Canonical Allele Identifier: CA2001167966
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412678T= , CM000673.2:g.113412678T= GRCh38
NC_000011.9:g.113283400T= , CM000673.1:g.113283400T= GRCh37
NC_000011.8:g.112788610T= NCBI36
NG_008841.1:g.67602A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1016A= MANE Select ENSP00000354859.3:p.Lys339=
ENST00000346454.7:c.929A= ENSP00000278597.5:p.Lys310=
ENST00000362072.7:c.1016A= ENSP00000354859.3:p.Lys339=
ENST00000538967.5:c.1022A= ENSP00000438215.1:p.Lys341=
ENST00000542968.5:c.1016A= ENSP00000442172.1:p.Lys339=
ENST00000544518.5:c.1013A= ENSP00000441068.1:p.Lys338=
NM_000795.3:c.1016A= NP_000786.1:p.Lys339=
NM_016574.3:c.929A= NP_057658.2:p.Lys310=
XM_017017296.2:c.1016A= XP_016872785.1:p.Lys339=
NM_000795.4:c.1016A= MANE Select NP_000786.1:p.Lys339=
NM_016574.4:c.929A= NP_057658.2:p.Lys310=