Canonical Allele Identifier: CA368857182

Gene: DLD

Linked Data

• dbSNP Id: rs2032249701
• gnomAD v3: 7-107915624-A-T
• gnomAD v4: 7-107915624-A-T
• MyVariant Identifiers: chr7:g.107556069A>T (hg19) ; chr7:g.107915624A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915624A>T , CM000669.2:g.107915624A>T	GRCh38
NC_000007.13:g.107556069A>T , CM000669.1:g.107556069A>T	GRCh37
NC_000007.12:g.107343305A>T	NCBI36
NG_008045.1:g.29484A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.803A>T MANE Select	ENSP00000205402.3:p.Gln268Leu
ENST00000205402.9:c.803A>T	ENSP00000205402.3:p.Gln268Leu
ENST00000415325.5:c.*477A>T	ENSP00000402593.1:n.*477A>T
ENST00000417551.5:c.803A>T	ENSP00000390667.1:p.Gln268Leu
ENST00000437604.6:c.659A>T	ENSP00000387542.2:p.Gln220Leu
ENST00000440410.5:c.734A>T	ENSP00000417016.1:p.Gln245Leu
NM_000108.4:c.803A>T	NP_000099.2:p.Gln268Leu
NM_001289750.1:c.506A>T	NP_001276679.1:p.Gln169Leu
NM_001289751.1:c.734A>T	NP_001276680.1:p.Gln245Leu
NM_001289752.1:c.659A>T	NP_001276681.1:p.Gln220Leu
NM_000108.5:c.803A>T MANE Select	NP_000099.2:p.Gln268Leu