Canonical Allele Identifier: CA1732860729
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919054_107919055delinsTG , CM000669.2:g.107919054_107919055delinsTG GRCh38
NC_000007.13:g.107559499_107559500delinsTG , CM000669.1:g.107559499_107559500delinsTG GRCh37
NC_000007.12:g.107346735_107346736delinsTG NCBI36
NG_008045.1:g.32914_32915delinsTG

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1419_1420delinsTG MANE Select ENSP00000205402.3:p.Tyr473=
ENST00000205402.9:c.1419_1420delinsTG ENSP00000205402.3:p.Tyr473=
ENST00000415325.5:c.*1093_*1094delinsTG ENSP00000402593.1:n.*1093_*1094delinsTG
ENST00000417551.5:c.1419_1420delinsTG ENSP00000390667.1:p.Tyr473=
ENST00000437604.6:c.1275_1276delinsTG ENSP00000387542.2:p.Tyr425=
ENST00000440410.5:c.1350_1351delinsTG ENSP00000417016.1:p.Tyr450=
NM_000108.4:c.1419_1420delinsTG NP_000099.2:p.Tyr473=
NM_001289750.1:c.1122_1123delinsTG NP_001276679.1:p.Tyr374=
NM_001289751.1:c.1350_1351delinsTG NP_001276680.1:p.Tyr450=
NM_001289752.1:c.1275_1276delinsTG NP_001276681.1:p.Tyr425=
NM_000108.5:c.1419_1420delinsTG MANE Select NP_000099.2:p.Tyr473=