Canonical Allele Identifier: CA1105645742
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032351147

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919267del , CM000669.2:g.107919267del GRCh38
NC_000007.13:g.107559712del , CM000669.1:g.107559712del GRCh37
NC_000007.12:g.107346948del NCBI36
NG_008045.1:g.33127del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*8del MANE Select ENSP00000205402.3:n.*8del
ENST00000205402.9:c.*8del ENSP00000205402.3:n.*8del
ENST00000415325.5:c.*1212del ENSP00000402593.1:n.*1212del
ENST00000417551.5:c.*8del ENSP00000390667.1:n.*8del
ENST00000437604.6:c.*8del ENSP00000387542.2:n.*8del
ENST00000440410.5:c.*8del ENSP00000417016.1:n.*8del
NM_000108.4:c.*8del NP_000099.2:n.*8del
NM_001289750.1:c.*8del NP_001276679.1:n.*8del
NM_001289751.1:c.*8del NP_001276680.1:n.*8del
NM_001289752.1:c.*8del NP_001276681.1:n.*8del
NM_000108.5:c.*8del MANE Select NP_000099.2:n.*8del