Canonical Allele Identifier: CA368859480

Gene: DLD

Linked Data

• COSMIC: COSM4677714 ; COSM4677715
• MyVariant Identifiers: chr7:g.107559503G>A (hg19) ; chr7:g.107919058G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919058G>A , CM000669.2:g.107919058G>A	GRCh38
NC_000007.13:g.107559503G>A , CM000669.1:g.107559503G>A	GRCh37
NC_000007.12:g.107346739G>A	NCBI36
NG_008045.1:g.32918G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1423G>A MANE Select	ENSP00000205402.3:p.Ala475Thr
ENST00000205402.9:c.1423G>A	ENSP00000205402.3:p.Ala475Thr
ENST00000415325.5:c.*1097G>A	ENSP00000402593.1:n.*1097G>A
ENST00000417551.5:c.1423G>A	ENSP00000390667.1:p.Ala475Thr
ENST00000437604.6:c.1279G>A	ENSP00000387542.2:p.Ala427Thr
ENST00000440410.5:c.1354G>A	ENSP00000417016.1:p.Ala452Thr
NM_000108.4:c.1423G>A	NP_000099.2:p.Ala475Thr
NM_001289750.1:c.1126G>A	NP_001276679.1:p.Ala376Thr
NM_001289751.1:c.1354G>A	NP_001276680.1:p.Ala452Thr
NM_001289752.1:c.1279G>A	NP_001276681.1:p.Ala427Thr
NM_000108.5:c.1423G>A MANE Select	NP_000099.2:p.Ala475Thr