Canonical Allele Identifier: CA1548139500

Gene: MAP3K1

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.56882200T= , CM000667.2:g.56882200T=	GRCh38
NC_000005.9:g.56178027T= , CM000667.1:g.56178027T=	GRCh37
NC_000005.8:g.56213784T=	NCBI36
NG_031884.1:g.72128T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399503.4:c.3000T= MANE Select	ENSP00000382423.3:p.Asp1000=
ENST00000399503.3:c.3000T=	ENSP00000382423.3:p.Asp1000=
NM_005921.1:c.3000T=	NP_005912.1:p.Asp1000=
XM_005248519.3:c.2622T=	XP_005248576.2:p.Asp874=
XM_011543406.1:c.2745T=	XP_011541708.1:p.Asp915=
XM_011543407.1:c.2721T=	XP_011541709.1:p.Asp907=
XM_011543408.1:c.3000T=	XP_011541710.1:p.Asp1000=
XM_017009484.1:c.2589T=	XP_016864973.1:p.Asp863=
XM_017009485.1:c.2511T=	XP_016864974.1:p.Asp837=
XR_001742068.2:n.3031T=
NM_005921.2:c.3000T= MANE Select	NP_005912.1:p.Asp1000=