Canonical Allele Identifier: CA671885521

Gene: DRD2

Linked Data

• dbSNP Id: rs1487481725
• gnomAD v3: 11-113442745-CTT-C
• gnomAD v4: 11-113442745-CTT-C
• MyVariant Identifiers: chr11:g.113313468_113313469del (hg19) ; chr11:g.113442746_113442747del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113442746_113442747del , CM000673.2:g.113442746_113442747del	GRCh38
NC_000011.9:g.113313468_113313469del , CM000673.1:g.113313468_113313469del	GRCh37
NC_000011.8:g.112818678_112818679del	NCBI36
NG_008841.1:g.37533_37534del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-18065_-31-18064del MANE Select	ENSP00000354859.3:n.-31-18065_-31-18064del
ENST00000346454.7:c.-31-18065_-31-18064del	ENSP00000278597.5:n.-31-18065_-31-18064del
ENST00000362072.7:c.-31-18065_-31-18064del	ENSP00000354859.3:n.-31-18065_-31-18064del
ENST00000540600.5:n.35-18065_35-18064del
ENST00000542616.1:c.-31-18065_-31-18064del	ENSP00000441474.1:n.-31-18065_-31-18064del
ENST00000543292.1:c.-32+4824_-32+4825del	ENSP00000438419.1:n.-32+4824_-32+4825del
NM_000795.3:c.-31-18065_-31-18064del	NP_000786.1:n.-31-18065_-31-18064del
NM_016574.3:c.-31-18065_-31-18064del	NP_057658.2:n.-31-18065_-31-18064del
XM_017017296.2:c.-31-18065_-31-18064del	XP_016872785.1:n.-31-18065_-31-18064del
NM_000795.4:c.-31-18065_-31-18064del MANE Select	NP_000786.1:n.-31-18065_-31-18064del
NM_016574.4:c.-31-18065_-31-18064del	NP_057658.2:n.-31-18065_-31-18064del