Canonical Allele Identifier: CA2001168886

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414626_113414627delinsGA , CM000673.2:g.113414626_113414627delinsGA	GRCh38
NC_000011.9:g.113285348_113285349delinsGA , CM000673.1:g.113285348_113285349delinsGA	GRCh37
NC_000011.8:g.112790558_112790559delinsGA	NCBI36
NG_008841.1:g.65653_65654delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-166_724-165delinsTC MANE Select	ENSP00000354859.3:n.724-166_724-165delinsTC
ENST00000346454.7:c.723+794_723+795delinsTC	ENSP00000278597.5:n.723+794_723+795delinsTC
ENST00000362072.7:c.724-166_724-165delinsTC	ENSP00000354859.3:n.724-166_724-165delinsTC
ENST00000535984.1:n.443-166_443-165delinsTC
ENST00000538967.5:c.724-166_724-165delinsTC	ENSP00000438215.1:n.724-166_724-165delinsTC
ENST00000540600.5:n.789-166_789-165delinsTC
ENST00000542968.5:c.724-166_724-165delinsTC	ENSP00000442172.1:n.724-166_724-165delinsTC
ENST00000544518.5:c.721-166_721-165delinsTC	ENSP00000441068.1:n.721-166_721-165delinsTC
NM_000795.3:c.724-166_724-165delinsTC	NP_000786.1:n.724-166_724-165delinsTC
NM_016574.3:c.723+794_723+795delinsTC	NP_057658.2:n.723+794_723+795delinsTC
XM_017017296.2:c.724-166_724-165delinsTC	XP_016872785.1:n.724-166_724-165delinsTC
NM_000795.4:c.724-166_724-165delinsTC MANE Select	NP_000786.1:n.724-166_724-165delinsTC
NM_016574.4:c.723+794_723+795delinsTC	NP_057658.2:n.723+794_723+795delinsTC