Canonical Allele Identifier: CA1732860033
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917335G= , CM000669.2:g.107917335G= GRCh38
NC_000007.13:g.107557780G= , CM000669.1:g.107557780G= GRCh37
NC_000007.12:g.107345016G= NCBI36
NG_008045.1:g.31195G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1109G= MANE Select ENSP00000205402.3:p.Gly370=
ENST00000205402.9:c.1109G= ENSP00000205402.3:p.Gly370=
ENST00000415325.5:c.*783G= ENSP00000402593.1:n.*783G=
ENST00000417551.5:c.1109G= ENSP00000390667.1:p.Gly370=
ENST00000437604.6:c.965G= ENSP00000387542.2:p.Gly322=
ENST00000440410.5:c.1040G= ENSP00000417016.1:p.Gly347=
NM_000108.4:c.1109G= NP_000099.2:p.Gly370=
NM_001289750.1:c.812G= NP_001276679.1:p.Gly271=
NM_001289751.1:c.1040G= NP_001276680.1:p.Gly347=
NM_001289752.1:c.965G= NP_001276681.1:p.Gly322=
NM_000108.5:c.1109G= MANE Select NP_000099.2:p.Gly370=