Canonical Allele Identifier: CA2793220813
Gene: PIWIL4 HGNC NCBI
PIWIL4-AS1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94579424_94579454del , CM000673.2:g.94579424_94579454del GRCh38
NC_000011.9:g.94312590_94312620del , CM000673.1:g.94312590_94312620del GRCh37
NC_000011.8:g.93952238_93952268del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000299001.11:c.513+1932_513+1962del (PIWIL4) MANE Select ENSP00000299001.6:n.513+1932_513+1962del
ENST00000299001.10:c.513+1932_513+1962del (PIWIL4) ENSP00000299001.6:n.513+1932_513+1962del
ENST00000446230.6:c.432+1932_432+1962del (PIWIL4) ENSP00000413838.2:n.432+1932_432+1962del
ENST00000543336.5:c.306+1932_306+1962del (PIWIL4) ENSP00000444575.1:n.306+1932_306+1962del
ENST00000545603.1:c.306+1932_306+1962del (PIWIL4) ENSP00000440499.1:n.306+1932_306+1962del
NM_152431.2:c.513+1932_513+1962del (PIWIL4) NP_689644.2:n.513+1932_513+1962del
NR_135093.1:n.524-33607_524-33577del (PIWIL4-AS1)
NR_135094.1:n.437-33128_437-33098del (PIWIL4-AS1)
NR_135096.1:n.623-3513_623-3483del (PIWIL4-AS1)
NM_152431.3:c.513+1932_513+1962del (PIWIL4) MANE Select NP_689644.2:n.513+1932_513+1962del