Canonical Allele Identifier: CA410980066

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144986T>G (hg19) ; chr22:g.24749019T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24749019T>G , CM000684.2:g.24749019T>G	GRCh38
NC_000022.10:g.25144986T>G , CM000684.1:g.25144986T>G	GRCh37
NC_000022.9:g.23474986T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1309A>C	ENSP00000435718.2:n.*1309A>C
ENST00000533313.6:c.*1263A>C	ENSP00000431843.2:n.*1263A>C
ENST00000616349.5:c.1337A>C MANE Select	ENSP00000479524.2:p.Asn446Thr
ENST00000332271.9:c.1337A>C	ENSP00000330031.5:p.Asn446Thr
ENST00000527701.5:c.1010A>C	ENSP00000435718.1:p.Asn337Thr
ENST00000532537.2:n.1758A>C
ENST00000533313.5:c.1010A>C	ENSP00000431843.1:p.Asn337Thr
ENST00000616349.4:c.1337A>C	ENSP00000479524.1:p.Asn446Thr
NM_001008496.3:c.1337A>C	NP_001008496.2:p.Asn446Thr
NM_001255975.1:c.1337A>C MANE Select	NP_001242904.1:p.Asn446Thr
NR_045648.1:n.1968A>C
NR_045649.1:n.1841A>C
NR_045649.2:n.1841A>C