Canonical Allele Identifier: CA1548129162

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859677T= , CM000667.2:g.56859677T=	GRCh38
NC_000005.9:g.56155504T= , CM000667.1:g.56155504T=	GRCh37
NC_000005.8:g.56191261T=	NCBI36
NG_031884.1:g.49605T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000399503.4:c.634-38T= MANE Select	ENSP00000382423.3:n.634-38T=
ENST00000399503.3:c.634-38T=	ENSP00000382423.3:n.634-38T=
NM_005921.1:c.634-38T=	NP_005912.1:n.634-38T=
XM_005248519.3:c.256-38T=	XP_005248576.2:n.256-38T=
XM_011543406.1:c.379-38T=	XP_011541708.1:n.379-38T=
XM_011543407.1:c.634-38T=	XP_011541709.1:n.634-38T=
XM_011543408.1:c.634-38T=	XP_011541710.1:n.634-38T=
XM_017009484.1:c.223-38T=	XP_016864973.1:n.223-38T=
XM_017009485.1:c.145-38T=	XP_016864974.1:n.145-38T=
XR_001742068.2:n.665-38T=
NM_005921.2:c.634-38T= MANE Select	NP_005912.1:n.634-38T=