Canonical Allele Identifier: CA368857130

Gene: DLD

Linked Data

• MyVariant Identifiers: chr7:g.107556053C>G (hg19) ; chr7:g.107915608C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915608C>G , CM000669.2:g.107915608C>G	GRCh38
NC_000007.13:g.107556053C>G , CM000669.1:g.107556053C>G	GRCh37
NC_000007.12:g.107343289C>G	NCBI36
NG_008045.1:g.29468C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.787C>G MANE Select	ENSP00000205402.3:p.Arg263Gly
ENST00000205402.9:c.787C>G	ENSP00000205402.3:p.Arg263Gly
ENST00000415325.5:c.*461C>G	ENSP00000402593.1:n.*461C>G
ENST00000417551.5:c.787C>G	ENSP00000390667.1:p.Arg263Gly
ENST00000437604.6:c.643C>G	ENSP00000387542.2:p.Arg215Gly
ENST00000440410.5:c.718C>G	ENSP00000417016.1:p.Arg240Gly
NM_000108.4:c.787C>G	NP_000099.2:p.Arg263Gly
NM_001289750.1:c.490C>G	NP_001276679.1:p.Arg164Gly
NM_001289751.1:c.718C>G	NP_001276680.1:p.Arg240Gly
NM_001289752.1:c.643C>G	NP_001276681.1:p.Arg215Gly
NM_000108.5:c.787C>G MANE Select	NP_000099.2:p.Arg263Gly