Canonical Allele Identifier: CA2793679101
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414614dup , CM000673.2:g.113414614dup GRCh38
NC_000011.9:g.113285336dup , CM000673.1:g.113285336dup GRCh37
NC_000011.8:g.112790546dup NCBI36
NG_008841.1:g.65670dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.724-149dup MANE Select ENSP00000354859.3:n.724-149dup
ENST00000346454.7:c.723+811dup ENSP00000278597.5:n.723+811dup
ENST00000362072.7:c.724-149dup ENSP00000354859.3:n.724-149dup
ENST00000535984.1:n.443-149dup
ENST00000538967.5:c.724-149dup ENSP00000438215.1:n.724-149dup
ENST00000540600.5:n.789-149dup
ENST00000542968.5:c.724-149dup ENSP00000442172.1:n.724-149dup
ENST00000544518.5:c.721-149dup ENSP00000441068.1:n.721-149dup
NM_000795.3:c.724-149dup NP_000786.1:n.724-149dup
NM_016574.3:c.723+811dup NP_057658.2:n.723+811dup
XM_017017296.2:c.724-149dup XP_016872785.1:n.724-149dup
NM_000795.4:c.724-149dup MANE Select NP_000786.1:n.724-149dup
NM_016574.4:c.723+811dup NP_057658.2:n.723+811dup