Canonical Allele Identifier: CA2001159558
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113439218_113439219delinsCT , CM000673.2:g.113439218_113439219delinsCT GRCh38
NC_000011.9:g.113309940_113309941delinsCT , CM000673.1:g.113309940_113309941delinsCT GRCh37
NC_000011.8:g.112815150_112815151delinsCT NCBI36
NG_008841.1:g.41061_41062delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000362072.8:c.-31-14537_-31-14536delinsAG MANE Select ENSP00000354859.3:n.-31-14537_-31-14536de...
ENST00000346454.7:c.-31-14537_-31-14536delinsAG ENSP00000278597.5:n.-31-14537_-31-14536de...
ENST00000362072.7:c.-31-14537_-31-14536delinsAG ENSP00000354859.3:n.-31-14537_-31-14536de...
ENST00000540600.5:n.35-14537_35-14536delinsAG
ENST00000542616.1:c.-31-14537_-31-14536delinsAG ENSP00000441474.1:n.-31-14537_-31-14536de...
ENST00000543292.1:c.-32+8352_-32+8353delinsAG ENSP00000438419.1:n.-32+8352_-32+8353deli...
NM_000795.3:c.-31-14537_-31-14536delinsAG NP_000786.1:n.-31-14537_-31-14536delinsAG...
NM_016574.3:c.-31-14537_-31-14536delinsAG NP_057658.2:n.-31-14537_-31-14536delinsAG...
XM_017017296.2:c.-31-14537_-31-14536delinsAG XP_016872785.1:n.-31-14537_-31-14536delin...
NM_000795.4:c.-31-14537_-31-14536delinsAG MANE Select NP_000786.1:n.-31-14537_-31-14536delinsAG...
NM_016574.4:c.-31-14537_-31-14536delinsAG NP_057658.2:n.-31-14537_-31-14536delinsAG...