Canonical Allele Identifier: CA2684463022
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920647C>A , CM000669.2:g.107920647C>A GRCh38
NC_000007.13:g.107561092C>A , CM000669.1:g.107561092C>A GRCh37
NC_000007.12:g.107348328C>A NCBI36
NG_008045.1:g.34507C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*1388C>A MANE Select ENSP00000205402.3:n.*1388C>A
ENST00000205402.9:c.*1388C>A ENSP00000205402.3:n.*1388C>A
ENST00000417551.5:c.*124+1264C>A ENSP00000390667.1:n.*124+1264C>A
NM_000108.4:c.*1388C>A NP_000099.2:n.*1388C>A
NM_001289750.1:c.*1388C>A NP_001276679.1:n.*1388C>A
NM_001289751.1:c.*1388C>A NP_001276680.1:n.*1388C>A
NM_001289752.1:c.*1388C>A NP_001276681.1:n.*1388C>A
NM_000108.5:c.*1388C>A MANE Select NP_000099.2:n.*1388C>A