Canonical Allele Identifier: CA1310286794
Gene: PDE11A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014289C= , CM000664.2:g.178014289C= GRCh38
NC_000002.11:g.178879016C= , CM000664.1:g.178879016C= GRCh37
NC_000002.10:g.178587262C= NCBI36
NG_012168.1:g.99051G=
NG_012168.2:g.99051G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.1071+13G= MANE Select ENSP00000286063.5:n.1071+13G=
ENST00000286063.10:c.1071+13G= ENSP00000286063.5:n.1071+13G=
ENST00000358450.8:c.321+13G= ENSP00000351232.4:n.321+13G=
NM_001077197.1:c.321+13G= NP_001070665.1:n.321+13G=
NM_016953.3:c.1071+13G= NP_058649.3:n.1071+13G=
NM_016953.4:c.1071+13G= MANE Select NP_058649.3:n.1071+13G=
NM_001077197.2:c.321+13G= NP_001070665.1:n.321+13G=
Search 100 bp 5'
Search 100 bp 3'