Canonical Allele Identifier: CA2715483350

Gene: DLD

Linked Data

• dbSNP Id: rs2116262668

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.107915340_107915357del , CM000669.2:g.107915340_107915357del	GRCh38
NC_000007.13:g.107555785_107555802del , CM000669.1:g.107555785_107555802del	GRCh37
NC_000007.12:g.107343021_107343038del	NCBI36
NG_008045.1:g.29200_29217del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000205402.10:c.685-166_685-149del MANE Select	ENSP00000205402.3:n.685-166_685-149del
ENST00000205402.9:c.685-166_685-149del	ENSP00000205402.3:n.685-166_685-149del
ENST00000415325.5:c.*359-166_*359-149del	ENSP00000402593.1:n.*359-166_*359-149del
ENST00000417551.5:c.685-166_685-149del	ENSP00000390667.1:n.685-166_685-149del
ENST00000437604.6:c.541-166_541-149del	ENSP00000387542.2:n.541-166_541-149del
ENST00000440410.5:c.616-166_616-149del	ENSP00000417016.1:n.616-166_616-149del
ENST00000451081.5:c.*428-166_*428-149del	ENSP00000388077.1:n.*428-166_*428-149del
NM_000108.4:c.685-166_685-149del	NP_000099.2:n.685-166_685-149del
NM_001289750.1:c.388-166_388-149del	NP_001276679.1:n.388-166_388-149del
NM_001289751.1:c.616-166_616-149del	NP_001276680.1:n.616-166_616-149del
NM_001289752.1:c.541-166_541-149del	NP_001276681.1:n.541-166_541-149del
NM_000108.5:c.685-166_685-149del MANE Select	NP_000099.2:n.685-166_685-149del