Canonical Allele Identifier: CA2793679591
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439625del , CM000673.2:g.113439625del GRCh38
NC_000011.9:g.113310347del , CM000673.1:g.113310347del GRCh37
NC_000011.8:g.112815557del NCBI36
NG_008841.1:g.40655del

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-31-14943del MANE Select ENSP00000354859.3:n.-31-14943del
ENST00000346454.7:c.-31-14943del ENSP00000278597.5:n.-31-14943del
ENST00000362072.7:c.-31-14943del ENSP00000354859.3:n.-31-14943del
ENST00000540600.5:n.35-14943del
ENST00000542616.1:c.-31-14943del ENSP00000441474.1:n.-31-14943del
ENST00000543292.1:c.-32+7946del ENSP00000438419.1:n.-32+7946del
NM_000795.3:c.-31-14943del NP_000786.1:n.-31-14943del
NM_016574.3:c.-31-14943del NP_057658.2:n.-31-14943del
XM_017017296.2:c.-31-14943del XP_016872785.1:n.-31-14943del
NM_000795.4:c.-31-14943del MANE Select NP_000786.1:n.-31-14943del
NM_016574.4:c.-31-14943del NP_057658.2:n.-31-14943del