Canonical Allele Identifier: CA831211126

Gene: DLD

Linked Data

• dbSNP Id: rs1243375261
• gnomAD v3: 7-107919160-T-C
• gnomAD v4: 7-107919160-T-C
• MyVariant Identifiers: chr7:g.107559605T>C (hg19) ; chr7:g.107919160T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919160T>C , CM000669.2:g.107919160T>C	GRCh38
NC_000007.13:g.107559605T>C , CM000669.1:g.107559605T>C	GRCh37
NC_000007.12:g.107346841T>C	NCBI36
NG_008045.1:g.33020T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1465-34T>C MANE Select	ENSP00000205402.3:n.1465-34T>C
ENST00000205402.9:c.1465-34T>C	ENSP00000205402.3:n.1465-34T>C
ENST00000415325.5:c.*1139-34T>C	ENSP00000402593.1:n.*1139-34T>C
ENST00000417551.5:c.1465-34T>C	ENSP00000390667.1:n.1465-34T>C
ENST00000437604.6:c.1321-34T>C	ENSP00000387542.2:n.1321-34T>C
ENST00000440410.5:c.1396-34T>C	ENSP00000417016.1:n.1396-34T>C
NM_000108.4:c.1465-34T>C	NP_000099.2:n.1465-34T>C
NM_001289750.1:c.1168-34T>C	NP_001276679.1:n.1168-34T>C
NM_001289751.1:c.1396-34T>C	NP_001276680.1:n.1396-34T>C
NM_001289752.1:c.1321-34T>C	NP_001276681.1:n.1321-34T>C
NM_000108.5:c.1465-34T>C MANE Select	NP_000099.2:n.1465-34T>C