Canonical Allele Identifier: CA10155626

Gene: PIWIL3

Linked Data

• dbSNP Id: rs377333935
• ExAC: 22:25144866 T / C
• gnomAD v2: 22-25144866-T-C
• gnomAD v3: 22-24748899-T-C
• gnomAD v4: 22-24748899-T-C
• MyVariant Identifiers: chr22:g.25144866T>C (hg19) ; chr22:g.24748899T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748899T>C , CM000684.2:g.24748899T>C	GRCh38
NC_000022.10:g.25144866T>C , CM000684.1:g.25144866T>C	GRCh37
NC_000022.9:g.23474866T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1421+8A>G	ENSP00000435718.2:n.*1421+8A>G
ENST00000533313.6:c.*1375+8A>G	ENSP00000431843.2:n.*1375+8A>G
ENST00000616349.5:c.1449+8A>G MANE Select	ENSP00000479524.2:n.1449+8A>G
ENST00000332271.9:c.1449+8A>G	ENSP00000330031.5:n.1449+8A>G
ENST00000527701.5:c.1122+8A>G	ENSP00000435718.1:n.1122+8A>G
ENST00000532537.2:n.1870+8A>G
ENST00000533313.5:c.1122+8A>G	ENSP00000431843.1:n.1122+8A>G
ENST00000616349.4:c.1449+8A>G	ENSP00000479524.1:n.1449+8A>G
NM_001008496.3:c.1449+8A>G	NP_001008496.2:n.1449+8A>G
NM_001255975.1:c.1449+8A>G MANE Select	NP_001242904.1:n.1449+8A>G
NR_045648.1:n.2080+8A>G
NR_045649.1:n.1953+8A>G
NR_045649.2:n.1953+8A>G