Canonical Allele Identifier: CA430205441
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879089A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014362A>C , CM000664.2:g.178014362A>C GRCh38
NC_000002.11:g.178879089A>C , CM000664.1:g.178879089A>C GRCh37
NC_000002.10:g.178587335A>C NCBI36
NG_012168.1:g.98978T>G
NG_012168.2:g.98978T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1011T>G MANE Select ENSP00000286063.5:p.Gly337=
ENST00000286063.10:c.1011T>G ENSP00000286063.5:p.Gly337=
ENST00000358450.8:c.261T>G ENSP00000351232.4:p.Gly87=
NM_001077197.1:c.261T>G NP_001070665.1:p.Gly87=
NM_016953.3:c.1011T>G NP_058649.3:p.Gly337=
NM_016953.4:c.1011T>G MANE Select NP_058649.3:p.Gly337=
NM_001077197.2:c.261T>G NP_001070665.1:p.Gly87=
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