Canonical Allele Identifier: CA1732861290
Gene: DLD HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920312G= , CM000669.2:g.107920312G= GRCh38
NC_000007.13:g.107560757G= , CM000669.1:g.107560757G= GRCh37
NC_000007.12:g.107347993G= NCBI36
NG_008045.1:g.34172G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*1053G= MANE Select ENSP00000205402.3:n.*1053G=
ENST00000205402.9:c.*1053G= ENSP00000205402.3:n.*1053G=
ENST00000417551.5:c.*124+929G= ENSP00000390667.1:n.*124+929G=
NM_000108.4:c.*1053G= NP_000099.2:n.*1053G=
NM_001289750.1:c.*1053G= NP_001276679.1:n.*1053G=
NM_001289751.1:c.*1053G= NP_001276680.1:n.*1053G=
NM_001289752.1:c.*1053G= NP_001276681.1:n.*1053G=
NM_000108.5:c.*1053G= MANE Select NP_000099.2:n.*1053G=
Search 100 bp 5'
Search 100 bp 3'