Canonical Allele Identifier: CA368857797

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107557361C>A (hg19) ; chr7:g.107916916C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916916C>A , CM000669.2:g.107916916C>A	GRCh38
NC_000007.13:g.107557361C>A , CM000669.1:g.107557361C>A	GRCh37
NC_000007.12:g.107344597C>A	NCBI36
NG_008045.1:g.30776C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.998C>A MANE Select	ENSP00000205402.3:p.Pro333His
ENST00000205402.9:c.998C>A	ENSP00000205402.3:p.Pro333His
ENST00000415325.5:c.*672C>A	ENSP00000402593.1:n.*672C>A
ENST00000417551.5:c.998C>A	ENSP00000390667.1:p.Pro333His
ENST00000437604.6:c.854C>A	ENSP00000387542.2:p.Pro285His
ENST00000440410.5:c.929C>A	ENSP00000417016.1:p.Pro310His
NM_000108.4:c.998C>A	NP_000099.2:p.Pro333His
NM_001289750.1:c.701C>A	NP_001276679.1:p.Pro234His
NM_001289751.1:c.929C>A	NP_001276680.1:p.Pro310His
NM_001289752.1:c.854C>A	NP_001276681.1:p.Pro285His
NM_000108.5:c.998C>A MANE Select	NP_000099.2:p.Pro333His