Canonical Allele Identifier: CA354324858

Gene: DRD3

Linked Data

• MyVariant Identifiers: chr3:g.113890715G>A (hg19) ; chr3:g.114171868G>A (hg38)

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