Canonical Allele Identifier: CA513860491

Gene: PIWIL3

Linked Data

• dbSNP Id: rs1924544354
• MyVariant Identifiers: chr22:g.25144976T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24749009T>C , CM000684.2:g.24749009T>C	GRCh38
NC_000022.10:g.25144976T>C , CM000684.1:g.25144976T>C	GRCh37
NC_000022.9:g.23474976T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1319A>G	ENSP00000435718.2:n.*1319A>G
ENST00000533313.6:c.*1273A>G	ENSP00000431843.2:n.*1273A>G
ENST00000616349.5:c.1347A>G MANE Select	ENSP00000479524.2:p.Val449=
ENST00000332271.9:c.1347A>G	ENSP00000330031.5:p.Val449=
ENST00000527701.5:c.1020A>G	ENSP00000435718.1:p.Val340=
ENST00000532537.2:n.1768A>G
ENST00000533313.5:c.1020A>G	ENSP00000431843.1:p.Val340=
ENST00000616349.4:c.1347A>G	ENSP00000479524.1:p.Val449=
NM_001008496.3:c.1347A>G	NP_001008496.2:p.Val449=
NM_001255975.1:c.1347A>G MANE Select	NP_001242904.1:p.Val449=
NR_045648.1:n.1978A>G
NR_045649.1:n.1851A>G
NR_045649.2:n.1851A>G