Canonical Allele Identifier: CA1548139441

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882078G= , CM000667.2:g.56882078G=	GRCh38
NC_000005.9:g.56177905G= , CM000667.1:g.56177905G=	GRCh37
NC_000005.8:g.56213662G=	NCBI36
NG_031884.1:g.72006G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2878G= MANE Select	ENSP00000382423.3:p.Gly960=
ENST00000399503.3:c.2878G=	ENSP00000382423.3:p.Gly960=
NM_005921.1:c.2878G=	NP_005912.1:p.Gly960=
XM_005248519.3:c.2500G=	XP_005248576.2:p.Gly834=
XM_011543406.1:c.2623G=	XP_011541708.1:p.Gly875=
XM_011543407.1:c.2599G=	XP_011541709.1:p.Gly867=
XM_011543408.1:c.2878G=	XP_011541710.1:p.Gly960=
XM_017009484.1:c.2467G=	XP_016864973.1:p.Gly823=
XM_017009485.1:c.2389G=	XP_016864974.1:p.Gly797=
XR_001742068.2:n.2909G=
NM_005921.2:c.2878G= MANE Select	NP_005912.1:p.Gly960=