Canonical Allele Identifier: CA10628053

Gene: DLD

Linked Data

• ClinVar Variation Id: 358574
• ClinVar RCV Id: RCV000307241 ; RCV000364131 ; RCV000404165
• dbSNP Id: rs886061909
• gnomAD v4: 7-107919426-T-C
• MyVariant Identifiers: chr7:g.107559871T>C (hg19) ; chr7:g.107919426T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919426T>C , CM000669.2:g.107919426T>C	GRCh38
NC_000007.13:g.107559871T>C , CM000669.1:g.107559871T>C	GRCh37
NC_000007.12:g.107347107T>C	NCBI36
NG_008045.1:g.33286T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.*167T>C MANE Select	ENSP00000205402.3:n.*167T>C
ENST00000205402.9:c.*167T>C	ENSP00000205402.3:n.*167T>C
ENST00000415325.5:c.*1371T>C	ENSP00000402593.1:n.*1371T>C
ENST00000417551.5:c.*124+43T>C	ENSP00000390667.1:n.*124+43T>C
ENST00000437604.6:c.*167T>C	ENSP00000387542.2:n.*167T>C
ENST00000440410.5:c.*167T>C	ENSP00000417016.1:n.*167T>C
NM_000108.4:c.*167T>C	NP_000099.2:n.*167T>C
NM_001289750.1:c.*167T>C	NP_001276679.1:n.*167T>C
NM_001289751.1:c.*167T>C	NP_001276680.1:n.*167T>C
NM_001289752.1:c.*167T>C	NP_001276681.1:n.*167T>C
NM_000108.5:c.*167T>C MANE Select	NP_000099.2:n.*167T>C