Canonical Allele Identifier: CA366387940

Gene: PDE10A

Linked Data

• ClinVar Variation Id: 488874
• ClinVar RCV Id: RCV000578525
• dbSNP Id: rs1554240201
• MyVariant Identifiers: chr6:g.165756886C>T (hg19) ; chr6:g.165343397C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.165343397C>T , CM000668.2:g.165343397C>T	GRCh38
NC_000006.11:g.165756886C>T , CM000668.1:g.165756886C>T	GRCh37
NC_000006.10:g.165676876C>T	NCBI36
NG_031878.2:g.323704G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366882.7:c.1239G>A	ENSP00000355847.3:p.Trp413Ter
ENST00000686660.1:n.336G>A
ENST00000366882.6:c.2091G>A	ENSP00000355847.2:p.Trp697Ter
ENST00000539869.4:c.2889G>A MANE Select	ENSP00000438284.3:p.Trp963Ter
ENST00000647590.1:c.2040G>A	ENSP00000497062.1:p.Trp680Ter
ENST00000647768.3:c.2265G>A	ENSP00000497930.3:p.Trp755Ter
ENST00000647837.1:c.2216G>A	ENSP00000497085.1:n.2216G>A
ENST00000647989.1:n.2295G>A
ENST00000648884.1:c.1851G>A	ENSP00000497392.1:p.Trp617Ter
ENST00000648917.1:c.2097G>A	ENSP00000497277.1:p.Trp699Ter
ENST00000649247.1:c.2206G>A
ENST00000649273.1:c.2013G>A
ENST00000649761.1:n.2247G>A
ENST00000672859.1:c.2142G>A	ENSP00000500900.1:p.Trp714Ter
ENST00000672902.1:c.2142G>A	ENSP00000500351.1:p.Trp714Ter
ENST00000676766.1:c.2130G>A	ENSP00000504611.1:p.Trp710Ter
ENST00000676767.1:c.2106G>A
ENST00000678161.1:c.*2030G>A	ENSP00000503721.1:n.*2030G>A
ENST00000366882.5:c.2061G>A	ENSP00000355847.1:p.Trp687Ter
ENST00000539869.2:c.2091G>A	ENSP00000438284.2:p.Trp697Ter
NM_001130690.2:c.2091G>A	NP_001124162.1:p.Trp697Ter
NM_006661.3:c.2061G>A	NP_006652.1:p.Trp687Ter
XM_006715321.2:c.2040G>A	XP_006715384.1:p.Trp680Ter
XM_011535387.1:c.2142G>A	XP_011533689.1:p.Trp714Ter
XM_011535388.1:c.2061G>A	XP_011533690.1:p.Trp687Ter
XM_011535389.1:c.2061G>A	XP_011533691.1:p.Trp687Ter
XM_011535390.1:c.1920G>A	XP_011533692.1:p.Trp640Ter
XM_011535391.1:c.1851G>A	XP_011533693.1:p.Trp617Ter
XM_011535392.1:c.1851G>A	XP_011533694.1:p.Trp617Ter
XM_011535393.1:c.1122G>A	XP_011533695.1:p.Trp374Ter
XM_006715321.4:c.2040G>A	XP_006715384.1:p.Trp680Ter
XM_011535387.3:c.2217G>A	XP_011533689.2:p.Trp739Ter
XM_011535388.3:c.2061G>A	XP_011533690.1:p.Trp687Ter
XM_011535393.3:c.1122G>A	XP_011533695.1:p.Trp374Ter
XM_017010194.2:c.2217G>A	XP_016865683.1:p.Trp739Ter
XM_017010195.2:c.1920G>A	XP_016865684.1:p.Trp640Ter
XM_017010196.2:c.1851G>A	XP_016865685.1:p.Trp617Ter
XM_024446311.1:c.2061G>A	XP_024302079.1:p.Trp687Ter
XM_024446312.1:c.1851G>A	XP_024302080.1:p.Trp617Ter
XR_001743121.2:n.4447G>A
NM_001130690.3:c.2091G>A	NP_001124162.1:p.Trp697Ter
NM_006661.4:c.2061G>A	NP_006652.1:p.Trp687Ter
NM_001385079.1:c.2889G>A MANE Select	NP_001372008.1:p.Trp963Ter