Canonical Allele Identifier: CA2001167139

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410755T= , CM000673.2:g.113410755T=	GRCh38
NC_000011.9:g.113281477T= , CM000673.1:g.113281477T=	GRCh37
NC_000011.8:g.112786687T=	NCBI36
NG_008841.1:g.69525A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1304A= MANE Select	ENSP00000354859.3:p.Lys435=
ENST00000346454.7:c.1217A=	ENSP00000278597.5:p.Lys406=
ENST00000362072.7:c.1304A=	ENSP00000354859.3:p.Lys435=
ENST00000538967.5:c.1310A=	ENSP00000438215.1:p.Lys437=
ENST00000542968.5:c.1304A=	ENSP00000442172.1:p.Lys435=
ENST00000544518.5:c.1301A=	ENSP00000441068.1:p.Lys434=
NM_000795.3:c.1304A=	NP_000786.1:p.Lys435=
NM_016574.3:c.1217A=	NP_057658.2:p.Lys406=
XM_017017296.2:c.1304A=	XP_016872785.1:p.Lys435=
NM_000795.4:c.1304A= MANE Select	NP_000786.1:p.Lys435=
NM_016574.4:c.1217A=	NP_057658.2:p.Lys406=