Canonical Allele Identifier: CA2502571167
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920612_107920614del , CM000669.2:g.107920612_107920614del GRCh38
NC_000007.13:g.107561057_107561059del , CM000669.1:g.107561057_107561059del GRCh37
NC_000007.12:g.107348293_107348295del NCBI36
NG_008045.1:g.34472_34474del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*1353_*1355del MANE Select ENSP00000205402.3:n.*1353_*1355del
ENST00000205402.9:c.*1353_*1355del ENSP00000205402.3:n.*1353_*1355del
ENST00000417551.5:c.*124+1229_*124+1231del ENSP00000390667.1:n.*124+1229_*124+1231del
NM_000108.4:c.*1353_*1355del NP_000099.2:n.*1353_*1355del
NM_001289750.1:c.*1353_*1355del NP_001276679.1:n.*1353_*1355del
NM_001289751.1:c.*1353_*1355del NP_001276680.1:n.*1353_*1355del
NM_001289752.1:c.*1353_*1355del NP_001276681.1:n.*1353_*1355del
NM_000108.5:c.*1353_*1355del MANE Select NP_000099.2:n.*1353_*1355del