Canonical Allele Identifier: CA513860526

Gene: PIWIL3

Linked Data

• MyVariant Identifiers: chr22:g.25144988A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24749021A>G , CM000684.2:g.24749021A>G	GRCh38
NC_000022.10:g.25144988A>G , CM000684.1:g.25144988A>G	GRCh37
NC_000022.9:g.23474988A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1307T>C	ENSP00000435718.2:n.*1307T>C
ENST00000533313.6:c.*1261T>C	ENSP00000431843.2:n.*1261T>C
ENST00000616349.5:c.1335T>C MANE Select	ENSP00000479524.2:p.Asp445=
ENST00000332271.9:c.1335T>C	ENSP00000330031.5:p.Asp445=
ENST00000527701.5:c.1008T>C	ENSP00000435718.1:p.Asp336=
ENST00000532537.2:n.1756T>C
ENST00000533313.5:c.1008T>C	ENSP00000431843.1:p.Asp336=
ENST00000616349.4:c.1335T>C	ENSP00000479524.1:p.Asp445=
NM_001008496.3:c.1335T>C	NP_001008496.2:p.Asp445=
NM_001255975.1:c.1335T>C MANE Select	NP_001242904.1:p.Asp445=
NR_045648.1:n.1966T>C
NR_045649.1:n.1839T>C
NR_045649.2:n.1839T>C