Canonical Allele Identifier: CA513860377

Gene: PIWIL3

Linked Data

• dbSNP Id: rs770608514
• gnomAD v3: 22-24748970-G-T
• gnomAD v4: 22-24748970-G-T
• MyVariant Identifiers: chr22:g.25144937G>T (hg19) ; chr22:g.24748970G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748970G>T , CM000684.2:g.24748970G>T	GRCh38
NC_000022.10:g.25144937G>T , CM000684.1:g.25144937G>T	GRCh37
NC_000022.9:g.23474937G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1358C>A	ENSP00000435718.2:n.*1358C>A
ENST00000533313.6:c.*1312C>A	ENSP00000431843.2:n.*1312C>A
ENST00000616349.5:c.1386C>A MANE Select	ENSP00000479524.2:p.Thr462=
ENST00000332271.9:c.1386C>A	ENSP00000330031.5:p.Thr462=
ENST00000527701.5:c.1059C>A	ENSP00000435718.1:p.Thr353=
ENST00000532537.2:n.1807C>A
ENST00000533313.5:c.1059C>A	ENSP00000431843.1:p.Thr353=
ENST00000616349.4:c.1386C>A	ENSP00000479524.1:p.Thr462=
NM_001008496.3:c.1386C>A	NP_001008496.2:p.Thr462=
NM_001255975.1:c.1386C>A MANE Select	NP_001242904.1:p.Thr462=
NR_045648.1:n.2017C>A
NR_045649.1:n.1890C>A
NR_045649.2:n.1890C>A