Canonical Allele Identifier: CA4434428

Gene: DLD

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107904676G>A , CM000669.2:g.107904676G>A	GRCh38
NC_000007.13:g.107545121G>A , CM000669.1:g.107545121G>A	GRCh37
NC_000007.12:g.107332357G>A	NCBI36
NG_008045.1:g.18536G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.338-282G>A MANE Select	ENSP00000205402.3:n.338-282G>A
ENST00000205402.9:c.338-282G>A	ENSP00000205402.3:n.338-282G>A
ENST00000415325.5:c.*12-282G>A	ENSP00000402593.1:n.*12-282G>A
ENST00000417551.5:c.338-282G>A	ENSP00000390667.1:n.338-282G>A
ENST00000437604.6:c.338-282G>A	ENSP00000387542.2:n.338-282G>A
ENST00000440410.5:c.269-282G>A	ENSP00000417016.1:n.269-282G>A
ENST00000450038.5:c.*6G>A	ENSP00000409590.1:n.*6G>A
ENST00000451081.5:c.338-187G>A	ENSP00000388077.1:n.338-187G>A
ENST00000453354.5:n.403-187G>A
ENST00000478414.1:n.46-282G>A
ENST00000489184.1:n.9G>A
ENST00000494441.1:n.483-187G>A
NM_000108.4:c.338-282G>A	NP_000099.2:n.338-282G>A
NM_001289750.1:c.41-282G>A	NP_001276679.1:n.41-282G>A
NM_001289751.1:c.269-282G>A	NP_001276680.1:n.269-282G>A
NM_001289752.1:c.338-282G>A	NP_001276681.1:n.338-282G>A
NM_000108.5:c.338-282G>A MANE Select	NP_000099.2:n.338-282G>A