Canonical Allele Identifier: CA1732859885
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916894G= , CM000669.2:g.107916894G= GRCh38
NC_000007.13:g.107557339G= , CM000669.1:g.107557339G= GRCh37
NC_000007.12:g.107344575G= NCBI36
NG_008045.1:g.30754G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.976G= MANE Select ENSP00000205402.3:p.Glu326=
ENST00000205402.9:c.976G= ENSP00000205402.3:p.Glu326=
ENST00000415325.5:c.*650G= ENSP00000402593.1:n.*650G=
ENST00000417551.5:c.976G= ENSP00000390667.1:p.Glu326=
ENST00000437604.6:c.832G= ENSP00000387542.2:p.Glu278=
ENST00000440410.5:c.907G= ENSP00000417016.1:p.Glu303=
NM_000108.4:c.976G= NP_000099.2:p.Glu326=
NM_001289750.1:c.679G= NP_001276679.1:p.Glu227=
NM_001289751.1:c.907G= NP_001276680.1:p.Glu303=
NM_001289752.1:c.832G= NP_001276681.1:p.Glu278=
NM_000108.5:c.976G= MANE Select NP_000099.2:p.Glu326=