Canonical Allele Identifier: CA1548139542
Gene: MAP3K1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.56882289A= , CM000667.2:g.56882289A= GRCh38
NC_000005.9:g.56178116A= , CM000667.1:g.56178116A= GRCh37
NC_000005.8:g.56213873A= NCBI36
NG_031884.1:g.72217A=

Transcript Alleles

HGVS Amino-acid change
ENST00000399503.4:c.3089A= MANE Select ENSP00000382423.3:p.His1030=
ENST00000399503.3:c.3089A= ENSP00000382423.3:p.His1030=
NM_005921.1:c.3089A= NP_005912.1:p.His1030=
XM_005248519.3:c.2711A= XP_005248576.2:p.His904=
XM_011543406.1:c.2834A= XP_011541708.1:p.His945=
XM_011543407.1:c.2810A= XP_011541709.1:p.His937=
XM_011543408.1:c.3089A= XP_011541710.1:p.His1030=
XM_017009484.1:c.2678A= XP_016864973.1:p.His893=
XM_017009485.1:c.2600A= XP_016864974.1:p.His867=
XR_001742068.2:n.3120A=
NM_005921.2:c.3089A= MANE Select NP_005912.1:p.His1030=