Canonical Allele Identifier: CA1732860040
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917349G= , CM000669.2:g.107917349G= GRCh38
NC_000007.13:g.107557794G= , CM000669.1:g.107557794G= GRCh37
NC_000007.12:g.107345030G= NCBI36
NG_008045.1:g.31209G=

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.1123G= MANE Select ENSP00000205402.3:p.Glu375=
ENST00000205402.9:c.1123G= ENSP00000205402.3:p.Glu375=
ENST00000415325.5:c.*797G= ENSP00000402593.1:n.*797G=
ENST00000417551.5:c.1123G= ENSP00000390667.1:p.Glu375=
ENST00000437604.6:c.979G= ENSP00000387542.2:p.Glu327=
ENST00000440410.5:c.1054G= ENSP00000417016.1:p.Glu352=
NM_000108.4:c.1123G= NP_000099.2:p.Glu375=
NM_001289750.1:c.826G= NP_001276679.1:p.Glu276=
NM_001289751.1:c.1054G= NP_001276680.1:p.Glu352=
NM_001289752.1:c.979G= NP_001276681.1:p.Glu327=
NM_000108.5:c.1123G= MANE Select NP_000099.2:p.Glu375=