Canonical Allele Identifier: CA2684458226
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916890_107916898del , CM000669.2:g.107916890_107916898del GRCh38
NC_000007.13:g.107557335_107557343del , CM000669.1:g.107557335_107557343del GRCh37
NC_000007.12:g.107344571_107344579del NCBI36
NG_008045.1:g.30750_30758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.972_980del MANE Select ENSP00000205402.3:p.Glu325_Leu327del
ENST00000205402.9:c.972_980del ENSP00000205402.3:p.Glu325_Leu327del
ENST00000415325.5:c.*646_*654del ENSP00000402593.1:n.*646_*654del
ENST00000417551.5:c.972_980del ENSP00000390667.1:p.Glu325_Leu327del
ENST00000437604.6:c.828_836del ENSP00000387542.2:p.Glu277_Leu279del
ENST00000440410.5:c.903_911del ENSP00000417016.1:p.Glu302_Leu304del
NM_000108.4:c.972_980del NP_000099.2:p.Glu325_Leu327del
NM_001289750.1:c.675_683del NP_001276679.1:p.Glu226_Leu228del
NM_001289751.1:c.903_911del NP_001276680.1:p.Glu302_Leu304del
NM_001289752.1:c.828_836del NP_001276681.1:p.Glu277_Leu279del
NM_000108.5:c.972_980del MANE Select NP_000099.2:p.Glu325_Leu327del