Canonical Allele Identifier: CA4336892
Community Standard Title: NM_005751.5(AKAP9):c.5680A>G (p.Lys1894Glu)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92061338A>G , CM000669.2:g.92061338A>G GRCh38
NC_000007.13:g.91690652A>G , CM000669.1:g.91690652A>G GRCh37
NC_000007.12:g.91528588A>G NCBI36
NG_011623.1:g.125464A>G , LRG_331:g.125464A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.5680A>G MANE Select NP_005742.4:p.Lys1894Glu
ENST00000356239.8:c.5680A>G MANE Select ENSP00000348573.3:p.Lys1894Glu
NM_001379277.1:c.325A>G NP_001366206.1:p.Lys109Glu
NM_005751.4:c.5680A>G , LRG_331t1:c.5680A>G NP_005742.4:p.Lys1894Glu
NM_147185.2:c.5680A>G NP_671714.1:p.Lys1894Glu
NM_147185.3:c.5680A>G NP_671714.1:p.Lys1894Glu
ENST00000356239.7:c.5680A>G ENSP00000348573.3:p.Lys1894Glu
ENST00000358100.6:c.5539A>G ENSP00000350813.3:p.Lys1847Glu
ENST00000359028.6:c.5713A>G ENSP00000351922.3:p.Lys1905Glu
ENST00000359028.7:c.5776A>G ENSP00000351922.4:p.Lys1926Glu
ENST00000491695.1:n.868A>G
ENST00000491695.2:c.325A>G ENSP00000494626.2:p.Lys109Glu
ENST00000674381.2:c.*5409A>G ENSP00000501536.2:n.*5409A>G
ENST00000679448.1:c.5680A>G ENSP00000505889.1:p.Lys1894Glu
ENST00000679457.1:c.5680A>G ENSP00000505450.1:p.Lys1894Glu
ENST00000679474.1:n.5902A>G
ENST00000679521.1:c.5626A>G ENSP00000505456.1:p.Lys1876Glu
ENST00000679554.1:c.*5465A>G ENSP00000506415.1:n.*5465A>G
ENST00000679722.1:n.5902A>G
ENST00000679821.1:c.5422A>G ENSP00000506040.1:p.Lys1808Glu
ENST00000680047.1:n.5902A>G
ENST00000680072.1:c.5680A>G ENSP00000506581.1:p.Lys1894Glu
ENST00000680074.1:n.5902A>G
ENST00000680181.1:c.5587A>G ENSP00000505548.1:p.Lys1863Glu
ENST00000680513.1:c.5539A>G ENSP00000505284.1:p.Lys1847Glu
ENST00000680534.1:c.5680A>G ENSP00000506674.1:p.Lys1894Glu
ENST00000680766.1:c.5680A>G ENSP00000505204.1:p.Lys1894Glu
ENST00000680952.1:c.5680A>G ENSP00000506407.1:p.Lys1894Glu
ENST00000681412.1:c.5680A>G ENSP00000506486.1:p.Lys1894Glu
ENST00000681722.1:c.5680A>G ENSP00000506566.1:p.Lys1894Glu
XM_006715827.1:c.5539A>G XP_006715890.1:p.Lys1847Glu
XM_011515709.1:c.5812A>G XP_011514011.1:p.Lys1938Glu
XM_011515710.1:c.5812A>G XP_011514012.1:p.Lys1938Glu
XM_011515711.1:c.5776A>G XP_011514013.1:p.Lys1926Glu
XM_011515712.1:c.5812A>G XP_011514014.1:p.Lys1938Glu
XM_011515713.1:c.5758A>G XP_011514015.1:p.Lys1920Glu
XM_011515714.1:c.5812A>G XP_011514016.1:p.Lys1938Glu
XM_011515716.1:c.5716A>G XP_011514018.1:p.Lys1906Glu
XM_011515717.1:c.5671A>G XP_011514019.1:p.Lys1891Glu
XM_011515718.1:c.5716A>G XP_011514020.1:p.Lys1906Glu
XM_011515719.1:c.5716A>G XP_011514021.1:p.Lys1906Glu
XM_011515720.1:c.5575A>G XP_011514022.1:p.Lys1859Glu
XM_011515721.1:c.325A>G XP_011514023.1:p.Lys109Glu
XM_011515722.1:c.325A>G XP_011514024.1:p.Lys109Glu
XM_017011642.2:c.5776A>G XP_016867131.1:p.Lys1926Glu
XM_017011643.2:c.5776A>G XP_016867132.1:p.Lys1926Glu
XM_017011644.2:c.5776A>G XP_016867133.1:p.Lys1926Glu
XM_017011645.2:c.5722A>G XP_016867134.1:p.Lys1908Glu
XM_017011646.2:c.5776A>G XP_016867135.1:p.Lys1926Glu
XM_017011647.2:c.5683A>G XP_016867136.1:p.Lys1895Glu
XM_017011648.2:c.5680A>G XP_016867137.1:p.Lys1894Glu
XM_017011649.2:c.5776A>G XP_016867138.1:p.Lys1926Glu
XM_017011650.2:c.5680A>G XP_016867139.1:p.Lys1894Glu
XM_017011651.2:c.5635A>G XP_016867140.1:p.Lys1879Glu
XM_017011652.2:c.5776A>G XP_016867141.1:p.Lys1926Glu
XM_017011653.2:c.5587A>G XP_016867142.1:p.Lys1863Glu
XM_017011654.2:c.5539A>G XP_016867143.1:p.Lys1847Glu
XM_017011655.2:c.5404A>G XP_016867144.1:p.Lys1802Glu
XM_017011656.2:c.5404A>G XP_016867145.1:p.Lys1802Glu
XM_017011657.2:c.1441A>G XP_016867146.1:p.Lys481Glu
XM_017011658.2:c.325A>G XP_016867147.1:p.Lys109Glu
XM_017011659.2:c.325A>G XP_016867148.1:p.Lys109Glu
XM_017011660.2:c.325A>G XP_016867149.1:p.Lys109Glu
XM_024446631.1:c.5539A>G XP_024302399.1:p.Lys1847Glu