.1:c.2494T= XP_016864973.1:p.Ser832=
XM_017009485.1:c.2416T= XP_016864974.1:p.Ser806=
XR_001742068.2:n.2936T=
NM_005921.2:c.2905T= MANE Select NP_005912.1:p.Ser969=