Canonical Allele Identifier: CA161885427
Community Standard Title: NM_005751.5(AKAP9):c.7363A>G (p.Ile2455Val)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92079496A>G , CM000669.2:g.92079496A>G GRCh38
NC_000007.13:g.91708810A>G , CM000669.1:g.91708810A>G GRCh37
NC_000007.12:g.91546746A>G NCBI36
NG_011623.1:g.143622A>G , LRG_331:g.143622A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.7363A>G MANE Select NP_005742.4:p.Ile2455Val
ENST00000356239.8:c.7363A>G MANE Select ENSP00000348573.3:p.Ile2455Val
NM_001379277.1:c.2008A>G NP_001366206.1:p.Ile670Val
NM_005751.4:c.7363A>G , LRG_331t1:c.7363A>G NP_005742.4:p.Ile2455Val
NM_147185.2:c.7339A>G NP_671714.1:p.Ile2447Val
NM_147185.3:c.7339A>G NP_671714.1:p.Ile2447Val
ENST00000356239.7:c.7363A>G ENSP00000348573.3:p.Ile2455Val
ENST00000358100.6:c.7222A>G ENSP00000350813.3:p.Ile2408Val
ENST00000359028.6:c.7396A>G ENSP00000351922.3:p.Ile2466Val
ENST00000359028.7:c.7435A>G ENSP00000351922.4:p.Ile2479Val
ENST00000394534.6:c.901A>G ENSP00000378042.2:p.Ile301Val
ENST00000394534.7:c.856A>G ENSP00000378042.3:p.Ile286Val
ENST00000491695.2:c.2008A>G ENSP00000494626.2:p.Ile670Val
ENST00000674381.2:c.*7092A>G ENSP00000501536.2:n.*7092A>G
ENST00000679448.1:c.7339A>G ENSP00000505889.1:p.Ile2447Val
ENST00000679457.1:c.7339A>G ENSP00000505450.1:p.Ile2447Val
ENST00000679474.1:n.7561A>G
ENST00000679521.1:c.7309A>G ENSP00000505456.1:p.Ile2437Val
ENST00000679554.1:c.*7148A>G ENSP00000506415.1:n.*7148A>G
ENST00000679722.1:n.7585A>G
ENST00000679821.1:c.7105A>G ENSP00000506040.1:p.Ile2369Val
ENST00000680047.1:n.7561A>G
ENST00000680072.1:c.7186A>G ENSP00000506581.1:p.Ile2396Val
ENST00000680181.1:c.7270A>G ENSP00000505548.1:p.Ile2424Val
ENST00000680365.1:c.856A>G ENSP00000506019.1:p.Ile286Val
ENST00000680513.1:c.7222A>G ENSP00000505284.1:p.Ile2408Val
ENST00000680534.1:c.7402A>G ENSP00000506674.1:p.Ile2468Val
ENST00000680766.1:c.7339A>G ENSP00000505204.1:p.Ile2447Val
ENST00000680952.1:c.7339A>G ENSP00000506407.1:p.Ile2447Val
ENST00000681216.1:c.856A>G ENSP00000505551.1:p.Ile286Val
ENST00000681412.1:c.7363A>G ENSP00000506486.1:p.Ile2455Val
ENST00000681722.1:c.7339A>G ENSP00000506566.1:p.Ile2447Val
XM_006715827.1:c.7222A>G XP_006715890.1:p.Ile2408Val
XM_011515709.1:c.7510A>G XP_011514011.1:p.Ile2504Val
XM_011515710.1:c.7534A>G XP_011514012.1:p.Ile2512Val
XM_011515711.1:c.7474A>G XP_011514013.1:p.Ile2492Val
XM_011515712.1:c.7471A>G XP_011514014.1:p.Ile2491Val
XM_011515713.1:c.7456A>G XP_011514015.1:p.Ile2486Val
XM_011515714.1:c.7495A>G XP_011514016.1:p.Ile2499Val
XM_011515716.1:c.7414A>G XP_011514018.1:p.Ile2472Val
XM_011515717.1:c.7369A>G XP_011514019.1:p.Ile2457Val
XM_011515718.1:c.7399A>G XP_011514020.1:p.Ile2467Val
XM_011515719.1:c.7375A>G XP_011514021.1:p.Ile2459Val
XM_011515720.1:c.7258A>G XP_011514022.1:p.Ile2420Val
XM_011515721.1:c.2023A>G XP_011514023.1:p.Ile675Val
XM_011515722.1:c.1984A>G XP_011514024.1:p.Ile662Val
XM_017011642.2:c.7498A>G XP_016867131.1:p.Ile2500Val
XM_017011643.2:c.7459A>G XP_016867132.1:p.Ile2487Val
XM_017011644.2:c.7498A>G XP_016867133.1:p.Ile2500Val
XM_017011645.2:c.7444A>G XP_016867134.1:p.Ile2482Val
XM_017011646.2:c.7459A>G XP_016867135.1:p.Ile2487Val
XM_017011647.2:c.7405A>G XP_016867136.1:p.Ile2469Val
XM_017011648.2:c.7402A>G XP_016867137.1:p.Ile2468Val
XM_017011649.2:c.7435A>G XP_016867138.1:p.Ile2479Val
XM_017011650.2:c.7363A>G XP_016867139.1:p.Ile2455Val
XM_017011651.2:c.7357A>G XP_016867140.1:p.Ile2453Val
XM_017011652.2:c.7498A>G XP_016867141.1:p.Ile2500Val
XM_017011653.2:c.7270A>G XP_016867142.1:p.Ile2424Val
XM_017011654.2:c.7222A>G XP_016867143.1:p.Ile2408Val
XM_017011655.2:c.7126A>G XP_016867144.1:p.Ile2376Val
XM_017011656.2:c.7126A>G XP_016867145.1:p.Ile2376Val
XM_017011657.2:c.3163A>G XP_016867146.1:p.Ile1055Val
XM_017011658.2:c.2047A>G XP_016867147.1:p.Ile683Val
XM_017011659.2:c.2008A>G XP_016867148.1:p.Ile670Val
XM_017011660.2:c.2008A>G XP_016867149.1:p.Ile670Val
XM_024446631.1:c.7261A>G XP_024302399.1:p.Ile2421Val