Canonical Allele Identifier: CA822131440

Gene: PDE10A

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.165521933A>C , CM000668.2:g.165521933A>C	GRCh38
NC_000006.11:g.165935421A>C , CM000668.1:g.165935421A>C	GRCh37
NC_000006.10:g.165855411A>C	NCBI36
NG_031878.2:g.145168T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366882.7:c.-486+21507T>G	ENSP00000355847.3:n.-486+21507T>G
ENST00000366882.6:c.196+21507T>G	ENSP00000355847.2:n.196+21507T>G
ENST00000539869.4:c.994+21507T>G MANE Select	ENSP00000438284.3:n.994+21507T>G
ENST00000647590.1:c.145+21507T>G	ENSP00000497062.1:n.145+21507T>G
ENST00000647768.3:c.370+21507T>G	ENSP00000497930.3:n.370+21507T>G
ENST00000647837.1:c.321+21507T>G	ENSP00000497085.1:n.321+21507T>G
ENST00000647989.1:n.400+21507T>G
ENST00000648884.1:c.-45+21507T>G	ENSP00000497392.1:n.-45+21507T>G
ENST00000648917.1:c.202+21507T>G	ENSP00000497277.1:n.202+21507T>G
ENST00000649247.1:c.198+21507T>G
ENST00000672859.1:c.247+21507T>G	ENSP00000500900.1:n.247+21507T>G
ENST00000672902.1:c.247+21507T>G	ENSP00000500351.1:n.247+21507T>G
ENST00000676766.1:c.235+21507T>G	ENSP00000504611.1:n.235+21507T>G
ENST00000676767.1:c.56+21507T>G
ENST00000678161.1:c.247+21507T>G	ENSP00000503721.1:n.247+21507T>G
ENST00000678462.1:c.67+21507T>G	ENSP00000503041.1:n.67+21507T>G
ENST00000366882.5:c.166+21507T>G	ENSP00000355847.1:n.166+21507T>G
ENST00000539869.2:c.196+21507T>G	ENSP00000438284.2:n.196+21507T>G
NM_001130690.2:c.196+21507T>G	NP_001124162.1:n.196+21507T>G
NM_006661.3:c.166+21507T>G	NP_006652.1:n.166+21507T>G
XM_006715321.2:c.145+21507T>G	XP_006715384.1:n.145+21507T>G
XM_011535387.1:c.247+21507T>G	XP_011533689.1:n.247+21507T>G
XM_011535388.1:c.166+21507T>G	XP_011533690.1:n.166+21507T>G
XM_011535389.1:c.166+21507T>G	XP_011533691.1:n.166+21507T>G
XM_011535390.1:c.25+16495T>G	XP_011533692.1:n.25+16495T>G
XM_011535391.1:c.-163+21507T>G	XP_011533693.1:n.-163+21507T>G
XM_006715321.4:c.145+21507T>G	XP_006715384.1:n.145+21507T>G
XM_011535387.3:c.322+21507T>G	XP_011533689.2:n.322+21507T>G
XM_011535388.3:c.166+21507T>G	XP_011533690.1:n.166+21507T>G
XM_011535393.3:c.-929+21507T>G	XP_011533695.1:n.-929+21507T>G
XM_017010194.2:c.322+21507T>G	XP_016865683.1:n.322+21507T>G
XM_017010195.2:c.25+16495T>G	XP_016865684.1:n.25+16495T>G
XM_017010196.2:c.-163+21507T>G	XP_016865685.1:n.-163+21507T>G
XM_017010197.2:c.322+21507T>G	XP_016865686.1:n.322+21507T>G
XM_024446311.1:c.166+21507T>G	XP_024302079.1:n.166+21507T>G
XM_024446312.1:c.-45+21507T>G	XP_024302080.1:n.-45+21507T>G
XR_001743121.2:n.2397+21507T>G
NM_001130690.3:c.196+21507T>G	NP_001124162.1:n.196+21507T>G
NM_006661.4:c.166+21507T>G	NP_006652.1:n.166+21507T>G
NM_001385079.1:c.994+21507T>G MANE Select	NP_001372008.1:n.994+21507T>G