Canonical Allele Identifier: CA1105646229
Gene: DLD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920242A>C , CM000669.2:g.107920242A>C GRCh38
NC_000007.13:g.107560687A>C , CM000669.1:g.107560687A>C GRCh37
NC_000007.12:g.107347923A>C NCBI36
NG_008045.1:g.34102A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000205402.10:c.*983A>C MANE Select ENSP00000205402.3:n.*983A>C
ENST00000205402.9:c.*983A>C ENSP00000205402.3:n.*983A>C
ENST00000417551.5:c.*124+859A>C ENSP00000390667.1:n.*124+859A>C
NM_000108.4:c.*983A>C NP_000099.2:n.*983A>C
NM_001289750.1:c.*983A>C NP_001276679.1:n.*983A>C
NM_001289751.1:c.*983A>C NP_001276680.1:n.*983A>C
NM_001289752.1:c.*983A>C NP_001276681.1:n.*983A>C
NM_000108.5:c.*983A>C MANE Select NP_000099.2:n.*983A>C