Canonical Allele Identifier: CA2398411414
Gene: PIWIL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.24748952C= , CM000684.2:g.24748952C= GRCh38
NC_000022.10:g.25144919C= , CM000684.1:g.25144919C= GRCh37
NC_000022.9:g.23474919C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527701.6:c.*1376G= ENSP00000435718.2:n.*1376G=
ENST00000533313.6:c.*1330G= ENSP00000431843.2:n.*1330G=
ENST00000616349.5:c.1404G= MANE Select ENSP00000479524.2:p.Pro468=
ENST00000332271.9:c.1404G= ENSP00000330031.5:p.Pro468=
ENST00000527701.5:c.1077G= ENSP00000435718.1:p.Pro359=
ENST00000532537.2:n.1825G=
ENST00000533313.5:c.1077G= ENSP00000431843.1:p.Pro359=
ENST00000616349.4:c.1404G= ENSP00000479524.1:p.Pro468=
NM_001008496.3:c.1404G= NP_001008496.2:p.Pro468=
NM_001255975.1:c.1404G= MANE Select NP_001242904.1:p.Pro468=
NR_045648.1:n.2035G=
NR_045649.1:n.1908G=
NR_045649.2:n.1908G=