Canonical Allele Identifier: CA1548139559

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882338T= , CM000667.2:g.56882338T=	GRCh38
NC_000005.9:g.56178165T= , CM000667.1:g.56178165T=	GRCh37
NC_000005.8:g.56213922T=	NCBI36
NG_031884.1:g.72266T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3138T= MANE Select	ENSP00000382423.3:p.Phe1046=
ENST00000399503.3:c.3138T=	ENSP00000382423.3:p.Phe1046=
NM_005921.1:c.3138T=	NP_005912.1:p.Phe1046=
XM_005248519.3:c.2760T=	XP_005248576.2:p.Phe920=
XM_011543406.1:c.2883T=	XP_011541708.1:p.Phe961=
XM_011543407.1:c.2859T=	XP_011541709.1:p.Phe953=
XM_011543408.1:c.3138T=	XP_011541710.1:p.Phe1046=
XM_017009484.1:c.2727T=	XP_016864973.1:p.Phe909=
XM_017009485.1:c.2649T=	XP_016864974.1:p.Phe883=
XR_001742068.2:n.3169T=
NM_005921.2:c.3138T= MANE Select	NP_005912.1:p.Phe1046=