Canonical Allele Identifier: CA1326691212

Gene: SPAG16

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.213973802C= , CM000664.2:g.213973802C=	GRCh38
NC_000002.11:g.214838526C= , CM000664.1:g.214838526C=	GRCh37
NC_000002.10:g.214546771C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1401-40149C= MANE Select	ENSP00000332592.5:n.1401-40149C=
ENST00000331683.9:c.1401-40149C=	ENSP00000332592.5:n.1401-40149C=
ENST00000406979.6:c.*1402-40149C=	ENSP00000385496.2:n.*1402-40149C=
ENST00000451561.1:c.273-40149C=	ENSP00000416600.1:n.273-40149C=
ENST00000452556.5:c.*967-40149C=	ENSP00000398926.1:n.*967-40149C=
ENST00000480494.1:n.143-40149C=
NM_024532.4:c.1401-40149C=	NP_078808.3:n.1401-40149C=
NR_047659.1:n.1681-40149C=
NR_047660.1:n.1387-40149C=
XM_011511814.1:c.1308-40149C=	XP_011510116.1:n.1308-40149C=
XM_011511815.1:c.1401-40149C=	XP_011510117.1:n.1401-40149C=
XM_011511816.1:c.1401-40149C=	XP_011510118.1:n.1401-40149C=
XM_011511817.1:c.1401-40149C=	XP_011510119.1:n.1401-40149C=
XM_011511818.1:c.1401-40149C=	XP_011510120.1:n.1401-40149C=
XM_011511819.1:c.1239-40149C=	XP_011510121.1:n.1239-40149C=
XM_011511820.1:c.1215-40149C=	XP_011510122.1:n.1215-40149C=
XM_011511821.1:c.1119-40149C=	XP_011510123.1:n.1119-40149C=
XM_011511822.1:c.1092-40149C=	XP_011510124.1:n.1092-40149C=
XM_011511823.1:c.1092-40149C=	XP_011510125.1:n.1092-40149C=
XM_011511824.1:c.1401-40149C=	XP_011510126.1:n.1401-40149C=
XM_011511825.1:c.1044-40149C=	XP_011510127.1:n.1044-40149C=
XM_011511826.1:c.1401-13772C=	XP_011510128.1:n.1401-13772C=
XM_011511835.1:c.477-40149C=	XP_011510137.1:n.477-40149C=
XM_011511836.1:c.477-40149C=	XP_011510138.1:n.477-40149C=
XM_011511815.2:c.1401-40149C=	XP_011510117.1:n.1401-40149C=
XM_011511816.3:c.1401-40149C=	XP_011510118.1:n.1401-40149C=
XM_011511817.2:c.1401-40149C=	XP_011510119.1:n.1401-40149C=
XM_011511818.2:c.1401-40149C=	XP_011510120.1:n.1401-40149C=
XM_011511819.2:c.1239-40149C=	XP_011510121.1:n.1239-40149C=
XM_011511820.2:c.1215-40149C=	XP_011510122.1:n.1215-40149C=
XM_011511821.2:c.1119-40149C=	XP_011510123.1:n.1119-40149C=
XM_011511823.3:c.1092-40149C=	XP_011510125.1:n.1092-40149C=
XM_011511824.2:c.1401-40149C=	XP_011510126.1:n.1401-40149C=
XM_017004896.1:c.1044-40149C=	XP_016860385.1:n.1044-40149C=
XM_017004897.1:c.1044-40149C=	XP_016860386.1:n.1044-40149C=
XM_017004898.1:c.678-40149C=	XP_016860387.1:n.678-40149C=
XM_024453140.1:c.483-40149C=	XP_024308908.1:n.483-40149C=
NM_024532.5:c.1401-40149C= MANE Select	NP_078808.3:n.1401-40149C=
NR_047659.2:n.1596-40149C=
NR_047660.2:n.1302-40149C=