Canonical Allele Identifier: CA382649019
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410772G>T , CM000673.2:g.113410772G>T GRCh38
NC_000011.9:g.113281494G>T , CM000673.1:g.113281494G>T GRCh37
NC_000011.8:g.112786704G>T NCBI36
NG_008841.1:g.69508C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1287C>A MANE Select ENSP00000354859.3:p.Phe429Leu
ENST00000346454.7:c.1200C>A ENSP00000278597.5:p.Phe400Leu
ENST00000362072.7:c.1287C>A ENSP00000354859.3:p.Phe429Leu
ENST00000538967.5:c.1293C>A ENSP00000438215.1:p.Phe431Leu
ENST00000542968.5:c.1287C>A ENSP00000442172.1:p.Phe429Leu
ENST00000544518.5:c.1284C>A ENSP00000441068.1:p.Phe428Leu
NM_000795.3:c.1287C>A NP_000786.1:p.Phe429Leu
NM_016574.3:c.1200C>A NP_057658.2:p.Phe400Leu
XM_017017296.2:c.1287C>A XP_016872785.1:p.Phe429Leu
NM_000795.4:c.1287C>A MANE Select NP_000786.1:p.Phe429Leu
NM_016574.4:c.1200C>A NP_057658.2:p.Phe400Leu