Canonical Allele Identifier: CA2715481972
Gene: DLD HGNC NCBI

Linked Data

dbSNP Id: rs2116281827

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919978C>T , CM000669.2:g.107919978C>T GRCh38
NC_000007.13:g.107560423C>T , CM000669.1:g.107560423C>T GRCh37
NC_000007.12:g.107347659C>T NCBI36
NG_008045.1:g.33838C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*719C>T MANE Select ENSP00000205402.3:n.*719C>T
ENST00000205402.9:c.*719C>T ENSP00000205402.3:n.*719C>T
ENST00000417551.5:c.*124+595C>T ENSP00000390667.1:n.*124+595C>T
NM_000108.4:c.*719C>T NP_000099.2:n.*719C>T
NM_001289750.1:c.*719C>T NP_001276679.1:n.*719C>T
NM_001289751.1:c.*719C>T NP_001276680.1:n.*719C>T
NM_001289752.1:c.*719C>T NP_001276681.1:n.*719C>T
NM_000108.5:c.*719C>T MANE Select NP_000099.2:n.*719C>T