Canonical Allele Identifier: CA2559541351
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919066_107919067del , CM000669.2:g.107919066_107919067del GRCh38
NC_000007.13:g.107559511_107559512del , CM000669.1:g.107559511_107559512del GRCh37
NC_000007.12:g.107346747_107346748del NCBI36
NG_008045.1:g.32926_32927del

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1431_1432del MANE Select ENSP00000205402.3:p.Cys477Ter
ENST00000205402.9:c.1431_1432del ENSP00000205402.3:p.Cys477Ter
ENST00000415325.5:c.*1105_*1106del ENSP00000402593.1:n.*1105_*1106del
ENST00000417551.5:c.1431_1432del ENSP00000390667.1:p.Cys477Ter
ENST00000437604.6:c.1287_1288del ENSP00000387542.2:p.Cys429Ter
ENST00000440410.5:c.1362_1363del ENSP00000417016.1:p.Cys454Ter
NM_000108.4:c.1431_1432del NP_000099.2:p.Cys477Ter
NM_001289750.1:c.1134_1135del NP_001276679.1:p.Cys378Ter
NM_001289751.1:c.1362_1363del NP_001276680.1:p.Cys454Ter
NM_001289752.1:c.1287_1288del NP_001276681.1:p.Cys429Ter
NM_000108.5:c.1431_1432del MANE Select NP_000099.2:p.Cys477Ter