Canonical Allele Identifier: CA601780333
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs1188919564

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113442584_113442585del , CM000673.2:g.113442584_113442585del GRCh38
NC_000011.9:g.113313306_113313307del , CM000673.1:g.113313306_113313307del GRCh37
NC_000011.8:g.112818516_112818517del NCBI36
NG_008841.1:g.37695_37696del

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-31-17903_-31-17902del MANE Select ENSP00000354859.3:n.-31-17903_-31-17902de...
ENST00000346454.7:c.-31-17903_-31-17902del ENSP00000278597.5:n.-31-17903_-31-17902de...
ENST00000362072.7:c.-31-17903_-31-17902del ENSP00000354859.3:n.-31-17903_-31-17902de...
ENST00000540600.5:n.35-17903_35-17902del
ENST00000542616.1:c.-31-17903_-31-17902del ENSP00000441474.1:n.-31-17903_-31-17902de...
ENST00000543292.1:c.-32+4986_-32+4987del ENSP00000438419.1:n.-32+4986_-32+4987del
NM_000795.3:c.-31-17903_-31-17902del NP_000786.1:n.-31-17903_-31-17902del
NM_016574.3:c.-31-17903_-31-17902del NP_057658.2:n.-31-17903_-31-17902del
XM_017017296.2:c.-31-17903_-31-17902del XP_016872785.1:n.-31-17903_-31-17902del
NM_000795.4:c.-31-17903_-31-17902del MANE Select NP_000786.1:n.-31-17903_-31-17902del
NM_016574.4:c.-31-17903_-31-17902del NP_057658.2:n.-31-17903_-31-17902del