Canonical Allele Identifier: CA1732861160
Gene: DLD HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.107920042_107920043delinsCT , CM000669.2:g.107920042_107920043delinsCT GRCh38
NC_000007.13:g.107560487_107560488delinsCT , CM000669.1:g.107560487_107560488delinsCT GRCh37
NC_000007.12:g.107347723_107347724delinsCT NCBI36
NG_008045.1:g.33902_33903delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000205402.10:c.*783_*784delinsCT MANE Select ENSP00000205402.3:n.*783_*784delinsCT
ENST00000205402.9:c.*783_*784delinsCT ENSP00000205402.3:n.*783_*784delinsCT
ENST00000417551.5:c.*124+659_*124+660delinsCT ENSP00000390667.1:n.*124+659_*124+660delinsCT
NM_000108.4:c.*783_*784delinsCT NP_000099.2:n.*783_*784delinsCT
NM_001289750.1:c.*783_*784delinsCT NP_001276679.1:n.*783_*784delinsCT
NM_001289751.1:c.*783_*784delinsCT NP_001276680.1:n.*783_*784delinsCT
NM_001289752.1:c.*783_*784delinsCT NP_001276681.1:n.*783_*784delinsCT
NM_000108.5:c.*783_*784delinsCT MANE Select NP_000099.2:n.*783_*784delinsCT