Canonical Allele Identifier: CA1105646270
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920281_107920282del , CM000669.2:g.107920281_107920282del GRCh38
NC_000007.13:g.107560726_107560727del , CM000669.1:g.107560726_107560727del GRCh37
NC_000007.12:g.107347962_107347963del NCBI36
NG_008045.1:g.34141_34142del

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*1022_*1023del MANE Select ENSP00000205402.3:n.*1022_*1023del
ENST00000205402.9:c.*1022_*1023del ENSP00000205402.3:n.*1022_*1023del
ENST00000417551.5:c.*124+898_*124+899del ENSP00000390667.1:n.*124+898_*124+899del
NM_000108.4:c.*1022_*1023del NP_000099.2:n.*1022_*1023del
NM_001289750.1:c.*1022_*1023del NP_001276679.1:n.*1022_*1023del
NM_001289751.1:c.*1022_*1023del NP_001276680.1:n.*1022_*1023del
NM_001289752.1:c.*1022_*1023del NP_001276681.1:n.*1022_*1023del
NM_000108.5:c.*1022_*1023del MANE Select NP_000099.2:n.*1022_*1023del