Canonical Allele Identifier: CA2001168877
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113414612_113414619delinsGGGAAGGC , CM000673.2:g.113414612_113414619delinsGGGAAGGC GRCh38
NC_000011.9:g.113285334_113285341delinsGGGAAGGC , CM000673.1:g.113285334_113285341delinsGGGAAGGC GRCh37
NC_000011.8:g.112790544_112790551delinsGGGAAGGC NCBI36
NG_008841.1:g.65661_65668delinsGCCTTCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.724-158_724-151delinsGCCTTCCC MANE Select ENSP00000354859.3:n.724-158_724-151delinsGCCTTCCC
ENST00000346454.7:c.723+802_723+809delinsGCCTTCCC ENSP00000278597.5:n.723+802_723+809delinsGCCTTCCC
ENST00000362072.7:c.724-158_724-151delinsGCCTTCCC ENSP00000354859.3:n.724-158_724-151delinsGCCTTCCC
ENST00000535984.1:n.443-158_443-151delinsGCCTTCCC
ENST00000538967.5:c.724-158_724-151delinsGCCTTCCC ENSP00000438215.1:n.724-158_724-151delinsGCCTTCCC
ENST00000540600.5:n.789-158_789-151delinsGCCTTCCC
ENST00000542968.5:c.724-158_724-151delinsGCCTTCCC ENSP00000442172.1:n.724-158_724-151delinsGCCTTCCC
ENST00000544518.5:c.721-158_721-151delinsGCCTTCCC ENSP00000441068.1:n.721-158_721-151delinsGCCTTCCC
NM_000795.3:c.724-158_724-151delinsGCCTTCCC NP_000786.1:n.724-158_724-151delinsGCCTTCCC
NM_016574.3:c.723+802_723+809delinsGCCTTCCC NP_057658.2:n.723+802_723+809delinsGCCTTCCC
XM_017017296.2:c.724-158_724-151delinsGCCTTCCC XP_016872785.1:n.724-158_724-151delinsGCCTTCCC
NM_000795.4:c.724-158_724-151delinsGCCTTCCC MANE Select NP_000786.1:n.724-158_724-151delinsGCCTTCCC
NM_016574.4:c.723+802_723+809delinsGCCTTCCC NP_057658.2:n.723+802_723+809delinsGCCTTCCC