Canonical Allele Identifier: CA671867405

Gene: DRD2

Linked Data

• dbSNP Id: rs1200183317
• gnomAD v3: 11-113414905-CCA-C
• gnomAD v4: 11-113414905-CCA-C
• MyVariant Identifiers: chr11:g.113285628_113285629del (hg19) ; chr11:g.113414906_113414907del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414911_113414912del , CM000673.2:g.113414911_113414912del	GRCh38
NC_000011.9:g.113285633_113285634del , CM000673.1:g.113285633_113285634del	GRCh37
NC_000011.8:g.112790843_112790844del	NCBI36
NG_008841.1:g.65373_65374del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-446_724-445del MANE Select	ENSP00000354859.3:n.724-446_724-445del
ENST00000346454.7:c.723+514_723+515del	ENSP00000278597.5:n.723+514_723+515del
ENST00000362072.7:c.724-446_724-445del	ENSP00000354859.3:n.724-446_724-445del
ENST00000535984.1:n.443-446_443-445del
ENST00000538967.5:c.724-446_724-445del	ENSP00000438215.1:n.724-446_724-445del
ENST00000540600.5:n.789-446_789-445del
ENST00000542968.5:c.724-446_724-445del	ENSP00000442172.1:n.724-446_724-445del
ENST00000544518.5:c.721-446_721-445del	ENSP00000441068.1:n.721-446_721-445del
NM_000795.3:c.724-446_724-445del	NP_000786.1:n.724-446_724-445del
NM_016574.3:c.723+514_723+515del	NP_057658.2:n.723+514_723+515del
XM_017017296.2:c.724-446_724-445del	XP_016872785.1:n.724-446_724-445del
NM_000795.4:c.724-446_724-445del MANE Select	NP_000786.1:n.724-446_724-445del
NM_016574.4:c.723+514_723+515del	NP_057658.2:n.723+514_723+515del