Canonical Allele Identifier: CA539703887

Gene: SPAG16

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.213852855C>G , CM000664.2:g.213852855C>G	GRCh38
NC_000002.11:g.214717579C>G , CM000664.1:g.214717579C>G	GRCh37
NC_000002.10:g.214425824C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000331683.10:c.1071-9630C>G MANE Select	ENSP00000332592.5:n.1071-9630C>G
ENST00000331683.9:c.1071-9630C>G	ENSP00000332592.5:n.1071-9630C>G
ENST00000406979.6:c.*1072-9630C>G	ENSP00000385496.2:n.*1072-9630C>G
ENST00000451561.1:c.129-9630C>G	ENSP00000416600.1:n.129-9630C>G
ENST00000452556.5:c.*637-9630C>G	ENSP00000398926.1:n.*637-9630C>G
NM_024532.4:c.1071-9630C>G	NP_078808.3:n.1071-9630C>G
NR_047659.1:n.1351-9630C>G
NR_047660.1:n.1057-9630C>G
XM_011511814.1:c.978-9630C>G	XP_011510116.1:n.978-9630C>G
XM_011511815.1:c.1071-9630C>G	XP_011510117.1:n.1071-9630C>G
XM_011511816.1:c.1071-9630C>G	XP_011510118.1:n.1071-9630C>G
XM_011511817.1:c.1071-9630C>G	XP_011510119.1:n.1071-9630C>G
XM_011511818.1:c.1071-9630C>G	XP_011510120.1:n.1071-9630C>G
XM_011511819.1:c.909-9630C>G	XP_011510121.1:n.909-9630C>G
XM_011511820.1:c.1071-9630C>G	XP_011510122.1:n.1071-9630C>G
XM_011511821.1:c.789-9630C>G	XP_011510123.1:n.789-9630C>G
XM_011511822.1:c.762-9630C>G	XP_011510124.1:n.762-9630C>G
XM_011511823.1:c.762-9630C>G	XP_011510125.1:n.762-9630C>G
XM_011511824.1:c.1071-9630C>G	XP_011510126.1:n.1071-9630C>G
XM_011511825.1:c.714-9630C>G	XP_011510127.1:n.714-9630C>G
XM_011511826.1:c.1071-9630C>G	XP_011510128.1:n.1071-9630C>G
XM_011511831.1:c.1071-5458C>G	XP_011510133.1:n.1071-5458C>G
XM_011511835.1:c.147-9630C>G	XP_011510137.1:n.147-9630C>G
XM_011511836.1:c.147-9630C>G	XP_011510138.1:n.147-9630C>G
XM_011511815.2:c.1071-9630C>G	XP_011510117.1:n.1071-9630C>G
XM_011511816.3:c.1071-9630C>G	XP_011510118.1:n.1071-9630C>G
XM_011511817.2:c.1071-9630C>G	XP_011510119.1:n.1071-9630C>G
XM_011511818.2:c.1071-9630C>G	XP_011510120.1:n.1071-9630C>G
XM_011511819.2:c.909-9630C>G	XP_011510121.1:n.909-9630C>G
XM_011511820.2:c.1071-9630C>G	XP_011510122.1:n.1071-9630C>G
XM_011511821.2:c.789-9630C>G	XP_011510123.1:n.789-9630C>G
XM_011511823.3:c.762-9630C>G	XP_011510125.1:n.762-9630C>G
XM_011511824.2:c.1071-9630C>G	XP_011510126.1:n.1071-9630C>G
XM_011511831.2:c.1071-5458C>G	XP_011510133.1:n.1071-5458C>G
XM_017004896.1:c.714-9630C>G	XP_016860385.1:n.714-9630C>G
XM_017004897.1:c.714-9630C>G	XP_016860386.1:n.714-9630C>G
XM_017004898.1:c.348-9630C>G	XP_016860387.1:n.348-9630C>G
XM_024453140.1:c.153-9630C>G	XP_024308908.1:n.153-9630C>G
NM_024532.5:c.1071-9630C>G MANE Select	NP_078808.3:n.1071-9630C>G
NR_047659.2:n.1266-9630C>G
NR_047660.2:n.972-9630C>G