Canonical Allele Identifier: CA10155641

Gene: PIWIL3

Linked Data

• dbSNP Id: rs767564752
• ExAC: 22:25144901 G / A
• gnomAD v2: 22-25144901-G-A
• gnomAD v3: 22-24748934-G-A
• gnomAD v4: 22-24748934-G-A
• COSMIC: COSM3310328
• MyVariant Identifiers: chr22:g.25144901G>A (hg19) ; chr22:g.24748934G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748934G>A , CM000684.2:g.24748934G>A	GRCh38
NC_000022.10:g.25144901G>A , CM000684.1:g.25144901G>A	GRCh37
NC_000022.9:g.23474901G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1394C>T	ENSP00000435718.2:n.*1394C>T
ENST00000533313.6:c.*1348C>T	ENSP00000431843.2:n.*1348C>T
ENST00000616349.5:c.1422C>T MANE Select	ENSP00000479524.2:p.Asn474=
ENST00000332271.9:c.1422C>T	ENSP00000330031.5:p.Asn474=
ENST00000527701.5:c.1095C>T	ENSP00000435718.1:p.Asn365=
ENST00000532537.2:n.1843C>T
ENST00000533313.5:c.1095C>T	ENSP00000431843.1:p.Asn365=
ENST00000616349.4:c.1422C>T	ENSP00000479524.1:p.Asn474=
NM_001008496.3:c.1422C>T	NP_001008496.2:p.Asn474=
NM_001255975.1:c.1422C>T MANE Select	NP_001242904.1:p.Asn474=
NR_045648.1:n.2053C>T
NR_045649.1:n.1926C>T
NR_045649.2:n.1926C>T