Canonical Allele Identifier: CA942361014

Gene: DRD2

Linked Data

• dbSNP Id: rs1950802882
• gnomAD v3: 11-113414502-GGATGGAGGGGGGACA-G
• gnomAD v4: 11-113414502-GGATGGAGGGGGGACA-G

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414505_113414519del , CM000673.2:g.113414505_113414519del	GRCh38
NC_000011.9:g.113285227_113285241del , CM000673.1:g.113285227_113285241del	GRCh37
NC_000011.8:g.112790437_112790451del	NCBI36
NG_008841.1:g.65763_65777del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-56_724-42del MANE Select	ENSP00000354859.3:n.724-56_724-42del
ENST00000346454.7:c.723+904_723+918del	ENSP00000278597.5:n.723+904_723+918del
ENST00000362072.7:c.724-56_724-42del	ENSP00000354859.3:n.724-56_724-42del
ENST00000535984.1:n.443-56_443-42del
ENST00000538967.5:c.724-56_724-42del	ENSP00000438215.1:n.724-56_724-42del
ENST00000540600.5:n.789-56_789-42del
ENST00000542968.5:c.724-56_724-42del	ENSP00000442172.1:n.724-56_724-42del
ENST00000544518.5:c.721-56_721-42del	ENSP00000441068.1:n.721-56_721-42del
NM_000795.3:c.724-56_724-42del	NP_000786.1:n.724-56_724-42del
NM_016574.3:c.723+904_723+918del	NP_057658.2:n.723+904_723+918del
XM_017017296.2:c.724-56_724-42del	XP_016872785.1:n.724-56_724-42del
NM_000795.4:c.724-56_724-42del MANE Select	NP_000786.1:n.724-56_724-42del
NM_016574.4:c.723+904_723+918del	NP_057658.2:n.723+904_723+918del