Canonical Allele Identifier: CA2511265931

Gene: DRD3

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.114130439_114130442del , CM000665.2:g.114130439_114130442del	GRCh38
NC_000003.11:g.113849286_113849289del , CM000665.1:g.113849286_113849289del	GRCh37
NC_000003.10:g.115331976_115331979del	NCBI36
NG_008842.2:g.73978_73981del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698213.1:c.*310+688_*310+691del	ENSP00000513607.1:n.*310+688_*310+691del
ENST00000383673.5:c.1006+688_1006+691del MANE Select	ENSP00000373169.2:n.1006+688_1006+691del
ENST00000295881.9:c.907+688_907+691del	ENSP00000295881.6:n.907+688_907+691del
ENST00000383673.4:c.1006+688_1006+691del	ENSP00000373169.2:n.1006+688_1006+691del
ENST00000460779.5:c.1006+688_1006+691del	ENSP00000419402.1:n.1006+688_1006+691del
ENST00000467632.5:c.1006+688_1006+691del	ENSP00000420662.1:n.1006+688_1006+691del
NM_000796.5:c.1006+688_1006+691del	NP_000787.2:n.1006+688_1006+691del
NM_001282563.2:c.1006+688_1006+691del	NP_001269492.1:n.1006+688_1006+691del
NM_001290809.1:c.1006+688_1006+691del	NP_001277738.1:n.1006+688_1006+691del
NM_033663.5:c.907+688_907+691del	NP_387512.3:n.907+688_907+691del
XM_011512510.1:c.1006+688_1006+691del	XP_011510812.1:n.1006+688_1006+691del
XM_011512511.1:c.1006+688_1006+691del	XP_011510813.1:n.1006+688_1006+691del
XM_011512512.1:c.1006+688_1006+691del	XP_011510814.1:n.1006+688_1006+691del
XM_017005829.1:c.1006+688_1006+691del	XP_016861318.1:n.1006+688_1006+691del
NM_000796.6:c.1006+688_1006+691del MANE Select	NP_000787.2:n.1006+688_1006+691del
NM_033663.6:c.907+688_907+691del	NP_387512.3:n.907+688_907+691del