Canonical Allele Identifier: CA382649122
Gene: DRD2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.113410818A>G , CM000673.2:g.113410818A>G GRCh38
NC_000011.9:g.113281540A>G , CM000673.1:g.113281540A>G GRCh37
NC_000011.8:g.112786750A>G NCBI36
NG_008841.1:g.69462T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000362072.8:c.1241T>C MANE Select ENSP00000354859.3:p.Leu414Pro
ENST00000346454.7:c.1154T>C ENSP00000278597.5:p.Leu385Pro
ENST00000362072.7:c.1241T>C ENSP00000354859.3:p.Leu414Pro
ENST00000538967.5:c.1247T>C ENSP00000438215.1:p.Leu416Pro
ENST00000542968.5:c.1241T>C ENSP00000442172.1:p.Leu414Pro
ENST00000544518.5:c.1238T>C ENSP00000441068.1:p.Leu413Pro
NM_000795.3:c.1241T>C NP_000786.1:p.Leu414Pro
NM_016574.3:c.1154T>C NP_057658.2:p.Leu385Pro
XM_017017296.2:c.1241T>C XP_016872785.1:p.Leu414Pro
NM_000795.4:c.1241T>C MANE Select NP_000786.1:p.Leu414Pro
NM_016574.4:c.1154T>C NP_057658.2:p.Leu385Pro