Canonical Allele Identifier: CA1326856073

Gene: SPAG16

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214324186_214324191delinsATTACT , CM000664.2:g.214324186_214324191delinsATTACT	GRCh38
NC_000002.11:g.215188910_215188915delinsATTACT , CM000664.1:g.215188910_215188915delinsATTACT	GRCh37
NC_000002.10:g.214897155_214897160delinsATTACT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1721-85954_1721-85949delinsATTACT MANE Select	ENSP00000332592.5:n.1721-85954_1721-85949delinsATTACT
ENST00000331683.9:c.1721-85954_1721-85949delinsATTACT	ENSP00000332592.5:n.1721-85954_1721-85949delinsATTACT
ENST00000406979.6:c.*1722-85954_*1722-85949delinsATTACT	ENSP00000385496.2:n.*1722-85954_*1722-85949delinsATTACT
ENST00000451561.1:c.593-85954_593-85949delinsATTACT	ENSP00000416600.1:n.593-85954_593-85949delinsATTACT
ENST00000480494.1:n.463-85954_463-85949delinsATTACT
NM_024532.4:c.1721-85954_1721-85949delinsATTACT	NP_078808.3:n.1721-85954_1721-85949delinsATTACT
NR_047659.1:n.2001-85954_2001-85949delinsATTACT
NR_047660.1:n.1707-85954_1707-85949delinsATTACT
XM_011511814.1:c.1628-85954_1628-85949delinsATTACT	XP_011510116.1:n.1628-85954_1628-85949delinsATTACT
XM_011511819.1:c.1559-85954_1559-85949delinsATTACT	XP_011510121.1:n.1559-85954_1559-85949delinsATTACT
XM_011511820.1:c.1535-85954_1535-85949delinsATTACT	XP_011510122.1:n.1535-85954_1535-85949delinsATTACT
XM_011511821.1:c.1439-85954_1439-85949delinsATTACT	XP_011510123.1:n.1439-85954_1439-85949delinsATTACT
XM_011511822.1:c.1412-85954_1412-85949delinsATTACT	XP_011510124.1:n.1412-85954_1412-85949delinsATTACT
XM_011511823.1:c.1412-85954_1412-85949delinsATTACT	XP_011510125.1:n.1412-85954_1412-85949delinsATTACT
XM_011511825.1:c.1364-85954_1364-85949delinsATTACT	XP_011510127.1:n.1364-85954_1364-85949delinsATTACT
XM_011511835.1:c.797-85954_797-85949delinsATTACT	XP_011510137.1:n.797-85954_797-85949delinsATTACT
XM_011511836.1:c.797-85954_797-85949delinsATTACT	XP_011510138.1:n.797-85954_797-85949delinsATTACT
XM_011511819.2:c.1559-85954_1559-85949delinsATTACT	XP_011510121.1:n.1559-85954_1559-85949delinsATTACT
XM_011511820.2:c.1535-85954_1535-85949delinsATTACT	XP_011510122.1:n.1535-85954_1535-85949delinsATTACT
XM_011511821.2:c.1439-85954_1439-85949delinsATTACT	XP_011510123.1:n.1439-85954_1439-85949delinsATTACT
XM_011511823.3:c.1412-85954_1412-85949delinsATTACT	XP_011510125.1:n.1412-85954_1412-85949delinsATTACT
XM_017004896.1:c.1364-85954_1364-85949delinsATTACT	XP_016860385.1:n.1364-85954_1364-85949delinsATTACT
XM_017004897.1:c.1364-85954_1364-85949delinsATTACT	XP_016860386.1:n.1364-85954_1364-85949delinsATTACT
XM_017004898.1:c.998-85954_998-85949delinsATTACT	XP_016860387.1:n.998-85954_998-85949delinsATTACT
XM_024453140.1:c.803-85954_803-85949delinsATTACT	XP_024308908.1:n.803-85954_803-85949delinsATTACT
NM_024532.5:c.1721-85954_1721-85949delinsATTACT MANE Select	NP_078808.3:n.1721-85954_1721-85949delinsATTACT
NR_047659.2:n.1916-85954_1916-85949delinsATTACT
NR_047660.2:n.1622-85954_1622-85949delinsATTACT