Canonical Allele Identifier: CA2578989969
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107893210del , CM000669.2:g.107893210del GRCh38
NC_000007.13:g.107533655del , CM000669.1:g.107533655del GRCh37
NC_000007.12:g.107320891del NCBI36
NG_008045.1:g.7070del

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.50del MANE Select ENSP00000205402.3:p.Phe17SerfsTer16
ENST00000639772.1:c.50del ENSP00000492159.1:p.Phe17SerfsTer16
ENST00000205402.9:c.50del ENSP00000205402.3:p.Phe17SerfsTer16
ENST00000415325.5:c.50del ENSP00000402593.1:p.Phe17SerfsTer16
ENST00000417551.5:c.50del ENSP00000390667.1:p.Phe17SerfsTer16
ENST00000437604.6:c.50del ENSP00000387542.2:p.Phe17SerfsTer16
ENST00000440410.5:c.50del ENSP00000417016.1:p.Phe17SerfsTer16
ENST00000450038.5:c.50del ENSP00000409590.1:p.Phe17SerfsTer16
ENST00000451081.5:c.50del ENSP00000388077.1:p.Phe17SerfsTer16
ENST00000453354.5:n.115del
ENST00000460577.5:n.84del
ENST00000485066.1:n.139del
ENST00000494441.1:n.195del
NM_000108.4:c.50del NP_000099.2:p.Phe17SerfsTer16
NM_001289750.1:c.-99del NP_001276679.1:n.-99del
NM_001289751.1:c.50del NP_001276680.1:p.Phe17SerfsTer16
NM_001289752.1:c.50del NP_001276681.1:p.Phe17SerfsTer16
NM_000108.5:c.50del MANE Select NP_000099.2:p.Phe17SerfsTer16