Canonical Allele Identifier: CA2001168011

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412768T= , CM000673.2:g.113412768T=	GRCh38
NC_000011.9:g.113283490T= , CM000673.1:g.113283490T=	GRCh37
NC_000011.8:g.112788700T=	NCBI36
NG_008841.1:g.67512A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.926A= MANE Select	ENSP00000354859.3:p.Asp309=
ENST00000346454.7:c.839A=	ENSP00000278597.5:p.Asp280=
ENST00000362072.7:c.926A=	ENSP00000354859.3:p.Asp309=
ENST00000538967.5:c.932A=	ENSP00000438215.1:p.Asp311=
ENST00000542968.5:c.926A=	ENSP00000442172.1:p.Asp309=
ENST00000544518.5:c.923A=	ENSP00000441068.1:p.Asp308=
NM_000795.3:c.926A=	NP_000786.1:p.Asp309=
NM_016574.3:c.839A=	NP_057658.2:p.Asp280=
XM_017017296.2:c.926A=	XP_016872785.1:p.Asp309=
NM_000795.4:c.926A= MANE Select	NP_000786.1:p.Asp309=
NM_016574.4:c.839A=	NP_057658.2:p.Asp280=