Canonical Allele Identifier: CA2001166996
Gene: DRD2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410495_113410496delinsTG , CM000673.2:g.113410495_113410496delinsTG GRCh38
NC_000011.9:g.113281217_113281218delinsTG , CM000673.1:g.113281217_113281218delinsTG GRCh37
NC_000011.8:g.112786427_112786428delinsTG NCBI36
NG_008841.1:g.69784_69785delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.*231_*232delinsCA MANE Select ENSP00000354859.3:n.*231_*232delinsCA
ENST00000346454.7:c.*231_*232delinsCA ENSP00000278597.5:n.*231_*232delinsCA
ENST00000362072.7:c.*231_*232delinsCA ENSP00000354859.3:n.*231_*232delinsCA
ENST00000542968.5:c.*231_*232delinsCA ENSP00000442172.1:n.*231_*232delinsCA
ENST00000544518.5:c.*231_*232delinsCA ENSP00000441068.1:n.*231_*232delinsCA
NM_000795.3:c.*231_*232delinsCA NP_000786.1:n.*231_*232delinsCA
NM_016574.3:c.*231_*232delinsCA NP_057658.2:n.*231_*232delinsCA
XM_017017296.2:c.*231_*232delinsCA XP_016872785.1:n.*231_*232delinsCA
NM_000795.4:c.*231_*232delinsCA MANE Select NP_000786.1:n.*231_*232delinsCA
NM_016574.4:c.*231_*232delinsCA NP_057658.2:n.*231_*232delinsCA
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