Canonical Allele Identifier: CA368856718
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915510C>T , CM000669.2:g.107915510C>T GRCh38
NC_000007.13:g.107555955C>T , CM000669.1:g.107555955C>T GRCh37
NC_000007.12:g.107343191C>T NCBI36
NG_008045.1:g.29370C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.689C>T MANE Select ENSP00000205402.3:p.Ser230Leu
ENST00000205402.9:c.689C>T ENSP00000205402.3:p.Ser230Leu
ENST00000415325.5:c.*363C>T ENSP00000402593.1:n.*363C>T
ENST00000417551.5:c.689C>T ENSP00000390667.1:p.Ser230Leu
ENST00000437604.6:c.545C>T ENSP00000387542.2:p.Ser182Leu
ENST00000440410.5:c.620C>T ENSP00000417016.1:p.Ser207Leu
ENST00000451081.5:c.*432C>T ENSP00000388077.1:n.*432C>T
NM_000108.4:c.689C>T NP_000099.2:p.Ser230Leu
NM_001289750.1:c.392C>T NP_001276679.1:p.Ser131Leu
NM_001289751.1:c.620C>T NP_001276680.1:p.Ser207Leu
NM_001289752.1:c.545C>T NP_001276681.1:p.Ser182Leu
NM_000108.5:c.689C>T MANE Select NP_000099.2:p.Ser230Leu