Canonical Allele Identifier: CA368140066
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92083640T>G , CM000669.2:g.92083640T>G GRCh38
NC_000007.13:g.91712954T>G , CM000669.1:g.91712954T>G GRCh37
NC_000007.12:g.91550890T>G NCBI36
NG_011623.1:g.147766T>G , LRG_331:g.147766T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356239.8:c.8631T>G MANE Select ENSP00000348573.3:p.Cys2877Trp
ENST00000359028.7:c.8703T>G ENSP00000351922.4:p.Cys2901Trp
ENST00000394534.7:c.2124T>G ENSP00000378042.3:p.Cys708Trp
ENST00000435423.2:n.471T>G
ENST00000491695.2:c.3276T>G ENSP00000494626.2:p.Cys1092Trp
ENST00000679448.1:c.8607T>G ENSP00000505889.1:p.Cys2869Trp
ENST00000679457.1:c.8607T>G ENSP00000505450.1:p.Cys2869Trp
ENST00000679474.1:n.8829T>G
ENST00000679521.1:c.8577T>G ENSP00000505456.1:p.Cys2859Trp
ENST00000679722.1:n.8853T>G
ENST00000679821.1:c.8373T>G ENSP00000506040.1:p.Cys2791Trp
ENST00000680047.1:n.8829T>G
ENST00000680072.1:c.8454T>G ENSP00000506581.1:p.Cys2818Trp
ENST00000680181.1:c.8538T>G ENSP00000505548.1:p.Cys2846Trp
ENST00000680365.1:c.2124T>G ENSP00000506019.1:p.Cys708Trp
ENST00000680513.1:c.8490T>G ENSP00000505284.1:p.Cys2830Trp
ENST00000680534.1:c.8670T>G ENSP00000506674.1:p.Cys2890Trp
ENST00000680766.1:c.8607T>G ENSP00000505204.1:p.Cys2869Trp
ENST00000680952.1:c.8607T>G ENSP00000506407.1:p.Cys2869Trp
ENST00000681216.1:c.1968T>G ENSP00000505551.1:p.Cys656Trp
ENST00000681412.1:c.8631T>G ENSP00000506486.1:p.Cys2877Trp
ENST00000681722.1:c.8607T>G ENSP00000506566.1:p.Cys2869Trp
ENST00000356239.7:c.8631T>G ENSP00000348573.3:p.Cys2877Trp
ENST00000358100.6:c.8490T>G ENSP00000350813.3:p.Cys2830Trp
ENST00000359028.6:c.8664T>G ENSP00000351922.3:p.Cys2888Trp
ENST00000394534.6:c.2169T>G ENSP00000378042.2:p.Cys723Trp
ENST00000435423.1:c.65T>G
NM_005751.4:c.8631T>G , LRG_331t1:c.8631T>G NP_005742.4:p.Cys2877Trp
NM_147185.2:c.8607T>G NP_671714.1:p.Cys2869Trp
XM_006715827.1:c.8490T>G XP_006715890.1:p.Cys2830Trp
XM_011515709.1:c.8778T>G XP_011514011.1:p.Cys2926Trp
XM_011515710.1:c.8802T>G XP_011514012.1:p.Cys2934Trp
XM_011515711.1:c.8742T>G XP_011514013.1:p.Cys2914Trp
XM_011515712.1:c.8739T>G XP_011514014.1:p.Cys2913Trp
XM_011515713.1:c.8724T>G XP_011514015.1:p.Cys2908Trp
XM_011515714.1:c.8763T>G XP_011514016.1:p.Cys2921Trp
XM_011515716.1:c.8682T>G XP_011514018.1:p.Cys2894Trp
XM_011515717.1:c.8637T>G XP_011514019.1:p.Cys2879Trp
XM_011515718.1:c.8667T>G XP_011514020.1:p.Cys2889Trp
XM_011515719.1:c.8643T>G XP_011514021.1:p.Cys2881Trp
XM_011515720.1:c.8526T>G XP_011514022.1:p.Cys2842Trp
XM_011515721.1:c.3291T>G XP_011514023.1:p.Cys1097Trp
XM_011515722.1:c.3252T>G XP_011514024.1:p.Cys1084Trp
XM_017011642.2:c.8766T>G XP_016867131.1:p.Cys2922Trp
XM_017011643.2:c.8727T>G XP_016867132.1:p.Cys2909Trp
XM_017011644.2:c.8766T>G XP_016867133.1:p.Cys2922Trp
XM_017011645.2:c.8712T>G XP_016867134.1:p.Cys2904Trp
XM_017011646.2:c.8727T>G XP_016867135.1:p.Cys2909Trp
XM_017011647.2:c.8673T>G XP_016867136.1:p.Cys2891Trp
XM_017011648.2:c.8670T>G XP_016867137.1:p.Cys2890Trp
XM_017011649.2:c.8703T>G XP_016867138.1:p.Cys2901Trp
XM_017011650.2:c.8631T>G XP_016867139.1:p.Cys2877Trp
XM_017011651.2:c.8625T>G XP_016867140.1:p.Cys2875Trp
XM_017011652.2:c.8766T>G XP_016867141.1:p.Cys2922Trp
XM_017011653.2:c.8538T>G XP_016867142.1:p.Cys2846Trp
XM_017011654.2:c.8490T>G XP_016867143.1:p.Cys2830Trp
XM_017011655.2:c.8394T>G XP_016867144.1:p.Cys2798Trp
XM_017011656.2:c.8394T>G XP_016867145.1:p.Cys2798Trp
XM_017011657.2:c.4431T>G XP_016867146.1:p.Cys1477Trp
XM_017011658.2:c.3315T>G XP_016867147.1:p.Cys1105Trp
XM_017011659.2:c.3276T>G XP_016867148.1:p.Cys1092Trp
XM_017011660.2:c.3276T>G XP_016867149.1:p.Cys1092Trp
XM_024446631.1:c.8529T>G XP_024302399.1:p.Cys2843Trp
NM_147185.3:c.8607T>G NP_671714.1:p.Cys2869Trp
NM_001379277.1:c.3276T>G NP_001366206.1:p.Cys1092Trp
NM_005751.5:c.8631T>G MANE Select NP_005742.4:p.Cys2877Trp