Canonical Allele Identifier: CA226534401
Gene: PIWIL4 HGNC NCBI
PIWIL4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs898644728
MyVariant Identifiers: chr11:g.94312383_94312393del (hg19) chr11:g.94579217_94579227del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94579218_94579228del , CM000673.2:g.94579218_94579228del GRCh38
NC_000011.9:g.94312384_94312394del , CM000673.1:g.94312384_94312394del GRCh37
NC_000011.8:g.93952032_93952042del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000299001.11:c.513+1726_513+1736del (PIWIL4) MANE Select ENSP00000299001.6:n.513+1726_513+1736del
ENST00000299001.10:c.513+1726_513+1736del (PIWIL4) ENSP00000299001.6:n.513+1726_513+1736del
ENST00000446230.6:c.432+1726_432+1736del (PIWIL4) ENSP00000413838.2:n.432+1726_432+1736del
ENST00000543336.5:c.306+1726_306+1736del (PIWIL4) ENSP00000444575.1:n.306+1726_306+1736del
ENST00000545603.1:c.306+1726_306+1736del (PIWIL4) ENSP00000440499.1:n.306+1726_306+1736del
NM_152431.2:c.513+1726_513+1736del (PIWIL4) NP_689644.2:n.513+1726_513+1736del
NR_135093.1:n.524-33381_524-33371del (PIWIL4-AS1)
NR_135094.1:n.437-32902_437-32892del (PIWIL4-AS1)
NR_135096.1:n.623-3287_623-3277del (PIWIL4-AS1)
NM_152431.3:c.513+1726_513+1736del (PIWIL4) MANE Select NP_689644.2:n.513+1726_513+1736del
Search 100 bp 5'
Search 100 bp 3'