Canonical Allele Identifier: CA1326856059
Gene: SPAG16 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214324133_214324134delinsTC , CM000664.2:g.214324133_214324134delinsTC GRCh38
NC_000002.11:g.215188857_215188858delinsTC , CM000664.1:g.215188857_215188858delinsTC GRCh37
NC_000002.10:g.214897102_214897103delinsTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331683.10:c.1721-86007_1721-86006delinsTC MANE Select ENSP00000332592.5:n.1721-86007_1721-86006delinsTC
ENST00000331683.9:c.1721-86007_1721-86006delinsTC ENSP00000332592.5:n.1721-86007_1721-86006delinsTC
ENST00000406979.6:c.*1722-86007_*1722-86006delinsTC ENSP00000385496.2:n.*1722-86007_*1722-86006delinsTC
ENST00000451561.1:c.593-86007_593-86006delinsTC ENSP00000416600.1:n.593-86007_593-86006delinsTC
ENST00000480494.1:n.463-86007_463-86006delinsTC
NM_024532.4:c.1721-86007_1721-86006delinsTC NP_078808.3:n.1721-86007_1721-86006delinsTC
NR_047659.1:n.2001-86007_2001-86006delinsTC
NR_047660.1:n.1707-86007_1707-86006delinsTC
XM_011511814.1:c.1628-86007_1628-86006delinsTC XP_011510116.1:n.1628-86007_1628-86006delinsTC
XM_011511819.1:c.1559-86007_1559-86006delinsTC XP_011510121.1:n.1559-86007_1559-86006delinsTC
XM_011511820.1:c.1535-86007_1535-86006delinsTC XP_011510122.1:n.1535-86007_1535-86006delinsTC
XM_011511821.1:c.1439-86007_1439-86006delinsTC XP_011510123.1:n.1439-86007_1439-86006delinsTC
XM_011511822.1:c.1412-86007_1412-86006delinsTC XP_011510124.1:n.1412-86007_1412-86006delinsTC
XM_011511823.1:c.1412-86007_1412-86006delinsTC XP_011510125.1:n.1412-86007_1412-86006delinsTC
XM_011511825.1:c.1364-86007_1364-86006delinsTC XP_011510127.1:n.1364-86007_1364-86006delinsTC
XM_011511835.1:c.797-86007_797-86006delinsTC XP_011510137.1:n.797-86007_797-86006delinsTC
XM_011511836.1:c.797-86007_797-86006delinsTC XP_011510138.1:n.797-86007_797-86006delinsTC
XM_011511819.2:c.1559-86007_1559-86006delinsTC XP_011510121.1:n.1559-86007_1559-86006delinsTC
XM_011511820.2:c.1535-86007_1535-86006delinsTC XP_011510122.1:n.1535-86007_1535-86006delinsTC
XM_011511821.2:c.1439-86007_1439-86006delinsTC XP_011510123.1:n.1439-86007_1439-86006delinsTC
XM_011511823.3:c.1412-86007_1412-86006delinsTC XP_011510125.1:n.1412-86007_1412-86006delinsTC
XM_017004896.1:c.1364-86007_1364-86006delinsTC XP_016860385.1:n.1364-86007_1364-86006delinsTC
XM_017004897.1:c.1364-86007_1364-86006delinsTC XP_016860386.1:n.1364-86007_1364-86006delinsTC
XM_017004898.1:c.998-86007_998-86006delinsTC XP_016860387.1:n.998-86007_998-86006delinsTC
XM_024453140.1:c.803-86007_803-86006delinsTC XP_024308908.1:n.803-86007_803-86006delinsTC
NM_024532.5:c.1721-86007_1721-86006delinsTC MANE Select NP_078808.3:n.1721-86007_1721-86006delinsTC
NR_047659.2:n.1916-86007_1916-86006delinsTC
NR_047660.2:n.1622-86007_1622-86006delinsTC