Canonical Allele Identifier: CA2001168908
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414668_113414669delinsGT , CM000673.2:g.113414668_113414669delinsGT GRCh38
NC_000011.9:g.113285390_113285391delinsGT , CM000673.1:g.113285390_113285391delinsGT GRCh37
NC_000011.8:g.112790600_112790601delinsGT NCBI36
NG_008841.1:g.65611_65612delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.724-208_724-207delinsAC MANE Select ENSP00000354859.3:n.724-208_724-207delinsAC
ENST00000346454.7:c.723+752_723+753delinsAC ENSP00000278597.5:n.723+752_723+753delinsAC
ENST00000362072.7:c.724-208_724-207delinsAC ENSP00000354859.3:n.724-208_724-207delinsAC
ENST00000535984.1:n.443-208_443-207delinsAC
ENST00000538967.5:c.724-208_724-207delinsAC ENSP00000438215.1:n.724-208_724-207delinsAC
ENST00000540600.5:n.789-208_789-207delinsAC
ENST00000542968.5:c.724-208_724-207delinsAC ENSP00000442172.1:n.724-208_724-207delinsAC
ENST00000544518.5:c.721-208_721-207delinsAC ENSP00000441068.1:n.721-208_721-207delinsAC
NM_000795.3:c.724-208_724-207delinsAC NP_000786.1:n.724-208_724-207delinsAC
NM_016574.3:c.723+752_723+753delinsAC NP_057658.2:n.723+752_723+753delinsAC
XM_017017296.2:c.724-208_724-207delinsAC XP_016872785.1:n.724-208_724-207delinsAC
NM_000795.4:c.724-208_724-207delinsAC MANE Select NP_000786.1:n.724-208_724-207delinsAC
NM_016574.4:c.723+752_723+753delinsAC NP_057658.2:n.723+752_723+753delinsAC