Canonical Allele Identifier: CA2001169438

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113415790G= , CM000673.2:g.113415790G=	GRCh38
NC_000011.9:g.113286512G= , CM000673.1:g.113286512G=	GRCh37
NC_000011.8:g.112791722G=	NCBI36
NG_008841.1:g.64490C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.533-179C= MANE Select	ENSP00000354859.3:n.533-179C=
ENST00000346454.7:c.533-179C=	ENSP00000278597.5:n.533-179C=
ENST00000362072.7:c.533-179C=	ENSP00000354859.3:n.533-179C=
ENST00000535984.1:n.252-179C=
ENST00000538967.5:c.533-179C=	ENSP00000438215.1:n.533-179C=
ENST00000539420.1:n.229-179C=
ENST00000540600.5:n.598-179C=
ENST00000542968.5:c.533-179C=	ENSP00000442172.1:n.533-179C=
ENST00000544518.5:c.530-179C=	ENSP00000441068.1:n.530-179C=
NM_000795.3:c.533-179C=	NP_000786.1:n.533-179C=
NM_016574.3:c.533-179C=	NP_057658.2:n.533-179C=
XM_017017296.2:c.533-179C=	XP_016872785.1:n.533-179C=
NM_000795.4:c.533-179C= MANE Select	NP_000786.1:n.533-179C=
NM_016574.4:c.533-179C=	NP_057658.2:n.533-179C=