Canonical Allele Identifier: CA349703830
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879094T>A (hg19) chr2:g.178014367T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014367T>A , CM000664.2:g.178014367T>A GRCh38
NC_000002.11:g.178879094T>A , CM000664.1:g.178879094T>A GRCh37
NC_000002.10:g.178587340T>A NCBI36
NG_012168.1:g.98973A>T
NG_012168.2:g.98973A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1006A>T MANE Select ENSP00000286063.5:p.Ile336Phe
ENST00000286063.10:c.1006A>T ENSP00000286063.5:p.Ile336Phe
ENST00000358450.8:c.256A>T ENSP00000351232.4:p.Ile86Phe
NM_001077197.1:c.256A>T NP_001070665.1:p.Ile86Phe
NM_016953.3:c.1006A>T NP_058649.3:p.Ile336Phe
NM_016953.4:c.1006A>T MANE Select NP_058649.3:p.Ile336Phe
NM_001077197.2:c.256A>T NP_001070665.1:p.Ile86Phe
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