Canonical Allele Identifier: CA2001168986

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414823_113414826delinsTAAG , CM000673.2:g.113414823_113414826delinsTAAG	GRCh38
NC_000011.9:g.113285545_113285548delinsTAAG , CM000673.1:g.113285545_113285548delinsTAAG	GRCh37
NC_000011.8:g.112790755_112790758delinsTAAG	NCBI36
NG_008841.1:g.65454_65457delinsCTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-365_724-362delinsCTTA MANE Select	ENSP00000354859.3:n.724-365_724-362delinsCTTA
ENST00000346454.7:c.723+595_723+598delinsCTTA	ENSP00000278597.5:n.723+595_723+598delinsCTTA
ENST00000362072.7:c.724-365_724-362delinsCTTA	ENSP00000354859.3:n.724-365_724-362delinsCTTA
ENST00000535984.1:n.443-365_443-362delinsCTTA
ENST00000538967.5:c.724-365_724-362delinsCTTA	ENSP00000438215.1:n.724-365_724-362delinsCTTA
ENST00000540600.5:n.789-365_789-362delinsCTTA
ENST00000542968.5:c.724-365_724-362delinsCTTA	ENSP00000442172.1:n.724-365_724-362delinsCTTA
ENST00000544518.5:c.721-365_721-362delinsCTTA	ENSP00000441068.1:n.721-365_721-362delinsCTTA
NM_000795.3:c.724-365_724-362delinsCTTA	NP_000786.1:n.724-365_724-362delinsCTTA
NM_016574.3:c.723+595_723+598delinsCTTA	NP_057658.2:n.723+595_723+598delinsCTTA
XM_017017296.2:c.724-365_724-362delinsCTTA	XP_016872785.1:n.724-365_724-362delinsCTTA
NM_000795.4:c.724-365_724-362delinsCTTA MANE Select	NP_000786.1:n.724-365_724-362delinsCTTA
NM_016574.4:c.723+595_723+598delinsCTTA	NP_057658.2:n.723+595_723+598delinsCTTA