Canonical Allele Identifier: CA349703814
Gene: PDE11A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014360A>C , CM000664.2:g.178014360A>C GRCh38
NC_000002.11:g.178879087A>C , CM000664.1:g.178879087A>C GRCh37
NC_000002.10:g.178587333A>C NCBI36
NG_012168.1:g.98980T>G
NG_012168.2:g.98980T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1013T>G MANE Select ENSP00000286063.5:p.Val338Gly
ENST00000286063.10:c.1013T>G ENSP00000286063.5:p.Val338Gly
ENST00000358450.8:c.263T>G ENSP00000351232.4:p.Val88Gly
NM_001077197.1:c.263T>G NP_001070665.1:p.Val88Gly
NM_016953.3:c.1013T>G NP_058649.3:p.Val338Gly
NM_016953.4:c.1013T>G MANE Select NP_058649.3:p.Val338Gly
NM_001077197.2:c.263T>G NP_001070665.1:p.Val88Gly