Canonical Allele Identifier: CA10155628

Gene: PIWIL3

Linked Data

• dbSNP Id: rs369653612
• ExAC: 22:25144875 A / G
• gnomAD v2: 22-25144875-A-G
• gnomAD v3: 22-24748908-A-G
• gnomAD v4: 22-24748908-A-G
• MyVariant Identifiers: chr22:g.25144875A>G (hg19) ; chr22:g.25144875_25144878delinsGTTC (hg19) ; chr22:g.24748908A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748908A>G , CM000684.2:g.24748908A>G	GRCh38
NC_000022.10:g.25144875A>G , CM000684.1:g.25144875A>G	GRCh37
NC_000022.9:g.23474875A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1420T>C	ENSP00000435718.2:n.*1420T>C
ENST00000533313.6:c.*1374T>C	ENSP00000431843.2:n.*1374T>C
ENST00000616349.5:c.1448T>C MANE Select	ENSP00000479524.2:p.Met483Thr
ENST00000332271.9:c.1448T>C	ENSP00000330031.5:p.Met483Thr
ENST00000527701.5:c.1121T>C	ENSP00000435718.1:p.Met374Thr
ENST00000532537.2:n.1869T>C
ENST00000533313.5:c.1121T>C	ENSP00000431843.1:p.Met374Thr
ENST00000616349.4:c.1448T>C	ENSP00000479524.1:p.Met483Thr
NM_001008496.3:c.1448T>C	NP_001008496.2:p.Met483Thr
NM_001255975.1:c.1448T>C MANE Select	NP_001242904.1:p.Met483Thr
NR_045648.1:n.2079T>C
NR_045649.1:n.1952T>C
NR_045649.2:n.1952T>C