Canonical Allele Identifier: CA1548139371

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881958T= , CM000667.2:g.56881958T=	GRCh38
NC_000005.9:g.56177785T= , CM000667.1:g.56177785T=	GRCh37
NC_000005.8:g.56213542T=	NCBI36
NG_031884.1:g.71886T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2758T= MANE Select	ENSP00000382423.3:p.Leu920=
ENST00000399503.3:c.2758T=	ENSP00000382423.3:p.Leu920=
NM_005921.1:c.2758T=	NP_005912.1:p.Leu920=
XM_005248519.3:c.2380T=	XP_005248576.2:p.Leu794=
XM_011543406.1:c.2503T=	XP_011541708.1:p.Leu835=
XM_011543407.1:c.2479T=	XP_011541709.1:p.Leu827=
XM_011543408.1:c.2758T=	XP_011541710.1:p.Leu920=
XM_017009484.1:c.2347T=	XP_016864973.1:p.Leu783=
XM_017009485.1:c.2269T=	XP_016864974.1:p.Leu757=
XR_001742068.2:n.2789T=
NM_005921.2:c.2758T= MANE Select	NP_005912.1:p.Leu920=