Canonical Allele Identifier: CA671883352

Gene: DRD2

Linked Data

• dbSNP Id: rs1418141786
• MyVariant Identifiers: chr11:g.113309858_113309865del (hg19) ; chr11:g.113439136_113439143del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439137_113439144del , CM000673.2:g.113439137_113439144del	GRCh38
NC_000011.9:g.113309859_113309866del , CM000673.1:g.113309859_113309866del	GRCh37
NC_000011.8:g.112815069_112815076del	NCBI36
NG_008841.1:g.41137_41144del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.-31-14461_-31-14454del MANE Select	ENSP00000354859.3:n.-31-14461_-31-14454del
ENST00000346454.7:c.-31-14461_-31-14454del	ENSP00000278597.5:n.-31-14461_-31-14454del
ENST00000362072.7:c.-31-14461_-31-14454del	ENSP00000354859.3:n.-31-14461_-31-14454del
ENST00000540600.5:n.35-14461_35-14454del
ENST00000542616.1:c.-31-14461_-31-14454del	ENSP00000441474.1:n.-31-14461_-31-14454del
ENST00000543292.1:c.-32+8428_-32+8435del	ENSP00000438419.1:n.-32+8428_-32+8435del
NM_000795.3:c.-31-14461_-31-14454del	NP_000786.1:n.-31-14461_-31-14454del
NM_016574.3:c.-31-14461_-31-14454del	NP_057658.2:n.-31-14461_-31-14454del
XM_017017296.2:c.-31-14461_-31-14454del	XP_016872785.1:n.-31-14461_-31-14454del
NM_000795.4:c.-31-14461_-31-14454del MANE Select	NP_000786.1:n.-31-14461_-31-14454del
NM_016574.4:c.-31-14461_-31-14454del	NP_057658.2:n.-31-14461_-31-14454del