Canonical Allele Identifier: CA1548139528

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882269C= , CM000667.2:g.56882269C=	GRCh38
NC_000005.9:g.56178096C= , CM000667.1:g.56178096C=	GRCh37
NC_000005.8:g.56213853C=	NCBI36
NG_031884.1:g.72197C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3069C= MANE Select	ENSP00000382423.3:p.Arg1023=
ENST00000399503.3:c.3069C=	ENSP00000382423.3:p.Arg1023=
NM_005921.1:c.3069C=	NP_005912.1:p.Arg1023=
XM_005248519.3:c.2691C=	XP_005248576.2:p.Arg897=
XM_011543406.1:c.2814C=	XP_011541708.1:p.Arg938=
XM_011543407.1:c.2790C=	XP_011541709.1:p.Arg930=
XM_011543408.1:c.3069C=	XP_011541710.1:p.Arg1023=
XM_017009484.1:c.2658C=	XP_016864973.1:p.Arg886=
XM_017009485.1:c.2580C=	XP_016864974.1:p.Arg860=
XR_001742068.2:n.3100C=
NM_005921.2:c.3069C= MANE Select	NP_005912.1:p.Arg1023=