Canonical Allele Identifier: CA349703733
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879048A>T (hg19) chr2:g.178014321A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014321A>T , CM000664.2:g.178014321A>T GRCh38
NC_000002.11:g.178879048A>T , CM000664.1:g.178879048A>T GRCh37
NC_000002.10:g.178587294A>T NCBI36
NG_012168.1:g.99019T>A
NG_012168.2:g.99019T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.1052T>A MANE Select ENSP00000286063.5:p.Phe351Tyr
ENST00000286063.10:c.1052T>A ENSP00000286063.5:p.Phe351Tyr
ENST00000358450.8:c.302T>A ENSP00000351232.4:p.Phe101Tyr
NM_001077197.1:c.302T>A NP_001070665.1:p.Phe101Tyr
NM_016953.3:c.1052T>A NP_058649.3:p.Phe351Tyr
NM_016953.4:c.1052T>A MANE Select NP_058649.3:p.Phe351Tyr
NM_001077197.2:c.302T>A NP_001070665.1:p.Phe101Tyr
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