Canonical Allele Identifier: CA1732859891
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916917C= , CM000669.2:g.107916917C= GRCh38
NC_000007.13:g.107557362C= , CM000669.1:g.107557362C= GRCh37
NC_000007.12:g.107344598C= NCBI36
NG_008045.1:g.30777C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.999C= MANE Select ENSP00000205402.3:p.Pro333=
ENST00000205402.9:c.999C= ENSP00000205402.3:p.Pro333=
ENST00000415325.5:c.*673C= ENSP00000402593.1:n.*673C=
ENST00000417551.5:c.999C= ENSP00000390667.1:p.Pro333=
ENST00000437604.6:c.855C= ENSP00000387542.2:p.Pro285=
ENST00000440410.5:c.930C= ENSP00000417016.1:p.Pro310=
NM_000108.4:c.999C= NP_000099.2:p.Pro333=
NM_001289750.1:c.702C= NP_001276679.1:p.Pro234=
NM_001289751.1:c.930C= NP_001276680.1:p.Pro310=
NM_001289752.1:c.855C= NP_001276681.1:p.Pro285=
NM_000108.5:c.999C= MANE Select NP_000099.2:p.Pro333=