Canonical Allele Identifier: CA2684464916
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915628del , CM000669.2:g.107915628del GRCh38
NC_000007.13:g.107556073del , CM000669.1:g.107556073del GRCh37
NC_000007.12:g.107343309del NCBI36
NG_008045.1:g.29488del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.807del MANE Select ENSP00000205402.3:p.Phe270LeufsTer5
ENST00000205402.9:c.807del ENSP00000205402.3:p.Phe270LeufsTer5
ENST00000415325.5:c.*481del ENSP00000402593.1:n.*481del
ENST00000417551.5:c.807del ENSP00000390667.1:p.Phe270LeufsTer5
ENST00000437604.6:c.663del ENSP00000387542.2:p.Phe222LeufsTer5
ENST00000440410.5:c.738del ENSP00000417016.1:p.Phe247LeufsTer5
NM_000108.4:c.807del NP_000099.2:p.Phe270LeufsTer5
NM_001289750.1:c.510del NP_001276679.1:p.Phe171LeufsTer5
NM_001289751.1:c.738del NP_001276680.1:p.Phe247LeufsTer5
NM_001289752.1:c.663del NP_001276681.1:p.Phe222LeufsTer5
NM_000108.5:c.807del MANE Select NP_000099.2:p.Phe270LeufsTer5