Canonical Allele Identifier: CA2616029231
Gene: DRD2 HGNC NCBI

Linked Data

gnomAD v4: 11-113410515-C-CA
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410515_113410516insA , CM000673.2:g.113410515_113410516insA GRCh38
NC_000011.9:g.113281237_113281238insA , CM000673.1:g.113281237_113281238insA GRCh37
NC_000011.8:g.112786447_112786448insA NCBI36
NG_008841.1:g.69764_69765insT

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.*211_*212insT MANE Select ENSP00000354859.3:n.*211_*212insT
ENST00000346454.7:c.*211_*212insT ENSP00000278597.5:n.*211_*212insT
ENST00000362072.7:c.*211_*212insT ENSP00000354859.3:n.*211_*212insT
ENST00000542968.5:c.*211_*212insT ENSP00000442172.1:n.*211_*212insT
ENST00000544518.5:c.*211_*212insT ENSP00000441068.1:n.*211_*212insT
NM_000795.3:c.*211_*212insT NP_000786.1:n.*211_*212insT
NM_016574.3:c.*211_*212insT NP_057658.2:n.*211_*212insT
XM_017017296.2:c.*211_*212insT XP_016872785.1:n.*211_*212insT
NM_000795.4:c.*211_*212insT MANE Select NP_000786.1:n.*211_*212insT
NM_016574.4:c.*211_*212insT NP_057658.2:n.*211_*212insT
Search 100 bp 5'
Search 100 bp 3'