Canonical Allele Identifier: CA1548136393

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56875092G= , CM000667.2:g.56875092G=	GRCh38
NC_000005.9:g.56170919G= , CM000667.1:g.56170919G=	GRCh37
NC_000005.8:g.56206676G=	NCBI36
NG_031884.1:g.65020G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.1747G= MANE Select	ENSP00000382423.3:p.Ala583=
ENST00000399503.3:c.1747G=	ENSP00000382423.3:p.Ala583=
NM_005921.1:c.1747G=	NP_005912.1:p.Ala583=
XM_005248519.3:c.1369G=	XP_005248576.2:p.Ala457=
XM_011543406.1:c.1492G=	XP_011541708.1:p.Ala498=
XM_011543407.1:c.1686+2087G=	XP_011541709.1:n.1686+2087G=
XM_011543408.1:c.1747G=	XP_011541710.1:p.Ala583=
XM_017009484.1:c.1336G=	XP_016864973.1:p.Ala446=
XM_017009485.1:c.1258G=	XP_016864974.1:p.Ala420=
XR_001742068.2:n.1778G=
NM_005921.2:c.1747G= MANE Select	NP_005912.1:p.Ala583=