Canonical Allele Identifier: CA1326856009

Gene: SPAG16

Linked Data

• dbSNP Id: rs1696298202

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214324006_214324007del , CM000664.2:g.214324006_214324007del	GRCh38
NC_000002.11:g.215188730_215188731del , CM000664.1:g.215188730_215188731del	GRCh37
NC_000002.10:g.214896975_214896976del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1721-86134_1721-86133del MANE Select	ENSP00000332592.5:n.1721-86134_1721-86133del
ENST00000331683.9:c.1721-86134_1721-86133del	ENSP00000332592.5:n.1721-86134_1721-86133del
ENST00000406979.6:c.*1722-86134_*1722-86133del	ENSP00000385496.2:n.*1722-86134_*1722-86133del
ENST00000451561.1:c.593-86134_593-86133del	ENSP00000416600.1:n.593-86134_593-86133del
ENST00000480494.1:n.463-86134_463-86133del
NM_024532.4:c.1721-86134_1721-86133del	NP_078808.3:n.1721-86134_1721-86133del
NR_047659.1:n.2001-86134_2001-86133del
NR_047660.1:n.1707-86134_1707-86133del
XM_011511814.1:c.1628-86134_1628-86133del	XP_011510116.1:n.1628-86134_1628-86133del
XM_011511819.1:c.1559-86134_1559-86133del	XP_011510121.1:n.1559-86134_1559-86133del
XM_011511820.1:c.1535-86134_1535-86133del	XP_011510122.1:n.1535-86134_1535-86133del
XM_011511821.1:c.1439-86134_1439-86133del	XP_011510123.1:n.1439-86134_1439-86133del
XM_011511822.1:c.1412-86134_1412-86133del	XP_011510124.1:n.1412-86134_1412-86133del
XM_011511823.1:c.1412-86134_1412-86133del	XP_011510125.1:n.1412-86134_1412-86133del
XM_011511825.1:c.1364-86134_1364-86133del	XP_011510127.1:n.1364-86134_1364-86133del
XM_011511835.1:c.797-86134_797-86133del	XP_011510137.1:n.797-86134_797-86133del
XM_011511836.1:c.797-86134_797-86133del	XP_011510138.1:n.797-86134_797-86133del
XM_011511819.2:c.1559-86134_1559-86133del	XP_011510121.1:n.1559-86134_1559-86133del
XM_011511820.2:c.1535-86134_1535-86133del	XP_011510122.1:n.1535-86134_1535-86133del
XM_011511821.2:c.1439-86134_1439-86133del	XP_011510123.1:n.1439-86134_1439-86133del
XM_011511823.3:c.1412-86134_1412-86133del	XP_011510125.1:n.1412-86134_1412-86133del
XM_017004896.1:c.1364-86134_1364-86133del	XP_016860385.1:n.1364-86134_1364-86133del
XM_017004897.1:c.1364-86134_1364-86133del	XP_016860386.1:n.1364-86134_1364-86133del
XM_017004898.1:c.998-86134_998-86133del	XP_016860387.1:n.998-86134_998-86133del
XM_024453140.1:c.803-86134_803-86133del	XP_024308908.1:n.803-86134_803-86133del
NM_024532.5:c.1721-86134_1721-86133del MANE Select	NP_078808.3:n.1721-86134_1721-86133del
NR_047659.2:n.1916-86134_1916-86133del
NR_047660.2:n.1622-86134_1622-86133del