Canonical Allele Identifier: CA368857345
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107915671A>C , CM000669.2:g.107915671A>C GRCh38
NC_000007.13:g.107556116A>C , CM000669.1:g.107556116A>C GRCh37
NC_000007.12:g.107343352A>C NCBI36
NG_008045.1:g.29531A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.850A>C MANE Select ENSP00000205402.3:p.Lys284Gln
ENST00000205402.9:c.850A>C ENSP00000205402.3:p.Lys284Gln
ENST00000415325.5:c.*524A>C ENSP00000402593.1:n.*524A>C
ENST00000417551.5:c.850A>C ENSP00000390667.1:p.Lys284Gln
ENST00000437604.6:c.706A>C ENSP00000387542.2:p.Lys236Gln
ENST00000440410.5:c.781A>C ENSP00000417016.1:p.Lys261Gln
NM_000108.4:c.850A>C NP_000099.2:p.Lys284Gln
NM_001289750.1:c.553A>C NP_001276679.1:p.Lys185Gln
NM_001289751.1:c.781A>C NP_001276680.1:p.Lys261Gln
NM_001289752.1:c.706A>C NP_001276681.1:p.Lys236Gln
NM_000108.5:c.850A>C MANE Select NP_000099.2:p.Lys284Gln