Canonical Allele Identifier: CA1548139448

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882095G= , CM000667.2:g.56882095G=	GRCh38
NC_000005.9:g.56177922G= , CM000667.1:g.56177922G=	GRCh37
NC_000005.8:g.56213679G=	NCBI36
NG_031884.1:g.72023G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2895G= MANE Select	ENSP00000382423.3:p.Gln965=
ENST00000399503.3:c.2895G=	ENSP00000382423.3:p.Gln965=
NM_005921.1:c.2895G=	NP_005912.1:p.Gln965=
XM_005248519.3:c.2517G=	XP_005248576.2:p.Gln839=
XM_011543406.1:c.2640G=	XP_011541708.1:p.Gln880=
XM_011543407.1:c.2616G=	XP_011541709.1:p.Gln872=
XM_011543408.1:c.2895G=	XP_011541710.1:p.Gln965=
XM_017009484.1:c.2484G=	XP_016864973.1:p.Gln828=
XM_017009485.1:c.2406G=	XP_016864974.1:p.Gln802=
XR_001742068.2:n.2926G=
NM_005921.2:c.2895G= MANE Select	NP_005912.1:p.Gln965=