Canonical Allele Identifier: CA2001167129

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410726G= , CM000673.2:g.113410726G=	GRCh38
NC_000011.9:g.113281448G= , CM000673.1:g.113281448G=	GRCh37
NC_000011.8:g.112786658G=	NCBI36
NG_008841.1:g.69554C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*1C= MANE Select	ENSP00000354859.3:n.*1C=
ENST00000346454.7:c.*1C=	ENSP00000278597.5:n.*1C=
ENST00000362072.7:c.*1C=	ENSP00000354859.3:n.*1C=
ENST00000538967.5:c.1339C=	ENSP00000438215.1:n.1339C=
ENST00000542968.5:c.*1C=	ENSP00000442172.1:n.*1C=
ENST00000544518.5:c.*1C=	ENSP00000441068.1:n.*1C=
NM_000795.3:c.*1C=	NP_000786.1:n.*1C=
NM_016574.3:c.*1C=	NP_057658.2:n.*1C=
XM_017017296.2:c.*1C=	XP_016872785.1:n.*1C=
NM_000795.4:c.*1C= MANE Select	NP_000786.1:n.*1C=
NM_016574.4:c.*1C=	NP_057658.2:n.*1C=