Canonical Allele Identifier: CA4434451

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107904995G>A , CM000669.2:g.107904995G>A	GRCh38
NC_000007.13:g.107545440G>A , CM000669.1:g.107545440G>A	GRCh37
NC_000007.12:g.107332676G>A	NCBI36
NG_008045.1:g.18855G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000108.5:c.375G>A MANE Select	NP_000099.2:p.Glu125=
ENST00000205402.10:c.375G>A MANE Select	ENSP00000205402.3:p.Glu125=
NM_000108.4:c.375G>A	NP_000099.2:p.Glu125=
NM_001289750.1:c.78G>A	NP_001276679.1:p.Glu26=
NM_001289751.1:c.306G>A	NP_001276680.1:p.Glu102=
NM_001289752.1:c.375G>A	NP_001276681.1:p.Glu125=
ENST00000205402.9:c.375G>A	ENSP00000205402.3:p.Glu125=
ENST00000415325.5:c.*49G>A	ENSP00000402593.1:n.*49G>A
ENST00000417551.5:c.375G>A	ENSP00000390667.1:p.Glu125=
ENST00000437604.6:c.375G>A	ENSP00000387542.2:p.Glu125=
ENST00000440410.5:c.306G>A	ENSP00000417016.1:p.Glu102=
ENST00000450038.5:c.*209G>A	ENSP00000409590.1:n.*209G>A
ENST00000451081.5:c.*122G>A	ENSP00000388077.1:n.*122G>A
ENST00000453354.5:n.535G>A
ENST00000478414.1:n.83G>A
ENST00000489184.1:n.328G>A
ENST00000494441.1:n.615G>A