Canonical Allele Identifier: CA1630834383

Gene: DRD3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114172195C= , CM000665.2:g.114172195C=	GRCh38
NC_000003.11:g.113891042C= , CM000665.1:g.113891042C=	GRCh37
NC_000003.10:g.115373732C=	NCBI36
NG_008842.2:g.32213G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698213.1:c.-35-168G=	ENSP00000513607.1:n.-35-168G=
ENST00000383673.5:c.-35-168G= MANE Select	ENSP00000373169.2:n.-35-168G=
ENST00000295881.9:c.-35-168G=	ENSP00000295881.6:n.-35-168G=
ENST00000383673.4:c.-35-168G=	ENSP00000373169.2:n.-35-168G=
ENST00000460779.5:c.-35-168G=	ENSP00000419402.1:n.-35-168G=
ENST00000467632.5:c.-35-168G=	ENSP00000420662.1:n.-35-168G=
NM_000796.5:c.-35-168G=	NP_000787.2:n.-35-168G=
NM_001282563.2:c.-35-168G=	NP_001269492.1:n.-35-168G=
NM_001290809.1:c.-35-168G=	NP_001277738.1:n.-35-168G=
NM_033663.5:c.-35-168G=	NP_387512.3:n.-35-168G=
XM_011512510.1:c.-35-168G=	XP_011510812.1:n.-35-168G=
XM_011512511.1:c.-35-168G=	XP_011510813.1:n.-35-168G=
XM_011512512.1:c.-35-168G=	XP_011510814.1:n.-35-168G=
XM_017005829.1:c.-35-168G=	XP_016861318.1:n.-35-168G=
NM_000796.6:c.-35-168G= MANE Select	NP_000787.2:n.-35-168G=
NM_033663.6:c.-35-168G=	NP_387512.3:n.-35-168G=