Canonical Allele Identifier: CA2616029180

Gene: DRD2

Linked Data

• gnomAD v4: 11-113410479-TGAGCTGCCCC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410480_113410489del , CM000673.2:g.113410480_113410489del	GRCh38
NC_000011.9:g.113281202_113281211del , CM000673.1:g.113281202_113281211del	GRCh37
NC_000011.8:g.112786412_112786421del	NCBI36
NG_008841.1:g.69791_69800del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.*238_*247del MANE Select	ENSP00000354859.3:n.*238_*247del
ENST00000346454.7:c.*238_*247del	ENSP00000278597.5:n.*238_*247del
ENST00000362072.7:c.*238_*247del	ENSP00000354859.3:n.*238_*247del
ENST00000542968.5:c.*238_*247del	ENSP00000442172.1:n.*238_*247del
ENST00000544518.5:c.*238_*247del	ENSP00000441068.1:n.*238_*247del
NM_000795.3:c.*238_*247del	NP_000786.1:n.*238_*247del
NM_016574.3:c.*238_*247del	NP_057658.2:n.*238_*247del
XM_017017296.2:c.*238_*247del	XP_016872785.1:n.*238_*247del
NM_000795.4:c.*238_*247del MANE Select	NP_000786.1:n.*238_*247del
NM_016574.4:c.*238_*247del	NP_057658.2:n.*238_*247del