Canonical Allele Identifier: CA368858194
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107917329A>G , CM000669.2:g.107917329A>G GRCh38
NC_000007.13:g.107557774A>G , CM000669.1:g.107557774A>G GRCh37
NC_000007.12:g.107345010A>G NCBI36
NG_008045.1:g.31189A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.1103A>G MANE Select ENSP00000205402.3:p.Asp368Gly
ENST00000205402.9:c.1103A>G ENSP00000205402.3:p.Asp368Gly
ENST00000415325.5:c.*777A>G ENSP00000402593.1:n.*777A>G
ENST00000417551.5:c.1103A>G ENSP00000390667.1:p.Asp368Gly
ENST00000437604.6:c.959A>G ENSP00000387542.2:p.Asp320Gly
ENST00000440410.5:c.1034A>G ENSP00000417016.1:p.Asp345Gly
NM_000108.4:c.1103A>G NP_000099.2:p.Asp368Gly
NM_001289750.1:c.806A>G NP_001276679.1:p.Asp269Gly
NM_001289751.1:c.1034A>G NP_001276680.1:p.Asp345Gly
NM_001289752.1:c.959A>G NP_001276681.1:p.Asp320Gly
NM_000108.5:c.1103A>G MANE Select NP_000099.2:p.Asp368Gly