Canonical Allele Identifier: CA2001168992

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113414836_113414838delinsCAA , CM000673.2:g.113414836_113414838delinsCAA	GRCh38
NC_000011.9:g.113285558_113285560delinsCAA , CM000673.1:g.113285558_113285560delinsCAA	GRCh37
NC_000011.8:g.112790768_112790770delinsCAA	NCBI36
NG_008841.1:g.65442_65444delinsTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.724-377_724-375delinsTTG MANE Select	ENSP00000354859.3:n.724-377_724-375delinsTTG
ENST00000346454.7:c.723+583_723+585delinsTTG	ENSP00000278597.5:n.723+583_723+585delinsTTG
ENST00000362072.7:c.724-377_724-375delinsTTG	ENSP00000354859.3:n.724-377_724-375delinsTTG
ENST00000535984.1:n.443-377_443-375delinsTTG
ENST00000538967.5:c.724-377_724-375delinsTTG	ENSP00000438215.1:n.724-377_724-375delinsTTG
ENST00000540600.5:n.789-377_789-375delinsTTG
ENST00000542968.5:c.724-377_724-375delinsTTG	ENSP00000442172.1:n.724-377_724-375delinsTTG
ENST00000544518.5:c.721-377_721-375delinsTTG	ENSP00000441068.1:n.721-377_721-375delinsTTG
NM_000795.3:c.724-377_724-375delinsTTG	NP_000786.1:n.724-377_724-375delinsTTG
NM_016574.3:c.723+583_723+585delinsTTG	NP_057658.2:n.723+583_723+585delinsTTG
XM_017017296.2:c.724-377_724-375delinsTTG	XP_016872785.1:n.724-377_724-375delinsTTG
NM_000795.4:c.724-377_724-375delinsTTG MANE Select	NP_000786.1:n.724-377_724-375delinsTTG
NM_016574.4:c.723+583_723+585delinsTTG	NP_057658.2:n.723+583_723+585delinsTTG