Canonical Allele Identifier: CA2793678798
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410500_113410501dup , CM000673.2:g.113410500_113410501dup GRCh38
NC_000011.9:g.113281222_113281223dup , CM000673.1:g.113281222_113281223dup GRCh37
NC_000011.8:g.112786432_112786433dup NCBI36
NG_008841.1:g.69783_69784dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*230_*231dup MANE Select ENSP00000354859.3:n.*230_*231dup
ENST00000346454.7:c.*230_*231dup ENSP00000278597.5:n.*230_*231dup
ENST00000362072.7:c.*230_*231dup ENSP00000354859.3:n.*230_*231dup
ENST00000542968.5:c.*230_*231dup ENSP00000442172.1:n.*230_*231dup
ENST00000544518.5:c.*230_*231dup ENSP00000441068.1:n.*230_*231dup
NM_000795.3:c.*230_*231dup NP_000786.1:n.*230_*231dup
NM_016574.3:c.*230_*231dup NP_057658.2:n.*230_*231dup
XM_017017296.2:c.*230_*231dup XP_016872785.1:n.*230_*231dup
NM_000795.4:c.*230_*231dup MANE Select NP_000786.1:n.*230_*231dup
NM_016574.4:c.*230_*231dup NP_057658.2:n.*230_*231dup