Canonical Allele Identifier: CA2681144230

Gene: PDE10A

Linked Data

• gnomAD v4: 6-165450184-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.165450189del , CM000668.2:g.165450189del	GRCh38
NC_000006.11:g.165863677del , CM000668.1:g.165863677del	GRCh37
NC_000006.10:g.165783667del	NCBI36
NG_031878.2:g.216916del

Transcript Alleles

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