Canonical Allele Identifier: CA654518895

Gene: DRD2

Linked Data

• COSMIC: COSN22865165

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414662_113414680del , CM000673.2:g.113414662_113414680del	GRCh38
NC_000011.9:g.113285384_113285402del , CM000673.1:g.113285384_113285402del	GRCh37
NC_000011.8:g.112790594_112790612del	NCBI36
NG_008841.1:g.65602_65620del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-217_724-199del MANE Select	ENSP00000354859.3:n.724-217_724-199del
ENST00000346454.7:c.723+743_723+761del	ENSP00000278597.5:n.723+743_723+761del
ENST00000362072.7:c.724-217_724-199del	ENSP00000354859.3:n.724-217_724-199del
ENST00000535984.1:n.443-217_443-199del
ENST00000538967.5:c.724-217_724-199del	ENSP00000438215.1:n.724-217_724-199del
ENST00000540600.5:n.789-217_789-199del
ENST00000542968.5:c.724-217_724-199del	ENSP00000442172.1:n.724-217_724-199del
ENST00000544518.5:c.721-217_721-199del	ENSP00000441068.1:n.721-217_721-199del
NM_000795.3:c.724-217_724-199del	NP_000786.1:n.724-217_724-199del
NM_016574.3:c.723+743_723+761del	NP_057658.2:n.723+743_723+761del
XM_017017296.2:c.724-217_724-199del	XP_016872785.1:n.724-217_724-199del
NM_000795.4:c.724-217_724-199del MANE Select	NP_000786.1:n.724-217_724-199del
NM_016574.4:c.723+743_723+761del	NP_057658.2:n.723+743_723+761del