Canonical Allele Identifier: CA1042157955
Gene: SPAG16 HGNC NCBI

Linked Data

dbSNP Id: rs1696294702

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.214323962_214323966dup , CM000664.2:g.214323962_214323966dup GRCh38
NC_000002.11:g.215188686_215188690dup , CM000664.1:g.215188686_215188690dup GRCh37
NC_000002.10:g.214896931_214896935dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000331683.10:c.1721-86178_1721-86174dup MANE Select ENSP00000332592.5:n.1721-86178_1721-86174dup
ENST00000331683.9:c.1721-86178_1721-86174dup ENSP00000332592.5:n.1721-86178_1721-86174dup
ENST00000406979.6:c.*1722-86178_*1722-86174dup ENSP00000385496.2:n.*1722-86178_*1722-86174dup
ENST00000451561.1:c.593-86178_593-86174dup ENSP00000416600.1:n.593-86178_593-86174dup
ENST00000480494.1:n.463-86178_463-86174dup
NM_024532.4:c.1721-86178_1721-86174dup NP_078808.3:n.1721-86178_1721-86174dup
NR_047659.1:n.2001-86178_2001-86174dup
NR_047660.1:n.1707-86178_1707-86174dup
XM_011511814.1:c.1628-86178_1628-86174dup XP_011510116.1:n.1628-86178_1628-86174dup
XM_011511819.1:c.1559-86178_1559-86174dup XP_011510121.1:n.1559-86178_1559-86174dup
XM_011511820.1:c.1535-86178_1535-86174dup XP_011510122.1:n.1535-86178_1535-86174dup
XM_011511821.1:c.1439-86178_1439-86174dup XP_011510123.1:n.1439-86178_1439-86174dup
XM_011511822.1:c.1412-86178_1412-86174dup XP_011510124.1:n.1412-86178_1412-86174dup
XM_011511823.1:c.1412-86178_1412-86174dup XP_011510125.1:n.1412-86178_1412-86174dup
XM_011511825.1:c.1364-86178_1364-86174dup XP_011510127.1:n.1364-86178_1364-86174dup
XM_011511835.1:c.797-86178_797-86174dup XP_011510137.1:n.797-86178_797-86174dup
XM_011511836.1:c.797-86178_797-86174dup XP_011510138.1:n.797-86178_797-86174dup
XM_011511819.2:c.1559-86178_1559-86174dup XP_011510121.1:n.1559-86178_1559-86174dup
XM_011511820.2:c.1535-86178_1535-86174dup XP_011510122.1:n.1535-86178_1535-86174dup
XM_011511821.2:c.1439-86178_1439-86174dup XP_011510123.1:n.1439-86178_1439-86174dup
XM_011511823.3:c.1412-86178_1412-86174dup XP_011510125.1:n.1412-86178_1412-86174dup
XM_017004896.1:c.1364-86178_1364-86174dup XP_016860385.1:n.1364-86178_1364-86174dup
XM_017004897.1:c.1364-86178_1364-86174dup XP_016860386.1:n.1364-86178_1364-86174dup
XM_017004898.1:c.998-86178_998-86174dup XP_016860387.1:n.998-86178_998-86174dup
XM_024453140.1:c.803-86178_803-86174dup XP_024308908.1:n.803-86178_803-86174dup
NM_024532.5:c.1721-86178_1721-86174dup MANE Select NP_078808.3:n.1721-86178_1721-86174dup
NR_047659.2:n.1916-86178_1916-86174dup
NR_047660.2:n.1622-86178_1622-86174dup