Canonical Allele Identifier: CA682122650
Gene: PIWIL4 HGNC NCBI
PIWIL4-AS1 HGNC NCBI

Linked Data

dbSNP Id: rs1441718512
MyVariant Identifiers: chr11:g.94312345T>C (hg19) chr11:g.94579179T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.94579179T>C , CM000673.2:g.94579179T>C GRCh38
NC_000011.9:g.94312345T>C , CM000673.1:g.94312345T>C GRCh37
NC_000011.8:g.93951993T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000299001.11:c.513+1687T>C (PIWIL4) MANE Select ENSP00000299001.6:n.513+1687T>C
ENST00000299001.10:c.513+1687T>C (PIWIL4) ENSP00000299001.6:n.513+1687T>C
ENST00000446230.6:c.432+1687T>C (PIWIL4) ENSP00000413838.2:n.432+1687T>C
ENST00000543336.5:c.306+1687T>C (PIWIL4) ENSP00000444575.1:n.306+1687T>C
ENST00000545603.1:c.306+1687T>C (PIWIL4) ENSP00000440499.1:n.306+1687T>C
NM_152431.2:c.513+1687T>C (PIWIL4) NP_689644.2:n.513+1687T>C
NR_135093.1:n.524-33333A>G (PIWIL4-AS1)
NR_135094.1:n.437-32854A>G (PIWIL4-AS1)
NR_135096.1:n.623-3239A>G (PIWIL4-AS1)
NM_152431.3:c.513+1687T>C (PIWIL4) MANE Select NP_689644.2:n.513+1687T>C
Search 100 bp 5'
Search 100 bp 3'