Canonical Allele Identifier: CA410979909

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144917C>A (hg19) ; chr22:g.24748950C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748950C>A , CM000684.2:g.24748950C>A	GRCh38
NC_000022.10:g.25144917C>A , CM000684.1:g.25144917C>A	GRCh37
NC_000022.9:g.23474917C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1378G>T	ENSP00000435718.2:n.*1378G>T
ENST00000533313.6:c.*1332G>T	ENSP00000431843.2:n.*1332G>T
ENST00000616349.5:c.1406G>T MANE Select	ENSP00000479524.2:p.Gly469Val
ENST00000332271.9:c.1406G>T	ENSP00000330031.5:p.Gly469Val
ENST00000527701.5:c.1079G>T	ENSP00000435718.1:p.Gly360Val
ENST00000532537.2:n.1827G>T
ENST00000533313.5:c.1079G>T	ENSP00000431843.1:p.Gly360Val
ENST00000616349.4:c.1406G>T	ENSP00000479524.1:p.Gly469Val
NM_001008496.3:c.1406G>T	NP_001008496.2:p.Gly469Val
NM_001255975.1:c.1406G>T MANE Select	NP_001242904.1:p.Gly469Val
NR_045648.1:n.2037G>T
NR_045649.1:n.1910G>T
NR_045649.2:n.1910G>T