Canonical Allele Identifier: CA2001168829

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414508_113414510delinsAGG , CM000673.2:g.113414508_113414510delinsAGG	GRCh38
NC_000011.9:g.113285230_113285232delinsAGG , CM000673.1:g.113285230_113285232delinsAGG	GRCh37
NC_000011.8:g.112790440_112790442delinsAGG	NCBI36
NG_008841.1:g.65770_65772delinsCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-49_724-47delinsCCT MANE Select	ENSP00000354859.3:n.724-49_724-47delinsCCT
ENST00000346454.7:c.723+911_723+913delinsCCT	ENSP00000278597.5:n.723+911_723+913delinsCCT
ENST00000362072.7:c.724-49_724-47delinsCCT	ENSP00000354859.3:n.724-49_724-47delinsCCT
ENST00000535984.1:n.443-49_443-47delinsCCT
ENST00000538967.5:c.724-49_724-47delinsCCT	ENSP00000438215.1:n.724-49_724-47delinsCCT
ENST00000540600.5:n.789-49_789-47delinsCCT
ENST00000542968.5:c.724-49_724-47delinsCCT	ENSP00000442172.1:n.724-49_724-47delinsCCT
ENST00000544518.5:c.721-49_721-47delinsCCT	ENSP00000441068.1:n.721-49_721-47delinsCCT
NM_000795.3:c.724-49_724-47delinsCCT	NP_000786.1:n.724-49_724-47delinsCCT
NM_016574.3:c.723+911_723+913delinsCCT	NP_057658.2:n.723+911_723+913delinsCCT
XM_017017296.2:c.724-49_724-47delinsCCT	XP_016872785.1:n.724-49_724-47delinsCCT
NM_000795.4:c.724-49_724-47delinsCCT MANE Select	NP_000786.1:n.724-49_724-47delinsCCT
NM_016574.4:c.723+911_723+913delinsCCT	NP_057658.2:n.723+911_723+913delinsCCT