Canonical Allele Identifier: CA226534523
Gene: PIWIL4 HGNC NCBI
PIWIL4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs59308481
gnomAD v2: 11-94312648-T-TA
gnomAD v3: 11-94579482-T-TA
gnomAD v4: 11-94579482-T-TA
MyVariant Identifiers: chr11:g.94312648_94312649insA (hg19) chr11:g.94579482_94579483insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94579483dup , CM000673.2:g.94579483dup GRCh38
NC_000011.9:g.94312649dup , CM000673.1:g.94312649dup GRCh37
NC_000011.8:g.93952297dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000299001.11:c.513+1991dup (PIWIL4) MANE Select ENSP00000299001.6:n.513+1991dup
ENST00000299001.10:c.513+1991dup (PIWIL4) ENSP00000299001.6:n.513+1991dup
ENST00000446230.6:c.432+1991dup (PIWIL4) ENSP00000413838.2:n.432+1991dup
ENST00000543336.5:c.306+1991dup (PIWIL4) ENSP00000444575.1:n.306+1991dup
ENST00000545603.1:c.306+1991dup (PIWIL4) ENSP00000440499.1:n.306+1991dup
NM_152431.2:c.513+1991dup (PIWIL4) NP_689644.2:n.513+1991dup
NR_135093.1:n.524-33637dup (PIWIL4-AS1)
NR_135094.1:n.437-33158dup (PIWIL4-AS1)
NR_135096.1:n.623-3543dup (PIWIL4-AS1)
NM_152431.3:c.513+1991dup (PIWIL4) MANE Select NP_689644.2:n.513+1991dup
Search 100 bp 5'
Search 100 bp 3'