Canonical Allele Identifier: CA1548139586

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882408A= , CM000667.2:g.56882408A=	GRCh38
NC_000005.9:g.56178235A= , CM000667.1:g.56178235A=	GRCh37
NC_000005.8:g.56213992A=	NCBI36
NG_031884.1:g.72336A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3208A= MANE Select	ENSP00000382423.3:p.Thr1070=
ENST00000399503.3:c.3208A=	ENSP00000382423.3:p.Thr1070=
NM_005921.1:c.3208A=	NP_005912.1:p.Thr1070=
XM_005248519.3:c.2830A=	XP_005248576.2:p.Thr944=
XM_011543406.1:c.2953A=	XP_011541708.1:p.Thr985=
XM_011543407.1:c.2929A=	XP_011541709.1:p.Thr977=
XM_011543408.1:c.3208A=	XP_011541710.1:p.Thr1070=
XM_017009484.1:c.2797A=	XP_016864973.1:p.Thr933=
XM_017009485.1:c.2719A=	XP_016864974.1:p.Thr907=
XR_001742068.2:n.3239A=
NM_005921.2:c.3208A= MANE Select	NP_005912.1:p.Thr1070=