Canonical Allele Identifier: CA654518877
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410675_113410676insT , CM000673.2:g.113410675_113410676insT GRCh38
NC_000011.9:g.113281397_113281398insT , CM000673.1:g.113281397_113281398insT GRCh37
NC_000011.8:g.112786607_112786608insT NCBI36
NG_008841.1:g.69604_69605insA

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.*51_*52insA MANE Select ENSP00000354859.3:n.*51_*52insA
ENST00000346454.7:c.*51_*52insA ENSP00000278597.5:n.*51_*52insA
ENST00000362072.7:c.*51_*52insA ENSP00000354859.3:n.*51_*52insA
ENST00000538967.5:c.1389_1390insA ENSP00000438215.1:n.1389_1390insA
ENST00000542968.5:c.*51_*52insA ENSP00000442172.1:n.*51_*52insA
ENST00000544518.5:c.*51_*52insA ENSP00000441068.1:n.*51_*52insA
NM_000795.3:c.*51_*52insA NP_000786.1:n.*51_*52insA
NM_016574.3:c.*51_*52insA NP_057658.2:n.*51_*52insA
XM_017017296.2:c.*51_*52insA XP_016872785.1:n.*51_*52insA
NM_000795.4:c.*51_*52insA MANE Select NP_000786.1:n.*51_*52insA
NM_016574.4:c.*51_*52insA NP_057658.2:n.*51_*52insA