Canonical Allele Identifier: CA410979918

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144921G>T (hg19) ; chr22:g.24748954G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748954G>T , CM000684.2:g.24748954G>T	GRCh38
NC_000022.10:g.25144921G>T , CM000684.1:g.25144921G>T	GRCh37
NC_000022.9:g.23474921G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1374C>A	ENSP00000435718.2:n.*1374C>A
ENST00000533313.6:c.*1328C>A	ENSP00000431843.2:n.*1328C>A
ENST00000616349.5:c.1402C>A MANE Select	ENSP00000479524.2:p.Pro468Thr
ENST00000332271.9:c.1402C>A	ENSP00000330031.5:p.Pro468Thr
ENST00000527701.5:c.1075C>A	ENSP00000435718.1:p.Pro359Thr
ENST00000532537.2:n.1823C>A
ENST00000533313.5:c.1075C>A	ENSP00000431843.1:p.Pro359Thr
ENST00000616349.4:c.1402C>A	ENSP00000479524.1:p.Pro468Thr
NM_001008496.3:c.1402C>A	NP_001008496.2:p.Pro468Thr
NM_001255975.1:c.1402C>A MANE Select	NP_001242904.1:p.Pro468Thr
NR_045648.1:n.2033C>A
NR_045649.1:n.1906C>A
NR_045649.2:n.1906C>A