Canonical Allele Identifier: CA2398411383

Gene: PIWIL3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748897_24748901delinsACTGT , CM000684.2:g.24748897_24748901delinsACTGT	GRCh38
NC_000022.10:g.25144864_25144868delinsACTGT , CM000684.1:g.25144864_25144868delinsACTGT	GRCh37
NC_000022.9:g.23474864_23474868delinsACTGT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1421+6_*1421+10delinsACAGT	ENSP00000435718.2:n.*1421+6_*1421+10delinsACAGT
ENST00000533313.6:c.*1375+6_*1375+10delinsACAGT	ENSP00000431843.2:n.*1375+6_*1375+10delinsACAGT
ENST00000616349.5:c.1449+6_1449+10delinsACAGT MANE Select	ENSP00000479524.2:n.1449+6_1449+10delinsACAGT
ENST00000332271.9:c.1449+6_1449+10delinsACAGT	ENSP00000330031.5:n.1449+6_1449+10delinsACAGT
ENST00000527701.5:c.1122+6_1122+10delinsACAGT	ENSP00000435718.1:n.1122+6_1122+10delinsACAGT
ENST00000532537.2:n.1870+6_1870+10delinsACAGT
ENST00000533313.5:c.1122+6_1122+10delinsACAGT	ENSP00000431843.1:n.1122+6_1122+10delinsACAGT
ENST00000616349.4:c.1449+6_1449+10delinsACAGT	ENSP00000479524.1:n.1449+6_1449+10delinsACAGT
NM_001008496.3:c.1449+6_1449+10delinsACAGT	NP_001008496.2:n.1449+6_1449+10delinsACAGT
NM_001255975.1:c.1449+6_1449+10delinsACAGT MANE Select	NP_001242904.1:n.1449+6_1449+10delinsACAGT
NR_045648.1:n.2080+6_2080+10delinsACAGT
NR_045649.1:n.1953+6_1953+10delinsACAGT
NR_045649.2:n.1953+6_1953+10delinsACAGT