Canonical Allele Identifier: CA368858279

Gene: DLD

Linked Data

• dbSNP Id: rs1182952578
• gnomAD v3: 7-107917352-G-C
• gnomAD v4: 7-107917352-G-C
• MyVariant Identifiers: chr7:g.107557797G>C (hg19) ; chr7:g.107917352G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107917352G>C , CM000669.2:g.107917352G>C	GRCh38
NC_000007.13:g.107557797G>C , CM000669.1:g.107557797G>C	GRCh37
NC_000007.12:g.107345033G>C	NCBI36
NG_008045.1:g.31212G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1126G>C MANE Select	ENSP00000205402.3:p.Gly376Arg
ENST00000205402.9:c.1126G>C	ENSP00000205402.3:p.Gly376Arg
ENST00000415325.5:c.*800G>C	ENSP00000402593.1:n.*800G>C
ENST00000417551.5:c.1126G>C	ENSP00000390667.1:p.Gly376Arg
ENST00000437604.6:c.982G>C	ENSP00000387542.2:p.Gly328Arg
ENST00000440410.5:c.1057G>C	ENSP00000417016.1:p.Gly353Arg
NM_000108.4:c.1126G>C	NP_000099.2:p.Gly376Arg
NM_001289750.1:c.829G>C	NP_001276679.1:p.Gly277Arg
NM_001289751.1:c.1057G>C	NP_001276680.1:p.Gly353Arg
NM_001289752.1:c.982G>C	NP_001276681.1:p.Gly328Arg
NM_000108.5:c.1126G>C MANE Select	NP_000099.2:p.Gly376Arg