Canonical Allele Identifier: CA682122602

Gene: PIWIL4 PIWIL4-AS1

Linked Data

• dbSNP Id: rs1379321378
• MyVariant Identifiers: chr11:g.94312215C>T (hg19) ; chr11:g.94579049C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94579049C>T , CM000673.2:g.94579049C>T	GRCh38
NC_000011.9:g.94312215C>T , CM000673.1:g.94312215C>T	GRCh37
NC_000011.8:g.93951863C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299001.11:c.513+1557C>T (PIWIL4) MANE Select	ENSP00000299001.6:n.513+1557C>T
ENST00000299001.10:c.513+1557C>T (PIWIL4)	ENSP00000299001.6:n.513+1557C>T
ENST00000446230.6:c.432+1557C>T (PIWIL4)	ENSP00000413838.2:n.432+1557C>T
ENST00000543336.5:c.306+1557C>T (PIWIL4)	ENSP00000444575.1:n.306+1557C>T
ENST00000545603.1:c.306+1557C>T (PIWIL4)	ENSP00000440499.1:n.306+1557C>T
NM_152431.2:c.513+1557C>T (PIWIL4)	NP_689644.2:n.513+1557C>T
NR_135093.1:n.524-33203G>A (PIWIL4-AS1)
NR_135094.1:n.437-32724G>A (PIWIL4-AS1)
NR_135096.1:n.623-3109G>A (PIWIL4-AS1)
NM_152431.3:c.513+1557C>T (PIWIL4) MANE Select	NP_689644.2:n.513+1557C>T