Canonical Allele Identifier: CA457109187

Gene: DLD

Linked Data

• ClinVar Variation Id: 2983751
• ClinVar RCV Id: RCV003840846
• MyVariant Identifiers: chr7:g.107557362C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107916917C>G , CM000669.2:g.107916917C>G	GRCh38
NC_000007.13:g.107557362C>G , CM000669.1:g.107557362C>G	GRCh37
NC_000007.12:g.107344598C>G	NCBI36
NG_008045.1:g.30777C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.999C>G MANE Select	ENSP00000205402.3:p.Pro333=
ENST00000205402.9:c.999C>G	ENSP00000205402.3:p.Pro333=
ENST00000415325.5:c.*673C>G	ENSP00000402593.1:n.*673C>G
ENST00000417551.5:c.999C>G	ENSP00000390667.1:p.Pro333=
ENST00000437604.6:c.855C>G	ENSP00000387542.2:p.Pro285=
ENST00000440410.5:c.930C>G	ENSP00000417016.1:p.Pro310=
NM_000108.4:c.999C>G	NP_000099.2:p.Pro333=
NM_001289750.1:c.702C>G	NP_001276679.1:p.Pro234=
NM_001289751.1:c.930C>G	NP_001276680.1:p.Pro310=
NM_001289752.1:c.855C>G	NP_001276681.1:p.Pro285=
NM_000108.5:c.999C>G MANE Select	NP_000099.2:p.Pro333=