Canonical Allele Identifier: CA410979899

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144911A>T (hg19) ; chr22:g.24748944A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748944A>T , CM000684.2:g.24748944A>T	GRCh38
NC_000022.10:g.25144911A>T , CM000684.1:g.25144911A>T	GRCh37
NC_000022.9:g.23474911A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1384T>A	ENSP00000435718.2:n.*1384T>A
ENST00000533313.6:c.*1338T>A	ENSP00000431843.2:n.*1338T>A
ENST00000616349.5:c.1412T>A MANE Select	ENSP00000479524.2:p.Val471Asp
ENST00000332271.9:c.1412T>A	ENSP00000330031.5:p.Val471Asp
ENST00000527701.5:c.1085T>A	ENSP00000435718.1:p.Val362Asp
ENST00000532537.2:n.1833T>A
ENST00000533313.5:c.1085T>A	ENSP00000431843.1:p.Val362Asp
ENST00000616349.4:c.1412T>A	ENSP00000479524.1:p.Val471Asp
NM_001008496.3:c.1412T>A	NP_001008496.2:p.Val471Asp
NM_001255975.1:c.1412T>A MANE Select	NP_001242904.1:p.Val471Asp
NR_045648.1:n.2043T>A
NR_045649.1:n.1916T>A
NR_045649.2:n.1916T>A