Canonical Allele Identifier: CA1732861264
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2032376592

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920256_107920258del , CM000669.2:g.107920256_107920258del GRCh38
NC_000007.13:g.107560701_107560703del , CM000669.1:g.107560701_107560703del GRCh37
NC_000007.12:g.107347937_107347939del NCBI36
NG_008045.1:g.34116_34118del

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*997_*999del MANE Select ENSP00000205402.3:n.*997_*999del
ENST00000205402.9:c.*997_*999del ENSP00000205402.3:n.*997_*999del
ENST00000417551.5:c.*124+873_*124+875del ENSP00000390667.1:n.*124+873_*124+875del
NM_000108.4:c.*997_*999del NP_000099.2:n.*997_*999del
NM_001289750.1:c.*997_*999del NP_001276679.1:n.*997_*999del
NM_001289751.1:c.*997_*999del NP_001276680.1:n.*997_*999del
NM_001289752.1:c.*997_*999del NP_001276681.1:n.*997_*999del
NM_000108.5:c.*997_*999del MANE Select NP_000099.2:n.*997_*999del