Canonical Allele Identifier: CA1732861137
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs948689084

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920012del , CM000669.2:g.107920012del GRCh38
NC_000007.13:g.107560457del , CM000669.1:g.107560457del GRCh37
NC_000007.12:g.107347693del NCBI36
NG_008045.1:g.33872del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*753del MANE Select ENSP00000205402.3:n.*753del
ENST00000205402.9:c.*753del ENSP00000205402.3:n.*753del
ENST00000417551.5:c.*124+629del ENSP00000390667.1:n.*124+629del
NM_000108.4:c.*753del NP_000099.2:n.*753del
NM_001289750.1:c.*753del NP_001276679.1:n.*753del
NM_001289751.1:c.*753del NP_001276680.1:n.*753del
NM_001289752.1:c.*753del NP_001276681.1:n.*753del
NM_000108.5:c.*753del MANE Select NP_000099.2:n.*753del