Canonical Allele Identifier: CA942360430

Gene: DRD2

Linked Data

• gnomAD v3: 11-113412779-C-CATTAAAAA
• gnomAD v4: 11-113412779-C-CATTAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113412780_113412781insTTAAAAAA , CM000673.2:g.113412780_113412781insTTAAAAAA	GRCh38
NC_000011.9:g.113283502_113283503insTTAAAAAA , CM000673.1:g.113283502_113283503insTTAAAAAA	GRCh37
NC_000011.8:g.112788712_112788713insTTAAAAAA	NCBI36
NG_008841.1:g.67500_67501insTTTTTAAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.914_915insTTTTTAAT MANE Select	ENSP00000354859.3:p.Thr306PhefsTer2
ENST00000346454.7:c.827_828insTTTTTAAT	ENSP00000278597.5:p.Thr277PhefsTer2
ENST00000362072.7:c.914_915insTTTTTAAT	ENSP00000354859.3:p.Thr306PhefsTer2
ENST00000538967.5:c.920_921insTTTTTAAT	ENSP00000438215.1:p.Thr308PhefsTer2
ENST00000542968.5:c.914_915insTTTTTAAT	ENSP00000442172.1:p.Thr306PhefsTer2
ENST00000544518.5:c.911_912insTTTTTAAT	ENSP00000441068.1:p.Thr305PhefsTer2
NM_000795.3:c.914_915insTTTTTAAT	NP_000786.1:p.Thr306PhefsTer2
NM_016574.3:c.827_828insTTTTTAAT	NP_057658.2:p.Thr277PhefsTer2
XM_017017296.2:c.914_915insTTTTTAAT	XP_016872785.1:p.Thr306PhefsTer2
NM_000795.4:c.914_915insTTTTTAAT MANE Select	NP_000786.1:p.Thr306PhefsTer2
NM_016574.4:c.827_828insTTTTTAAT	NP_057658.2:p.Thr277PhefsTer2