Canonical Allele Identifier: CA1548139336

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881856C= , CM000667.2:g.56881856C=	GRCh38
NC_000005.9:g.56177683C= , CM000667.1:g.56177683C=	GRCh37
NC_000005.8:g.56213440C=	NCBI36
NG_031884.1:g.71784C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2656C= MANE Select	ENSP00000382423.3:p.Gln886=
ENST00000399503.3:c.2656C=	ENSP00000382423.3:p.Gln886=
NM_005921.1:c.2656C=	NP_005912.1:p.Gln886=
XM_005248519.3:c.2278C=	XP_005248576.2:p.Gln760=
XM_011543406.1:c.2401C=	XP_011541708.1:p.Gln801=
XM_011543407.1:c.2377C=	XP_011541709.1:p.Gln793=
XM_011543408.1:c.2656C=	XP_011541710.1:p.Gln886=
XM_017009484.1:c.2245C=	XP_016864973.1:p.Gln749=
XM_017009485.1:c.2167C=	XP_016864974.1:p.Gln723=
XR_001742068.2:n.2687C=
NM_005921.2:c.2656C= MANE Select	NP_005912.1:p.Gln886=