Canonical Allele Identifier: CA2001159404
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113438952_113438959delinsCTTAATAG , CM000673.2:g.113438952_113438959delinsCTTAATAG GRCh38
NC_000011.9:g.113309674_113309681delinsCTTAATAG , CM000673.1:g.113309674_113309681delinsCTTAATAG GRCh37
NC_000011.8:g.112814884_112814891delinsCTTAATAG NCBI36
NG_008841.1:g.41321_41328delinsCTATTAAG

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-31-14277_-31-14270delinsCTATTAAG MANE Select ENSP00000354859.3:n.-31-14277_-31-14270de...
ENST00000346454.7:c.-31-14277_-31-14270delinsCTATTAAG ENSP00000278597.5:n.-31-14277_-31-14270de...
ENST00000362072.7:c.-31-14277_-31-14270delinsCTATTAAG ENSP00000354859.3:n.-31-14277_-31-14270de...
ENST00000540600.5:n.35-14277_35-14270delinsCTATTAAG
ENST00000542616.1:c.-31-14277_-31-14270delinsCTATTAAG ENSP00000441474.1:n.-31-14277_-31-14270de...
ENST00000543292.1:c.-32+8612_-32+8619delinsCTATTAAG ENSP00000438419.1:n.-32+8612_-32+8619deli...
NM_000795.3:c.-31-14277_-31-14270delinsCTATTAAG NP_000786.1:n.-31-14277_-31-14270delinsCT...
NM_016574.3:c.-31-14277_-31-14270delinsCTATTAAG NP_057658.2:n.-31-14277_-31-14270delinsCT...
XM_017017296.2:c.-31-14277_-31-14270delinsCTATTAAG XP_016872785.1:n.-31-14277_-31-14270delin...
NM_000795.4:c.-31-14277_-31-14270delinsCTATTAAG MANE Select NP_000786.1:n.-31-14277_-31-14270delinsCT...
NM_016574.4:c.-31-14277_-31-14270delinsCTATTAAG NP_057658.2:n.-31-14277_-31-14270delinsCT...