Canonical Allele Identifier: CA2578840133

Gene: PDE10A

Linked Data

• gnomAD v4: 6-165450184-C-CTT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.165450188_165450189dup , CM000668.2:g.165450188_165450189dup	GRCh38
NC_000006.11:g.165863676_165863677dup , CM000668.1:g.165863676_165863677dup	GRCh37
NC_000006.10:g.165783666_165783667dup	NCBI36
NG_031878.2:g.216915_216916dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000366882.7:c.-456-14809_-456-14808dup	ENSP00000355847.3:n.-456-14809_-456-14808dup
ENST00000366882.6:c.346+56_346+57dup	ENSP00000355847.2:n.346+56_346+57dup
ENST00000539869.4:c.1144+56_1144+57dup MANE Select	ENSP00000438284.3:n.1144+56_1144+57dup
ENST00000647590.1:c.295+56_295+57dup	ENSP00000497062.1:n.295+56_295+57dup
ENST00000647768.3:c.520+56_520+57dup	ENSP00000497930.3:n.520+56_520+57dup
ENST00000647837.1:c.471+56_471+57dup	ENSP00000497085.1:n.471+56_471+57dup
ENST00000647989.1:n.550+56_550+57dup
ENST00000648884.1:c.106+56_106+57dup	ENSP00000497392.1:n.106+56_106+57dup
ENST00000648917.1:c.352+56_352+57dup	ENSP00000497277.1:n.352+56_352+57dup
ENST00000649247.1:c.461+56_461+57dup
ENST00000649273.1:c.268+56_268+57dup
ENST00000649761.1:n.502+56_502+57dup
ENST00000672859.1:c.397+56_397+57dup	ENSP00000500900.1:n.397+56_397+57dup
ENST00000672902.1:c.397+56_397+57dup	ENSP00000500351.1:n.397+56_397+57dup
ENST00000676766.1:c.385+56_385+57dup	ENSP00000504611.1:n.385+56_385+57dup
ENST00000676767.1:c.206+56_206+57dup
ENST00000678161.1:c.*86+56_*86+57dup	ENSP00000503721.1:n.*86+56_*86+57dup
ENST00000678462.1:c.217+56_217+57dup	ENSP00000503041.1:n.217+56_217+57dup
ENST00000366882.5:c.316+56_316+57dup	ENSP00000355847.1:n.316+56_316+57dup
ENST00000539869.2:c.346+56_346+57dup	ENSP00000438284.2:n.346+56_346+57dup
NM_001130690.2:c.346+56_346+57dup	NP_001124162.1:n.346+56_346+57dup
NM_006661.3:c.316+56_316+57dup	NP_006652.1:n.316+56_316+57dup
XM_006715321.2:c.295+56_295+57dup	XP_006715384.1:n.295+56_295+57dup
XM_011535387.1:c.397+56_397+57dup	XP_011533689.1:n.397+56_397+57dup
XM_011535388.1:c.316+56_316+57dup	XP_011533690.1:n.316+56_316+57dup
XM_011535389.1:c.316+56_316+57dup	XP_011533691.1:n.316+56_316+57dup
XM_011535390.1:c.175+56_175+57dup	XP_011533692.1:n.175+56_175+57dup
XM_011535391.1:c.106+56_106+57dup	XP_011533693.1:n.106+56_106+57dup
XM_011535392.1:c.106+56_106+57dup	XP_011533694.1:n.106+56_106+57dup
XM_006715321.4:c.295+56_295+57dup	XP_006715384.1:n.295+56_295+57dup
XM_011535387.3:c.472+56_472+57dup	XP_011533689.2:n.472+56_472+57dup
XM_011535388.3:c.316+56_316+57dup	XP_011533690.1:n.316+56_316+57dup
XM_011535393.3:c.-779+56_-779+57dup	XP_011533695.1:n.-779+56_-779+57dup
XM_017010194.2:c.472+56_472+57dup	XP_016865683.1:n.472+56_472+57dup
XM_017010195.2:c.175+56_175+57dup	XP_016865684.1:n.175+56_175+57dup
XM_017010196.2:c.106+56_106+57dup	XP_016865685.1:n.106+56_106+57dup
XM_017010197.2:c.472+56_472+57dup	XP_016865686.1:n.472+56_472+57dup
XM_024446311.1:c.316+56_316+57dup	XP_024302079.1:n.316+56_316+57dup
XM_024446312.1:c.106+56_106+57dup	XP_024302080.1:n.106+56_106+57dup
XR_001743121.2:n.2547+56_2547+57dup
NM_001130690.3:c.346+56_346+57dup	NP_001124162.1:n.346+56_346+57dup
NM_006661.4:c.316+56_316+57dup	NP_006652.1:n.316+56_316+57dup
NM_001385079.1:c.1144+56_1144+57dup MANE Select	NP_001372008.1:n.1144+56_1144+57dup