Canonical Allele Identifier: CA1024571147

Gene: PIWIL3

Linked Data

• dbSNP Id: rs1924532860
• gnomAD v3: 22-24748882-CATG-C
• gnomAD v4: 22-24748882-CATG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748888_24748890del , CM000684.2:g.24748888_24748890del	GRCh38
NC_000022.10:g.25144855_25144857del , CM000684.1:g.25144855_25144857del	GRCh37
NC_000022.9:g.23474855_23474857del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1421+22_*1421+24del	ENSP00000435718.2:n.*1421+22_*1421+24del
ENST00000533313.6:c.*1375+22_*1375+24del	ENSP00000431843.2:n.*1375+22_*1375+24del
ENST00000616349.5:c.1449+22_1449+24del MANE Select	ENSP00000479524.2:n.1449+22_1449+24del
ENST00000332271.9:c.1449+22_1449+24del	ENSP00000330031.5:n.1449+22_1449+24del
ENST00000527701.5:c.1122+22_1122+24del	ENSP00000435718.1:n.1122+22_1122+24del
ENST00000532537.2:n.1870+22_1870+24del
ENST00000533313.5:c.1122+22_1122+24del	ENSP00000431843.1:n.1122+22_1122+24del
ENST00000616349.4:c.1449+22_1449+24del	ENSP00000479524.1:n.1449+22_1449+24del
NM_001008496.3:c.1449+22_1449+24del	NP_001008496.2:n.1449+22_1449+24del
NM_001255975.1:c.1449+22_1449+24del MANE Select	NP_001242904.1:n.1449+22_1449+24del
NR_045648.1:n.2080+22_2080+24del
NR_045649.1:n.1953+22_1953+24del
NR_045649.2:n.1953+22_1953+24del