Canonical Allele Identifier: CA638728884

Gene: PIWIL3

Linked Data

• dbSNP Id: rs1279063160
• gnomAD v2: 22-25144828-C-T
• gnomAD v4: 22-24748861-C-T
• MyVariant Identifiers: chr22:g.25144828C>T (hg19) ; chr22:g.24748861C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748861C>T , CM000684.2:g.24748861C>T	GRCh38
NC_000022.10:g.25144828C>T , CM000684.1:g.25144828C>T	GRCh37
NC_000022.9:g.23474828C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1421+46G>A	ENSP00000435718.2:n.*1421+46G>A
ENST00000533313.6:c.*1375+46G>A	ENSP00000431843.2:n.*1375+46G>A
ENST00000616349.5:c.1449+46G>A MANE Select	ENSP00000479524.2:n.1449+46G>A
ENST00000332271.9:c.1449+46G>A	ENSP00000330031.5:n.1449+46G>A
ENST00000527701.5:c.1122+46G>A	ENSP00000435718.1:n.1122+46G>A
ENST00000532537.2:n.1870+46G>A
ENST00000533313.5:c.1122+46G>A	ENSP00000431843.1:n.1122+46G>A
ENST00000616349.4:c.1449+46G>A	ENSP00000479524.1:n.1449+46G>A
NM_001008496.3:c.1449+46G>A	NP_001008496.2:n.1449+46G>A
NM_001255975.1:c.1449+46G>A MANE Select	NP_001242904.1:n.1449+46G>A
NR_045648.1:n.2080+46G>A
NR_045649.1:n.1953+46G>A
NR_045649.2:n.1953+46G>A