Canonical Allele Identifier: CA1732861669
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107921185_107921186delinsGT , CM000669.2:g.107921185_107921186delinsGT GRCh38
NC_000007.13:g.107561630_107561631delinsGT , CM000669.1:g.107561630_107561631delinsGT GRCh37
NC_000007.12:g.107348866_107348867delinsGT NCBI36
NG_008045.1:g.35045_35046delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*1926_*1927delinsGT MANE Select ENSP00000205402.3:n.*1926_*1927delinsGT
ENST00000205402.9:c.*1926_*1927delinsGT ENSP00000205402.3:n.*1926_*1927delinsGT
ENST00000417551.5:c.*124+1802_*124+1803delinsGT ENSP00000390667.1:n.*124+1802_*124+1803delinsGT
NM_000108.4:c.*1926_*1927delinsGT NP_000099.2:n.*1926_*1927delinsGT
NM_001289750.1:c.*1926_*1927delinsGT NP_001276679.1:n.*1926_*1927delinsGT
NM_001289751.1:c.*1926_*1927delinsGT NP_001276680.1:n.*1926_*1927delinsGT
NM_001289752.1:c.*1926_*1927delinsGT NP_001276681.1:n.*1926_*1927delinsGT
NM_000108.5:c.*1926_*1927delinsGT MANE Select NP_000099.2:n.*1926_*1927delinsGT