Canonical Allele Identifier: CA10627979
Gene: DLD HGNC NCBI

Linked Data

ClinVar Variation Id: 358575
ClinVar RCV Id: RCV000267242 RCV000324559 RCV000358247
dbSNP Id: rs4564
gnomAD v2: 7-107559911-G-A
gnomAD v3: 7-107919466-G-A
gnomAD v4: 7-107919466-G-A
MyVariant Identifiers: chr7:g.107559911G>A (hg19) chr7:g.107919466G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919466G>A , CM000669.2:g.107919466G>A GRCh38
NC_000007.13:g.107559911G>A , CM000669.1:g.107559911G>A GRCh37
NC_000007.12:g.107347147G>A NCBI36
NG_008045.1:g.33326G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*207G>A MANE Select ENSP00000205402.3:n.*207G>A
ENST00000205402.9:c.*207G>A ENSP00000205402.3:n.*207G>A
ENST00000415325.5:c.*1411G>A ENSP00000402593.1:n.*1411G>A
ENST00000417551.5:c.*124+83G>A ENSP00000390667.1:n.*124+83G>A
ENST00000437604.6:c.*207G>A ENSP00000387542.2:n.*207G>A
ENST00000440410.5:c.*207G>A ENSP00000417016.1:n.*207G>A
NM_000108.4:c.*207G>A NP_000099.2:n.*207G>A
NM_001289750.1:c.*207G>A NP_001276679.1:n.*207G>A
NM_001289751.1:c.*207G>A NP_001276680.1:n.*207G>A
NM_001289752.1:c.*207G>A NP_001276681.1:n.*207G>A
NM_000108.5:c.*207G>A MANE Select NP_000099.2:n.*207G>A
Search 100 bp 5'
Search 100 bp 3'