Canonical Allele Identifier: CA368856715
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915509T>G , CM000669.2:g.107915509T>G GRCh38
NC_000007.13:g.107555954T>G , CM000669.1:g.107555954T>G GRCh37
NC_000007.12:g.107343190T>G NCBI36
NG_008045.1:g.29369T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.688T>G MANE Select ENSP00000205402.3:p.Ser230Ala
ENST00000205402.9:c.688T>G ENSP00000205402.3:p.Ser230Ala
ENST00000415325.5:c.*362T>G ENSP00000402593.1:n.*362T>G
ENST00000417551.5:c.688T>G ENSP00000390667.1:p.Ser230Ala
ENST00000437604.6:c.544T>G ENSP00000387542.2:p.Ser182Ala
ENST00000440410.5:c.619T>G ENSP00000417016.1:p.Ser207Ala
ENST00000451081.5:c.*431T>G ENSP00000388077.1:n.*431T>G
NM_000108.4:c.688T>G NP_000099.2:p.Ser230Ala
NM_001289750.1:c.391T>G NP_001276679.1:p.Ser131Ala
NM_001289751.1:c.619T>G NP_001276680.1:p.Ser207Ala
NM_001289752.1:c.544T>G NP_001276681.1:p.Ser182Ala
NM_000108.5:c.688T>G MANE Select NP_000099.2:p.Ser230Ala