Canonical Allele Identifier: CA1548139301

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881786G= , CM000667.2:g.56881786G=	GRCh38
NC_000005.9:g.56177613G= , CM000667.1:g.56177613G=	GRCh37
NC_000005.8:g.56213370G=	NCBI36
NG_031884.1:g.71714G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2586G= MANE Select	ENSP00000382423.3:p.Glu862=
ENST00000399503.3:c.2586G=	ENSP00000382423.3:p.Glu862=
NM_005921.1:c.2586G=	NP_005912.1:p.Glu862=
XM_005248519.3:c.2208G=	XP_005248576.2:p.Glu736=
XM_011543406.1:c.2331G=	XP_011541708.1:p.Glu777=
XM_011543407.1:c.2307G=	XP_011541709.1:p.Glu769=
XM_011543408.1:c.2586G=	XP_011541710.1:p.Glu862=
XM_017009484.1:c.2175G=	XP_016864973.1:p.Glu725=
XM_017009485.1:c.2097G=	XP_016864974.1:p.Glu699=
XR_001742068.2:n.2617G=
NM_005921.2:c.2586G= MANE Select	NP_005912.1:p.Glu862=