Canonical Allele Identifier: CA2001167513

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113411573T= , CM000673.2:g.113411573T=	GRCh38
NC_000011.9:g.113282295T= , CM000673.1:g.113282295T=	GRCh37
NC_000011.8:g.112787505T=	NCBI36
NG_008841.1:g.68707A=

Transcript Alleles

HGVS	Amino-acid Change
NM_000795.4:c.1139-653A= MANE Select	NP_000786.1:n.1139-653A=
ENST00000362072.8:c.1139-653A= MANE Select	ENSP00000354859.3:n.1139-653A=
NM_000795.3:c.1139-653A=	NP_000786.1:n.1139-653A=
NM_016574.3:c.1052-653A=	NP_057658.2:n.1052-653A=
NM_016574.4:c.1052-653A=	NP_057658.2:n.1052-653A=
ENST00000346454.7:c.1052-653A=	ENSP00000278597.5:n.1052-653A=
ENST00000362072.7:c.1139-653A=	ENSP00000354859.3:n.1139-653A=
ENST00000538967.5:c.1145-653A=	ENSP00000438215.1:n.1145-653A=
ENST00000542968.5:c.1139-653A=	ENSP00000442172.1:n.1139-653A=
ENST00000544518.5:c.1136-653A=	ENSP00000441068.1:n.1136-653A=
XM_017017296.2:c.1139-653A=	XP_016872785.1:n.1139-653A=