Canonical Allele Identifier: CA382650154

Gene: DRD2

Linked Data

• gnomAD v4: 11-113412730-G-T
• MyVariant Identifiers: chr11:g.113283452G>T (hg19) ; chr11:g.113412730G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.964C>A MANE Select	ENSP00000354859.3:p.Pro322Thr
ENST00000346454.7:c.877C>A	ENSP00000278597.5:p.Pro293Thr
ENST00000362072.7:c.964C>A	ENSP00000354859.3:p.Pro322Thr
ENST00000538967.5:c.970C>A	ENSP00000438215.1:p.Pro324Thr
ENST00000542968.5:c.964C>A	ENSP00000442172.1:p.Pro322Thr
ENST00000544518.5:c.961C>A	ENSP00000441068.1:p.Pro321Thr
NM_000795.3:c.964C>A	NP_000786.1:p.Pro322Thr
NM_016574.3:c.877C>A	NP_057658.2:p.Pro293Thr
XM_017017296.2:c.964C>A	XP_016872785.1:p.Pro322Thr
NM_000795.4:c.964C>A MANE Select	NP_000786.1:p.Pro322Thr
NM_016574.4:c.877C>A	NP_057658.2:p.Pro293Thr