Canonical Allele Identifier: CA2001168961

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414761_113414762delinsTG , CM000673.2:g.113414761_113414762delinsTG	GRCh38
NC_000011.9:g.113285483_113285484delinsTG , CM000673.1:g.113285483_113285484delinsTG	GRCh37
NC_000011.8:g.112790693_112790694delinsTG	NCBI36
NG_008841.1:g.65518_65519delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-301_724-300delinsCA MANE Select	ENSP00000354859.3:n.724-301_724-300delinsCA
ENST00000346454.7:c.723+659_723+660delinsCA	ENSP00000278597.5:n.723+659_723+660delinsCA
ENST00000362072.7:c.724-301_724-300delinsCA	ENSP00000354859.3:n.724-301_724-300delinsCA
ENST00000535984.1:n.443-301_443-300delinsCA
ENST00000538967.5:c.724-301_724-300delinsCA	ENSP00000438215.1:n.724-301_724-300delinsCA
ENST00000540600.5:n.789-301_789-300delinsCA
ENST00000542968.5:c.724-301_724-300delinsCA	ENSP00000442172.1:n.724-301_724-300delinsCA
ENST00000544518.5:c.721-301_721-300delinsCA	ENSP00000441068.1:n.721-301_721-300delinsCA
NM_000795.3:c.724-301_724-300delinsCA	NP_000786.1:n.724-301_724-300delinsCA
NM_016574.3:c.723+659_723+660delinsCA	NP_057658.2:n.723+659_723+660delinsCA
XM_017017296.2:c.724-301_724-300delinsCA	XP_016872785.1:n.724-301_724-300delinsCA
NM_000795.4:c.724-301_724-300delinsCA MANE Select	NP_000786.1:n.724-301_724-300delinsCA
NM_016574.4:c.723+659_723+660delinsCA	NP_057658.2:n.723+659_723+660delinsCA