Canonical Allele Identifier: CA382650156

Gene: DRD2

Linked Data

• MyVariant Identifiers: chr11:g.113283452G>C (hg19) ; chr11:g.113412730G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412730G>C , CM000673.2:g.113412730G>C	GRCh38
NC_000011.9:g.113283452G>C , CM000673.1:g.113283452G>C	GRCh37
NC_000011.8:g.112788662G>C	NCBI36
NG_008841.1:g.67550C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.964C>G MANE Select	ENSP00000354859.3:p.Pro322Ala
ENST00000346454.7:c.877C>G	ENSP00000278597.5:p.Pro293Ala
ENST00000362072.7:c.964C>G	ENSP00000354859.3:p.Pro322Ala
ENST00000538967.5:c.970C>G	ENSP00000438215.1:p.Pro324Ala
ENST00000542968.5:c.964C>G	ENSP00000442172.1:p.Pro322Ala
ENST00000544518.5:c.961C>G	ENSP00000441068.1:p.Pro321Ala
NM_000795.3:c.964C>G	NP_000786.1:p.Pro322Ala
NM_016574.3:c.877C>G	NP_057658.2:p.Pro293Ala
XM_017017296.2:c.964C>G	XP_016872785.1:p.Pro322Ala
NM_000795.4:c.964C>G MANE Select	NP_000786.1:p.Pro322Ala
NM_016574.4:c.877C>G	NP_057658.2:p.Pro293Ala