Canonical Allele Identifier: CA1548139292

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881761G= , CM000667.2:g.56881761G=	GRCh38
NC_000005.9:g.56177588G= , CM000667.1:g.56177588G=	GRCh37
NC_000005.8:g.56213345G=	NCBI36
NG_031884.1:g.71689G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2561G= MANE Select	ENSP00000382423.3:p.Arg854=
ENST00000399503.3:c.2561G=	ENSP00000382423.3:p.Arg854=
NM_005921.1:c.2561G=	NP_005912.1:p.Arg854=
XM_005248519.3:c.2183G=	XP_005248576.2:p.Arg728=
XM_011543406.1:c.2306G=	XP_011541708.1:p.Arg769=
XM_011543407.1:c.2282G=	XP_011541709.1:p.Arg761=
XM_011543408.1:c.2561G=	XP_011541710.1:p.Arg854=
XM_017009484.1:c.2150G=	XP_016864973.1:p.Arg717=
XM_017009485.1:c.2072G=	XP_016864974.1:p.Arg691=
XR_001742068.2:n.2592G=
NM_005921.2:c.2561G= MANE Select	NP_005912.1:p.Arg854=