Canonical Allele Identifier: CA1732859262
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032242988

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915434del , CM000669.2:g.107915434del GRCh38
NC_000007.13:g.107555879del , CM000669.1:g.107555879del GRCh37
NC_000007.12:g.107343115del NCBI36
NG_008045.1:g.29294del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.685-72del MANE Select ENSP00000205402.3:n.685-72del
ENST00000205402.9:c.685-72del ENSP00000205402.3:n.685-72del
ENST00000415325.5:c.*359-72del ENSP00000402593.1:n.*359-72del
ENST00000417551.5:c.685-72del ENSP00000390667.1:n.685-72del
ENST00000437604.6:c.541-72del ENSP00000387542.2:n.541-72del
ENST00000440410.5:c.616-72del ENSP00000417016.1:n.616-72del
ENST00000451081.5:c.*428-72del ENSP00000388077.1:n.*428-72del
NM_000108.4:c.685-72del NP_000099.2:n.685-72del
NM_001289750.1:c.388-72del NP_001276679.1:n.388-72del
NM_001289751.1:c.616-72del NP_001276680.1:n.616-72del
NM_001289752.1:c.541-72del NP_001276681.1:n.541-72del
NM_000108.5:c.685-72del MANE Select NP_000099.2:n.685-72del