Canonical Allele Identifier: CA942360420
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412775_113412777del , CM000673.2:g.113412775_113412777del GRCh38
NC_000011.9:g.113283497_113283499del , CM000673.1:g.113283497_113283499del GRCh37
NC_000011.8:g.112788707_112788709del NCBI36
NG_008841.1:g.67503_67505del

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.917_919del MANE Select ENSP00000354859.3:p.Thr306_Leu307delinsIle
ENST00000346454.7:c.830_832del ENSP00000278597.5:p.Thr277_Leu278delinsIle
ENST00000362072.7:c.917_919del ENSP00000354859.3:p.Thr306_Leu307delinsIle
ENST00000538967.5:c.923_925del ENSP00000438215.1:p.Thr308_Leu309delinsIle
ENST00000542968.5:c.917_919del ENSP00000442172.1:p.Thr306_Leu307delinsIle
ENST00000544518.5:c.914_916del ENSP00000441068.1:p.Thr305_Leu306delinsIle
NM_000795.3:c.917_919del NP_000786.1:p.Thr306_Leu307delinsIle
NM_016574.3:c.830_832del NP_057658.2:p.Thr277_Leu278delinsIle
XM_017017296.2:c.917_919del XP_016872785.1:p.Thr306_Leu307delinsIle
NM_000795.4:c.917_919del MANE Select NP_000786.1:p.Thr306_Leu307delinsIle
NM_016574.4:c.830_832del NP_057658.2:p.Thr277_Leu278delinsIle