Canonical Allele Identifier: CA1732860037
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917344G= , CM000669.2:g.107917344G= GRCh38
NC_000007.13:g.107557789G= , CM000669.1:g.107557789G= GRCh37
NC_000007.12:g.107345025G= NCBI36
NG_008045.1:g.31204G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1118G= MANE Select ENSP00000205402.3:p.Cys373=
ENST00000205402.9:c.1118G= ENSP00000205402.3:p.Cys373=
ENST00000415325.5:c.*792G= ENSP00000402593.1:n.*792G=
ENST00000417551.5:c.1118G= ENSP00000390667.1:p.Cys373=
ENST00000437604.6:c.974G= ENSP00000387542.2:p.Cys325=
ENST00000440410.5:c.1049G= ENSP00000417016.1:p.Cys350=
NM_000108.4:c.1118G= NP_000099.2:p.Cys373=
NM_001289750.1:c.821G= NP_001276679.1:p.Cys274=
NM_001289751.1:c.1049G= NP_001276680.1:p.Cys350=
NM_001289752.1:c.974G= NP_001276681.1:p.Cys325=
NM_000108.5:c.1118G= MANE Select NP_000099.2:p.Cys373=