Canonical Allele Identifier: CA410979901

Gene: PIWIL3

Linked Data

• dbSNP Id: rs11703684
• gnomAD v3: 22-24748945-C-G
• gnomAD v4: 22-24748945-C-G
• MyVariant Identifiers: chr22:g.25144912C>G (hg19) ; chr22:g.24748945C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748945C>G , CM000684.2:g.24748945C>G	GRCh38
NC_000022.10:g.25144912C>G , CM000684.1:g.25144912C>G	GRCh37
NC_000022.9:g.23474912C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000527701.6:c.*1383G>C	ENSP00000435718.2:n.*1383G>C
ENST00000533313.6:c.*1337G>C	ENSP00000431843.2:n.*1337G>C
ENST00000616349.5:c.1411G>C MANE Select	ENSP00000479524.2:p.Val471Leu
ENST00000332271.9:c.1411G>C	ENSP00000330031.5:p.Val471Leu
ENST00000527701.5:c.1084G>C	ENSP00000435718.1:p.Val362Leu
ENST00000532537.2:n.1832G>C
ENST00000533313.5:c.1084G>C	ENSP00000431843.1:p.Val362Leu
ENST00000616349.4:c.1411G>C	ENSP00000479524.1:p.Val471Leu
NM_001008496.3:c.1411G>C	NP_001008496.2:p.Val471Leu
NM_001255975.1:c.1411G>C MANE Select	NP_001242904.1:p.Val471Leu
NR_045648.1:n.2042G>C
NR_045649.2:n.1915G>C