Canonical Allele Identifier: CA2001167163

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410811A= , CM000673.2:g.113410811A=	GRCh38
NC_000011.9:g.113281533A= , CM000673.1:g.113281533A=	GRCh37
NC_000011.8:g.112786743A=	NCBI36
NG_008841.1:g.69469T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1248T= MANE Select	ENSP00000354859.3:p.Tyr416=
ENST00000346454.7:c.1161T=	ENSP00000278597.5:p.Tyr387=
ENST00000362072.7:c.1248T=	ENSP00000354859.3:p.Tyr416=
ENST00000538967.5:c.1254T=	ENSP00000438215.1:p.Tyr418=
ENST00000542968.5:c.1248T=	ENSP00000442172.1:p.Tyr416=
ENST00000544518.5:c.1245T=	ENSP00000441068.1:p.Tyr415=
NM_000795.3:c.1248T=	NP_000786.1:p.Tyr416=
NM_016574.3:c.1161T=	NP_057658.2:p.Tyr387=
XM_017017296.2:c.1248T=	XP_016872785.1:p.Tyr416=
NM_000795.4:c.1248T= MANE Select	NP_000786.1:p.Tyr416=
NM_016574.4:c.1161T=	NP_057658.2:p.Tyr387=