Canonical Allele Identifier: CA671883399

Gene: DRD2

Linked Data

• dbSNP Id: rs1281911134
• MyVariant Identifiers: chr11:g.113309941del (hg19) ; chr11:g.113439219del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113439220del , CM000673.2:g.113439220del	GRCh38
NC_000011.9:g.113309942del , CM000673.1:g.113309942del	GRCh37
NC_000011.8:g.112815152del	NCBI36
NG_008841.1:g.41061del

Transcript Alleles

HGVS	Amino-acid change
ENST00000362072.8:c.-31-14537del MANE Select	ENSP00000354859.3:n.-31-14537del
ENST00000346454.7:c.-31-14537del	ENSP00000278597.5:n.-31-14537del
ENST00000362072.7:c.-31-14537del	ENSP00000354859.3:n.-31-14537del
ENST00000540600.5:n.35-14537del
ENST00000542616.1:c.-31-14537del	ENSP00000441474.1:n.-31-14537del
ENST00000543292.1:c.-32+8352del	ENSP00000438419.1:n.-32+8352del
NM_000795.3:c.-31-14537del	NP_000786.1:n.-31-14537del
NM_016574.3:c.-31-14537del	NP_057658.2:n.-31-14537del
XM_017017296.2:c.-31-14537del	XP_016872785.1:n.-31-14537del
NM_000795.4:c.-31-14537del MANE Select	NP_000786.1:n.-31-14537del
NM_016574.4:c.-31-14537del	NP_057658.2:n.-31-14537del