Canonical Allele Identifier: CA2684464842
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915584_107915585del , CM000669.2:g.107915584_107915585del GRCh38
NC_000007.13:g.107556029_107556030del , CM000669.1:g.107556029_107556030del GRCh37
NC_000007.12:g.107343265_107343266del NCBI36
NG_008045.1:g.29444_29445del

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.763_764del MANE Select ENSP00000205402.3:p.Met255GlyfsTer4
ENST00000205402.9:c.763_764del ENSP00000205402.3:p.Met255GlyfsTer4
ENST00000415325.5:c.*437_*438del ENSP00000402593.1:n.*437_*438del
ENST00000417551.5:c.763_764del ENSP00000390667.1:p.Met255GlyfsTer4
ENST00000437604.6:c.619_620del ENSP00000387542.2:p.Met207GlyfsTer4
ENST00000440410.5:c.694_695del ENSP00000417016.1:p.Met232GlyfsTer4
ENST00000451081.5:c.*506_*507del ENSP00000388077.1:n.*506_*507del
NM_000108.4:c.763_764del NP_000099.2:p.Met255GlyfsTer4
NM_001289750.1:c.466_467del NP_001276679.1:p.Met156GlyfsTer4
NM_001289751.1:c.694_695del NP_001276680.1:p.Met232GlyfsTer4
NM_001289752.1:c.619_620del NP_001276681.1:p.Met207GlyfsTer4
NM_000108.5:c.763_764del MANE Select NP_000099.2:p.Met255GlyfsTer4