Canonical Allele Identifier: CA2602854213
Gene: DRD2 HGNC NCBI

Linked Data

dbSNP Id: rs2119847717

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439420_113439423del , CM000673.2:g.113439420_113439423del GRCh38
NC_000011.9:g.113310142_113310145del , CM000673.1:g.113310142_113310145del GRCh37
NC_000011.8:g.112815352_112815355del NCBI36
NG_008841.1:g.40863_40866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-31-14735_-31-14732del MANE Select ENSP00000354859.3:n.-31-14735_-31-14732del
ENST00000346454.7:c.-31-14735_-31-14732del ENSP00000278597.5:n.-31-14735_-31-14732del
ENST00000362072.7:c.-31-14735_-31-14732del ENSP00000354859.3:n.-31-14735_-31-14732del
ENST00000540600.5:n.35-14735_35-14732del
ENST00000542616.1:c.-31-14735_-31-14732del ENSP00000441474.1:n.-31-14735_-31-14732del
ENST00000543292.1:c.-32+8154_-32+8157del ENSP00000438419.1:n.-32+8154_-32+8157del
NM_000795.3:c.-31-14735_-31-14732del NP_000786.1:n.-31-14735_-31-14732del
NM_016574.3:c.-31-14735_-31-14732del NP_057658.2:n.-31-14735_-31-14732del
XM_017017296.2:c.-31-14735_-31-14732del XP_016872785.1:n.-31-14735_-31-14732del
NM_000795.4:c.-31-14735_-31-14732del MANE Select NP_000786.1:n.-31-14735_-31-14732del
NM_016574.4:c.-31-14735_-31-14732del NP_057658.2:n.-31-14735_-31-14732del