Canonical Allele Identifier: CA1548139554

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882322A= , CM000667.2:g.56882322A=	GRCh38
NC_000005.9:g.56178149A= , CM000667.1:g.56178149A=	GRCh37
NC_000005.8:g.56213906A=	NCBI36
NG_031884.1:g.72250A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3122A= MANE Select	ENSP00000382423.3:p.Lys1041=
ENST00000399503.3:c.3122A=	ENSP00000382423.3:p.Lys1041=
NM_005921.1:c.3122A=	NP_005912.1:p.Lys1041=
XM_005248519.3:c.2744A=	XP_005248576.2:p.Lys915=
XM_011543406.1:c.2867A=	XP_011541708.1:p.Lys956=
XM_011543407.1:c.2843A=	XP_011541709.1:p.Lys948=
XM_011543408.1:c.3122A=	XP_011541710.1:p.Lys1041=
XM_017009484.1:c.2711A=	XP_016864973.1:p.Lys904=
XM_017009485.1:c.2633A=	XP_016864974.1:p.Lys878=
XR_001742068.2:n.3153A=
NM_005921.2:c.3122A= MANE Select	NP_005912.1:p.Lys1041=