Canonical Allele Identifier: CA2573141459

Gene: DLD

Linked Data

• ClinVar Variation Id: 1602029
• ClinVar RCV Id: RCV002127680
• dbSNP Id: rs2116278286

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919116T>C , CM000669.2:g.107919116T>C	GRCh38
NC_000007.13:g.107559561T>C , CM000669.1:g.107559561T>C	GRCh37
NC_000007.12:g.107346797T>C	NCBI36
NG_008045.1:g.32976T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1464+17T>C MANE Select	ENSP00000205402.3:n.1464+17T>C
ENST00000205402.9:c.1464+17T>C	ENSP00000205402.3:n.1464+17T>C
ENST00000415325.5:c.*1138+17T>C	ENSP00000402593.1:n.*1138+17T>C
ENST00000417551.5:c.1464+17T>C	ENSP00000390667.1:n.1464+17T>C
ENST00000437604.6:c.1320+17T>C	ENSP00000387542.2:n.1320+17T>C
ENST00000440410.5:c.1395+17T>C	ENSP00000417016.1:n.1395+17T>C
NM_000108.4:c.1464+17T>C	NP_000099.2:n.1464+17T>C
NM_001289750.1:c.1167+17T>C	NP_001276679.1:n.1167+17T>C
NM_001289751.1:c.1395+17T>C	NP_001276680.1:n.1395+17T>C
NM_001289752.1:c.1320+17T>C	NP_001276681.1:n.1320+17T>C
NM_000108.5:c.1464+17T>C MANE Select	NP_000099.2:n.1464+17T>C