Canonical Allele Identifier: CA1310286812
Gene: PDE11A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014340T= , CM000664.2:g.178014340T= GRCh38
NC_000002.11:g.178879067T= , CM000664.1:g.178879067T= GRCh37
NC_000002.10:g.178587313T= NCBI36
NG_012168.1:g.99000A=
NG_012168.2:g.99000A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.1033A= MANE Select ENSP00000286063.5:p.Ile345=
ENST00000286063.10:c.1033A= ENSP00000286063.5:p.Ile345=
ENST00000358450.8:c.283A= ENSP00000351232.4:p.Ile95=
NM_001077197.1:c.283A= NP_001070665.1:p.Ile95=
NM_016953.3:c.1033A= NP_058649.3:p.Ile345=
NM_016953.4:c.1033A= MANE Select NP_058649.3:p.Ile345=
NM_001077197.2:c.283A= NP_001070665.1:p.Ile95=