Canonical Allele Identifier: CA1548136394

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875093C= , CM000667.2:g.56875093C=	GRCh38
NC_000005.9:g.56170920C= , CM000667.1:g.56170920C=	GRCh37
NC_000005.8:g.56206677C=	NCBI36
NG_031884.1:g.65021C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1748C= MANE Select	ENSP00000382423.3:p.Ala583=
ENST00000399503.3:c.1748C=	ENSP00000382423.3:p.Ala583=
NM_005921.1:c.1748C=	NP_005912.1:p.Ala583=
XM_005248519.3:c.1370C=	XP_005248576.2:p.Ala457=
XM_011543406.1:c.1493C=	XP_011541708.1:p.Ala498=
XM_011543407.1:c.1686+2088C=	XP_011541709.1:n.1686+2088C=
XM_011543408.1:c.1748C=	XP_011541710.1:p.Ala583=
XM_017009484.1:c.1337C=	XP_016864973.1:p.Ala446=
XM_017009485.1:c.1259C=	XP_016864974.1:p.Ala420=
XR_001742068.2:n.1779C=
NM_005921.2:c.1748C= MANE Select	NP_005912.1:p.Ala583=