Canonical Allele Identifier: CA2001168975
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414798_113414799delinsGC , CM000673.2:g.113414798_113414799delinsGC GRCh38
NC_000011.9:g.113285520_113285521delinsGC , CM000673.1:g.113285520_113285521delinsGC GRCh37
NC_000011.8:g.112790730_112790731delinsGC NCBI36
NG_008841.1:g.65481_65482delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.724-338_724-337delinsGC MANE Select ENSP00000354859.3:n.724-338_724-337delinsGC
ENST00000346454.7:c.723+622_723+623delinsGC ENSP00000278597.5:n.723+622_723+623delinsGC
ENST00000362072.7:c.724-338_724-337delinsGC ENSP00000354859.3:n.724-338_724-337delinsGC
ENST00000535984.1:n.443-338_443-337delinsGC
ENST00000538967.5:c.724-338_724-337delinsGC ENSP00000438215.1:n.724-338_724-337delinsGC
ENST00000540600.5:n.789-338_789-337delinsGC
ENST00000542968.5:c.724-338_724-337delinsGC ENSP00000442172.1:n.724-338_724-337delinsGC
ENST00000544518.5:c.721-338_721-337delinsGC ENSP00000441068.1:n.721-338_721-337delinsGC
NM_000795.3:c.724-338_724-337delinsGC NP_000786.1:n.724-338_724-337delinsGC
NM_016574.3:c.723+622_723+623delinsGC NP_057658.2:n.723+622_723+623delinsGC
XM_017017296.2:c.724-338_724-337delinsGC XP_016872785.1:n.724-338_724-337delinsGC
NM_000795.4:c.724-338_724-337delinsGC MANE Select NP_000786.1:n.724-338_724-337delinsGC
NM_016574.4:c.723+622_723+623delinsGC NP_057658.2:n.723+622_723+623delinsGC