Canonical Allele Identifier: CA1725747792
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92077835C= , CM000669.2:g.92077835C= GRCh38
NC_000007.13:g.91707149C= , CM000669.1:g.91707149C= GRCh37
NC_000007.12:g.91545085C= NCBI36
NG_011623.1:g.141961C= , LRG_331:g.141961C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000356239.8:c.6905C= MANE Select ENSP00000348573.3:p.Thr2302=
ENST00000359028.7:c.6977C= ENSP00000351922.4:p.Thr2326=
ENST00000394534.7:c.398C= ENSP00000378042.3:p.Thr133=
ENST00000491695.2:c.1550C= ENSP00000494626.2:p.Thr517=
ENST00000674381.2:c.*6634C= ENSP00000501536.2:n.*6634C=
ENST00000679448.1:c.6881C= ENSP00000505889.1:p.Thr2294=
ENST00000679457.1:c.6881C= ENSP00000505450.1:p.Thr2294=
ENST00000679474.1:n.7103C=
ENST00000679521.1:c.6851C= ENSP00000505456.1:p.Thr2284=
ENST00000679554.1:c.*6690C= ENSP00000506415.1:n.*6690C=
ENST00000679722.1:n.7127C=
ENST00000679821.1:c.6647C= ENSP00000506040.1:p.Thr2216=
ENST00000680047.1:n.7103C=
ENST00000680072.1:c.6728C= ENSP00000506581.1:p.Thr2243=
ENST00000680181.1:c.6812C= ENSP00000505548.1:p.Thr2271=
ENST00000680365.1:c.398C= ENSP00000506019.1:p.Thr133=
ENST00000680513.1:c.6764C= ENSP00000505284.1:p.Thr2255=
ENST00000680534.1:c.6944C= ENSP00000506674.1:p.Thr2315=
ENST00000680766.1:c.6881C= ENSP00000505204.1:p.Thr2294=
ENST00000680952.1:c.6881C= ENSP00000506407.1:p.Thr2294=
ENST00000681216.1:c.398C= ENSP00000505551.1:p.Thr133=
ENST00000681412.1:c.6905C= ENSP00000506486.1:p.Thr2302=
ENST00000681722.1:c.6881C= ENSP00000506566.1:p.Thr2294=
ENST00000356239.7:c.6905C= ENSP00000348573.3:p.Thr2302=
ENST00000358100.6:c.6764C= ENSP00000350813.3:p.Thr2255=
ENST00000359028.6:c.6938C= ENSP00000351922.3:p.Thr2313=
ENST00000394534.6:c.443C= ENSP00000378042.2:p.Thr148=
NM_005751.4:c.6905C= , LRG_331t1:c.6905C= NP_005742.4:p.Thr2302=
NM_147185.2:c.6881C= NP_671714.1:p.Thr2294=
XM_006715827.1:c.6764C= XP_006715890.1:p.Thr2255=
XM_011515709.1:c.7052C= XP_011514011.1:p.Thr2351=
XM_011515710.1:c.7076C= XP_011514012.1:p.Thr2359=
XM_011515711.1:c.7016C= XP_011514013.1:p.Thr2339=
XM_011515712.1:c.7013C= XP_011514014.1:p.Thr2338=
XM_011515713.1:c.6998C= XP_011514015.1:p.Thr2333=
XM_011515714.1:c.7037C= XP_011514016.1:p.Thr2346=
XM_011515716.1:c.6956C= XP_011514018.1:p.Thr2319=
XM_011515717.1:c.6911C= XP_011514019.1:p.Thr2304=
XM_011515718.1:c.6941C= XP_011514020.1:p.Thr2314=
XM_011515719.1:c.6917C= XP_011514021.1:p.Thr2306=
XM_011515720.1:c.6800C= XP_011514022.1:p.Thr2267=
XM_011515721.1:c.1565C= XP_011514023.1:p.Thr522=
XM_011515722.1:c.1526C= XP_011514024.1:p.Thr509=
XM_017011642.2:c.7040C= XP_016867131.1:p.Thr2347=
XM_017011643.2:c.7001C= XP_016867132.1:p.Thr2334=
XM_017011644.2:c.7040C= XP_016867133.1:p.Thr2347=
XM_017011645.2:c.6986C= XP_016867134.1:p.Thr2329=
XM_017011646.2:c.7001C= XP_016867135.1:p.Thr2334=
XM_017011647.2:c.6947C= XP_016867136.1:p.Thr2316=
XM_017011648.2:c.6944C= XP_016867137.1:p.Thr2315=
XM_017011649.2:c.6977C= XP_016867138.1:p.Thr2326=
XM_017011650.2:c.6905C= XP_016867139.1:p.Thr2302=
XM_017011651.2:c.6899C= XP_016867140.1:p.Thr2300=
XM_017011652.2:c.7040C= XP_016867141.1:p.Thr2347=
XM_017011653.2:c.6812C= XP_016867142.1:p.Thr2271=
XM_017011654.2:c.6764C= XP_016867143.1:p.Thr2255=
XM_017011655.2:c.6668C= XP_016867144.1:p.Thr2223=
XM_017011656.2:c.6668C= XP_016867145.1:p.Thr2223=
XM_017011657.2:c.2705C= XP_016867146.1:p.Thr902=
XM_017011658.2:c.1589C= XP_016867147.1:p.Thr530=
XM_017011659.2:c.1550C= XP_016867148.1:p.Thr517=
XM_017011660.2:c.1550C= XP_016867149.1:p.Thr517=
XM_024446631.1:c.6803C= XP_024302399.1:p.Thr2268=
NM_147185.3:c.6881C= NP_671714.1:p.Thr2294=
NM_001379277.1:c.1550C= NP_001366206.1:p.Thr517=
NM_005751.5:c.6905C= MANE Select NP_005742.4:p.Thr2302=