Canonical Allele Identifier: CA4337456
Community Standard Title: NM_005751.5(AKAP9):c.8221G>A (p.Ala2741Thr)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92083230G>A , CM000669.2:g.92083230G>A GRCh38
NC_000007.13:g.91712544G>A , CM000669.1:g.91712544G>A GRCh37
NC_000007.12:g.91550480G>A NCBI36
NG_011623.1:g.147356G>A , LRG_331:g.147356G>A

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8221G>A MANE Select NP_005742.4:p.Ala2741Thr
ENST00000356239.8:c.8221G>A MANE Select ENSP00000348573.3:p.Ala2741Thr
NM_001379277.1:c.2866G>A NP_001366206.1:p.Ala956Thr
NM_005751.4:c.8221G>A , LRG_331t1:c.8221G>A NP_005742.4:p.Ala2741Thr
NM_147185.2:c.8197G>A NP_671714.1:p.Ala2733Thr
NM_147185.3:c.8197G>A NP_671714.1:p.Ala2733Thr
ENST00000356239.7:c.8221G>A ENSP00000348573.3:p.Ala2741Thr
ENST00000358100.6:c.8080G>A ENSP00000350813.3:p.Ala2694Thr
ENST00000359028.6:c.8254G>A ENSP00000351922.3:p.Ala2752Thr
ENST00000359028.7:c.8293G>A ENSP00000351922.4:p.Ala2765Thr
ENST00000394534.6:c.1759G>A ENSP00000378042.2:p.Ala587Thr
ENST00000394534.7:c.1714G>A ENSP00000378042.3:p.Ala572Thr
ENST00000435423.2:n.61G>A
ENST00000491695.2:c.2866G>A ENSP00000494626.2:p.Ala956Thr
ENST00000674381.2:c.*7950G>A ENSP00000501536.2:n.*7950G>A
ENST00000679448.1:c.8197G>A ENSP00000505889.1:p.Ala2733Thr
ENST00000679457.1:c.8197G>A ENSP00000505450.1:p.Ala2733Thr
ENST00000679474.1:n.8419G>A
ENST00000679521.1:c.8167G>A ENSP00000505456.1:p.Ala2723Thr
ENST00000679554.1:c.*8006G>A ENSP00000506415.1:n.*8006G>A
ENST00000679722.1:n.8443G>A
ENST00000679821.1:c.7963G>A ENSP00000506040.1:p.Ala2655Thr
ENST00000680047.1:n.8419G>A
ENST00000680072.1:c.8044G>A ENSP00000506581.1:p.Ala2682Thr
ENST00000680181.1:c.8128G>A ENSP00000505548.1:p.Ala2710Thr
ENST00000680365.1:c.1714G>A ENSP00000506019.1:p.Ala572Thr
ENST00000680513.1:c.8080G>A ENSP00000505284.1:p.Ala2694Thr
ENST00000680534.1:c.8260G>A ENSP00000506674.1:p.Ala2754Thr
ENST00000680766.1:c.8197G>A ENSP00000505204.1:p.Ala2733Thr
ENST00000680952.1:c.8197G>A ENSP00000506407.1:p.Ala2733Thr
ENST00000681216.1:c.1714G>A ENSP00000505551.1:p.Ala572Thr
ENST00000681412.1:c.8221G>A ENSP00000506486.1:p.Ala2741Thr
ENST00000681722.1:c.8197G>A ENSP00000506566.1:p.Ala2733Thr
XM_006715827.1:c.8080G>A XP_006715890.1:p.Ala2694Thr
XM_011515709.1:c.8368G>A XP_011514011.1:p.Ala2790Thr
XM_011515710.1:c.8392G>A XP_011514012.1:p.Ala2798Thr
XM_011515711.1:c.8332G>A XP_011514013.1:p.Ala2778Thr
XM_011515712.1:c.8329G>A XP_011514014.1:p.Ala2777Thr
XM_011515713.1:c.8314G>A XP_011514015.1:p.Ala2772Thr
XM_011515714.1:c.8353G>A XP_011514016.1:p.Ala2785Thr
XM_011515716.1:c.8272G>A XP_011514018.1:p.Ala2758Thr
XM_011515717.1:c.8227G>A XP_011514019.1:p.Ala2743Thr
XM_011515718.1:c.8257G>A XP_011514020.1:p.Ala2753Thr
XM_011515719.1:c.8233G>A XP_011514021.1:p.Ala2745Thr
XM_011515720.1:c.8116G>A XP_011514022.1:p.Ala2706Thr
XM_011515721.1:c.2881G>A XP_011514023.1:p.Ala961Thr
XM_011515722.1:c.2842G>A XP_011514024.1:p.Ala948Thr
XM_017011642.2:c.8356G>A XP_016867131.1:p.Ala2786Thr
XM_017011643.2:c.8317G>A XP_016867132.1:p.Ala2773Thr
XM_017011644.2:c.8356G>A XP_016867133.1:p.Ala2786Thr
XM_017011645.2:c.8302G>A XP_016867134.1:p.Ala2768Thr
XM_017011646.2:c.8317G>A XP_016867135.1:p.Ala2773Thr
XM_017011647.2:c.8263G>A XP_016867136.1:p.Ala2755Thr
XM_017011648.2:c.8260G>A XP_016867137.1:p.Ala2754Thr
XM_017011649.2:c.8293G>A XP_016867138.1:p.Ala2765Thr
XM_017011650.2:c.8221G>A XP_016867139.1:p.Ala2741Thr
XM_017011651.2:c.8215G>A XP_016867140.1:p.Ala2739Thr
XM_017011652.2:c.8356G>A XP_016867141.1:p.Ala2786Thr
XM_017011653.2:c.8128G>A XP_016867142.1:p.Ala2710Thr
XM_017011654.2:c.8080G>A XP_016867143.1:p.Ala2694Thr
XM_017011655.2:c.7984G>A XP_016867144.1:p.Ala2662Thr
XM_017011656.2:c.7984G>A XP_016867145.1:p.Ala2662Thr
XM_017011657.2:c.4021G>A XP_016867146.1:p.Ala1341Thr
XM_017011658.2:c.2905G>A XP_016867147.1:p.Ala969Thr
XM_017011659.2:c.2866G>A XP_016867148.1:p.Ala956Thr
XM_017011660.2:c.2866G>A XP_016867149.1:p.Ala956Thr
XM_024446631.1:c.8119G>A XP_024302399.1:p.Ala2707Thr