Canonical Allele Identifier: CA226534350

Gene: PIWIL4 PIWIL4-AS1

Linked Data

• dbSNP Id: rs979772529
• MyVariant Identifiers: chr11:g.94312221A>C (hg19) ; chr11:g.94579055A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.94579055A>C , CM000673.2:g.94579055A>C	GRCh38
NC_000011.9:g.94312221A>C , CM000673.1:g.94312221A>C	GRCh37
NC_000011.8:g.93951869A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299001.11:c.513+1563A>C (PIWIL4) MANE Select	ENSP00000299001.6:n.513+1563A>C
ENST00000299001.10:c.513+1563A>C (PIWIL4)	ENSP00000299001.6:n.513+1563A>C
ENST00000446230.6:c.432+1563A>C (PIWIL4)	ENSP00000413838.2:n.432+1563A>C
ENST00000543336.5:c.306+1563A>C (PIWIL4)	ENSP00000444575.1:n.306+1563A>C
ENST00000545603.1:c.306+1563A>C (PIWIL4)	ENSP00000440499.1:n.306+1563A>C
NM_152431.2:c.513+1563A>C (PIWIL4)	NP_689644.2:n.513+1563A>C
NR_135093.1:n.524-33209T>G (PIWIL4-AS1)
NR_135094.1:n.437-32730T>G (PIWIL4-AS1)
NR_135096.1:n.623-3115T>G (PIWIL4-AS1)
NM_152431.3:c.513+1563A>C (PIWIL4) MANE Select	NP_689644.2:n.513+1563A>C