Canonical Allele Identifier: CA368131269
Community Standard Title: NM_005751.5(AKAP9):c.5528T>C (p.Met1843Thr)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92052885T>C , CM000669.2:g.92052885T>C GRCh38
NC_000007.13:g.91682199T>C , CM000669.1:g.91682199T>C GRCh37
NC_000007.12:g.91520135T>C NCBI36
NG_011623.1:g.117011T>C , LRG_331:g.117011T>C

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.5528T>C MANE Select NP_005742.4:p.Met1843Thr
ENST00000356239.8:c.5528T>C MANE Select ENSP00000348573.3:p.Met1843Thr
NM_005751.4:c.5528T>C , LRG_331t1:c.5528T>C NP_005742.4:p.Met1843Thr
NM_147185.2:c.5528T>C NP_671714.1:p.Met1843Thr
NM_147185.3:c.5528T>C NP_671714.1:p.Met1843Thr
ENST00000356239.7:c.5528T>C ENSP00000348573.3:p.Met1843Thr
ENST00000358100.6:c.5387T>C ENSP00000350813.3:p.Met1796Thr
ENST00000359028.6:c.5561T>C ENSP00000351922.3:p.Met1854Thr
ENST00000359028.7:c.5624T>C ENSP00000351922.4:p.Met1875Thr
ENST00000674381.2:c.*5257T>C ENSP00000501536.2:n.*5257T>C
ENST00000679448.1:c.5528T>C ENSP00000505889.1:p.Met1843Thr
ENST00000679457.1:c.5528T>C ENSP00000505450.1:p.Met1843Thr
ENST00000679474.1:n.5750T>C
ENST00000679521.1:c.5474T>C ENSP00000505456.1:p.Met1825Thr
ENST00000679554.1:c.*5313T>C ENSP00000506415.1:n.*5313T>C
ENST00000679722.1:n.5750T>C
ENST00000679821.1:c.5270T>C ENSP00000506040.1:p.Met1757Thr
ENST00000680047.1:n.5750T>C
ENST00000680072.1:c.5528T>C ENSP00000506581.1:p.Met1843Thr
ENST00000680074.1:n.5750T>C
ENST00000680181.1:c.5435T>C ENSP00000505548.1:p.Met1812Thr
ENST00000680513.1:c.5387T>C ENSP00000505284.1:p.Met1796Thr
ENST00000680534.1:c.5528T>C ENSP00000506674.1:p.Met1843Thr
ENST00000680766.1:c.5528T>C ENSP00000505204.1:p.Met1843Thr
ENST00000680952.1:c.5528T>C ENSP00000506407.1:p.Met1843Thr
ENST00000681412.1:c.5528T>C ENSP00000506486.1:p.Met1843Thr
ENST00000681722.1:c.5528T>C ENSP00000506566.1:p.Met1843Thr
XM_006715827.1:c.5387T>C XP_006715890.1:p.Met1796Thr
XM_011515709.1:c.5660T>C XP_011514011.1:p.Met1887Thr
XM_011515710.1:c.5660T>C XP_011514012.1:p.Met1887Thr
XM_011515711.1:c.5624T>C XP_011514013.1:p.Met1875Thr
XM_011515712.1:c.5660T>C XP_011514014.1:p.Met1887Thr
XM_011515713.1:c.5606T>C XP_011514015.1:p.Met1869Thr
XM_011515714.1:c.5660T>C XP_011514016.1:p.Met1887Thr
XM_011515716.1:c.5564T>C XP_011514018.1:p.Met1855Thr
XM_011515717.1:c.5519T>C XP_011514019.1:p.Met1840Thr
XM_011515718.1:c.5564T>C XP_011514020.1:p.Met1855Thr
XM_011515719.1:c.5564T>C XP_011514021.1:p.Met1855Thr
XM_011515720.1:c.5423T>C XP_011514022.1:p.Met1808Thr
XM_017011642.2:c.5624T>C XP_016867131.1:p.Met1875Thr
XM_017011643.2:c.5624T>C XP_016867132.1:p.Met1875Thr
XM_017011644.2:c.5624T>C XP_016867133.1:p.Met1875Thr
XM_017011645.2:c.5570T>C XP_016867134.1:p.Met1857Thr
XM_017011646.2:c.5624T>C XP_016867135.1:p.Met1875Thr
XM_017011647.2:c.5531T>C XP_016867136.1:p.Met1844Thr
XM_017011648.2:c.5528T>C XP_016867137.1:p.Met1843Thr
XM_017011649.2:c.5624T>C XP_016867138.1:p.Met1875Thr
XM_017011650.2:c.5528T>C XP_016867139.1:p.Met1843Thr
XM_017011651.2:c.5483T>C XP_016867140.1:p.Met1828Thr
XM_017011652.2:c.5624T>C XP_016867141.1:p.Met1875Thr
XM_017011653.2:c.5435T>C XP_016867142.1:p.Met1812Thr
XM_017011654.2:c.5387T>C XP_016867143.1:p.Met1796Thr
XM_017011655.2:c.5252T>C XP_016867144.1:p.Met1751Thr
XM_017011656.2:c.5252T>C XP_016867145.1:p.Met1751Thr
XM_017011657.2:c.1289T>C XP_016867146.1:p.Met430Thr
XM_024446631.1:c.5387T>C XP_024302399.1:p.Met1796Thr