Canonical Allele Identifier: CA1679549638
Gene: PDE10A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.165715150G= , CM000668.2:g.165715150G= GRCh38
NC_000006.11:g.166128638G= , CM000668.1:g.166128638G= GRCh37
NC_000006.10:g.166048628G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000366882.7:c.-614-171582C= ENSP00000355847.3:n.-614-171582C=
ENST00000685292.1:n.572-3997C=
ENST00000647768.3:c.107-3997C= ENSP00000497930.3:n.107-3997C=
ENST00000649882.1:n.551-3997C=
ENST00000672859.1:c.-17-3997C= ENSP00000500900.1:n.-17-3997C=
ENST00000672902.1:c.-17-3997C= ENSP00000500351.1:n.-17-3997C=
ENST00000676766.1:c.107-171582C= ENSP00000504611.1:n.107-171582C=
ENST00000678161.1:c.-17-3997C= ENSP00000503721.1:n.-17-3997C=
ENST00000580695.1:n.497-171582C=
XM_011535387.3:c.59-3997C= XP_011533689.2:n.59-3997C=
XM_017010194.2:c.59-3997C= XP_016865683.1:n.59-3997C=
XM_017010197.2:c.59-3997C= XP_016865686.1:n.59-3997C=
XR_001743121.2:n.2134-3997C=