Canonical Allele Identifier: CA2001169025

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414903_113414904delinsGC , CM000673.2:g.113414903_113414904delinsGC	GRCh38
NC_000011.9:g.113285625_113285626delinsGC , CM000673.1:g.113285625_113285626delinsGC	GRCh37
NC_000011.8:g.112790835_112790836delinsGC	NCBI36
NG_008841.1:g.65376_65377delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.724-443_724-442delinsGC MANE Select	ENSP00000354859.3:n.724-443_724-442delinsGC
ENST00000346454.7:c.723+517_723+518delinsGC	ENSP00000278597.5:n.723+517_723+518delinsGC
ENST00000362072.7:c.724-443_724-442delinsGC	ENSP00000354859.3:n.724-443_724-442delinsGC
ENST00000535984.1:n.443-443_443-442delinsGC
ENST00000538967.5:c.724-443_724-442delinsGC	ENSP00000438215.1:n.724-443_724-442delinsGC
ENST00000540600.5:n.789-443_789-442delinsGC
ENST00000542968.5:c.724-443_724-442delinsGC	ENSP00000442172.1:n.724-443_724-442delinsGC
ENST00000544518.5:c.721-443_721-442delinsGC	ENSP00000441068.1:n.721-443_721-442delinsGC
NM_000795.3:c.724-443_724-442delinsGC	NP_000786.1:n.724-443_724-442delinsGC
NM_016574.3:c.723+517_723+518delinsGC	NP_057658.2:n.723+517_723+518delinsGC
XM_017017296.2:c.724-443_724-442delinsGC	XP_016872785.1:n.724-443_724-442delinsGC
NM_000795.4:c.724-443_724-442delinsGC MANE Select	NP_000786.1:n.724-443_724-442delinsGC
NM_016574.4:c.723+517_723+518delinsGC	NP_057658.2:n.723+517_723+518delinsGC