Canonical Allele Identifier: CA2001167985

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412719T= , CM000673.2:g.113412719T=	GRCh38
NC_000011.9:g.113283441T= , CM000673.1:g.113283441T=	GRCh37
NC_000011.8:g.112788651T=	NCBI36
NG_008841.1:g.67561A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.975A= MANE Select	ENSP00000354859.3:p.Pro325=
ENST00000346454.7:c.888A=	ENSP00000278597.5:p.Pro296=
ENST00000362072.7:c.975A=	ENSP00000354859.3:p.Pro325=
ENST00000538967.5:c.981A=	ENSP00000438215.1:p.Pro327=
ENST00000542968.5:c.975A=	ENSP00000442172.1:p.Pro325=
ENST00000544518.5:c.972A=	ENSP00000441068.1:p.Pro324=
NM_000795.3:c.975A=	NP_000786.1:p.Pro325=
NM_016574.3:c.888A=	NP_057658.2:p.Pro296=
XM_017017296.2:c.975A=	XP_016872785.1:p.Pro325=
NM_000795.4:c.975A= MANE Select	NP_000786.1:p.Pro325=
NM_016574.4:c.888A=	NP_057658.2:p.Pro296=