Canonical Allele Identifier: CA942359624

Gene: DRD2

Linked Data

• dbSNP Id: rs1950762176
• gnomAD v3: 11-113410812-T-TTAAAAA
• gnomAD v4: 11-113410812-T-TTAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410812_113410813insTAAAAA , CM000673.2:g.113410812_113410813insTAAAAA	GRCh38
NC_000011.9:g.113281534_113281535insTAAAAA , CM000673.1:g.113281534_113281535insTAAAAA	GRCh37
NC_000011.8:g.112786744_112786745insTAAAAA	NCBI36
NG_008841.1:g.69467_69468insTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1246_1247insTTTTTA MANE Select	ENSP00000354859.3:p.Tyr416delinsPhePheAsn
ENST00000346454.7:c.1159_1160insTTTTTA	ENSP00000278597.5:p.Tyr387delinsPhePheAsn
ENST00000362072.7:c.1246_1247insTTTTTA	ENSP00000354859.3:p.Tyr416delinsPhePheAsn
ENST00000538967.5:c.1252_1253insTTTTTA	ENSP00000438215.1:p.Tyr418delinsPhePheAsn
ENST00000542968.5:c.1246_1247insTTTTTA	ENSP00000442172.1:p.Tyr416delinsPhePheAsn
ENST00000544518.5:c.1243_1244insTTTTTA	ENSP00000441068.1:p.Tyr415delinsPhePheAsn
NM_000795.3:c.1246_1247insTTTTTA	NP_000786.1:p.Tyr416delinsPhePheAsn
NM_016574.3:c.1159_1160insTTTTTA	NP_057658.2:p.Tyr387delinsPhePheAsn
XM_017017296.2:c.1246_1247insTTTTTA	XP_016872785.1:p.Tyr416delinsPhePheAsn
NM_000795.4:c.1246_1247insTTTTTA MANE Select	NP_000786.1:p.Tyr416delinsPhePheAsn
NM_016574.4:c.1159_1160insTTTTTA	NP_057658.2:p.Tyr387delinsPhePheAsn