Canonical Allele Identifier: CA457109775

Gene: DLD

Linked Data

• ClinVar Variation Id: 1534150
• ClinVar RCV Id: RCV002082908
• dbSNP Id: rs2032340474
• gnomAD v4: 7-107919012-T-A
• MyVariant Identifiers: chr7:g.107559457T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107919012T>A , CM000669.2:g.107919012T>A	GRCh38
NC_000007.13:g.107559457T>A , CM000669.1:g.107559457T>A	GRCh37
NC_000007.12:g.107346693T>A	NCBI36
NG_008045.1:g.32872T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000205402.10:c.1377T>A MANE Select	ENSP00000205402.3:p.Gly459=
ENST00000205402.9:c.1377T>A	ENSP00000205402.3:p.Gly459=
ENST00000415325.5:c.*1051T>A	ENSP00000402593.1:n.*1051T>A
ENST00000417551.5:c.1377T>A	ENSP00000390667.1:p.Gly459=
ENST00000437604.6:c.1233T>A	ENSP00000387542.2:p.Gly411=
ENST00000440410.5:c.1308T>A	ENSP00000417016.1:p.Gly436=
NM_000108.4:c.1377T>A	NP_000099.2:p.Gly459=
NM_001289750.1:c.1080T>A	NP_001276679.1:p.Gly360=
NM_001289751.1:c.1308T>A	NP_001276680.1:p.Gly436=
NM_001289752.1:c.1233T>A	NP_001276681.1:p.Gly411=
NM_000108.5:c.1377T>A MANE Select	NP_000099.2:p.Gly459=