Canonical Allele Identifier: CA1548139578

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882390A= , CM000667.2:g.56882390A=	GRCh38
NC_000005.9:g.56178217A= , CM000667.1:g.56178217A=	GRCh37
NC_000005.8:g.56213974A=	NCBI36
NG_031884.1:g.72318A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3190A= MANE Select	ENSP00000382423.3:p.Arg1064=
ENST00000399503.3:c.3190A=	ENSP00000382423.3:p.Arg1064=
NM_005921.1:c.3190A=	NP_005912.1:p.Arg1064=
XM_005248519.3:c.2812A=	XP_005248576.2:p.Arg938=
XM_011543406.1:c.2935A=	XP_011541708.1:p.Arg979=
XM_011543407.1:c.2911A=	XP_011541709.1:p.Arg971=
XM_011543408.1:c.3190A=	XP_011541710.1:p.Arg1064=
XM_017009484.1:c.2779A=	XP_016864973.1:p.Arg927=
XM_017009485.1:c.2701A=	XP_016864974.1:p.Arg901=
XR_001742068.2:n.3221A=
NM_005921.2:c.3190A= MANE Select	NP_005912.1:p.Arg1064=