Canonical Allele Identifier: CA1326855917

Gene: SPAG16

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214323811_214323826delinsCTAGGAAAGATCAAAT , CM000664.2:g.214323811_214323826delinsCTAGGAAAGATCAAAT	GRCh38
NC_000002.11:g.215188535_215188550delinsCTAGGAAAGATCAAAT , CM000664.1:g.215188535_215188550delinsCTAGGAAAGATCAAAT	GRCh37
NC_000002.10:g.214896780_214896795delinsCTAGGAAAGATCAAAT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1721-86329_1721-86314delinsCTAGGAAAGATCAAAT MANE Select	ENSP00000332592.5:n.1721-86329_1721-86314delinsCTAGGAAAGATCAA...
ENST00000331683.9:c.1721-86329_1721-86314delinsCTAGGAAAGATCAAAT	ENSP00000332592.5:n.1721-86329_1721-86314delinsCTAGGAAAGATCAA...
ENST00000406979.6:c.*1722-86329_*1722-86314delinsCTAGGAAAGATCAAAT	ENSP00000385496.2:n.*1722-86329_*1722-86314delinsCTAGGAAAGATC...
ENST00000451561.1:c.593-86329_593-86314delinsCTAGGAAAGATCAAAT	ENSP00000416600.1:n.593-86329_593-86314delinsCTAGGAAAGATCAAAT...
ENST00000480494.1:n.463-86329_463-86314delinsCTAGGAAAGATCAAAT
NM_024532.4:c.1721-86329_1721-86314delinsCTAGGAAAGATCAAAT	NP_078808.3:n.1721-86329_1721-86314delinsCTAGGAAAGATCAAAT
NR_047659.1:n.2001-86329_2001-86314delinsCTAGGAAAGATCAAAT
NR_047660.1:n.1707-86329_1707-86314delinsCTAGGAAAGATCAAAT
XM_011511814.1:c.1628-86329_1628-86314delinsCTAGGAAAGATCAAAT	XP_011510116.1:n.1628-86329_1628-86314delinsCTAGGAAAGATCAAAT
XM_011511819.1:c.1559-86329_1559-86314delinsCTAGGAAAGATCAAAT	XP_011510121.1:n.1559-86329_1559-86314delinsCTAGGAAAGATCAAAT
XM_011511820.1:c.1535-86329_1535-86314delinsCTAGGAAAGATCAAAT	XP_011510122.1:n.1535-86329_1535-86314delinsCTAGGAAAGATCAAAT
XM_011511821.1:c.1439-86329_1439-86314delinsCTAGGAAAGATCAAAT	XP_011510123.1:n.1439-86329_1439-86314delinsCTAGGAAAGATCAAAT
XM_011511822.1:c.1412-86329_1412-86314delinsCTAGGAAAGATCAAAT	XP_011510124.1:n.1412-86329_1412-86314delinsCTAGGAAAGATCAAAT
XM_011511823.1:c.1412-86329_1412-86314delinsCTAGGAAAGATCAAAT	XP_011510125.1:n.1412-86329_1412-86314delinsCTAGGAAAGATCAAAT
XM_011511825.1:c.1364-86329_1364-86314delinsCTAGGAAAGATCAAAT	XP_011510127.1:n.1364-86329_1364-86314delinsCTAGGAAAGATCAAAT
XM_011511835.1:c.797-86329_797-86314delinsCTAGGAAAGATCAAAT	XP_011510137.1:n.797-86329_797-86314delinsCTAGGAAAGATCAAAT
XM_011511836.1:c.797-86329_797-86314delinsCTAGGAAAGATCAAAT	XP_011510138.1:n.797-86329_797-86314delinsCTAGGAAAGATCAAAT
XM_011511819.2:c.1559-86329_1559-86314delinsCTAGGAAAGATCAAAT	XP_011510121.1:n.1559-86329_1559-86314delinsCTAGGAAAGATCAAAT
XM_011511820.2:c.1535-86329_1535-86314delinsCTAGGAAAGATCAAAT	XP_011510122.1:n.1535-86329_1535-86314delinsCTAGGAAAGATCAAAT
XM_011511821.2:c.1439-86329_1439-86314delinsCTAGGAAAGATCAAAT	XP_011510123.1:n.1439-86329_1439-86314delinsCTAGGAAAGATCAAAT
XM_011511823.3:c.1412-86329_1412-86314delinsCTAGGAAAGATCAAAT	XP_011510125.1:n.1412-86329_1412-86314delinsCTAGGAAAGATCAAAT
XM_017004896.1:c.1364-86329_1364-86314delinsCTAGGAAAGATCAAAT	XP_016860385.1:n.1364-86329_1364-86314delinsCTAGGAAAGATCAAAT
XM_017004897.1:c.1364-86329_1364-86314delinsCTAGGAAAGATCAAAT	XP_016860386.1:n.1364-86329_1364-86314delinsCTAGGAAAGATCAAAT
XM_017004898.1:c.998-86329_998-86314delinsCTAGGAAAGATCAAAT	XP_016860387.1:n.998-86329_998-86314delinsCTAGGAAAGATCAAAT
XM_024453140.1:c.803-86329_803-86314delinsCTAGGAAAGATCAAAT	XP_024308908.1:n.803-86329_803-86314delinsCTAGGAAAGATCAAAT
NM_024532.5:c.1721-86329_1721-86314delinsCTAGGAAAGATCAAAT MANE Select	NP_078808.3:n.1721-86329_1721-86314delinsCTAGGAAAGATCAAAT
NR_047659.2:n.1916-86329_1916-86314delinsCTAGGAAAGATCAAAT
NR_047660.2:n.1622-86329_1622-86314delinsCTAGGAAAGATCAAAT