Canonical Allele Identifier: CA2398411327

Gene: PIWIL3

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748802A= , CM000684.2:g.24748802A=	GRCh38
NC_000022.10:g.25144769A= , CM000684.1:g.25144769A=	GRCh37
NC_000022.9:g.23474769A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1421+105T=	ENSP00000435718.2:n.*1421+105T=
ENST00000533313.6:c.*1375+105T=	ENSP00000431843.2:n.*1375+105T=
ENST00000616349.5:c.1449+105T= MANE Select	ENSP00000479524.2:n.1449+105T=
ENST00000332271.9:c.1449+105T=	ENSP00000330031.5:n.1449+105T=
ENST00000527701.5:c.1122+105T=	ENSP00000435718.1:n.1122+105T=
ENST00000532537.2:n.1870+105T=
ENST00000533313.5:c.1122+105T=	ENSP00000431843.1:n.1122+105T=
ENST00000616349.4:c.1449+105T=	ENSP00000479524.1:n.1449+105T=
NM_001008496.3:c.1449+105T=	NP_001008496.2:n.1449+105T=
NM_001255975.1:c.1449+105T= MANE Select	NP_001242904.1:n.1449+105T=
NR_045648.1:n.2080+105T=
NR_045649.1:n.1953+105T=
NR_045649.2:n.1953+105T=