Canonical Allele Identifier: CA368859388

Gene: DLD

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919017G>C , CM000669.2:g.107919017G>C	GRCh38
NC_000007.13:g.107559462G>C , CM000669.1:g.107559462G>C	GRCh37
NC_000007.12:g.107346698G>C	NCBI36
NG_008045.1:g.32877G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.1382G>C MANE Select	ENSP00000205402.3:p.Gly461Ala
ENST00000205402.9:c.1382G>C	ENSP00000205402.3:p.Gly461Ala
ENST00000415325.5:c.*1056G>C	ENSP00000402593.1:n.*1056G>C
ENST00000417551.5:c.1382G>C	ENSP00000390667.1:p.Gly461Ala
ENST00000437604.6:c.1238G>C	ENSP00000387542.2:p.Gly413Ala
ENST00000440410.5:c.1313G>C	ENSP00000417016.1:p.Gly438Ala
NM_000108.4:c.1382G>C	NP_000099.2:p.Gly461Ala
NM_001289750.1:c.1085G>C	NP_001276679.1:p.Gly362Ala
NM_001289751.1:c.1313G>C	NP_001276680.1:p.Gly438Ala
NM_001289752.1:c.1238G>C	NP_001276681.1:p.Gly413Ala
NM_000108.5:c.1382G>C MANE Select	NP_000099.2:p.Gly461Ala