Canonical Allele Identifier: CA2001167144
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410775G= , CM000673.2:g.113410775G= GRCh38
NC_000011.9:g.113281497G= , CM000673.1:g.113281497G= GRCh37
NC_000011.8:g.112786707G= NCBI36
NG_008841.1:g.69505C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1284C= MANE Select ENSP00000354859.3:p.Thr428=
ENST00000346454.7:c.1197C= ENSP00000278597.5:p.Thr399=
ENST00000362072.7:c.1284C= ENSP00000354859.3:p.Thr428=
ENST00000538967.5:c.1290C= ENSP00000438215.1:p.Thr430=
ENST00000542968.5:c.1284C= ENSP00000442172.1:p.Thr428=
ENST00000544518.5:c.1281C= ENSP00000441068.1:p.Thr427=
NM_000795.3:c.1284C= NP_000786.1:p.Thr428=
NM_016574.3:c.1197C= NP_057658.2:p.Thr399=
XM_017017296.2:c.1284C= XP_016872785.1:p.Thr428=
NM_000795.4:c.1284C= MANE Select NP_000786.1:p.Thr428=
NM_016574.4:c.1197C= NP_057658.2:p.Thr399=