Canonical Allele Identifier: CA2001171797

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113420921C= , CM000673.2:g.113420921C=	GRCh38
NC_000011.9:g.113291643C= , CM000673.1:g.113291643C=	GRCh37
NC_000011.8:g.112796853C=	NCBI36
NG_008841.1:g.59359G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.286-2785G= MANE Select	ENSP00000354859.3:n.286-2785G=
ENST00000346454.7:c.286-2785G=	ENSP00000278597.5:n.286-2785G=
ENST00000362072.7:c.286-2785G=	ENSP00000354859.3:n.286-2785G=
ENST00000535984.1:n.142-2785G=
ENST00000538967.5:c.286-2785G=	ENSP00000438215.1:n.286-2785G=
ENST00000540600.5:n.351-2785G=
ENST00000542968.5:c.286-2785G=	ENSP00000442172.1:n.286-2785G=
ENST00000543292.1:c.286-2785G=	ENSP00000438419.1:n.286-2785G=
ENST00000544518.5:c.290-2792G=	ENSP00000441068.1:n.290-2792G=
NM_000795.3:c.286-2785G=	NP_000786.1:n.286-2785G=
NM_016574.3:c.286-2785G=	NP_057658.2:n.286-2785G=
XM_017017296.2:c.286-2785G=	XP_016872785.1:n.286-2785G=
NM_000795.4:c.286-2785G= MANE Select	NP_000786.1:n.286-2785G=
NM_016574.4:c.286-2785G=	NP_057658.2:n.286-2785G=