Canonical Allele Identifier: CA2578990156
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915515del , CM000669.2:g.107915515del GRCh38
NC_000007.13:g.107555960del , CM000669.1:g.107555960del GRCh37
NC_000007.12:g.107343196del NCBI36
NG_008045.1:g.29375del

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.694del MANE Select ENSP00000205402.3:p.Trp232GlyfsTer8
ENST00000205402.9:c.694del ENSP00000205402.3:p.Trp232GlyfsTer8
ENST00000415325.5:c.*368del ENSP00000402593.1:n.*368del
ENST00000417551.5:c.694del ENSP00000390667.1:p.Trp232GlyfsTer8
ENST00000437604.6:c.550del ENSP00000387542.2:p.Trp184GlyfsTer8
ENST00000440410.5:c.625del ENSP00000417016.1:p.Trp209GlyfsTer8
ENST00000451081.5:c.*437del ENSP00000388077.1:n.*437del
NM_000108.4:c.694del NP_000099.2:p.Trp232GlyfsTer8
NM_001289750.1:c.397del NP_001276679.1:p.Trp133GlyfsTer8
NM_001289751.1:c.625del NP_001276680.1:p.Trp209GlyfsTer8
NM_001289752.1:c.550del NP_001276681.1:p.Trp184GlyfsTer8
NM_000108.5:c.694del MANE Select NP_000099.2:p.Trp232GlyfsTer8