Canonical Allele Identifier: CA368857904
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107916948C>A , CM000669.2:g.107916948C>A GRCh38
NC_000007.13:g.107557393C>A , CM000669.1:g.107557393C>A GRCh37
NC_000007.12:g.107344629C>A NCBI36
NG_008045.1:g.30808C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1030C>A MANE Select ENSP00000205402.3:p.Gln344Lys
ENST00000205402.9:c.1030C>A ENSP00000205402.3:p.Gln344Lys
ENST00000415325.5:c.*704C>A ENSP00000402593.1:n.*704C>A
ENST00000417551.5:c.1030C>A ENSP00000390667.1:p.Gln344Lys
ENST00000437604.6:c.886C>A ENSP00000387542.2:p.Gln296Lys
ENST00000440410.5:c.961C>A ENSP00000417016.1:p.Gln321Lys
NM_000108.4:c.1030C>A NP_000099.2:p.Gln344Lys
NM_001289750.1:c.733C>A NP_001276679.1:p.Gln245Lys
NM_001289751.1:c.961C>A NP_001276680.1:p.Gln321Lys
NM_001289752.1:c.886C>A NP_001276681.1:p.Gln296Lys
NM_000108.5:c.1030C>A MANE Select NP_000099.2:p.Gln344Lys