Canonical Allele Identifier: CA410980172

Gene: PIWIL3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24749441G>T , CM000684.2:g.24749441G>T	GRCh38
NC_000022.10:g.25145408G>T , CM000684.1:g.25145408G>T	GRCh37
NC_000022.9:g.23475408G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_001255975.1:c.1297C>A MANE Select	NP_001242904.1:p.His433Asn
ENST00000616349.5:c.1297C>A MANE Select	ENSP00000479524.2:p.His433Asn
NM_001008496.3:c.1297C>A	NP_001008496.2:p.His433Asn
NR_045648.1:n.1928C>A
NR_045649.1:n.1801C>A
NR_045649.2:n.1801C>A
ENST00000332271.9:c.1297C>A	ENSP00000330031.5:p.His433Asn
ENST00000527701.5:c.970C>A	ENSP00000435718.1:p.His324Asn
ENST00000527701.6:c.*1269C>A	ENSP00000435718.2:n.*1269C>A
ENST00000532537.2:n.1718C>A
ENST00000533313.5:c.970C>A	ENSP00000431843.1:p.His324Asn
ENST00000533313.6:c.*1223C>A	ENSP00000431843.2:n.*1223C>A
ENST00000616349.4:c.1297C>A	ENSP00000479524.1:p.His433Asn