Canonical Allele Identifier: CA2398411326
Gene: PIWIL3 HGNC NCBI

Linked Data

dbSNP Id: rs1924523717

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.24748806del , CM000684.2:g.24748806del GRCh38
NC_000022.10:g.25144773del , CM000684.1:g.25144773del GRCh37
NC_000022.9:g.23474773del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527701.6:c.*1421+106del ENSP00000435718.2:n.*1421+106del
ENST00000533313.6:c.*1375+106del ENSP00000431843.2:n.*1375+106del
ENST00000616349.5:c.1449+106del MANE Select ENSP00000479524.2:n.1449+106del
ENST00000332271.9:c.1449+106del ENSP00000330031.5:n.1449+106del
ENST00000527701.5:c.1122+106del ENSP00000435718.1:n.1122+106del
ENST00000532537.2:n.1870+106del
ENST00000533313.5:c.1122+106del ENSP00000431843.1:n.1122+106del
ENST00000616349.4:c.1449+106del ENSP00000479524.1:n.1449+106del
NM_001008496.3:c.1449+106del NP_001008496.2:n.1449+106del
NM_001255975.1:c.1449+106del MANE Select NP_001242904.1:n.1449+106del
NR_045648.1:n.2080+106del
NR_045649.1:n.1953+106del
NR_045649.2:n.1953+106del