Canonical Allele Identifier: CA600863508
Gene: PIWIL4 HGNC NCBI
PIWIL4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1445497789
gnomAD v2: 11-94312574-TTAC-T
gnomAD v3: 11-94579408-TTAC-T
gnomAD v4: 11-94579408-TTAC-T
MyVariant Identifiers: chr11:g.94312575_94312577del (hg19) chr11:g.94579409_94579411del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94579412_94579414del , CM000673.2:g.94579412_94579414del GRCh38
NC_000011.9:g.94312578_94312580del , CM000673.1:g.94312578_94312580del GRCh37
NC_000011.8:g.93952226_93952228del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000299001.11:c.513+1920_513+1922del (PIWIL4) MANE Select ENSP00000299001.6:n.513+1920_513+1922del
ENST00000299001.10:c.513+1920_513+1922del (PIWIL4) ENSP00000299001.6:n.513+1920_513+1922del
ENST00000446230.6:c.432+1920_432+1922del (PIWIL4) ENSP00000413838.2:n.432+1920_432+1922del
ENST00000543336.5:c.306+1920_306+1922del (PIWIL4) ENSP00000444575.1:n.306+1920_306+1922del
ENST00000545603.1:c.306+1920_306+1922del (PIWIL4) ENSP00000440499.1:n.306+1920_306+1922del
NM_152431.2:c.513+1920_513+1922del (PIWIL4) NP_689644.2:n.513+1920_513+1922del
NR_135093.1:n.524-33565_524-33563del (PIWIL4-AS1)
NR_135094.1:n.437-33086_437-33084del (PIWIL4-AS1)
NR_135096.1:n.623-3471_623-3469del (PIWIL4-AS1)
NM_152431.3:c.513+1920_513+1922del (PIWIL4) MANE Select NP_689644.2:n.513+1920_513+1922del
Search 100 bp 5'
Search 100 bp 3'