Canonical Allele Identifier: CA1105646231
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920244_107920245del , CM000669.2:g.107920244_107920245del GRCh38
NC_000007.13:g.107560689_107560690del , CM000669.1:g.107560689_107560690del GRCh37
NC_000007.12:g.107347925_107347926del NCBI36
NG_008045.1:g.34104_34105del

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*985_*986del MANE Select ENSP00000205402.3:n.*985_*986del
ENST00000205402.9:c.*985_*986del ENSP00000205402.3:n.*985_*986del
ENST00000417551.5:c.*124+861_*124+862del ENSP00000390667.1:n.*124+861_*124+862del
NM_000108.4:c.*985_*986del NP_000099.2:n.*985_*986del
NM_001289750.1:c.*985_*986del NP_001276679.1:n.*985_*986del
NM_001289751.1:c.*985_*986del NP_001276680.1:n.*985_*986del
NM_001289752.1:c.*985_*986del NP_001276681.1:n.*985_*986del
NM_000108.5:c.*985_*986del MANE Select NP_000099.2:n.*985_*986del