Canonical Allele Identifier: CA368857149

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556059C>G (hg19) ; chr7:g.107915614C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915614C>G , CM000669.2:g.107915614C>G	GRCh38
NC_000007.13:g.107556059C>G , CM000669.1:g.107556059C>G	GRCh37
NC_000007.12:g.107343295C>G	NCBI36
NG_008045.1:g.29474C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.793C>G MANE Select	ENSP00000205402.3:p.Leu265Val
ENST00000205402.9:c.793C>G	ENSP00000205402.3:p.Leu265Val
ENST00000415325.5:c.*467C>G	ENSP00000402593.1:n.*467C>G
ENST00000417551.5:c.793C>G	ENSP00000390667.1:p.Leu265Val
ENST00000437604.6:c.649C>G	ENSP00000387542.2:p.Leu217Val
ENST00000440410.5:c.724C>G	ENSP00000417016.1:p.Leu242Val
NM_000108.4:c.793C>G	NP_000099.2:p.Leu265Val
NM_001289750.1:c.496C>G	NP_001276679.1:p.Leu166Val
NM_001289751.1:c.724C>G	NP_001276680.1:p.Leu242Val
NM_001289752.1:c.649C>G	NP_001276681.1:p.Leu217Val
NM_000108.5:c.793C>G MANE Select	NP_000099.2:p.Leu265Val