Canonical Allele Identifier: CA349703825
Gene: PDE11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014364C>T , CM000664.2:g.178014364C>T GRCh38
NC_000002.11:g.178879091C>T , CM000664.1:g.178879091C>T GRCh37
NC_000002.10:g.178587337C>T NCBI36
NG_012168.1:g.98976G>A
NG_012168.2:g.98976G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1009G>A MANE Select ENSP00000286063.5:p.Gly337Ser
ENST00000286063.10:c.1009G>A ENSP00000286063.5:p.Gly337Ser
ENST00000358450.8:c.259G>A ENSP00000351232.4:p.Gly87Ser
NM_001077197.1:c.259G>A NP_001070665.1:p.Gly87Ser
NM_016953.3:c.1009G>A NP_058649.3:p.Gly337Ser
NM_016953.4:c.1009G>A MANE Select NP_058649.3:p.Gly337Ser
NM_001077197.2:c.259G>A NP_001070665.1:p.Gly87Ser