Canonical Allele Identifier: CA4337346
Community Standard Title: NM_005751.5(AKAP9):c.7783G>T (p.Asp2595Tyr)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92079916G>T , CM000669.2:g.92079916G>T GRCh38
NC_000007.13:g.91709230G>T , CM000669.1:g.91709230G>T GRCh37
NC_000007.12:g.91547166G>T NCBI36
NG_011623.1:g.144042G>T , LRG_331:g.144042G>T

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.7783G>T MANE Select NP_005742.4:p.Asp2595Tyr
ENST00000356239.8:c.7783G>T MANE Select ENSP00000348573.3:p.Asp2595Tyr
NM_001379277.1:c.2428G>T NP_001366206.1:p.Asp810Tyr
NM_005751.4:c.7783G>T , LRG_331t1:c.7783G>T NP_005742.4:p.Asp2595Tyr
NM_147185.2:c.7759G>T NP_671714.1:p.Asp2587Tyr
NM_147185.3:c.7759G>T NP_671714.1:p.Asp2587Tyr
ENST00000356239.7:c.7783G>T ENSP00000348573.3:p.Asp2595Tyr
ENST00000358100.6:c.7642G>T ENSP00000350813.3:p.Asp2548Tyr
ENST00000359028.6:c.7816G>T ENSP00000351922.3:p.Asp2606Tyr
ENST00000359028.7:c.7855G>T ENSP00000351922.4:p.Asp2619Tyr
ENST00000394534.6:c.1321G>T ENSP00000378042.2:p.Asp441Tyr
ENST00000394534.7:c.1276G>T ENSP00000378042.3:p.Asp426Tyr
ENST00000491695.2:c.2428G>T ENSP00000494626.2:p.Asp810Tyr
ENST00000674381.2:c.*7512G>T ENSP00000501536.2:n.*7512G>T
ENST00000679448.1:c.7759G>T ENSP00000505889.1:p.Asp2587Tyr
ENST00000679457.1:c.7759G>T ENSP00000505450.1:p.Asp2587Tyr
ENST00000679474.1:n.7981G>T
ENST00000679521.1:c.7729G>T ENSP00000505456.1:p.Asp2577Tyr
ENST00000679554.1:c.*7568G>T ENSP00000506415.1:n.*7568G>T
ENST00000679722.1:n.8005G>T
ENST00000679821.1:c.7525G>T ENSP00000506040.1:p.Asp2509Tyr
ENST00000680047.1:n.7981G>T
ENST00000680072.1:c.7606G>T ENSP00000506581.1:p.Asp2536Tyr
ENST00000680181.1:c.7690G>T ENSP00000505548.1:p.Asp2564Tyr
ENST00000680365.1:c.1276G>T ENSP00000506019.1:p.Asp426Tyr
ENST00000680513.1:c.7642G>T ENSP00000505284.1:p.Asp2548Tyr
ENST00000680534.1:c.7822G>T ENSP00000506674.1:p.Asp2608Tyr
ENST00000680766.1:c.7759G>T ENSP00000505204.1:p.Asp2587Tyr
ENST00000680952.1:c.7759G>T ENSP00000506407.1:p.Asp2587Tyr
ENST00000681216.1:c.1276G>T ENSP00000505551.1:p.Asp426Tyr
ENST00000681412.1:c.7783G>T ENSP00000506486.1:p.Asp2595Tyr
ENST00000681722.1:c.7759G>T ENSP00000506566.1:p.Asp2587Tyr
XM_006715827.1:c.7642G>T XP_006715890.1:p.Asp2548Tyr
XM_011515709.1:c.7930G>T XP_011514011.1:p.Asp2644Tyr
XM_011515710.1:c.7954G>T XP_011514012.1:p.Asp2652Tyr
XM_011515711.1:c.7894G>T XP_011514013.1:p.Asp2632Tyr
XM_011515712.1:c.7891G>T XP_011514014.1:p.Asp2631Tyr
XM_011515713.1:c.7876G>T XP_011514015.1:p.Asp2626Tyr
XM_011515714.1:c.7915G>T XP_011514016.1:p.Asp2639Tyr
XM_011515716.1:c.7834G>T XP_011514018.1:p.Asp2612Tyr
XM_011515717.1:c.7789G>T XP_011514019.1:p.Asp2597Tyr
XM_011515718.1:c.7819G>T XP_011514020.1:p.Asp2607Tyr
XM_011515719.1:c.7795G>T XP_011514021.1:p.Asp2599Tyr
XM_011515720.1:c.7678G>T XP_011514022.1:p.Asp2560Tyr
XM_011515721.1:c.2443G>T XP_011514023.1:p.Asp815Tyr
XM_011515722.1:c.2404G>T XP_011514024.1:p.Asp802Tyr
XM_017011642.2:c.7918G>T XP_016867131.1:p.Asp2640Tyr
XM_017011643.2:c.7879G>T XP_016867132.1:p.Asp2627Tyr
XM_017011644.2:c.7918G>T XP_016867133.1:p.Asp2640Tyr
XM_017011645.2:c.7864G>T XP_016867134.1:p.Asp2622Tyr
XM_017011646.2:c.7879G>T XP_016867135.1:p.Asp2627Tyr
XM_017011647.2:c.7825G>T XP_016867136.1:p.Asp2609Tyr
XM_017011648.2:c.7822G>T XP_016867137.1:p.Asp2608Tyr
XM_017011649.2:c.7855G>T XP_016867138.1:p.Asp2619Tyr
XM_017011650.2:c.7783G>T XP_016867139.1:p.Asp2595Tyr
XM_017011651.2:c.7777G>T XP_016867140.1:p.Asp2593Tyr
XM_017011652.2:c.7918G>T XP_016867141.1:p.Asp2640Tyr
XM_017011653.2:c.7690G>T XP_016867142.1:p.Asp2564Tyr
XM_017011654.2:c.7642G>T XP_016867143.1:p.Asp2548Tyr
XM_017011655.2:c.7546G>T XP_016867144.1:p.Asp2516Tyr
XM_017011656.2:c.7546G>T XP_016867145.1:p.Asp2516Tyr
XM_017011657.2:c.3583G>T XP_016867146.1:p.Asp1195Tyr
XM_017011658.2:c.2467G>T XP_016867147.1:p.Asp823Tyr
XM_017011659.2:c.2428G>T XP_016867148.1:p.Asp810Tyr
XM_017011660.2:c.2428G>T XP_016867149.1:p.Asp810Tyr
XM_024446631.1:c.7681G>T XP_024302399.1:p.Asp2561Tyr