Canonical Allele Identifier: CA1548129257

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56859886G= , CM000667.2:g.56859886G=	GRCh38
NC_000005.9:g.56155713G= , CM000667.1:g.56155713G=	GRCh37
NC_000005.8:g.56191470G=	NCBI36
NG_031884.1:g.49814G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.805G= MANE Select	ENSP00000382423.3:p.Val269=
ENST00000399503.3:c.805G=	ENSP00000382423.3:p.Val269=
NM_005921.1:c.805G=	NP_005912.1:p.Val269=
XM_005248519.3:c.427G=	XP_005248576.2:p.Val143=
XM_011543406.1:c.550G=	XP_011541708.1:p.Val184=
XM_011543407.1:c.805G=	XP_011541709.1:p.Val269=
XM_011543408.1:c.805G=	XP_011541710.1:p.Val269=
XM_017009484.1:c.394G=	XP_016864973.1:p.Val132=
XM_017009485.1:c.316G=	XP_016864974.1:p.Val106=
XR_001742068.2:n.836G=
NM_005921.2:c.805G= MANE Select	NP_005912.1:p.Val269=