Canonical Allele Identifier: CA1310286816
Gene: PDE11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014354T= , CM000664.2:g.178014354T= GRCh38
NC_000002.11:g.178879081T= , CM000664.1:g.178879081T= GRCh37
NC_000002.10:g.178587327T= NCBI36
NG_012168.1:g.98986A=
NG_012168.2:g.98986A=

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1019A= MANE Select ENSP00000286063.5:p.Gln340=
ENST00000286063.10:c.1019A= ENSP00000286063.5:p.Gln340=
ENST00000358450.8:c.269A= ENSP00000351232.4:p.Gln90=
NM_001077197.1:c.269A= NP_001070665.1:p.Gln90=
NM_016953.3:c.1019A= NP_058649.3:p.Gln340=
NM_016953.4:c.1019A= MANE Select NP_058649.3:p.Gln340=
NM_001077197.2:c.269A= NP_001070665.1:p.Gln90=