Canonical Allele Identifier: CA1548139587

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882409C= , CM000667.2:g.56882409C=	GRCh38
NC_000005.9:g.56178236C= , CM000667.1:g.56178236C=	GRCh37
NC_000005.8:g.56213993C=	NCBI36
NG_031884.1:g.72337C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3209C= MANE Select	ENSP00000382423.3:p.Thr1070=
ENST00000399503.3:c.3209C=	ENSP00000382423.3:p.Thr1070=
NM_005921.1:c.3209C=	NP_005912.1:p.Thr1070=
XM_005248519.3:c.2831C=	XP_005248576.2:p.Thr944=
XM_011543406.1:c.2954C=	XP_011541708.1:p.Thr985=
XM_011543407.1:c.2930C=	XP_011541709.1:p.Thr977=
XM_011543408.1:c.3209C=	XP_011541710.1:p.Thr1070=
XM_017009484.1:c.2798C=	XP_016864973.1:p.Thr933=
XM_017009485.1:c.2720C=	XP_016864974.1:p.Thr907=
XR_001742068.2:n.3240C=
NM_005921.2:c.3209C= MANE Select	NP_005912.1:p.Thr1070=