Canonical Allele Identifier: CA4337577
Community Standard Title: NM_005751.5(AKAP9):c.8747C>A (p.Thr2916Lys)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92084855C>A , CM000669.2:g.92084855C>A GRCh38
NC_000007.13:g.91714169C>A , CM000669.1:g.91714169C>A GRCh37
NC_000007.12:g.91552105C>A NCBI36
NG_011623.1:g.148981C>A , LRG_331:g.148981C>A

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8747C>A MANE Select NP_005742.4:p.Thr2916Lys
ENST00000356239.8:c.8747C>A MANE Select ENSP00000348573.3:p.Thr2916Lys
NM_001379277.1:c.3392C>A NP_001366206.1:p.Thr1131Lys
NM_005751.4:c.8747C>A , LRG_331t1:c.8747C>A NP_005742.4:p.Thr2916Lys
NM_147185.2:c.8723C>A NP_671714.1:p.Thr2908Lys
NM_147185.3:c.8723C>A NP_671714.1:p.Thr2908Lys
ENST00000356239.7:c.8747C>A ENSP00000348573.3:p.Thr2916Lys
ENST00000358100.6:c.8606C>A ENSP00000350813.3:p.Thr2869Lys
ENST00000359028.6:c.8756C>A ENSP00000351922.3:p.Thr2919Lys
ENST00000359028.7:c.8819C>A ENSP00000351922.4:p.Thr2940Lys
ENST00000394534.6:c.2285C>A ENSP00000378042.2:p.Thr762Lys
ENST00000394534.7:c.2240C>A ENSP00000378042.3:p.Thr747Lys
ENST00000435423.1:c.181C>A
ENST00000435423.2:n.587C>A
ENST00000491695.2:c.3392C>A ENSP00000494626.2:p.Thr1131Lys
ENST00000679448.1:c.8723C>A ENSP00000505889.1:p.Thr2908Lys
ENST00000679457.1:c.8723C>A ENSP00000505450.1:p.Thr2908Lys
ENST00000679474.1:n.8945C>A
ENST00000679521.1:c.8693C>A ENSP00000505456.1:p.Thr2898Lys
ENST00000679722.1:n.8969C>A
ENST00000679821.1:c.8489C>A ENSP00000506040.1:p.Thr2830Lys
ENST00000680047.1:n.8945C>A
ENST00000680072.1:c.8570C>A ENSP00000506581.1:p.Thr2857Lys
ENST00000680181.1:c.8654C>A ENSP00000505548.1:p.Thr2885Lys
ENST00000680365.1:c.2240C>A ENSP00000506019.1:p.Thr747Lys
ENST00000680513.1:c.8606C>A ENSP00000505284.1:p.Thr2869Lys
ENST00000680534.1:c.8786C>A ENSP00000506674.1:p.Thr2929Lys
ENST00000680766.1:c.8723C>A ENSP00000505204.1:p.Thr2908Lys
ENST00000680952.1:c.8723C>A ENSP00000506407.1:p.Thr2908Lys
ENST00000681216.1:c.2084C>A ENSP00000505551.1:p.Thr695Lys
ENST00000681412.1:c.8747C>A ENSP00000506486.1:p.Thr2916Lys
ENST00000681722.1:c.8723C>A ENSP00000506566.1:p.Thr2908Lys
XM_006715827.1:c.8606C>A XP_006715890.1:p.Thr2869Lys
XM_011515709.1:c.8894C>A XP_011514011.1:p.Thr2965Lys
XM_011515710.1:c.8918C>A XP_011514012.1:p.Thr2973Lys
XM_011515711.1:c.8858C>A XP_011514013.1:p.Thr2953Lys
XM_011515712.1:c.8855C>A XP_011514014.1:p.Thr2952Lys
XM_011515713.1:c.8840C>A XP_011514015.1:p.Thr2947Lys
XM_011515714.1:c.8879C>A XP_011514016.1:p.Thr2960Lys
XM_011515716.1:c.8798C>A XP_011514018.1:p.Thr2933Lys
XM_011515717.1:c.8753C>A XP_011514019.1:p.Thr2918Lys
XM_011515718.1:c.8783C>A XP_011514020.1:p.Thr2928Lys
XM_011515719.1:c.8759C>A XP_011514021.1:p.Thr2920Lys
XM_011515720.1:c.8642C>A XP_011514022.1:p.Thr2881Lys
XM_011515721.1:c.3407C>A XP_011514023.1:p.Thr1136Lys
XM_011515722.1:c.3368C>A XP_011514024.1:p.Thr1123Lys
XM_017011642.2:c.8882C>A XP_016867131.1:p.Thr2961Lys
XM_017011643.2:c.8843C>A XP_016867132.1:p.Thr2948Lys
XM_017011644.2:c.8882C>A XP_016867133.1:p.Thr2961Lys
XM_017011645.2:c.8828C>A XP_016867134.1:p.Thr2943Lys
XM_017011646.2:c.8843C>A XP_016867135.1:p.Thr2948Lys
XM_017011647.2:c.8789C>A XP_016867136.1:p.Thr2930Lys
XM_017011648.2:c.8786C>A XP_016867137.1:p.Thr2929Lys
XM_017011649.2:c.8819C>A XP_016867138.1:p.Thr2940Lys
XM_017011650.2:c.8747C>A XP_016867139.1:p.Thr2916Lys
XM_017011651.2:c.8741C>A XP_016867140.1:p.Thr2914Lys
XM_017011652.2:c.8882C>A XP_016867141.1:p.Thr2961Lys
XM_017011653.2:c.8654C>A XP_016867142.1:p.Thr2885Lys
XM_017011654.2:c.8606C>A XP_016867143.1:p.Thr2869Lys
XM_017011655.2:c.8510C>A XP_016867144.1:p.Thr2837Lys
XM_017011656.2:c.8510C>A XP_016867145.1:p.Thr2837Lys
XM_017011657.2:c.4547C>A XP_016867146.1:p.Thr1516Lys
XM_017011658.2:c.3431C>A XP_016867147.1:p.Thr1144Lys
XM_017011659.2:c.3392C>A XP_016867148.1:p.Thr1131Lys
XM_017011660.2:c.3392C>A XP_016867149.1:p.Thr1131Lys
XM_024446631.1:c.8645C>A XP_024302399.1:p.Thr2882Lys