Canonical Allele Identifier: CA2793678817

Gene: DRD2

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.113410715_113410735dup , CM000673.2:g.113410715_113410735dup	GRCh38
NC_000011.9:g.113281437_113281457dup , CM000673.1:g.113281437_113281457dup	GRCh37
NC_000011.8:g.112786647_112786667dup	NCBI36
NG_008841.1:g.69546_69566dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000362072.8:c.1325_*13dup MANE Select	ENSP00000354859.3:n.1325_*13dup
ENST00000346454.7:c.1238_*13dup	ENSP00000278597.5:n.1238_*13dup
ENST00000362072.7:c.1325_*13dup	ENSP00000354859.3:n.1325_*13dup
ENST00000538967.5:c.1331_1351dup	ENSP00000438215.1:n.1331_1351dup
ENST00000542968.5:c.1325_*13dup	ENSP00000442172.1:n.1325_*13dup
ENST00000544518.5:c.1322_*13dup	ENSP00000441068.1:n.1322_*13dup
NM_000795.3:c.1325_*13dup	NP_000786.1:n.1325_*13dup
NM_016574.3:c.1238_*13dup	NP_057658.2:n.1238_*13dup
XM_017017296.2:c.1325_*13dup	XP_016872785.1:n.1325_*13dup
NM_000795.4:c.1325_*13dup MANE Select	NP_000786.1:n.1325_*13dup
NM_016574.4:c.1238_*13dup	NP_057658.2:n.1238_*13dup