Canonical Allele Identifier: CA10155647

Gene: PIWIL3

Linked Data

• dbSNP Id: rs779264127
• ExAC: 22:25144922 G / A
• gnomAD v2: 22-25144922-G-A
• gnomAD v3: 22-24748955-G-A
• gnomAD v4: 22-24748955-G-A
• MyVariant Identifiers: chr22:g.25144922G>A (hg19) ; chr22:g.24748955G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748955G>A , CM000684.2:g.24748955G>A	GRCh38
NC_000022.10:g.25144922G>A , CM000684.1:g.25144922G>A	GRCh37
NC_000022.9:g.23474922G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1373C>T	ENSP00000435718.2:n.*1373C>T
ENST00000533313.6:c.*1327C>T	ENSP00000431843.2:n.*1327C>T
ENST00000616349.5:c.1401C>T MANE Select	ENSP00000479524.2:p.Val467=
ENST00000332271.9:c.1401C>T	ENSP00000330031.5:p.Val467=
ENST00000527701.5:c.1074C>T	ENSP00000435718.1:p.Val358=
ENST00000532537.2:n.1822C>T
ENST00000533313.5:c.1074C>T	ENSP00000431843.1:p.Val358=
ENST00000616349.4:c.1401C>T	ENSP00000479524.1:p.Val467=
NM_001008496.3:c.1401C>T	NP_001008496.2:p.Val467=
NM_001255975.1:c.1401C>T MANE Select	NP_001242904.1:p.Val467=
NR_045648.1:n.2032C>T
NR_045649.1:n.1905C>T
NR_045649.2:n.1905C>T