Canonical Allele Identifier: CA1732849049

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107901759T= , CM000669.2:g.107901759T=	GRCh38
NC_000007.13:g.107542204T= , CM000669.1:g.107542204T=	GRCh37
NC_000007.12:g.107329440T=	NCBI36
NG_008045.1:g.15619T=

Transcript Alleles

HGVS	Amino-acid Change
NM_000108.5:c.140T= MANE Select	NP_000099.2:p.Ile47=
ENST00000205402.10:c.140T= MANE Select	ENSP00000205402.3:p.Ile47=
NM_000108.4:c.140T=	NP_000099.2:p.Ile47=
NM_001289750.1:c.-30-1719T=	NP_001276679.1:n.-30-1719T=
NM_001289751.1:c.140T=	NP_001276680.1:p.Ile47=
NM_001289752.1:c.140T=	NP_001276681.1:p.Ile47=
ENST00000205402.9:c.140T=	ENSP00000205402.3:p.Ile47=
ENST00000415325.5:c.119-1719T=	ENSP00000402593.1:n.119-1719T=
ENST00000417551.5:c.140T=	ENSP00000390667.1:p.Ile47=
ENST00000437604.6:c.140T=	ENSP00000387542.2:p.Ile47=
ENST00000440410.5:c.140T=	ENSP00000417016.1:p.Ile47=
ENST00000450038.5:c.140T=	ENSP00000409590.1:p.Ile47=
ENST00000451081.5:c.140T=	ENSP00000388077.1:p.Ile47=
ENST00000453354.5:n.205T=
ENST00000460577.5:n.174T=
ENST00000494441.1:n.285T=
ENST00000639772.1:c.140T=	ENSP00000492159.1:p.Ile47=