Canonical Allele Identifier: CA1310286817
Gene: PDE11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014356G= , CM000664.2:g.178014356G= GRCh38
NC_000002.11:g.178879083G= , CM000664.1:g.178879083G= GRCh37
NC_000002.10:g.178587329G= NCBI36
NG_012168.1:g.98984C=
NG_012168.2:g.98984C=

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1017C= MANE Select ENSP00000286063.5:p.Ala339=
ENST00000286063.10:c.1017C= ENSP00000286063.5:p.Ala339=
ENST00000358450.8:c.267C= ENSP00000351232.4:p.Ala89=
NM_001077197.1:c.267C= NP_001070665.1:p.Ala89=
NM_016953.3:c.1017C= NP_058649.3:p.Ala339=
NM_016953.4:c.1017C= MANE Select NP_058649.3:p.Ala339=
NM_001077197.2:c.267C= NP_001070665.1:p.Ala89=