Canonical Allele Identifier: CA1548139226

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56881570G= , CM000667.2:g.56881570G=	GRCh38
NC_000005.9:g.56177397G= , CM000667.1:g.56177397G=	GRCh37
NC_000005.8:g.56213154G=	NCBI36
NG_031884.1:g.71498G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.2370G= MANE Select	ENSP00000382423.3:p.Arg790=
ENST00000399503.3:c.2370G=	ENSP00000382423.3:p.Arg790=
NM_005921.1:c.2370G=	NP_005912.1:p.Arg790=
XM_005248519.3:c.1992G=	XP_005248576.2:p.Arg664=
XM_011543406.1:c.2115G=	XP_011541708.1:p.Arg705=
XM_011543407.1:c.2091G=	XP_011541709.1:p.Arg697=
XM_011543408.1:c.2370G=	XP_011541710.1:p.Arg790=
XM_017009484.1:c.1959G=	XP_016864973.1:p.Arg653=
XM_017009485.1:c.1881G=	XP_016864974.1:p.Arg627=
XR_001742068.2:n.2401G=
NM_005921.2:c.2370G= MANE Select	NP_005912.1:p.Arg790=