Canonical Allele Identifier: CA410979952

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144938G>C (hg19) ; chr22:g.24748971G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748971G>C , CM000684.2:g.24748971G>C	GRCh38
NC_000022.10:g.25144938G>C , CM000684.1:g.25144938G>C	GRCh37
NC_000022.9:g.23474938G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1357C>G	ENSP00000435718.2:n.*1357C>G
ENST00000533313.6:c.*1311C>G	ENSP00000431843.2:n.*1311C>G
ENST00000616349.5:c.1385C>G MANE Select	ENSP00000479524.2:p.Thr462Ser
ENST00000332271.9:c.1385C>G	ENSP00000330031.5:p.Thr462Ser
ENST00000527701.5:c.1058C>G	ENSP00000435718.1:p.Thr353Ser
ENST00000532537.2:n.1806C>G
ENST00000533313.5:c.1058C>G	ENSP00000431843.1:p.Thr353Ser
ENST00000616349.4:c.1385C>G	ENSP00000479524.1:p.Thr462Ser
NM_001008496.3:c.1385C>G	NP_001008496.2:p.Thr462Ser
NM_001255975.1:c.1385C>G MANE Select	NP_001242904.1:p.Thr462Ser
NR_045648.1:n.2016C>G
NR_045649.1:n.1889C>G
NR_045649.2:n.1889C>G