Canonical Allele Identifier: CA368856708

Gene: DLD

Linked Data

• dbSNP Id: rs121964990
• gnomAD v3: 7-107915506-G-A
• gnomAD v4: 7-107915506-G-A
• MyVariant Identifiers: chr7:g.107555951G>A (hg19) ; chr7:g.107915506G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915506G>A , CM000669.2:g.107915506G>A	GRCh38
NC_000007.13:g.107555951G>A , CM000669.1:g.107555951G>A	GRCh37
NC_000007.12:g.107343187G>A	NCBI36
NG_008045.1:g.29366G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.685G>A MANE Select	ENSP00000205402.3:p.Gly229Ser
ENST00000205402.9:c.685G>A	ENSP00000205402.3:p.Gly229Ser
ENST00000415325.5:c.*359G>A	ENSP00000402593.1:n.*359G>A
ENST00000417551.5:c.685G>A	ENSP00000390667.1:p.Gly229Ser
ENST00000437604.6:c.541G>A	ENSP00000387542.2:p.Gly181Ser
ENST00000440410.5:c.616G>A	ENSP00000417016.1:p.Gly206Ser
ENST00000451081.5:c.*428G>A	ENSP00000388077.1:n.*428G>A
NM_000108.4:c.685G>A	NP_000099.2:p.Gly229Ser
NM_001289750.1:c.388G>A	NP_001276679.1:p.Gly130Ser
NM_001289751.1:c.616G>A	NP_001276680.1:p.Gly206Ser
NM_001289752.1:c.541G>A	NP_001276681.1:p.Gly181Ser
NM_000108.5:c.685G>A MANE Select	NP_000099.2:p.Gly229Ser