Canonical Allele Identifier: CA2001167997
Gene: DRD2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113412751G= , CM000673.2:g.113412751G= GRCh38
NC_000011.9:g.113283473G= , CM000673.1:g.113283473G= GRCh37
NC_000011.8:g.112788683G= NCBI36
NG_008841.1:g.67529C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.943C= MANE Select ENSP00000354859.3:p.Leu315=
ENST00000346454.7:c.856C= ENSP00000278597.5:p.Leu286=
ENST00000362072.7:c.943C= ENSP00000354859.3:p.Leu315=
ENST00000538967.5:c.949C= ENSP00000438215.1:p.Leu317=
ENST00000542968.5:c.943C= ENSP00000442172.1:p.Leu315=
ENST00000544518.5:c.940C= ENSP00000441068.1:p.Leu314=
NM_000795.3:c.943C= NP_000786.1:p.Leu315=
NM_016574.3:c.856C= NP_057658.2:p.Leu286=
XM_017017296.2:c.943C= XP_016872785.1:p.Leu315=
NM_000795.4:c.943C= MANE Select NP_000786.1:p.Leu315=
NM_016574.4:c.856C= NP_057658.2:p.Leu286=