Canonical Allele Identifier: CA2838294596

Gene: DRD3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114157513G>T , CM000665.2:g.114157513G>T	GRCh38
NC_000003.11:g.113876360G>T , CM000665.1:g.113876360G>T	GRCh37
NC_000003.10:g.115359050G>T	NCBI36
NG_008842.2:g.46895C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698213.1:c.383+2242C>A	ENSP00000513607.1:n.383+2242C>A
ENST00000383673.5:c.383+2242C>A MANE Select	ENSP00000373169.2:n.383+2242C>A
ENST00000295881.9:c.383+2242C>A	ENSP00000295881.6:n.383+2242C>A
ENST00000383673.4:c.383+2242C>A	ENSP00000373169.2:n.383+2242C>A
ENST00000460779.5:c.383+2242C>A	ENSP00000419402.1:n.383+2242C>A
ENST00000467632.5:c.383+2242C>A	ENSP00000420662.1:n.383+2242C>A
NM_000796.5:c.383+2242C>A	NP_000787.2:n.383+2242C>A
NM_001282563.2:c.383+2242C>A	NP_001269492.1:n.383+2242C>A
NM_001290809.1:c.383+2242C>A	NP_001277738.1:n.383+2242C>A
NM_033663.5:c.383+2242C>A	NP_387512.3:n.383+2242C>A
XM_011512510.1:c.383+2242C>A	XP_011510812.1:n.383+2242C>A
XM_011512511.1:c.383+2242C>A	XP_011510813.1:n.383+2242C>A
XM_011512512.1:c.383+2242C>A	XP_011510814.1:n.383+2242C>A
XM_017005829.1:c.383+2242C>A	XP_016861318.1:n.383+2242C>A
NM_000796.6:c.383+2242C>A MANE Select	NP_000787.2:n.383+2242C>A
NM_033663.6:c.383+2242C>A	NP_387512.3:n.383+2242C>A