Canonical Allele Identifier: CA2655805920
Gene: PIWIL3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.24748818G>T , CM000684.2:g.24748818G>T GRCh38
NC_000022.10:g.25144785G>T , CM000684.1:g.25144785G>T GRCh37
NC_000022.9:g.23474785G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527701.6:c.*1421+89C>A ENSP00000435718.2:n.*1421+89C>A
ENST00000533313.6:c.*1375+89C>A ENSP00000431843.2:n.*1375+89C>A
ENST00000616349.5:c.1449+89C>A MANE Select ENSP00000479524.2:n.1449+89C>A
ENST00000332271.9:c.1449+89C>A ENSP00000330031.5:n.1449+89C>A
ENST00000527701.5:c.1122+89C>A ENSP00000435718.1:n.1122+89C>A
ENST00000532537.2:n.1870+89C>A
ENST00000533313.5:c.1122+89C>A ENSP00000431843.1:n.1122+89C>A
ENST00000616349.4:c.1449+89C>A ENSP00000479524.1:n.1449+89C>A
NM_001008496.3:c.1449+89C>A NP_001008496.2:n.1449+89C>A
NM_001255975.1:c.1449+89C>A MANE Select NP_001242904.1:n.1449+89C>A
NR_045648.1:n.2080+89C>A
NR_045649.1:n.1953+89C>A
NR_045649.2:n.1953+89C>A