Canonical Allele Identifier: CA4337451
Community Standard Title: NM_005751.5(AKAP9):c.8206G>A (p.Val2736Ile)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92083215G>A , CM000669.2:g.92083215G>A GRCh38
NC_000007.13:g.91712529G>A , CM000669.1:g.91712529G>A GRCh37
NC_000007.12:g.91550465G>A NCBI36
NG_011623.1:g.147341G>A , LRG_331:g.147341G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8206G>A MANE Select NP_005742.4:p.Val2736Ile
ENST00000356239.8:c.8206G>A MANE Select ENSP00000348573.3:p.Val2736Ile
NM_001379277.1:c.2851G>A NP_001366206.1:p.Val951Ile
NM_005751.4:c.8206G>A , LRG_331t1:c.8206G>A NP_005742.4:p.Val2736Ile
NM_147185.2:c.8182G>A NP_671714.1:p.Val2728Ile
NM_147185.3:c.8182G>A NP_671714.1:p.Val2728Ile
ENST00000356239.7:c.8206G>A ENSP00000348573.3:p.Val2736Ile
ENST00000358100.6:c.8065G>A ENSP00000350813.3:p.Val2689Ile
ENST00000359028.6:c.8239G>A ENSP00000351922.3:p.Val2747Ile
ENST00000359028.7:c.8278G>A ENSP00000351922.4:p.Val2760Ile
ENST00000394534.6:c.1744G>A ENSP00000378042.2:p.Val582Ile
ENST00000394534.7:c.1699G>A ENSP00000378042.3:p.Val567Ile
ENST00000435423.2:n.46G>A
ENST00000491695.2:c.2851G>A ENSP00000494626.2:p.Val951Ile
ENST00000674381.2:c.*7935G>A ENSP00000501536.2:n.*7935G>A
ENST00000679448.1:c.8182G>A ENSP00000505889.1:p.Val2728Ile
ENST00000679457.1:c.8182G>A ENSP00000505450.1:p.Val2728Ile
ENST00000679474.1:n.8404G>A
ENST00000679521.1:c.8152G>A ENSP00000505456.1:p.Val2718Ile
ENST00000679554.1:c.*7991G>A ENSP00000506415.1:n.*7991G>A
ENST00000679722.1:n.8428G>A
ENST00000679821.1:c.7948G>A ENSP00000506040.1:p.Val2650Ile
ENST00000680047.1:n.8404G>A
ENST00000680072.1:c.8029G>A ENSP00000506581.1:p.Val2677Ile
ENST00000680181.1:c.8113G>A ENSP00000505548.1:p.Val2705Ile
ENST00000680365.1:c.1699G>A ENSP00000506019.1:p.Val567Ile
ENST00000680513.1:c.8065G>A ENSP00000505284.1:p.Val2689Ile
ENST00000680534.1:c.8245G>A ENSP00000506674.1:p.Val2749Ile
ENST00000680766.1:c.8182G>A ENSP00000505204.1:p.Val2728Ile
ENST00000680952.1:c.8182G>A ENSP00000506407.1:p.Val2728Ile
ENST00000681216.1:c.1699G>A ENSP00000505551.1:p.Val567Ile
ENST00000681412.1:c.8206G>A ENSP00000506486.1:p.Val2736Ile
ENST00000681722.1:c.8182G>A ENSP00000506566.1:p.Val2728Ile
XM_006715827.1:c.8065G>A XP_006715890.1:p.Val2689Ile
XM_011515709.1:c.8353G>A XP_011514011.1:p.Val2785Ile
XM_011515710.1:c.8377G>A XP_011514012.1:p.Val2793Ile
XM_011515711.1:c.8317G>A XP_011514013.1:p.Val2773Ile
XM_011515712.1:c.8314G>A XP_011514014.1:p.Val2772Ile
XM_011515713.1:c.8299G>A XP_011514015.1:p.Val2767Ile
XM_011515714.1:c.8338G>A XP_011514016.1:p.Val2780Ile
XM_011515716.1:c.8257G>A XP_011514018.1:p.Val2753Ile
XM_011515717.1:c.8212G>A XP_011514019.1:p.Val2738Ile
XM_011515718.1:c.8242G>A XP_011514020.1:p.Val2748Ile
XM_011515719.1:c.8218G>A XP_011514021.1:p.Val2740Ile
XM_011515720.1:c.8101G>A XP_011514022.1:p.Val2701Ile
XM_011515721.1:c.2866G>A XP_011514023.1:p.Val956Ile
XM_011515722.1:c.2827G>A XP_011514024.1:p.Val943Ile
XM_017011642.2:c.8341G>A XP_016867131.1:p.Val2781Ile
XM_017011643.2:c.8302G>A XP_016867132.1:p.Val2768Ile
XM_017011644.2:c.8341G>A XP_016867133.1:p.Val2781Ile
XM_017011645.2:c.8287G>A XP_016867134.1:p.Val2763Ile
XM_017011646.2:c.8302G>A XP_016867135.1:p.Val2768Ile
XM_017011647.2:c.8248G>A XP_016867136.1:p.Val2750Ile
XM_017011648.2:c.8245G>A XP_016867137.1:p.Val2749Ile
XM_017011649.2:c.8278G>A XP_016867138.1:p.Val2760Ile
XM_017011650.2:c.8206G>A XP_016867139.1:p.Val2736Ile
XM_017011651.2:c.8200G>A XP_016867140.1:p.Val2734Ile
XM_017011652.2:c.8341G>A XP_016867141.1:p.Val2781Ile
XM_017011653.2:c.8113G>A XP_016867142.1:p.Val2705Ile
XM_017011654.2:c.8065G>A XP_016867143.1:p.Val2689Ile
XM_017011655.2:c.7969G>A XP_016867144.1:p.Val2657Ile
XM_017011656.2:c.7969G>A XP_016867145.1:p.Val2657Ile
XM_017011657.2:c.4006G>A XP_016867146.1:p.Val1336Ile
XM_017011658.2:c.2890G>A XP_016867147.1:p.Val964Ile
XM_017011659.2:c.2851G>A XP_016867148.1:p.Val951Ile
XM_017011660.2:c.2851G>A XP_016867149.1:p.Val951Ile
XM_024446631.1:c.8104G>A XP_024302399.1:p.Val2702Ile