Canonical Allele Identifier: CA1548139523

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882258C= , CM000667.2:g.56882258C=	GRCh38
NC_000005.9:g.56178085C= , CM000667.1:g.56178085C=	GRCh37
NC_000005.8:g.56213842C=	NCBI36
NG_031884.1:g.72186C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3058C= MANE Select	ENSP00000382423.3:p.Gln1020=
ENST00000399503.3:c.3058C=	ENSP00000382423.3:p.Gln1020=
NM_005921.1:c.3058C=	NP_005912.1:p.Gln1020=
XM_005248519.3:c.2680C=	XP_005248576.2:p.Gln894=
XM_011543406.1:c.2803C=	XP_011541708.1:p.Gln935=
XM_011543407.1:c.2779C=	XP_011541709.1:p.Gln927=
XM_011543408.1:c.3058C=	XP_011541710.1:p.Gln1020=
XM_017009484.1:c.2647C=	XP_016864973.1:p.Gln883=
XM_017009485.1:c.2569C=	XP_016864974.1:p.Gln857=
XR_001742068.2:n.3089C=
NM_005921.2:c.3058C= MANE Select	NP_005912.1:p.Gln1020=