Canonical Allele Identifier: CA2001159405

Gene: DRD2

Linked Data

• dbSNP Id: rs1951062747

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113438959_113438965del , CM000673.2:g.113438959_113438965del	GRCh38
NC_000011.9:g.113309681_113309687del , CM000673.1:g.113309681_113309687del	GRCh37
NC_000011.8:g.112814891_112814897del	NCBI36
NG_008841.1:g.41321_41327del

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-14277_-31-14271del MANE Select	ENSP00000354859.3:n.-31-14277_-31-14271de...
ENST00000346454.7:c.-31-14277_-31-14271del	ENSP00000278597.5:n.-31-14277_-31-14271de...
ENST00000362072.7:c.-31-14277_-31-14271del	ENSP00000354859.3:n.-31-14277_-31-14271de...
ENST00000540600.5:n.35-14277_35-14271del
ENST00000542616.1:c.-31-14277_-31-14271del	ENSP00000441474.1:n.-31-14277_-31-14271de...
ENST00000543292.1:c.-32+8612_-32+8618del	ENSP00000438419.1:n.-32+8612_-32+8618del
NM_000795.3:c.-31-14277_-31-14271del	NP_000786.1:n.-31-14277_-31-14271del
NM_016574.3:c.-31-14277_-31-14271del	NP_057658.2:n.-31-14277_-31-14271del
XM_017017296.2:c.-31-14277_-31-14271del	XP_016872785.1:n.-31-14277_-31-14271del
NM_000795.4:c.-31-14277_-31-14271del MANE Select	NP_000786.1:n.-31-14277_-31-14271del
NM_016574.4:c.-31-14277_-31-14271del	NP_057658.2:n.-31-14277_-31-14271del