Canonical Allele Identifier: CA368857706

Gene: DLD

Linked Data

• dbSNP Id: rs2116270210
• MyVariant Identifiers: chr7:g.107557333C>G (hg19) ; chr7:g.107916888C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916888C>G , CM000669.2:g.107916888C>G	GRCh38
NC_000007.13:g.107557333C>G , CM000669.1:g.107557333C>G	GRCh37
NC_000007.12:g.107344569C>G	NCBI36
NG_008045.1:g.30748C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.970C>G MANE Select	ENSP00000205402.3:p.Leu324Val
ENST00000205402.9:c.970C>G	ENSP00000205402.3:p.Leu324Val
ENST00000415325.5:c.*644C>G	ENSP00000402593.1:n.*644C>G
ENST00000417551.5:c.970C>G	ENSP00000390667.1:p.Leu324Val
ENST00000437604.6:c.826C>G	ENSP00000387542.2:p.Leu276Val
ENST00000440410.5:c.901C>G	ENSP00000417016.1:p.Leu301Val
NM_000108.4:c.970C>G	NP_000099.2:p.Leu324Val
NM_001289750.1:c.673C>G	NP_001276679.1:p.Leu225Val
NM_001289751.1:c.901C>G	NP_001276680.1:p.Leu301Val
NM_001289752.1:c.826C>G	NP_001276681.1:p.Leu276Val
NM_000108.5:c.970C>G MANE Select	NP_000099.2:p.Leu324Val