Canonical Allele Identifier: CA368859449

Gene: DLD

Linked Data

• dbSNP Id: rs2032341369
• gnomAD v4: 7-107919044-C-G
• MyVariant Identifiers: chr7:g.107559489C>G (hg19) ; chr7:g.107919044C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919044C>G , CM000669.2:g.107919044C>G	GRCh38
NC_000007.13:g.107559489C>G , CM000669.1:g.107559489C>G	GRCh37
NC_000007.12:g.107346725C>G	NCBI36
NG_008045.1:g.32904C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1409C>G MANE Select	ENSP00000205402.3:p.Ala470Gly
ENST00000205402.9:c.1409C>G	ENSP00000205402.3:p.Ala470Gly
ENST00000415325.5:c.*1083C>G	ENSP00000402593.1:n.*1083C>G
ENST00000417551.5:c.1409C>G	ENSP00000390667.1:p.Ala470Gly
ENST00000437604.6:c.1265C>G	ENSP00000387542.2:p.Ala422Gly
ENST00000440410.5:c.1340C>G	ENSP00000417016.1:p.Ala447Gly
NM_000108.4:c.1409C>G	NP_000099.2:p.Ala470Gly
NM_001289750.1:c.1112C>G	NP_001276679.1:p.Ala371Gly
NM_001289751.1:c.1340C>G	NP_001276680.1:p.Ala447Gly
NM_001289752.1:c.1265C>G	NP_001276681.1:p.Ala422Gly
NM_000108.5:c.1409C>G MANE Select	NP_000099.2:p.Ala470Gly