Canonical Allele Identifier: CA1326856074

Gene: SPAG16

Linked Data

• dbSNP Id: rs1696308872

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214324192_214324196del , CM000664.2:g.214324192_214324196del	GRCh38
NC_000002.11:g.215188916_215188920del , CM000664.1:g.215188916_215188920del	GRCh37
NC_000002.10:g.214897161_214897165del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1721-85948_1721-85944del MANE Select	ENSP00000332592.5:n.1721-85948_1721-85944del
ENST00000331683.9:c.1721-85948_1721-85944del	ENSP00000332592.5:n.1721-85948_1721-85944del
ENST00000406979.6:c.*1722-85948_*1722-85944del	ENSP00000385496.2:n.*1722-85948_*1722-85944del
ENST00000451561.1:c.593-85948_593-85944del	ENSP00000416600.1:n.593-85948_593-85944del
ENST00000480494.1:n.463-85948_463-85944del
NM_024532.4:c.1721-85948_1721-85944del	NP_078808.3:n.1721-85948_1721-85944del
NR_047659.1:n.2001-85948_2001-85944del
NR_047660.1:n.1707-85948_1707-85944del
XM_011511814.1:c.1628-85948_1628-85944del	XP_011510116.1:n.1628-85948_1628-85944del
XM_011511819.1:c.1559-85948_1559-85944del	XP_011510121.1:n.1559-85948_1559-85944del
XM_011511820.1:c.1535-85948_1535-85944del	XP_011510122.1:n.1535-85948_1535-85944del
XM_011511821.1:c.1439-85948_1439-85944del	XP_011510123.1:n.1439-85948_1439-85944del
XM_011511822.1:c.1412-85948_1412-85944del	XP_011510124.1:n.1412-85948_1412-85944del
XM_011511823.1:c.1412-85948_1412-85944del	XP_011510125.1:n.1412-85948_1412-85944del
XM_011511825.1:c.1364-85948_1364-85944del	XP_011510127.1:n.1364-85948_1364-85944del
XM_011511835.1:c.797-85948_797-85944del	XP_011510137.1:n.797-85948_797-85944del
XM_011511836.1:c.797-85948_797-85944del	XP_011510138.1:n.797-85948_797-85944del
XM_011511819.2:c.1559-85948_1559-85944del	XP_011510121.1:n.1559-85948_1559-85944del
XM_011511820.2:c.1535-85948_1535-85944del	XP_011510122.1:n.1535-85948_1535-85944del
XM_011511821.2:c.1439-85948_1439-85944del	XP_011510123.1:n.1439-85948_1439-85944del
XM_011511823.3:c.1412-85948_1412-85944del	XP_011510125.1:n.1412-85948_1412-85944del
XM_017004896.1:c.1364-85948_1364-85944del	XP_016860385.1:n.1364-85948_1364-85944del
XM_017004897.1:c.1364-85948_1364-85944del	XP_016860386.1:n.1364-85948_1364-85944del
XM_017004898.1:c.998-85948_998-85944del	XP_016860387.1:n.998-85948_998-85944del
XM_024453140.1:c.803-85948_803-85944del	XP_024308908.1:n.803-85948_803-85944del
NM_024532.5:c.1721-85948_1721-85944del MANE Select	NP_078808.3:n.1721-85948_1721-85944del
NR_047659.2:n.1916-85948_1916-85944del
NR_047660.2:n.1622-85948_1622-85944del