Canonical Allele Identifier: CA1548139333

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881851T= , CM000667.2:g.56881851T=	GRCh38
NC_000005.9:g.56177678T= , CM000667.1:g.56177678T=	GRCh37
NC_000005.8:g.56213435T=	NCBI36
NG_031884.1:g.71779T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2651T= MANE Select	ENSP00000382423.3:p.Phe884=
ENST00000399503.3:c.2651T=	ENSP00000382423.3:p.Phe884=
NM_005921.1:c.2651T=	NP_005912.1:p.Phe884=
XM_005248519.3:c.2273T=	XP_005248576.2:p.Phe758=
XM_011543406.1:c.2396T=	XP_011541708.1:p.Phe799=
XM_011543407.1:c.2372T=	XP_011541709.1:p.Phe791=
XM_011543408.1:c.2651T=	XP_011541710.1:p.Phe884=
XM_017009484.1:c.2240T=	XP_016864973.1:p.Phe747=
XM_017009485.1:c.2162T=	XP_016864974.1:p.Phe721=
XR_001742068.2:n.2682T=
NM_005921.2:c.2651T= MANE Select	NP_005912.1:p.Phe884=