Canonical Allele Identifier: CA6281212

Gene: DRD2

Linked Data

• dbSNP Id: rs765345269
• ExAC: 11:113283432 ATTC / A
• gnomAD v2: 11-113283432-ATTC-A
• gnomAD v4: 11-113412710-ATTC-A
• MyVariant Identifiers: chr11:g.113283433_113283435del (hg19) ; chr11:g.113412711_113412713del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412715_113412717del , CM000673.2:g.113412715_113412717del	GRCh38
NC_000011.9:g.113283437_113283439del , CM000673.1:g.113283437_113283439del	GRCh37
NC_000011.8:g.112788647_112788649del	NCBI36
NG_008841.1:g.67567_67569del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.981_983del MANE Select	ENSP00000354859.3:p.Lys327del
ENST00000346454.7:c.894_896del	ENSP00000278597.5:p.Lys298del
ENST00000362072.7:c.981_983del	ENSP00000354859.3:p.Lys327del
ENST00000538967.5:c.987_989del	ENSP00000438215.1:p.Lys329del
ENST00000542968.5:c.981_983del	ENSP00000442172.1:p.Lys327del
ENST00000544518.5:c.978_980del	ENSP00000441068.1:p.Lys326del
NM_000795.3:c.981_983del	NP_000786.1:p.Lys327del
NM_016574.3:c.894_896del	NP_057658.2:p.Lys298del
XM_017017296.2:c.981_983del	XP_016872785.1:p.Lys327del
NM_000795.4:c.981_983del MANE Select	NP_000786.1:p.Lys327del
NM_016574.4:c.894_896del	NP_057658.2:p.Lys298del