Canonical Allele Identifier: CA2684461147
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919270del , CM000669.2:g.107919270del GRCh38
NC_000007.13:g.107559715del , CM000669.1:g.107559715del GRCh37
NC_000007.12:g.107346951del NCBI36
NG_008045.1:g.33130del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*11del MANE Select ENSP00000205402.3:n.*11del
ENST00000205402.9:c.*11del ENSP00000205402.3:n.*11del
ENST00000415325.5:c.*1215del ENSP00000402593.1:n.*1215del
ENST00000417551.5:c.*11del ENSP00000390667.1:n.*11del
ENST00000437604.6:c.*11del ENSP00000387542.2:n.*11del
ENST00000440410.5:c.*11del ENSP00000417016.1:n.*11del
NM_000108.4:c.*11del NP_000099.2:n.*11del
NM_001289750.1:c.*11del NP_001276679.1:n.*11del
NM_001289751.1:c.*11del NP_001276680.1:n.*11del
NM_001289752.1:c.*11del NP_001276681.1:n.*11del
NM_000108.5:c.*11del MANE Select NP_000099.2:n.*11del