Canonical Allele Identifier: CA2001168008

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412765G= , CM000673.2:g.113412765G=	GRCh38
NC_000011.9:g.113283487G= , CM000673.1:g.113283487G=	GRCh37
NC_000011.8:g.112788697G=	NCBI36
NG_008841.1:g.67515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.929C= MANE Select	ENSP00000354859.3:p.Pro310=
ENST00000346454.7:c.842C=	ENSP00000278597.5:p.Pro281=
ENST00000362072.7:c.929C=	ENSP00000354859.3:p.Pro310=
ENST00000538967.5:c.935C=	ENSP00000438215.1:p.Pro312=
ENST00000542968.5:c.929C=	ENSP00000442172.1:p.Pro310=
ENST00000544518.5:c.926C=	ENSP00000441068.1:p.Pro309=
NM_000795.3:c.929C=	NP_000786.1:p.Pro310=
NM_016574.3:c.842C=	NP_057658.2:p.Pro281=
XM_017017296.2:c.929C=	XP_016872785.1:p.Pro310=
NM_000795.4:c.929C= MANE Select	NP_000786.1:p.Pro310=
NM_016574.4:c.842C=	NP_057658.2:p.Pro281=