Canonical Allele Identifier: CA2684458381
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916996del , CM000669.2:g.107916996del GRCh38
NC_000007.13:g.107557441del , CM000669.1:g.107557441del GRCh37
NC_000007.12:g.107344677del NCBI36
NG_008045.1:g.30856del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1046+32del MANE Select ENSP00000205402.3:n.1046+32del
ENST00000205402.9:c.1046+32del ENSP00000205402.3:n.1046+32del
ENST00000415325.5:c.*720+32del ENSP00000402593.1:n.*720+32del
ENST00000417551.5:c.1046+32del ENSP00000390667.1:n.1046+32del
ENST00000437604.6:c.902+32del ENSP00000387542.2:n.902+32del
ENST00000440410.5:c.977+32del ENSP00000417016.1:n.977+32del
NM_000108.4:c.1046+32del NP_000099.2:n.1046+32del
NM_001289750.1:c.749+32del NP_001276679.1:n.749+32del
NM_001289751.1:c.977+32del NP_001276680.1:n.977+32del
NM_001289752.1:c.902+32del NP_001276681.1:n.902+32del
NM_000108.5:c.1046+32del MANE Select NP_000099.2:n.1046+32del