Canonical Allele Identifier: CA671867065

Gene: DRD2

Linked Data

• dbSNP Id: rs1379005238
• gnomAD v4: 11-113414517-AG-A
• MyVariant Identifiers: chr11:g.113285240del (hg19) ; chr11:g.113414518del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414518del , CM000673.2:g.113414518del	GRCh38
NC_000011.9:g.113285240del , CM000673.1:g.113285240del	GRCh37
NC_000011.8:g.112790450del	NCBI36
NG_008841.1:g.65762del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-57del MANE Select	ENSP00000354859.3:n.724-57del
ENST00000346454.7:c.723+903del	ENSP00000278597.5:n.723+903del
ENST00000362072.7:c.724-57del	ENSP00000354859.3:n.724-57del
ENST00000535984.1:n.443-57del
ENST00000538967.5:c.724-57del	ENSP00000438215.1:n.724-57del
ENST00000540600.5:n.789-57del
ENST00000542968.5:c.724-57del	ENSP00000442172.1:n.724-57del
ENST00000544518.5:c.721-57del	ENSP00000441068.1:n.721-57del
NM_000795.3:c.724-57del	NP_000786.1:n.724-57del
NM_016574.3:c.723+903del	NP_057658.2:n.723+903del
XM_017017296.2:c.724-57del	XP_016872785.1:n.724-57del
NM_000795.4:c.724-57del MANE Select	NP_000786.1:n.724-57del
NM_016574.4:c.723+903del	NP_057658.2:n.723+903del