Canonical Allele Identifier: CA2398411450
Gene: PIWIL3 HGNC NCBI

Linked Data

dbSNP Id: rs1924546206
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.24749036A>G , CM000684.2:g.24749036A>G GRCh38
NC_000022.10:g.25145003A>G , CM000684.1:g.25145003A>G GRCh37
NC_000022.9:g.23475003A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527701.6:c.*1307-15T>C ENSP00000435718.2:n.*1307-15T>C
ENST00000533313.6:c.*1261-15T>C ENSP00000431843.2:n.*1261-15T>C
ENST00000616349.5:c.1335-15T>C MANE Select ENSP00000479524.2:n.1335-15T>C
ENST00000332271.9:c.1335-15T>C ENSP00000330031.5:n.1335-15T>C
ENST00000527701.5:c.1008-15T>C ENSP00000435718.1:n.1008-15T>C
ENST00000532537.2:n.1756-15T>C
ENST00000533313.5:c.1008-15T>C ENSP00000431843.1:n.1008-15T>C
ENST00000616349.4:c.1335-15T>C ENSP00000479524.1:n.1335-15T>C
NM_001008496.3:c.1335-15T>C NP_001008496.2:n.1335-15T>C
NM_001255975.1:c.1335-15T>C MANE Select NP_001242904.1:n.1335-15T>C
NR_045648.1:n.1966-15T>C
NR_045649.1:n.1839-15T>C
NR_045649.2:n.1839-15T>C
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