Canonical Allele Identifier: CA410979878

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144902T>A (hg19) ; chr22:g.24748935T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748935T>A , CM000684.2:g.24748935T>A	GRCh38
NC_000022.10:g.25144902T>A , CM000684.1:g.25144902T>A	GRCh37
NC_000022.9:g.23474902T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1393A>T	ENSP00000435718.2:n.*1393A>T
ENST00000533313.6:c.*1347A>T	ENSP00000431843.2:n.*1347A>T
ENST00000616349.5:c.1421A>T MANE Select	ENSP00000479524.2:p.Asn474Ile
ENST00000332271.9:c.1421A>T	ENSP00000330031.5:p.Asn474Ile
ENST00000527701.5:c.1094A>T	ENSP00000435718.1:p.Asn365Ile
ENST00000532537.2:n.1842A>T
ENST00000533313.5:c.1094A>T	ENSP00000431843.1:p.Asn365Ile
ENST00000616349.4:c.1421A>T	ENSP00000479524.1:p.Asn474Ile
NM_001008496.3:c.1421A>T	NP_001008496.2:p.Asn474Ile
NM_001255975.1:c.1421A>T MANE Select	NP_001242904.1:p.Asn474Ile
NR_045648.1:n.2052A>T
NR_045649.1:n.1925A>T
NR_045649.2:n.1925A>T