Canonical Allele Identifier: CA2001159689
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439412_113439414delinsCTG , CM000673.2:g.113439412_113439414delinsCTG GRCh38
NC_000011.9:g.113310134_113310136delinsCTG , CM000673.1:g.113310134_113310136delinsCTG GRCh37
NC_000011.8:g.112815344_112815346delinsCTG NCBI36
NG_008841.1:g.40866_40868delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.-31-14732_-31-14730delinsCAG MANE Select ENSP00000354859.3:n.-31-14732_-31-14730delinsCAG
ENST00000346454.7:c.-31-14732_-31-14730delinsCAG ENSP00000278597.5:n.-31-14732_-31-14730delinsCAG
ENST00000362072.7:c.-31-14732_-31-14730delinsCAG ENSP00000354859.3:n.-31-14732_-31-14730delinsCAG
ENST00000540600.5:n.35-14732_35-14730delinsCAG
ENST00000542616.1:c.-31-14732_-31-14730delinsCAG ENSP00000441474.1:n.-31-14732_-31-14730delinsCAG
ENST00000543292.1:c.-32+8157_-32+8159delinsCAG ENSP00000438419.1:n.-32+8157_-32+8159delinsCAG
NM_000795.3:c.-31-14732_-31-14730delinsCAG NP_000786.1:n.-31-14732_-31-14730delinsCAG
NM_016574.3:c.-31-14732_-31-14730delinsCAG NP_057658.2:n.-31-14732_-31-14730delinsCAG
XM_017017296.2:c.-31-14732_-31-14730delinsCAG XP_016872785.1:n.-31-14732_-31-14730delinsCAG
NM_000795.4:c.-31-14732_-31-14730delinsCAG MANE Select NP_000786.1:n.-31-14732_-31-14730delinsCAG
NM_016574.4:c.-31-14732_-31-14730delinsCAG NP_057658.2:n.-31-14732_-31-14730delinsCAG