Canonical Allele Identifier: CA368856927

Gene: DLD

Linked Data

• COSMIC: COSM484613 ; COSM1137605
• MyVariant Identifiers: chr7:g.107556003G>C (hg19) ; chr7:g.107915558G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915558G>C , CM000669.2:g.107915558G>C	GRCh38
NC_000007.13:g.107556003G>C , CM000669.1:g.107556003G>C	GRCh37
NC_000007.12:g.107343239G>C	NCBI36
NG_008045.1:g.29418G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.737G>C MANE Select	ENSP00000205402.3:p.Gly246Ala
ENST00000205402.9:c.737G>C	ENSP00000205402.3:p.Gly246Ala
ENST00000415325.5:c.*411G>C	ENSP00000402593.1:n.*411G>C
ENST00000417551.5:c.737G>C	ENSP00000390667.1:p.Gly246Ala
ENST00000437604.6:c.593G>C	ENSP00000387542.2:p.Gly198Ala
ENST00000440410.5:c.668G>C	ENSP00000417016.1:p.Gly223Ala
ENST00000451081.5:c.*480G>C	ENSP00000388077.1:n.*480G>C
NM_000108.4:c.737G>C	NP_000099.2:p.Gly246Ala
NM_001289750.1:c.440G>C	NP_001276679.1:p.Gly147Ala
NM_001289751.1:c.668G>C	NP_001276680.1:p.Gly223Ala
NM_001289752.1:c.593G>C	NP_001276681.1:p.Gly198Ala
NM_000108.5:c.737G>C MANE Select	NP_000099.2:p.Gly246Ala