Canonical Allele Identifier: CA4337309
Community Standard Title: NM_005751.5(AKAP9):c.7565T>G (p.Ile2522Arg)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92079698T>G , CM000669.2:g.92079698T>G GRCh38
NC_000007.13:g.91709012T>G , CM000669.1:g.91709012T>G GRCh37
NC_000007.12:g.91546948T>G NCBI36
NG_011623.1:g.143824T>G , LRG_331:g.143824T>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.7565T>G MANE Select NP_005742.4:p.Ile2522Arg
ENST00000356239.8:c.7565T>G MANE Select ENSP00000348573.3:p.Ile2522Arg
NM_001379277.1:c.2210T>G NP_001366206.1:p.Ile737Arg
NM_005751.4:c.7565T>G , LRG_331t1:c.7565T>G NP_005742.4:p.Ile2522Arg
NM_147185.2:c.7541T>G NP_671714.1:p.Ile2514Arg
NM_147185.3:c.7541T>G NP_671714.1:p.Ile2514Arg
ENST00000356239.7:c.7565T>G ENSP00000348573.3:p.Ile2522Arg
ENST00000358100.6:c.7424T>G ENSP00000350813.3:p.Ile2475Arg
ENST00000359028.6:c.7598T>G ENSP00000351922.3:p.Ile2533Arg
ENST00000359028.7:c.7637T>G ENSP00000351922.4:p.Ile2546Arg
ENST00000394534.6:c.1103T>G ENSP00000378042.2:p.Ile368Arg
ENST00000394534.7:c.1058T>G ENSP00000378042.3:p.Ile353Arg
ENST00000491695.2:c.2210T>G ENSP00000494626.2:p.Ile737Arg
ENST00000674381.2:c.*7294T>G ENSP00000501536.2:n.*7294T>G
ENST00000679448.1:c.7541T>G ENSP00000505889.1:p.Ile2514Arg
ENST00000679457.1:c.7541T>G ENSP00000505450.1:p.Ile2514Arg
ENST00000679474.1:n.7763T>G
ENST00000679521.1:c.7511T>G ENSP00000505456.1:p.Ile2504Arg
ENST00000679554.1:c.*7350T>G ENSP00000506415.1:n.*7350T>G
ENST00000679722.1:n.7787T>G
ENST00000679821.1:c.7307T>G ENSP00000506040.1:p.Ile2436Arg
ENST00000680047.1:n.7763T>G
ENST00000680072.1:c.7388T>G ENSP00000506581.1:p.Ile2463Arg
ENST00000680181.1:c.7472T>G ENSP00000505548.1:p.Ile2491Arg
ENST00000680365.1:c.1058T>G ENSP00000506019.1:p.Ile353Arg
ENST00000680513.1:c.7424T>G ENSP00000505284.1:p.Ile2475Arg
ENST00000680534.1:c.7604T>G ENSP00000506674.1:p.Ile2535Arg
ENST00000680766.1:c.7541T>G ENSP00000505204.1:p.Ile2514Arg
ENST00000680952.1:c.7541T>G ENSP00000506407.1:p.Ile2514Arg
ENST00000681216.1:c.1058T>G ENSP00000505551.1:p.Ile353Arg
ENST00000681412.1:c.7565T>G ENSP00000506486.1:p.Ile2522Arg
ENST00000681722.1:c.7541T>G ENSP00000506566.1:p.Ile2514Arg
XM_006715827.1:c.7424T>G XP_006715890.1:p.Ile2475Arg
XM_011515709.1:c.7712T>G XP_011514011.1:p.Ile2571Arg
XM_011515710.1:c.7736T>G XP_011514012.1:p.Ile2579Arg
XM_011515711.1:c.7676T>G XP_011514013.1:p.Ile2559Arg
XM_011515712.1:c.7673T>G XP_011514014.1:p.Ile2558Arg
XM_011515713.1:c.7658T>G XP_011514015.1:p.Ile2553Arg
XM_011515714.1:c.7697T>G XP_011514016.1:p.Ile2566Arg
XM_011515716.1:c.7616T>G XP_011514018.1:p.Ile2539Arg
XM_011515717.1:c.7571T>G XP_011514019.1:p.Ile2524Arg
XM_011515718.1:c.7601T>G XP_011514020.1:p.Ile2534Arg
XM_011515719.1:c.7577T>G XP_011514021.1:p.Ile2526Arg
XM_011515720.1:c.7460T>G XP_011514022.1:p.Ile2487Arg
XM_011515721.1:c.2225T>G XP_011514023.1:p.Ile742Arg
XM_011515722.1:c.2186T>G XP_011514024.1:p.Ile729Arg
XM_017011642.2:c.7700T>G XP_016867131.1:p.Ile2567Arg
XM_017011643.2:c.7661T>G XP_016867132.1:p.Ile2554Arg
XM_017011644.2:c.7700T>G XP_016867133.1:p.Ile2567Arg
XM_017011645.2:c.7646T>G XP_016867134.1:p.Ile2549Arg
XM_017011646.2:c.7661T>G XP_016867135.1:p.Ile2554Arg
XM_017011647.2:c.7607T>G XP_016867136.1:p.Ile2536Arg
XM_017011648.2:c.7604T>G XP_016867137.1:p.Ile2535Arg
XM_017011649.2:c.7637T>G XP_016867138.1:p.Ile2546Arg
XM_017011650.2:c.7565T>G XP_016867139.1:p.Ile2522Arg
XM_017011651.2:c.7559T>G XP_016867140.1:p.Ile2520Arg
XM_017011652.2:c.7700T>G XP_016867141.1:p.Ile2567Arg
XM_017011653.2:c.7472T>G XP_016867142.1:p.Ile2491Arg
XM_017011654.2:c.7424T>G XP_016867143.1:p.Ile2475Arg
XM_017011655.2:c.7328T>G XP_016867144.1:p.Ile2443Arg
XM_017011656.2:c.7328T>G XP_016867145.1:p.Ile2443Arg
XM_017011657.2:c.3365T>G XP_016867146.1:p.Ile1122Arg
XM_017011658.2:c.2249T>G XP_016867147.1:p.Ile750Arg
XM_017011659.2:c.2210T>G XP_016867148.1:p.Ile737Arg
XM_017011660.2:c.2210T>G XP_016867149.1:p.Ile737Arg
XM_024446631.1:c.7463T>G XP_024302399.1:p.Ile2488Arg