Canonical Allele Identifier: CA410979931

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144929A>C (hg19) ; chr22:g.24748962A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748962A>C , CM000684.2:g.24748962A>C	GRCh38
NC_000022.10:g.25144929A>C , CM000684.1:g.25144929A>C	GRCh37
NC_000022.9:g.23474929A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1366T>G	ENSP00000435718.2:n.*1366T>G
ENST00000533313.6:c.*1320T>G	ENSP00000431843.2:n.*1320T>G
ENST00000616349.5:c.1394T>G MANE Select	ENSP00000479524.2:p.Leu465Trp
ENST00000332271.9:c.1394T>G	ENSP00000330031.5:p.Leu465Trp
ENST00000527701.5:c.1067T>G	ENSP00000435718.1:p.Leu356Trp
ENST00000532537.2:n.1815T>G
ENST00000533313.5:c.1067T>G	ENSP00000431843.1:p.Leu356Trp
ENST00000616349.4:c.1394T>G	ENSP00000479524.1:p.Leu465Trp
NM_001008496.3:c.1394T>G	NP_001008496.2:p.Leu465Trp
NM_001255975.1:c.1394T>G MANE Select	NP_001242904.1:p.Leu465Trp
NR_045648.1:n.2025T>G
NR_045649.1:n.1898T>G
NR_045649.2:n.1898T>G