Canonical Allele Identifier: CA638728901

Gene: PIWIL3

Linked Data

• dbSNP Id: rs1450407971
• gnomAD v2: 22-25144991-G-A
• gnomAD v4: 22-24749024-G-A
• MyVariant Identifiers: chr22:g.25144991G>A (hg19) ; chr22:g.24749024G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24749024G>A , CM000684.2:g.24749024G>A	GRCh38
NC_000022.10:g.25144991G>A , CM000684.1:g.25144991G>A	GRCh37
NC_000022.9:g.23474991G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1307-3C>T	ENSP00000435718.2:n.*1307-3C>T
ENST00000533313.6:c.*1261-3C>T	ENSP00000431843.2:n.*1261-3C>T
ENST00000616349.5:c.1335-3C>T MANE Select	ENSP00000479524.2:n.1335-3C>T
ENST00000332271.9:c.1335-3C>T	ENSP00000330031.5:n.1335-3C>T
ENST00000527701.5:c.1008-3C>T	ENSP00000435718.1:n.1008-3C>T
ENST00000532537.2:n.1756-3C>T
ENST00000533313.5:c.1008-3C>T	ENSP00000431843.1:n.1008-3C>T
ENST00000616349.4:c.1335-3C>T	ENSP00000479524.1:n.1335-3C>T
NM_001008496.3:c.1335-3C>T	NP_001008496.2:n.1335-3C>T
NM_001255975.1:c.1335-3C>T MANE Select	NP_001242904.1:n.1335-3C>T
NR_045648.1:n.1966-3C>T
NR_045649.1:n.1839-3C>T
NR_045649.2:n.1839-3C>T