Canonical Allele Identifier: CA682122660
Gene: PIWIL4 HGNC NCBI
PIWIL4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1421243444
gnomAD v3: 11-94579202-CGTTT-C
gnomAD v4: 11-94579202-CGTTT-C
MyVariant Identifiers: chr11:g.94312369_94312372del (hg19) chr11:g.94579203_94579206del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94579203_94579206del , CM000673.2:g.94579203_94579206del GRCh38
NC_000011.9:g.94312369_94312372del , CM000673.1:g.94312369_94312372del GRCh37
NC_000011.8:g.93952017_93952020del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000299001.11:c.513+1711_513+1714del (PIWIL4) MANE Select ENSP00000299001.6:n.513+1711_513+1714del
ENST00000299001.10:c.513+1711_513+1714del (PIWIL4) ENSP00000299001.6:n.513+1711_513+1714del
ENST00000446230.6:c.432+1711_432+1714del (PIWIL4) ENSP00000413838.2:n.432+1711_432+1714del
ENST00000543336.5:c.306+1711_306+1714del (PIWIL4) ENSP00000444575.1:n.306+1711_306+1714del
ENST00000545603.1:c.306+1711_306+1714del (PIWIL4) ENSP00000440499.1:n.306+1711_306+1714del
NM_152431.2:c.513+1711_513+1714del (PIWIL4) NP_689644.2:n.513+1711_513+1714del
NR_135093.1:n.524-33360_524-33357del (PIWIL4-AS1)
NR_135094.1:n.437-32881_437-32878del (PIWIL4-AS1)
NR_135096.1:n.623-3266_623-3263del (PIWIL4-AS1)
NM_152431.3:c.513+1711_513+1714del (PIWIL4) MANE Select NP_689644.2:n.513+1711_513+1714del
Search 100 bp 5'
Search 100 bp 3'