Canonical Allele Identifier: CA354324858
Gene: DRD3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.114171868G>A , CM000665.2:g.114171868G>A GRCh38
NC_000003.11:g.113890715G>A , CM000665.1:g.113890715G>A GRCh37
NC_000003.10:g.115373405G>A NCBI36
NG_008842.2:g.32540C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698213.1:c.125C>T ENSP00000513607.1:p.Ala42Val
ENST00000383673.5:c.125C>T MANE Select ENSP00000373169.2:p.Ala42Val
ENST00000295881.9:c.125C>T ENSP00000295881.6:p.Ala42Val
ENST00000383673.4:c.125C>T ENSP00000373169.2:p.Ala42Val
ENST00000460779.5:c.125C>T ENSP00000419402.1:p.Ala42Val
ENST00000467632.5:c.125C>T ENSP00000420662.1:p.Ala42Val
NM_000796.5:c.125C>T NP_000787.2:p.Ala42Val
NM_001282563.2:c.125C>T NP_001269492.1:p.Ala42Val
NM_001290809.1:c.125C>T NP_001277738.1:p.Ala42Val
NM_033663.5:c.125C>T NP_387512.3:p.Ala42Val
XM_011512510.1:c.125C>T XP_011510812.1:p.Ala42Val
XM_011512511.1:c.125C>T XP_011510813.1:p.Ala42Val
XM_011512512.1:c.125C>T XP_011510814.1:p.Ala42Val
XM_017005829.1:c.125C>T XP_016861318.1:p.Ala42Val
NM_000796.6:c.125C>T MANE Select NP_000787.2:p.Ala42Val
NM_033663.6:c.125C>T NP_387512.3:p.Ala42Val