Canonical Allele Identifier: CA2509378362
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920623_107920624insTTAAA , CM000669.2:g.107920623_107920624insTTAAA GRCh38
NC_000007.13:g.107561068_107561069insTTAAA , CM000669.1:g.107561068_107561069insTTAAA GRCh37
NC_000007.12:g.107348304_107348305insTTAAA NCBI36
NG_008045.1:g.34483_34484insTTAAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*1364_*1365insTTAAA MANE Select ENSP00000205402.3:n.*1364_*1365insTTAAA
ENST00000205402.9:c.*1364_*1365insTTAAA ENSP00000205402.3:n.*1364_*1365insTTAAA
ENST00000417551.5:c.*124+1240_*124+1241insTTAAA ENSP00000390667.1:n.*124+1240_*124+1241insTTAAA
NM_000108.4:c.*1364_*1365insTTAAA NP_000099.2:n.*1364_*1365insTTAAA
NM_001289750.1:c.*1364_*1365insTTAAA NP_001276679.1:n.*1364_*1365insTTAAA
NM_001289751.1:c.*1364_*1365insTTAAA NP_001276680.1:n.*1364_*1365insTTAAA
NM_001289752.1:c.*1364_*1365insTTAAA NP_001276681.1:n.*1364_*1365insTTAAA
NM_000108.5:c.*1364_*1365insTTAAA MANE Select NP_000099.2:n.*1364_*1365insTTAAA