Canonical Allele Identifier: CA1310286798
Gene: PDE11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014304T= , CM000664.2:g.178014304T= GRCh38
NC_000002.11:g.178879031T= , CM000664.1:g.178879031T= GRCh37
NC_000002.10:g.178587277T= NCBI36
NG_012168.1:g.99036A=
NG_012168.2:g.99036A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.1069A= MANE Select ENSP00000286063.5:p.Lys357=
ENST00000286063.10:c.1069A= ENSP00000286063.5:p.Lys357=
ENST00000358450.8:c.319A= ENSP00000351232.4:p.Lys107=
NM_001077197.1:c.319A= NP_001070665.1:p.Lys107=
NM_016953.3:c.1069A= NP_058649.3:p.Lys357=
NM_016953.4:c.1069A= MANE Select NP_058649.3:p.Lys357=
NM_001077197.2:c.319A= NP_001070665.1:p.Lys107=