Canonical Allele Identifier: CA368133601
Gene: AKAP9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92077727A>T , CM000669.2:g.92077727A>T GRCh38
NC_000007.13:g.91707041A>T , CM000669.1:g.91707041A>T GRCh37
NC_000007.12:g.91544977A>T NCBI36
NG_011623.1:g.141853A>T , LRG_331:g.141853A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000356239.8:c.6797A>T MANE Select ENSP00000348573.3:p.Lys2266Met
ENST00000359028.7:c.6869A>T ENSP00000351922.4:p.Lys2290Met
ENST00000394534.7:c.290A>T ENSP00000378042.3:p.Lys97Met
ENST00000491695.2:c.1442A>T ENSP00000494626.2:p.Lys481Met
ENST00000674381.2:c.*6526A>T ENSP00000501536.2:n.*6526A>T
ENST00000679448.1:c.6773A>T ENSP00000505889.1:p.Lys2258Met
ENST00000679457.1:c.6773A>T ENSP00000505450.1:p.Lys2258Met
ENST00000679474.1:n.6995A>T
ENST00000679521.1:c.6743A>T ENSP00000505456.1:p.Lys2248Met
ENST00000679554.1:c.*6582A>T ENSP00000506415.1:n.*6582A>T
ENST00000679722.1:n.7019A>T
ENST00000679821.1:c.6539A>T ENSP00000506040.1:p.Lys2180Met
ENST00000680047.1:n.6995A>T
ENST00000680072.1:c.6620A>T ENSP00000506581.1:p.Lys2207Met
ENST00000680181.1:c.6704A>T ENSP00000505548.1:p.Lys2235Met
ENST00000680365.1:c.290A>T ENSP00000506019.1:p.Lys97Met
ENST00000680513.1:c.6656A>T ENSP00000505284.1:p.Lys2219Met
ENST00000680534.1:c.6836A>T ENSP00000506674.1:p.Lys2279Met
ENST00000680766.1:c.6773A>T ENSP00000505204.1:p.Lys2258Met
ENST00000680952.1:c.6773A>T ENSP00000506407.1:p.Lys2258Met
ENST00000681216.1:c.290A>T ENSP00000505551.1:p.Lys97Met
ENST00000681412.1:c.6797A>T ENSP00000506486.1:p.Lys2266Met
ENST00000681722.1:c.6773A>T ENSP00000506566.1:p.Lys2258Met
ENST00000356239.7:c.6797A>T ENSP00000348573.3:p.Lys2266Met
ENST00000358100.6:c.6656A>T ENSP00000350813.3:p.Lys2219Met
ENST00000359028.6:c.6830A>T ENSP00000351922.3:p.Lys2277Met
ENST00000394534.6:c.335A>T ENSP00000378042.2:p.Lys112Met
NM_005751.4:c.6797A>T , LRG_331t1:c.6797A>T NP_005742.4:p.Lys2266Met
NM_147185.2:c.6773A>T NP_671714.1:p.Lys2258Met
XM_006715827.1:c.6656A>T XP_006715890.1:p.Lys2219Met
XM_011515709.1:c.6944A>T XP_011514011.1:p.Lys2315Met
XM_011515710.1:c.6968A>T XP_011514012.1:p.Lys2323Met
XM_011515711.1:c.6908A>T XP_011514013.1:p.Lys2303Met
XM_011515712.1:c.6905A>T XP_011514014.1:p.Lys2302Met
XM_011515713.1:c.6890A>T XP_011514015.1:p.Lys2297Met
XM_011515714.1:c.6929A>T XP_011514016.1:p.Lys2310Met
XM_011515716.1:c.6848A>T XP_011514018.1:p.Lys2283Met
XM_011515717.1:c.6803A>T XP_011514019.1:p.Lys2268Met
XM_011515718.1:c.6833A>T XP_011514020.1:p.Lys2278Met
XM_011515719.1:c.6809A>T XP_011514021.1:p.Lys2270Met
XM_011515720.1:c.6692A>T XP_011514022.1:p.Lys2231Met
XM_011515721.1:c.1457A>T XP_011514023.1:p.Lys486Met
XM_011515722.1:c.1418A>T XP_011514024.1:p.Lys473Met
XM_017011642.2:c.6932A>T XP_016867131.1:p.Lys2311Met
XM_017011643.2:c.6893A>T XP_016867132.1:p.Lys2298Met
XM_017011644.2:c.6932A>T XP_016867133.1:p.Lys2311Met
XM_017011645.2:c.6878A>T XP_016867134.1:p.Lys2293Met
XM_017011646.2:c.6893A>T XP_016867135.1:p.Lys2298Met
XM_017011647.2:c.6839A>T XP_016867136.1:p.Lys2280Met
XM_017011648.2:c.6836A>T XP_016867137.1:p.Lys2279Met
XM_017011649.2:c.6869A>T XP_016867138.1:p.Lys2290Met
XM_017011650.2:c.6797A>T XP_016867139.1:p.Lys2266Met
XM_017011651.2:c.6791A>T XP_016867140.1:p.Lys2264Met
XM_017011652.2:c.6932A>T XP_016867141.1:p.Lys2311Met
XM_017011653.2:c.6704A>T XP_016867142.1:p.Lys2235Met
XM_017011654.2:c.6656A>T XP_016867143.1:p.Lys2219Met
XM_017011655.2:c.6560A>T XP_016867144.1:p.Lys2187Met
XM_017011656.2:c.6560A>T XP_016867145.1:p.Lys2187Met
XM_017011657.2:c.2597A>T XP_016867146.1:p.Lys866Met
XM_017011658.2:c.1481A>T XP_016867147.1:p.Lys494Met
XM_017011659.2:c.1442A>T XP_016867148.1:p.Lys481Met
XM_017011660.2:c.1442A>T XP_016867149.1:p.Lys481Met
XM_024446631.1:c.6695A>T XP_024302399.1:p.Lys2232Met
NM_147185.3:c.6773A>T NP_671714.1:p.Lys2258Met
NM_001379277.1:c.1442A>T NP_001366206.1:p.Lys481Met
NM_005751.5:c.6797A>T MANE Select NP_005742.4:p.Lys2266Met