Canonical Allele Identifier: CA368857701

Gene: DLD

Linked Data

• gnomAD v4: 7-107916886-G-C
• MyVariant Identifiers: chr7:g.107557331G>C (hg19) ; chr7:g.107916886G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916886G>C , CM000669.2:g.107916886G>C	GRCh38
NC_000007.13:g.107557331G>C , CM000669.1:g.107557331G>C	GRCh37
NC_000007.12:g.107344567G>C	NCBI36
NG_008045.1:g.30746G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.968G>C MANE Select	ENSP00000205402.3:p.Gly323Ala
ENST00000205402.9:c.968G>C	ENSP00000205402.3:p.Gly323Ala
ENST00000415325.5:c.*642G>C	ENSP00000402593.1:n.*642G>C
ENST00000417551.5:c.968G>C	ENSP00000390667.1:p.Gly323Ala
ENST00000437604.6:c.824G>C	ENSP00000387542.2:p.Gly275Ala
ENST00000440410.5:c.899G>C	ENSP00000417016.1:p.Gly300Ala
NM_000108.4:c.968G>C	NP_000099.2:p.Gly323Ala
NM_001289750.1:c.671G>C	NP_001276679.1:p.Gly224Ala
NM_001289751.1:c.899G>C	NP_001276680.1:p.Gly300Ala
NM_001289752.1:c.824G>C	NP_001276681.1:p.Gly275Ala
NM_000108.5:c.968G>C MANE Select	NP_000099.2:p.Gly323Ala