Canonical Allele Identifier: CA10155625

Gene: PIWIL3

Linked Data

• dbSNP Id: rs746212688
• ExAC: 22:25144864 ACTGT / A
• gnomAD v2: 22-25144864-ACTGT-A
• gnomAD v3: 22-24748897-ACTGT-A
• gnomAD v4: 22-24748897-ACTGT-A
• MyVariant Identifiers: chr22:g.25144865_25144868del (hg19) ; chr22:g.24748898_24748901del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.24748900_24748903del , CM000684.2:g.24748900_24748903del	GRCh38
NC_000022.10:g.25144867_25144870del , CM000684.1:g.25144867_25144870del	GRCh37
NC_000022.9:g.23474867_23474870del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527701.6:c.*1421+6_*1421+9del	ENSP00000435718.2:n.*1421+6_*1421+9del
ENST00000533313.6:c.*1375+6_*1375+9del	ENSP00000431843.2:n.*1375+6_*1375+9del
ENST00000616349.5:c.1449+6_1449+9del MANE Select	ENSP00000479524.2:n.1449+6_1449+9del
ENST00000332271.9:c.1449+6_1449+9del	ENSP00000330031.5:n.1449+6_1449+9del
ENST00000527701.5:c.1122+6_1122+9del	ENSP00000435718.1:n.1122+6_1122+9del
ENST00000532537.2:n.1870+6_1870+9del
ENST00000533313.5:c.1122+6_1122+9del	ENSP00000431843.1:n.1122+6_1122+9del
ENST00000616349.4:c.1449+6_1449+9del	ENSP00000479524.1:n.1449+6_1449+9del
NM_001008496.3:c.1449+6_1449+9del	NP_001008496.2:n.1449+6_1449+9del
NM_001255975.1:c.1449+6_1449+9del MANE Select	NP_001242904.1:n.1449+6_1449+9del
NR_045648.1:n.2080+6_2080+9del
NR_045649.1:n.1953+6_1953+9del
NR_045649.2:n.1953+6_1953+9del