Canonical Allele Identifier: CA430205440
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879086C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014359C>T , CM000664.2:g.178014359C>T GRCh38
NC_000002.11:g.178879086C>T , CM000664.1:g.178879086C>T GRCh37
NC_000002.10:g.178587332C>T NCBI36
NG_012168.1:g.98981G>A
NG_012168.2:g.98981G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000286063.11:c.1014G>A MANE Select ENSP00000286063.5:p.Val338=
ENST00000286063.10:c.1014G>A ENSP00000286063.5:p.Val338=
ENST00000358450.8:c.264G>A ENSP00000351232.4:p.Val88=
NM_001077197.1:c.264G>A NP_001070665.1:p.Val88=
NM_016953.3:c.1014G>A NP_058649.3:p.Val338=
NM_016953.4:c.1014G>A MANE Select NP_058649.3:p.Val338=
NM_001077197.2:c.264G>A NP_001070665.1:p.Val88=
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