Canonical Allele Identifier: CA1326856076

Gene: SPAG16

Linked Data

• dbSNP Id: rs1696309062

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214324189_214324200del , CM000664.2:g.214324189_214324200del	GRCh38
NC_000002.11:g.215188913_215188924del , CM000664.1:g.215188913_215188924del	GRCh37
NC_000002.10:g.214897158_214897169del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1721-85951_1721-85940del MANE Select	ENSP00000332592.5:n.1721-85951_1721-85940del
ENST00000331683.9:c.1721-85951_1721-85940del	ENSP00000332592.5:n.1721-85951_1721-85940del
ENST00000406979.6:c.*1722-85951_*1722-85940del	ENSP00000385496.2:n.*1722-85951_*1722-85940del
ENST00000451561.1:c.593-85951_593-85940del	ENSP00000416600.1:n.593-85951_593-85940del
ENST00000480494.1:n.463-85951_463-85940del
NM_024532.4:c.1721-85951_1721-85940del	NP_078808.3:n.1721-85951_1721-85940del
NR_047659.1:n.2001-85951_2001-85940del
NR_047660.1:n.1707-85951_1707-85940del
XM_011511814.1:c.1628-85951_1628-85940del	XP_011510116.1:n.1628-85951_1628-85940del
XM_011511819.1:c.1559-85951_1559-85940del	XP_011510121.1:n.1559-85951_1559-85940del
XM_011511820.1:c.1535-85951_1535-85940del	XP_011510122.1:n.1535-85951_1535-85940del
XM_011511821.1:c.1439-85951_1439-85940del	XP_011510123.1:n.1439-85951_1439-85940del
XM_011511822.1:c.1412-85951_1412-85940del	XP_011510124.1:n.1412-85951_1412-85940del
XM_011511823.1:c.1412-85951_1412-85940del	XP_011510125.1:n.1412-85951_1412-85940del
XM_011511825.1:c.1364-85951_1364-85940del	XP_011510127.1:n.1364-85951_1364-85940del
XM_011511835.1:c.797-85951_797-85940del	XP_011510137.1:n.797-85951_797-85940del
XM_011511836.1:c.797-85951_797-85940del	XP_011510138.1:n.797-85951_797-85940del
XM_011511819.2:c.1559-85951_1559-85940del	XP_011510121.1:n.1559-85951_1559-85940del
XM_011511820.2:c.1535-85951_1535-85940del	XP_011510122.1:n.1535-85951_1535-85940del
XM_011511821.2:c.1439-85951_1439-85940del	XP_011510123.1:n.1439-85951_1439-85940del
XM_011511823.3:c.1412-85951_1412-85940del	XP_011510125.1:n.1412-85951_1412-85940del
XM_017004896.1:c.1364-85951_1364-85940del	XP_016860385.1:n.1364-85951_1364-85940del
XM_017004897.1:c.1364-85951_1364-85940del	XP_016860386.1:n.1364-85951_1364-85940del
XM_017004898.1:c.998-85951_998-85940del	XP_016860387.1:n.998-85951_998-85940del
XM_024453140.1:c.803-85951_803-85940del	XP_024308908.1:n.803-85951_803-85940del
NM_024532.5:c.1721-85951_1721-85940del MANE Select	NP_078808.3:n.1721-85951_1721-85940del
NR_047659.2:n.1916-85951_1916-85940del
NR_047660.2:n.1622-85951_1622-85940del