Canonical Allele Identifier: CA2574982178
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410649_113410650del , CM000673.2:g.113410649_113410650del GRCh38
NC_000011.9:g.113281371_113281372del , CM000673.1:g.113281371_113281372del GRCh37
NC_000011.8:g.112786581_112786582del NCBI36
NG_008841.1:g.69631_69632del

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*78_*79del MANE Select ENSP00000354859.3:n.*78_*79del
ENST00000346454.7:c.*78_*79del ENSP00000278597.5:n.*78_*79del
ENST00000362072.7:c.*78_*79del ENSP00000354859.3:n.*78_*79del
ENST00000538967.5:c.1416_1417del ENSP00000438215.1:n.1416_1417del
ENST00000542968.5:c.*78_*79del ENSP00000442172.1:n.*78_*79del
ENST00000544518.5:c.*78_*79del ENSP00000441068.1:n.*78_*79del
NM_000795.3:c.*78_*79del NP_000786.1:n.*78_*79del
NM_016574.3:c.*78_*79del NP_057658.2:n.*78_*79del
XM_017017296.2:c.*78_*79del XP_016872785.1:n.*78_*79del
NM_000795.4:c.*78_*79del MANE Select NP_000786.1:n.*78_*79del
NM_016574.4:c.*78_*79del NP_057658.2:n.*78_*79del