Canonical Allele Identifier: CA1104444566
Gene: AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92040689_92040690insTTTTTTTTTTTTTT , CM000669.2:g.92040689_92040690insTTTTTTTTTTTTTT GRCh38
NC_000007.13:g.91670003_91670004insTTTTTTTTTTTTTT , CM000669.1:g.91670003_91670004insTTTTTTTTTTTTTT GRCh37
NC_000007.12:g.91507939_91507940insTTTTTTTTTTTTTT NCBI36
NG_011623.1:g.104815_104816insTTTTTTTTTTTTTT , LRG_331:g.104815_104816insTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000356239.8:c.4708_4709insTTTTTTTTTTTTTT MANE Select ENSP00000348573.3:p.Ser1570PhefsTer16
ENST00000359028.7:c.4708_4709insTTTTTTTTTTTTTT ENSP00000351922.4:p.Ser1570PhefsTer16
ENST00000674381.2:c.*4437_*4438insTTTTTTTTTTTTTT ENSP00000501536.2:n.*4437_*4438insTTTTTTTTTTTTTT
ENST00000679448.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000505889.1:p.Ser1570PhefsTer16
ENST00000679457.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000505450.1:p.Ser1570PhefsTer16
ENST00000679474.1:n.4930_4931insTTTTTTTTTTTTTT
ENST00000679521.1:c.4654_4655insTTTTTTTTTTTTTT ENSP00000505456.1:p.Ser1552PhefsTer16
ENST00000679554.1:c.*4493_*4494insTTTTTTTTTTTTTT ENSP00000506415.1:n.*4493_*4494insTTTTTTTTTTTTTT
ENST00000679722.1:n.4930_4931insTTTTTTTTTTTTTT
ENST00000679821.1:c.4450_4451insTTTTTTTTTTTTTT ENSP00000506040.1:p.Ser1484PhefsTer16
ENST00000680047.1:n.4930_4931insTTTTTTTTTTTTTT
ENST00000680072.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000506581.1:p.Ser1570PhefsTer16
ENST00000680074.1:n.4930_4931insTTTTTTTTTTTTTT
ENST00000680181.1:c.4615_4616insTTTTTTTTTTTTTT ENSP00000505548.1:p.Ser1539PhefsTer16
ENST00000680513.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000505284.1:p.Ser1570PhefsTer16
ENST00000680534.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000506674.1:p.Ser1570PhefsTer16
ENST00000680766.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000505204.1:p.Ser1570PhefsTer16
ENST00000680952.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000506407.1:p.Ser1570PhefsTer16
ENST00000681412.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000506486.1:p.Ser1570PhefsTer16
ENST00000681722.1:c.4708_4709insTTTTTTTTTTTTTT ENSP00000506566.1:p.Ser1570PhefsTer16
ENST00000356239.7:c.4708_4709insTTTTTTTTTTTTTT ENSP00000348573.3:p.Ser1570PhefsTer16
ENST00000358100.6:c.4708_4709insTTTTTTTTTTTTTT ENSP00000350813.3:p.Ser1570PhefsTer16
ENST00000359028.6:c.4741_4742insTTTTTTTTTTTTTT ENSP00000351922.3:p.Ser1581PhefsTer16
ENST00000493453.1:n.4928_4929insTTTTTTTTTTTTTT
ENST00000619023.4:c.4732_4733insTTTTTTTTTTTTTT ENSP00000480807.1:p.Ser1578PhefsTer16
NM_005751.4:c.4708_4709insTTTTTTTTTTTTTT , LRG_331t1:c.4708_4709insTTTTTTTTTTTTTT NP_005742.4:p.Ser1570PhefsTer16
NM_147185.2:c.4708_4709insTTTTTTTTTTTTTT NP_671714.1:p.Ser1570PhefsTer16
XM_006715827.1:c.4708_4709insTTTTTTTTTTTTTT XP_006715890.1:p.Ser1570PhefsTer16
XM_011515709.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514011.1:p.Ser1582PhefsTer16
XM_011515710.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514012.1:p.Ser1582PhefsTer16
XM_011515711.1:c.4708_4709insTTTTTTTTTTTTTT XP_011514013.1:p.Ser1570PhefsTer16
XM_011515712.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514014.1:p.Ser1582PhefsTer16
XM_011515713.1:c.4690_4691insTTTTTTTTTTTTTT XP_011514015.1:p.Ser1564PhefsTer16
XM_011515714.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514016.1:p.Ser1582PhefsTer16
XM_011515716.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514018.1:p.Ser1582PhefsTer16
XM_011515717.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514019.1:p.Ser1582PhefsTer16
XM_011515718.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514020.1:p.Ser1582PhefsTer16
XM_011515719.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514021.1:p.Ser1582PhefsTer16
XM_011515720.1:c.4744_4745insTTTTTTTTTTTTTT XP_011514022.1:p.Ser1582PhefsTer16
XM_017011642.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867131.1:p.Ser1570PhefsTer16
XM_017011643.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867132.1:p.Ser1570PhefsTer16
XM_017011644.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867133.1:p.Ser1570PhefsTer16
XM_017011645.2:c.4654_4655insTTTTTTTTTTTTTT XP_016867134.1:p.Ser1552PhefsTer16
XM_017011646.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867135.1:p.Ser1570PhefsTer16
XM_017011647.2:c.4615_4616insTTTTTTTTTTTTTT XP_016867136.1:p.Ser1539PhefsTer16
XM_017011648.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867137.1:p.Ser1570PhefsTer16
XM_017011649.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867138.1:p.Ser1570PhefsTer16
XM_017011650.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867139.1:p.Ser1570PhefsTer16
XM_017011651.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867140.1:p.Ser1570PhefsTer16
XM_017011652.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867141.1:p.Ser1570PhefsTer16
XM_017011653.2:c.4615_4616insTTTTTTTTTTTTTT XP_016867142.1:p.Ser1539PhefsTer16
XM_017011654.2:c.4708_4709insTTTTTTTTTTTTTT XP_016867143.1:p.Ser1570PhefsTer16
XM_017011655.2:c.4336_4337insTTTTTTTTTTTTTT XP_016867144.1:p.Ser1446PhefsTer16
XM_017011656.2:c.4336_4337insTTTTTTTTTTTTTT XP_016867145.1:p.Ser1446PhefsTer16
XM_017011657.2:c.373_374insTTTTTTTTTTTTTT XP_016867146.1:p.Ser125PhefsTer16
XM_024446631.1:c.4708_4709insTTTTTTTTTTTTTT XP_024302399.1:p.Ser1570PhefsTer16
NM_147185.3:c.4708_4709insTTTTTTTTTTTTTT NP_671714.1:p.Ser1570PhefsTer16
NM_005751.5:c.4708_4709insTTTTTTTTTTTTTT MANE Select NP_005742.4:p.Ser1570PhefsTer16