Canonical Allele Identifier: CA2001167961

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412657A= , CM000673.2:g.113412657A=	GRCh38
NC_000011.9:g.113283379A= , CM000673.1:g.113283379A=	GRCh37
NC_000011.8:g.112788589A=	NCBI36
NG_008841.1:g.67623T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.1037T= MANE Select	ENSP00000354859.3:p.Met346=
ENST00000346454.7:c.950T=	ENSP00000278597.5:p.Met317=
ENST00000362072.7:c.1037T=	ENSP00000354859.3:p.Met346=
ENST00000538967.5:c.1043T=	ENSP00000438215.1:p.Met348=
ENST00000542968.5:c.1037T=	ENSP00000442172.1:p.Met346=
ENST00000544518.5:c.1034T=	ENSP00000441068.1:p.Met345=
NM_000795.3:c.1037T=	NP_000786.1:p.Met346=
NM_016574.3:c.950T=	NP_057658.2:p.Met317=
XM_017017296.2:c.1037T=	XP_016872785.1:p.Met346=
NM_000795.4:c.1037T= MANE Select	NP_000786.1:p.Met346=
NM_016574.4:c.950T=	NP_057658.2:p.Met317=