Canonical Allele Identifier: CA2616029348
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410623_113410625del , CM000673.2:g.113410623_113410625del GRCh38
NC_000011.9:g.113281345_113281347del , CM000673.1:g.113281345_113281347del GRCh37
NC_000011.8:g.112786555_112786557del NCBI36
NG_008841.1:g.69659_69661del

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.*106_*108del MANE Select ENSP00000354859.3:n.*106_*108del
ENST00000346454.7:c.*106_*108del ENSP00000278597.5:n.*106_*108del
ENST00000362072.7:c.*106_*108del ENSP00000354859.3:n.*106_*108del
ENST00000538967.5:c.1444_1446del ENSP00000438215.1:n.1444_1446del
ENST00000542968.5:c.*106_*108del ENSP00000442172.1:n.*106_*108del
ENST00000544518.5:c.*106_*108del ENSP00000441068.1:n.*106_*108del
NM_000795.3:c.*106_*108del NP_000786.1:n.*106_*108del
NM_016574.3:c.*106_*108del NP_057658.2:n.*106_*108del
XM_017017296.2:c.*106_*108del XP_016872785.1:n.*106_*108del
NM_000795.4:c.*106_*108del MANE Select NP_000786.1:n.*106_*108del
NM_016574.4:c.*106_*108del NP_057658.2:n.*106_*108del