Canonical Allele Identifier: CA4337586
Community Standard Title: NM_005751.5(AKAP9):c.8783G>A (p.Arg2928Gln)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92084891G>A , CM000669.2:g.92084891G>A GRCh38
NC_000007.13:g.91714205G>A , CM000669.1:g.91714205G>A GRCh37
NC_000007.12:g.91552141G>A NCBI36
NG_011623.1:g.149017G>A , LRG_331:g.149017G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8783G>A MANE Select NP_005742.4:p.Arg2928Gln
ENST00000356239.8:c.8783G>A MANE Select ENSP00000348573.3:p.Arg2928Gln
NM_001379277.1:c.3428G>A NP_001366206.1:p.Arg1143Gln
NM_005751.4:c.8783G>A , LRG_331t1:c.8783G>A NP_005742.4:p.Arg2928Gln
NM_147185.2:c.8759G>A NP_671714.1:p.Arg2920Gln
NM_147185.3:c.8759G>A NP_671714.1:p.Arg2920Gln
ENST00000356239.7:c.8783G>A ENSP00000348573.3:p.Arg2928Gln
ENST00000358100.6:c.8642G>A ENSP00000350813.3:p.Arg2881Gln
ENST00000359028.6:c.8792G>A ENSP00000351922.3:p.Arg2931Gln
ENST00000359028.7:c.8855G>A ENSP00000351922.4:p.Arg2952Gln
ENST00000394534.6:c.2321G>A ENSP00000378042.2:p.Arg774Gln
ENST00000394534.7:c.2276G>A ENSP00000378042.3:p.Arg759Gln
ENST00000435423.1:c.217G>A
ENST00000435423.2:n.623G>A
ENST00000491695.2:c.3428G>A ENSP00000494626.2:p.Arg1143Gln
ENST00000679448.1:c.8759G>A ENSP00000505889.1:p.Arg2920Gln
ENST00000679457.1:c.8759G>A ENSP00000505450.1:p.Arg2920Gln
ENST00000679474.1:n.8981G>A
ENST00000679521.1:c.8729G>A ENSP00000505456.1:p.Arg2910Gln
ENST00000679722.1:n.9005G>A
ENST00000679821.1:c.8525G>A ENSP00000506040.1:p.Arg2842Gln
ENST00000680047.1:n.8981G>A
ENST00000680072.1:c.8606G>A ENSP00000506581.1:p.Arg2869Gln
ENST00000680181.1:c.8690G>A ENSP00000505548.1:p.Arg2897Gln
ENST00000680365.1:c.2276G>A ENSP00000506019.1:p.Arg759Gln
ENST00000680513.1:c.8642G>A ENSP00000505284.1:p.Arg2881Gln
ENST00000680534.1:c.8822G>A ENSP00000506674.1:p.Arg2941Gln
ENST00000680766.1:c.8759G>A ENSP00000505204.1:p.Arg2920Gln
ENST00000680952.1:c.8759G>A ENSP00000506407.1:p.Arg2920Gln
ENST00000681216.1:c.2120G>A ENSP00000505551.1:p.Arg707Gln
ENST00000681412.1:c.8783G>A ENSP00000506486.1:p.Arg2928Gln
ENST00000681722.1:c.8759G>A ENSP00000506566.1:p.Arg2920Gln
XM_006715827.1:c.8642G>A XP_006715890.1:p.Arg2881Gln
XM_011515709.1:c.8930G>A XP_011514011.1:p.Arg2977Gln
XM_011515710.1:c.8954G>A XP_011514012.1:p.Arg2985Gln
XM_011515711.1:c.8894G>A XP_011514013.1:p.Arg2965Gln
XM_011515712.1:c.8891G>A XP_011514014.1:p.Arg2964Gln
XM_011515713.1:c.8876G>A XP_011514015.1:p.Arg2959Gln
XM_011515714.1:c.8915G>A XP_011514016.1:p.Arg2972Gln
XM_011515716.1:c.8834G>A XP_011514018.1:p.Arg2945Gln
XM_011515717.1:c.8789G>A XP_011514019.1:p.Arg2930Gln
XM_011515718.1:c.8819G>A XP_011514020.1:p.Arg2940Gln
XM_011515719.1:c.8795G>A XP_011514021.1:p.Arg2932Gln
XM_011515720.1:c.8678G>A XP_011514022.1:p.Arg2893Gln
XM_011515721.1:c.3443G>A XP_011514023.1:p.Arg1148Gln
XM_011515722.1:c.3404G>A XP_011514024.1:p.Arg1135Gln
XM_017011642.2:c.8918G>A XP_016867131.1:p.Arg2973Gln
XM_017011643.2:c.8879G>A XP_016867132.1:p.Arg2960Gln
XM_017011644.2:c.8918G>A XP_016867133.1:p.Arg2973Gln
XM_017011645.2:c.8864G>A XP_016867134.1:p.Arg2955Gln
XM_017011646.2:c.8879G>A XP_016867135.1:p.Arg2960Gln
XM_017011647.2:c.8825G>A XP_016867136.1:p.Arg2942Gln
XM_017011648.2:c.8822G>A XP_016867137.1:p.Arg2941Gln
XM_017011649.2:c.8855G>A XP_016867138.1:p.Arg2952Gln
XM_017011650.2:c.8783G>A XP_016867139.1:p.Arg2928Gln
XM_017011651.2:c.8777G>A XP_016867140.1:p.Arg2926Gln
XM_017011652.2:c.8918G>A XP_016867141.1:p.Arg2973Gln
XM_017011653.2:c.8690G>A XP_016867142.1:p.Arg2897Gln
XM_017011654.2:c.8642G>A XP_016867143.1:p.Arg2881Gln
XM_017011655.2:c.8546G>A XP_016867144.1:p.Arg2849Gln
XM_017011656.2:c.8546G>A XP_016867145.1:p.Arg2849Gln
XM_017011657.2:c.4583G>A XP_016867146.1:p.Arg1528Gln
XM_017011658.2:c.3467G>A XP_016867147.1:p.Arg1156Gln
XM_017011659.2:c.3428G>A XP_016867148.1:p.Arg1143Gln
XM_017011660.2:c.3428G>A XP_016867149.1:p.Arg1143Gln
XM_024446631.1:c.8681G>A XP_024302399.1:p.Arg2894Gln