Canonical Allele Identifier: CA2616029380

Gene: DRD2

Linked Data

• gnomAD v4: 11-113410671-TGGCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410676_113410679del , CM000673.2:g.113410676_113410679del	GRCh38
NC_000011.9:g.113281398_113281401del , CM000673.1:g.113281398_113281401del	GRCh37
NC_000011.8:g.112786608_112786611del	NCBI36
NG_008841.1:g.69605_69608del

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.*52_*55del MANE Select	ENSP00000354859.3:n.*52_*55del
ENST00000346454.7:c.*52_*55del	ENSP00000278597.5:n.*52_*55del
ENST00000362072.7:c.*52_*55del	ENSP00000354859.3:n.*52_*55del
ENST00000538967.5:c.1390_1393del	ENSP00000438215.1:n.1390_1393del
ENST00000542968.5:c.*52_*55del	ENSP00000442172.1:n.*52_*55del
ENST00000544518.5:c.*52_*55del	ENSP00000441068.1:n.*52_*55del
NM_000795.3:c.*52_*55del	NP_000786.1:n.*52_*55del
NM_016574.3:c.*52_*55del	NP_057658.2:n.*52_*55del
XM_017017296.2:c.*52_*55del	XP_016872785.1:n.*52_*55del
NM_000795.4:c.*52_*55del MANE Select	NP_000786.1:n.*52_*55del
NM_016574.4:c.*52_*55del	NP_057658.2:n.*52_*55del