Canonical Allele Identifier: CA2818558609
Gene: PIWIL3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.24749021_24749022insT , CM000684.2:g.24749021_24749022insT GRCh38
NC_000022.10:g.25144988_25144989insT , CM000684.1:g.25144988_25144989insT GRCh37
NC_000022.9:g.23474988_23474989insT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000527701.6:c.*1307-1_*1307insA ENSP00000435718.2:n.*1307-1_*1307insA
ENST00000533313.6:c.*1261-1_*1261insA ENSP00000431843.2:n.*1261-1_*1261insA
ENST00000616349.5:c.1335-1_1335insA MANE Select ENSP00000479524.2:n.1335-1_1335insA
ENST00000332271.9:c.1335-1_1335insA ENSP00000330031.5:n.1335-1_1335insA
ENST00000527701.5:c.1008-1_1008insA ENSP00000435718.1:n.1008-1_1008insA
ENST00000532537.2:n.1756-1_1756insA
ENST00000533313.5:c.1008-1_1008insA ENSP00000431843.1:n.1008-1_1008insA
ENST00000616349.4:c.1335-1_1335insA ENSP00000479524.1:n.1335-1_1335insA
NM_001008496.3:c.1335-1_1335insA NP_001008496.2:n.1335-1_1335insA
NM_001255975.1:c.1335-1_1335insA MANE Select NP_001242904.1:n.1335-1_1335insA
NR_045648.1:n.1966-1_1966insA
NR_045649.1:n.1839-1_1839insA
NR_045649.2:n.1839-1_1839insA