Canonical Allele Identifier: CA1548139227

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881572A= , CM000667.2:g.56881572A=	GRCh38
NC_000005.9:g.56177399A= , CM000667.1:g.56177399A=	GRCh37
NC_000005.8:g.56213156A=	NCBI36
NG_031884.1:g.71500A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2372A= MANE Select	ENSP00000382423.3:p.Tyr791=
ENST00000399503.3:c.2372A=	ENSP00000382423.3:p.Tyr791=
NM_005921.1:c.2372A=	NP_005912.1:p.Tyr791=
XM_005248519.3:c.1994A=	XP_005248576.2:p.Tyr665=
XM_011543406.1:c.2117A=	XP_011541708.1:p.Tyr706=
XM_011543407.1:c.2093A=	XP_011541709.1:p.Tyr698=
XM_011543408.1:c.2372A=	XP_011541710.1:p.Tyr791=
XM_017009484.1:c.1961A=	XP_016864973.1:p.Tyr654=
XM_017009485.1:c.1883A=	XP_016864974.1:p.Tyr628=
XR_001742068.2:n.2403A=
NM_005921.2:c.2372A= MANE Select	NP_005912.1:p.Tyr791=