Canonical Allele Identifier: CA10155638

Gene: PIWIL3

Linked Data

• dbSNP Id: rs149033400
• ExAC: 22:25144894 T / C
• gnomAD v2: 22-25144894-T-C
• gnomAD v3: 22-24748927-T-C
• gnomAD v4: 22-24748927-T-C
• MyVariant Identifiers: chr22:g.25144894T>C (hg19) ; chr22:g.24748927T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748927T>C , CM000684.2:g.24748927T>C	GRCh38
NC_000022.10:g.25144894T>C , CM000684.1:g.25144894T>C	GRCh37
NC_000022.9:g.23474894T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1401A>G	ENSP00000435718.2:n.*1401A>G
ENST00000533313.6:c.*1355A>G	ENSP00000431843.2:n.*1355A>G
ENST00000616349.5:c.1429A>G MANE Select	ENSP00000479524.2:p.Ile477Val
ENST00000332271.9:c.1429A>G	ENSP00000330031.5:p.Ile477Val
ENST00000527701.5:c.1102A>G	ENSP00000435718.1:p.Ile368Val
ENST00000532537.2:n.1850A>G
ENST00000533313.5:c.1102A>G	ENSP00000431843.1:p.Ile368Val
ENST00000616349.4:c.1429A>G	ENSP00000479524.1:p.Ile477Val
NM_001008496.3:c.1429A>G	NP_001008496.2:p.Ile477Val
NM_001255975.1:c.1429A>G MANE Select	NP_001242904.1:p.Ile477Val
NR_045648.1:n.2060A>G
NR_045649.1:n.1933A>G
NR_045649.2:n.1933A>G