Canonical Allele Identifier: CA349703734
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879049A>C (hg19) chr2:g.178014322A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014322A>C , CM000664.2:g.178014322A>C GRCh38
NC_000002.11:g.178879049A>C , CM000664.1:g.178879049A>C GRCh37
NC_000002.10:g.178587295A>C NCBI36
NG_012168.1:g.99018T>G
NG_012168.2:g.99018T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.1051T>G MANE Select ENSP00000286063.5:p.Phe351Val
ENST00000286063.10:c.1051T>G ENSP00000286063.5:p.Phe351Val
ENST00000358450.8:c.301T>G ENSP00000351232.4:p.Phe101Val
NM_001077197.1:c.301T>G NP_001070665.1:p.Phe101Val
NM_016953.3:c.1051T>G NP_058649.3:p.Phe351Val
NM_016953.4:c.1051T>G MANE Select NP_058649.3:p.Phe351Val
NM_001077197.2:c.301T>G NP_001070665.1:p.Phe101Val
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