Canonical Allele Identifier: CA368137426
Community Standard Title: NM_005751.5(AKAP9):c.8134G>A (p.Ala2712Thr)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92082636G>A , CM000669.2:g.92082636G>A GRCh38
NC_000007.13:g.91711950G>A , CM000669.1:g.91711950G>A GRCh37
NC_000007.12:g.91549886G>A NCBI36
NG_011623.1:g.146762G>A , LRG_331:g.146762G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8134G>A MANE Select NP_005742.4:p.Ala2712Thr
ENST00000356239.8:c.8134G>A MANE Select ENSP00000348573.3:p.Ala2712Thr
NM_001379277.1:c.2779G>A NP_001366206.1:p.Ala927Thr
NM_005751.4:c.8134G>A , LRG_331t1:c.8134G>A NP_005742.4:p.Ala2712Thr
NM_147185.2:c.8110G>A NP_671714.1:p.Ala2704Thr
NM_147185.3:c.8110G>A NP_671714.1:p.Ala2704Thr
ENST00000356239.7:c.8134G>A ENSP00000348573.3:p.Ala2712Thr
ENST00000358100.6:c.7993G>A ENSP00000350813.3:p.Ala2665Thr
ENST00000359028.6:c.8167G>A ENSP00000351922.3:p.Ala2723Thr
ENST00000359028.7:c.8206G>A ENSP00000351922.4:p.Ala2736Thr
ENST00000394534.6:c.1672G>A ENSP00000378042.2:p.Ala558Thr
ENST00000394534.7:c.1627G>A ENSP00000378042.3:p.Ala543Thr
ENST00000491695.2:c.2779G>A ENSP00000494626.2:p.Ala927Thr
ENST00000674381.2:c.*7863G>A ENSP00000501536.2:n.*7863G>A
ENST00000679448.1:c.8110G>A ENSP00000505889.1:p.Ala2704Thr
ENST00000679457.1:c.8110G>A ENSP00000505450.1:p.Ala2704Thr
ENST00000679474.1:n.8332G>A
ENST00000679521.1:c.8080G>A ENSP00000505456.1:p.Ala2694Thr
ENST00000679554.1:c.*7919G>A ENSP00000506415.1:n.*7919G>A
ENST00000679722.1:n.8356G>A
ENST00000679821.1:c.7876G>A ENSP00000506040.1:p.Ala2626Thr
ENST00000680047.1:n.8332G>A
ENST00000680072.1:c.7957G>A ENSP00000506581.1:p.Ala2653Thr
ENST00000680181.1:c.8041G>A ENSP00000505548.1:p.Ala2681Thr
ENST00000680365.1:c.1627G>A ENSP00000506019.1:p.Ala543Thr
ENST00000680513.1:c.7993G>A ENSP00000505284.1:p.Ala2665Thr
ENST00000680534.1:c.8173G>A ENSP00000506674.1:p.Ala2725Thr
ENST00000680766.1:c.8110G>A ENSP00000505204.1:p.Ala2704Thr
ENST00000680952.1:c.8110G>A ENSP00000506407.1:p.Ala2704Thr
ENST00000681216.1:c.1627G>A ENSP00000505551.1:p.Ala543Thr
ENST00000681412.1:c.8134G>A ENSP00000506486.1:p.Ala2712Thr
ENST00000681722.1:c.8110G>A ENSP00000506566.1:p.Ala2704Thr
XM_006715827.1:c.7993G>A XP_006715890.1:p.Ala2665Thr
XM_011515709.1:c.8281G>A XP_011514011.1:p.Ala2761Thr
XM_011515710.1:c.8305G>A XP_011514012.1:p.Ala2769Thr
XM_011515711.1:c.8245G>A XP_011514013.1:p.Ala2749Thr
XM_011515712.1:c.8242G>A XP_011514014.1:p.Ala2748Thr
XM_011515713.1:c.8227G>A XP_011514015.1:p.Ala2743Thr
XM_011515714.1:c.8266G>A XP_011514016.1:p.Ala2756Thr
XM_011515716.1:c.8185G>A XP_011514018.1:p.Ala2729Thr
XM_011515717.1:c.8140G>A XP_011514019.1:p.Ala2714Thr
XM_011515718.1:c.8170G>A XP_011514020.1:p.Ala2724Thr
XM_011515719.1:c.8146G>A XP_011514021.1:p.Ala2716Thr
XM_011515720.1:c.8029G>A XP_011514022.1:p.Ala2677Thr
XM_011515721.1:c.2794G>A XP_011514023.1:p.Ala932Thr
XM_011515722.1:c.2755G>A XP_011514024.1:p.Ala919Thr
XM_017011642.2:c.8269G>A XP_016867131.1:p.Ala2757Thr
XM_017011643.2:c.8230G>A XP_016867132.1:p.Ala2744Thr
XM_017011644.2:c.8269G>A XP_016867133.1:p.Ala2757Thr
XM_017011645.2:c.8215G>A XP_016867134.1:p.Ala2739Thr
XM_017011646.2:c.8230G>A XP_016867135.1:p.Ala2744Thr
XM_017011647.2:c.8176G>A XP_016867136.1:p.Ala2726Thr
XM_017011648.2:c.8173G>A XP_016867137.1:p.Ala2725Thr
XM_017011649.2:c.8206G>A XP_016867138.1:p.Ala2736Thr
XM_017011650.2:c.8134G>A XP_016867139.1:p.Ala2712Thr
XM_017011651.2:c.8128G>A XP_016867140.1:p.Ala2710Thr
XM_017011652.2:c.8269G>A XP_016867141.1:p.Ala2757Thr
XM_017011653.2:c.8041G>A XP_016867142.1:p.Ala2681Thr
XM_017011654.2:c.7993G>A XP_016867143.1:p.Ala2665Thr
XM_017011655.2:c.7897G>A XP_016867144.1:p.Ala2633Thr
XM_017011656.2:c.7897G>A XP_016867145.1:p.Ala2633Thr
XM_017011657.2:c.3934G>A XP_016867146.1:p.Ala1312Thr
XM_017011658.2:c.2818G>A XP_016867147.1:p.Ala940Thr
XM_017011659.2:c.2779G>A XP_016867148.1:p.Ala927Thr
XM_017011660.2:c.2779G>A XP_016867149.1:p.Ala927Thr
XM_024446631.1:c.8032G>A XP_024302399.1:p.Ala2678Thr