Canonical Allele Identifier: CA1326691232

Gene: SPAG16

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.213973870T= , CM000664.2:g.213973870T=	GRCh38
NC_000002.11:g.214838594T= , CM000664.1:g.214838594T=	GRCh37
NC_000002.10:g.214546839T=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1401-40081T= MANE Select	ENSP00000332592.5:n.1401-40081T=
ENST00000331683.9:c.1401-40081T=	ENSP00000332592.5:n.1401-40081T=
ENST00000406979.6:c.*1402-40081T=	ENSP00000385496.2:n.*1402-40081T=
ENST00000451561.1:c.273-40081T=	ENSP00000416600.1:n.273-40081T=
ENST00000452556.5:c.*967-40081T=	ENSP00000398926.1:n.*967-40081T=
ENST00000480494.1:n.143-40081T=
NM_024532.4:c.1401-40081T=	NP_078808.3:n.1401-40081T=
NR_047659.1:n.1681-40081T=
NR_047660.1:n.1387-40081T=
XM_011511814.1:c.1308-40081T=	XP_011510116.1:n.1308-40081T=
XM_011511815.1:c.1401-40081T=	XP_011510117.1:n.1401-40081T=
XM_011511816.1:c.1401-40081T=	XP_011510118.1:n.1401-40081T=
XM_011511817.1:c.1401-40081T=	XP_011510119.1:n.1401-40081T=
XM_011511818.1:c.1401-40081T=	XP_011510120.1:n.1401-40081T=
XM_011511819.1:c.1239-40081T=	XP_011510121.1:n.1239-40081T=
XM_011511820.1:c.1215-40081T=	XP_011510122.1:n.1215-40081T=
XM_011511821.1:c.1119-40081T=	XP_011510123.1:n.1119-40081T=
XM_011511822.1:c.1092-40081T=	XP_011510124.1:n.1092-40081T=
XM_011511823.1:c.1092-40081T=	XP_011510125.1:n.1092-40081T=
XM_011511824.1:c.1401-40081T=	XP_011510126.1:n.1401-40081T=
XM_011511825.1:c.1044-40081T=	XP_011510127.1:n.1044-40081T=
XM_011511826.1:c.1401-13704T=	XP_011510128.1:n.1401-13704T=
XM_011511835.1:c.477-40081T=	XP_011510137.1:n.477-40081T=
XM_011511836.1:c.477-40081T=	XP_011510138.1:n.477-40081T=
XM_011511815.2:c.1401-40081T=	XP_011510117.1:n.1401-40081T=
XM_011511816.3:c.1401-40081T=	XP_011510118.1:n.1401-40081T=
XM_011511817.2:c.1401-40081T=	XP_011510119.1:n.1401-40081T=
XM_011511818.2:c.1401-40081T=	XP_011510120.1:n.1401-40081T=
XM_011511819.2:c.1239-40081T=	XP_011510121.1:n.1239-40081T=
XM_011511820.2:c.1215-40081T=	XP_011510122.1:n.1215-40081T=
XM_011511821.2:c.1119-40081T=	XP_011510123.1:n.1119-40081T=
XM_011511823.3:c.1092-40081T=	XP_011510125.1:n.1092-40081T=
XM_011511824.2:c.1401-40081T=	XP_011510126.1:n.1401-40081T=
XM_017004896.1:c.1044-40081T=	XP_016860385.1:n.1044-40081T=
XM_017004897.1:c.1044-40081T=	XP_016860386.1:n.1044-40081T=
XM_017004898.1:c.678-40081T=	XP_016860387.1:n.678-40081T=
XM_024453140.1:c.483-40081T=	XP_024308908.1:n.483-40081T=
NM_024532.5:c.1401-40081T= MANE Select	NP_078808.3:n.1401-40081T=
NR_047659.2:n.1596-40081T=
NR_047660.2:n.1302-40081T=