Canonical Allele Identifier: CA1310160754
Gene: PDE11A HGNC NCBI
PDE11A-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.177727670G= , CM000664.2:g.177727670G= GRCh38
NC_000002.11:g.178592398G= , CM000664.1:g.178592398G= GRCh37
NC_000002.10:g.178300644G= NCBI36
NG_012168.1:g.385669C=
NG_012168.2:g.385670C=

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.2031C= (PDE11A) MANE Select ENSP00000286063.5:p.Phe677=
ENST00000286063.10:c.2031C= (PDE11A) ENSP00000286063.5:p.Phe677=
ENST00000358450.8:c.1281C= (PDE11A) ENSP00000351232.4:p.Phe427=
ENST00000389683.7:c.699C= (PDE11A) ENSP00000374333.3:p.Phe233=
ENST00000409504.5:c.957C= (PDE11A) ENSP00000386539.1:p.Phe319=
ENST00000433879.1:c.854C= (PDE11A)
ENST00000497003.5:n.1073C= (PDE11A)
NM_001077196.1:c.699C= (PDE11A) NP_001070664.1:p.Phe233=
NM_001077197.1:c.1281C= (PDE11A) NP_001070665.1:p.Phe427=
NM_001077358.1:c.957C= (PDE11A) NP_001070826.1:p.Phe319=
NM_016953.3:c.2031C= (PDE11A) NP_058649.3:p.Phe677=
XM_011512284.1:c.*35-392G= (PDE11A-AS1) XP_011510586.1:n.*35-392G=
NM_016953.4:c.2031C= (PDE11A) MANE Select NP_058649.3:p.Phe677=
NM_001077196.2:c.699C= (PDE11A) NP_001070664.1:p.Phe233=
NM_001077197.2:c.1281C= (PDE11A) NP_001070665.1:p.Phe427=
NM_001077358.2:c.957C= (PDE11A) NP_001070826.1:p.Phe319=