Canonical Allele Identifier: CA2684459018
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917463_107917464insGTATTGAGTACAAAGTTGGGAAAT , CM000669.2:g.107917463_107917464insGTATTGAGTACAAAGTTGGGAAAT GRCh38
NC_000007.13:g.107557908_107557909insGTATTGAGTACAAAGTTGGGAAAT , CM000669.1:g.107557908_107557909insGTATTGAGTACAAAGTTGGGAAAT GRCh37
NC_000007.12:g.107345144_107345145insGTATTGAGTACAAAGTTGGGAAAT NCBI36
NG_008045.1:g.31323_31324insGTATTGAGTACAAAGTTGGGAAAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT MANE Select ENSP00000205402.3:n.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT
ENST00000205402.9:c.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT ENSP00000205402.3:n.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT
ENST00000415325.5:c.*910+1_*910+2insGTATTGAGTACAAAGTTGGGAAAT ENSP00000402593.1:n.*910+1_*910+2insGTATTGAGTACAAAGTTGGGAAAT
ENST00000417551.5:c.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT ENSP00000390667.1:n.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT
ENST00000437604.6:c.1092+1_1092+2insGTATTGAGTACAAAGTTGGGAAAT ENSP00000387542.2:n.1092+1_1092+2insGTATTGAGTACAAAGTTGGGAAAT
ENST00000440410.5:c.1167+1_1167+2insGTATTGAGTACAAAGTTGGGAAAT ENSP00000417016.1:n.1167+1_1167+2insGTATTGAGTACAAAGTTGGGAAAT
NM_000108.4:c.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT NP_000099.2:n.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT
NM_001289750.1:c.939+1_939+2insGTATTGAGTACAAAGTTGGGAAAT NP_001276679.1:n.939+1_939+2insGTATTGAGTACAAAGTTGGGAAAT
NM_001289751.1:c.1167+1_1167+2insGTATTGAGTACAAAGTTGGGAAAT NP_001276680.1:n.1167+1_1167+2insGTATTGAGTACAAAGTTGGGAAAT
NM_001289752.1:c.1092+1_1092+2insGTATTGAGTACAAAGTTGGGAAAT NP_001276681.1:n.1092+1_1092+2insGTATTGAGTACAAAGTTGGGAAAT
NM_000108.5:c.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT MANE Select NP_000099.2:n.1236+1_1236+2insGTATTGAGTACAAAGTTGGGAAAT