Canonical Allele Identifier: CA682122667
Gene: PIWIL4 HGNC NCBI
PIWIL4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1268750598

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94579237_94579238del , CM000673.2:g.94579237_94579238del GRCh38
NC_000011.9:g.94312403_94312404del , CM000673.1:g.94312403_94312404del GRCh37
NC_000011.8:g.93952051_93952052del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000299001.11:c.513+1745_513+1746del (PIWIL4) MANE Select ENSP00000299001.6:n.513+1745_513+1746del
ENST00000299001.10:c.513+1745_513+1746del (PIWIL4) ENSP00000299001.6:n.513+1745_513+1746del
ENST00000446230.6:c.432+1745_432+1746del (PIWIL4) ENSP00000413838.2:n.432+1745_432+1746del
ENST00000543336.5:c.306+1745_306+1746del (PIWIL4) ENSP00000444575.1:n.306+1745_306+1746del
ENST00000545603.1:c.306+1745_306+1746del (PIWIL4) ENSP00000440499.1:n.306+1745_306+1746del
NM_152431.2:c.513+1745_513+1746del (PIWIL4) NP_689644.2:n.513+1745_513+1746del
NR_135093.1:n.524-33391_524-33390del (PIWIL4-AS1)
NR_135094.1:n.437-32912_437-32911del (PIWIL4-AS1)
NR_135096.1:n.623-3297_623-3296del (PIWIL4-AS1)
NM_152431.3:c.513+1745_513+1746del (PIWIL4) MANE Select NP_689644.2:n.513+1745_513+1746del