Canonical Allele Identifier: CA1548139532

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882273T= , CM000667.2:g.56882273T=	GRCh38
NC_000005.9:g.56178100T= , CM000667.1:g.56178100T=	GRCh37
NC_000005.8:g.56213857T=	NCBI36
NG_031884.1:g.72201T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3073T= MANE Select	ENSP00000382423.3:p.Phe1025=
ENST00000399503.3:c.3073T=	ENSP00000382423.3:p.Phe1025=
NM_005921.1:c.3073T=	NP_005912.1:p.Phe1025=
XM_005248519.3:c.2695T=	XP_005248576.2:p.Phe899=
XM_011543406.1:c.2818T=	XP_011541708.1:p.Phe940=
XM_011543407.1:c.2794T=	XP_011541709.1:p.Phe932=
XM_011543408.1:c.3073T=	XP_011541710.1:p.Phe1025=
XM_017009484.1:c.2662T=	XP_016864973.1:p.Phe888=
XM_017009485.1:c.2584T=	XP_016864974.1:p.Phe862=
XR_001742068.2:n.3104T=
NM_005921.2:c.3073T= MANE Select	NP_005912.1:p.Phe1025=