Canonical Allele Identifier: CA2777357466
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107919961A>T , CM000669.2:g.107919961A>T GRCh38
NC_000007.13:g.107560406A>T , CM000669.1:g.107560406A>T GRCh37
NC_000007.12:g.107347642A>T NCBI36
NG_008045.1:g.33821A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*702A>T MANE Select ENSP00000205402.3:n.*702A>T
ENST00000205402.9:c.*702A>T ENSP00000205402.3:n.*702A>T
ENST00000417551.5:c.*124+578A>T ENSP00000390667.1:n.*124+578A>T
NM_000108.4:c.*702A>T NP_000099.2:n.*702A>T
NM_001289750.1:c.*702A>T NP_001276679.1:n.*702A>T
NM_001289751.1:c.*702A>T NP_001276680.1:n.*702A>T
NM_001289752.1:c.*702A>T NP_001276681.1:n.*702A>T
NM_000108.5:c.*702A>T MANE Select NP_000099.2:n.*702A>T