Canonical Allele Identifier: CA2684476709
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893323_107893324del , CM000669.2:g.107893323_107893324del GRCh38
NC_000007.13:g.107533768_107533769del , CM000669.1:g.107533768_107533769del GRCh37
NC_000007.12:g.107321004_107321005del NCBI36
NG_008045.1:g.7183_7184del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.118+45_118+46del MANE Select ENSP00000205402.3:n.118+45_118+46del
ENST00000639772.1:c.118+45_118+46del ENSP00000492159.1:n.118+45_118+46del
ENST00000205402.9:c.118+45_118+46del ENSP00000205402.3:n.118+45_118+46del
ENST00000415325.5:c.118+45_118+46del ENSP00000402593.1:n.118+45_118+46del
ENST00000417551.5:c.118+45_118+46del ENSP00000390667.1:n.118+45_118+46del
ENST00000437604.6:c.118+45_118+46del ENSP00000387542.2:n.118+45_118+46del
ENST00000440410.5:c.118+45_118+46del ENSP00000417016.1:n.118+45_118+46del
ENST00000450038.5:c.118+45_118+46del ENSP00000409590.1:n.118+45_118+46del
ENST00000451081.5:c.118+45_118+46del ENSP00000388077.1:n.118+45_118+46del
ENST00000453354.5:n.183+45_183+46del
ENST00000460577.5:n.152+45_152+46del
ENST00000485066.1:n.252_253del
ENST00000494441.1:n.263+45_263+46del
NM_000108.4:c.118+45_118+46del NP_000099.2:n.118+45_118+46del
NM_001289750.1:c.-31+45_-31+46del NP_001276679.1:n.-31+45_-31+46del
NM_001289751.1:c.118+45_118+46del NP_001276680.1:n.118+45_118+46del
NM_001289752.1:c.118+45_118+46del NP_001276681.1:n.118+45_118+46del
NM_000108.5:c.118+45_118+46del MANE Select NP_000099.2:n.118+45_118+46del