Canonical Allele Identifier: CA349704038
Gene: PDE11A HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.178879188C>T (hg19) chr2:g.178014461C>T (hg38)
PubMed: PMID:28135719
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.178014461C>T , CM000664.2:g.178014461C>T GRCh38
NC_000002.11:g.178879188C>T , CM000664.1:g.178879188C>T GRCh37
NC_000002.10:g.178587434C>T NCBI36
NG_012168.1:g.98879G>A
NG_012168.2:g.98879G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000286063.11:c.913-1G>A MANE Select ENSP00000286063.5:n.913-1G>A
ENST00000286063.10:c.913-1G>A ENSP00000286063.5:n.913-1G>A
ENST00000358450.8:c.163-1G>A ENSP00000351232.4:n.163-1G>A
NM_001077197.1:c.163-1G>A NP_001070665.1:n.163-1G>A
NM_016953.3:c.913-1G>A NP_058649.3:n.913-1G>A
NM_016953.4:c.913-1G>A MANE Select NP_058649.3:n.913-1G>A
NM_001077197.2:c.163-1G>A NP_001070665.1:n.163-1G>A
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