Canonical Allele Identifier: CA368859378

Gene: DLD

Linked Data

• dbSNP Id: rs1444880572
• gnomAD v2: 7-107559456-G-T
• gnomAD v4: 7-107919011-G-T
• MyVariant Identifiers: chr7:g.107559456G>T (hg19) ; chr7:g.107919011G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919011G>T , CM000669.2:g.107919011G>T	GRCh38
NC_000007.13:g.107559456G>T , CM000669.1:g.107559456G>T	GRCh37
NC_000007.12:g.107346692G>T	NCBI36
NG_008045.1:g.32871G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1376G>T MANE Select	ENSP00000205402.3:p.Gly459Val
ENST00000205402.9:c.1376G>T	ENSP00000205402.3:p.Gly459Val
ENST00000415325.5:c.*1050G>T	ENSP00000402593.1:n.*1050G>T
ENST00000417551.5:c.1376G>T	ENSP00000390667.1:p.Gly459Val
ENST00000437604.6:c.1232G>T	ENSP00000387542.2:p.Gly411Val
ENST00000440410.5:c.1307G>T	ENSP00000417016.1:p.Gly436Val
NM_000108.4:c.1376G>T	NP_000099.2:p.Gly459Val
NM_001289750.1:c.1079G>T	NP_001276679.1:p.Gly360Val
NM_001289751.1:c.1307G>T	NP_001276680.1:p.Gly436Val
NM_001289752.1:c.1232G>T	NP_001276681.1:p.Gly411Val
NM_000108.5:c.1376G>T MANE Select	NP_000099.2:p.Gly459Val