Canonical Allele Identifier: CA671867253

Gene: DRD2

Linked Data

• dbSNP Id: rs1365806274
• MyVariant Identifiers: chr11:g.113285484del (hg19) ; chr11:g.113414762del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414763del , CM000673.2:g.113414763del	GRCh38
NC_000011.9:g.113285485del , CM000673.1:g.113285485del	GRCh37
NC_000011.8:g.112790695del	NCBI36
NG_008841.1:g.65518del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-301del MANE Select	ENSP00000354859.3:n.724-301del
ENST00000346454.7:c.723+659del	ENSP00000278597.5:n.723+659del
ENST00000362072.7:c.724-301del	ENSP00000354859.3:n.724-301del
ENST00000535984.1:n.443-301del
ENST00000538967.5:c.724-301del	ENSP00000438215.1:n.724-301del
ENST00000540600.5:n.789-301del
ENST00000542968.5:c.724-301del	ENSP00000442172.1:n.724-301del
ENST00000544518.5:c.721-301del	ENSP00000441068.1:n.721-301del
NM_000795.3:c.724-301del	NP_000786.1:n.724-301del
NM_016574.3:c.723+659del	NP_057658.2:n.723+659del
XM_017017296.2:c.724-301del	XP_016872785.1:n.724-301del
NM_000795.4:c.724-301del MANE Select	NP_000786.1:n.724-301del
NM_016574.4:c.723+659del	NP_057658.2:n.723+659del