Canonical Allele Identifier: CA4337354
Community Standard Title: NM_005751.5(AKAP9):c.7821A>T (p.Arg2607Ser)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92079954A>T , CM000669.2:g.92079954A>T GRCh38
NC_000007.13:g.91709268A>T , CM000669.1:g.91709268A>T GRCh37
NC_000007.12:g.91547204A>T NCBI36
NG_011623.1:g.144080A>T , LRG_331:g.144080A>T

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.7821A>T MANE Select NP_005742.4:p.Arg2607Ser
ENST00000356239.8:c.7821A>T MANE Select ENSP00000348573.3:p.Arg2607Ser
NM_001379277.1:c.2466A>T NP_001366206.1:p.Arg822Ser
NM_005751.4:c.7821A>T , LRG_331t1:c.7821A>T NP_005742.4:p.Arg2607Ser
NM_147185.2:c.7797A>T NP_671714.1:p.Arg2599Ser
NM_147185.3:c.7797A>T NP_671714.1:p.Arg2599Ser
ENST00000356239.7:c.7821A>T ENSP00000348573.3:p.Arg2607Ser
ENST00000358100.6:c.7680A>T ENSP00000350813.3:p.Arg2560Ser
ENST00000359028.6:c.7854A>T ENSP00000351922.3:p.Arg2618Ser
ENST00000359028.7:c.7893A>T ENSP00000351922.4:p.Arg2631Ser
ENST00000394534.6:c.1359A>T ENSP00000378042.2:p.Arg453Ser
ENST00000394534.7:c.1314A>T ENSP00000378042.3:p.Arg438Ser
ENST00000491695.2:c.2466A>T ENSP00000494626.2:p.Arg822Ser
ENST00000674381.2:c.*7550A>T ENSP00000501536.2:n.*7550A>T
ENST00000679448.1:c.7797A>T ENSP00000505889.1:p.Arg2599Ser
ENST00000679457.1:c.7797A>T ENSP00000505450.1:p.Arg2599Ser
ENST00000679474.1:n.8019A>T
ENST00000679521.1:c.7767A>T ENSP00000505456.1:p.Arg2589Ser
ENST00000679554.1:c.*7606A>T ENSP00000506415.1:n.*7606A>T
ENST00000679722.1:n.8043A>T
ENST00000679821.1:c.7563A>T ENSP00000506040.1:p.Arg2521Ser
ENST00000680047.1:n.8019A>T
ENST00000680072.1:c.7644A>T ENSP00000506581.1:p.Arg2548Ser
ENST00000680181.1:c.7728A>T ENSP00000505548.1:p.Arg2576Ser
ENST00000680365.1:c.1314A>T ENSP00000506019.1:p.Arg438Ser
ENST00000680513.1:c.7680A>T ENSP00000505284.1:p.Arg2560Ser
ENST00000680534.1:c.7860A>T ENSP00000506674.1:p.Arg2620Ser
ENST00000680766.1:c.7797A>T ENSP00000505204.1:p.Arg2599Ser
ENST00000680952.1:c.7797A>T ENSP00000506407.1:p.Arg2599Ser
ENST00000681216.1:c.1314A>T ENSP00000505551.1:p.Arg438Ser
ENST00000681412.1:c.7821A>T ENSP00000506486.1:p.Arg2607Ser
ENST00000681722.1:c.7797A>T ENSP00000506566.1:p.Arg2599Ser
XM_006715827.1:c.7680A>T XP_006715890.1:p.Arg2560Ser
XM_011515709.1:c.7968A>T XP_011514011.1:p.Arg2656Ser
XM_011515710.1:c.7992A>T XP_011514012.1:p.Arg2664Ser
XM_011515711.1:c.7932A>T XP_011514013.1:p.Arg2644Ser
XM_011515712.1:c.7929A>T XP_011514014.1:p.Arg2643Ser
XM_011515713.1:c.7914A>T XP_011514015.1:p.Arg2638Ser
XM_011515714.1:c.7953A>T XP_011514016.1:p.Arg2651Ser
XM_011515716.1:c.7872A>T XP_011514018.1:p.Arg2624Ser
XM_011515717.1:c.7827A>T XP_011514019.1:p.Arg2609Ser
XM_011515718.1:c.7857A>T XP_011514020.1:p.Arg2619Ser
XM_011515719.1:c.7833A>T XP_011514021.1:p.Arg2611Ser
XM_011515720.1:c.7716A>T XP_011514022.1:p.Arg2572Ser
XM_011515721.1:c.2481A>T XP_011514023.1:p.Arg827Ser
XM_011515722.1:c.2442A>T XP_011514024.1:p.Arg814Ser
XM_017011642.2:c.7956A>T XP_016867131.1:p.Arg2652Ser
XM_017011643.2:c.7917A>T XP_016867132.1:p.Arg2639Ser
XM_017011644.2:c.7956A>T XP_016867133.1:p.Arg2652Ser
XM_017011645.2:c.7902A>T XP_016867134.1:p.Arg2634Ser
XM_017011646.2:c.7917A>T XP_016867135.1:p.Arg2639Ser
XM_017011647.2:c.7863A>T XP_016867136.1:p.Arg2621Ser
XM_017011648.2:c.7860A>T XP_016867137.1:p.Arg2620Ser
XM_017011649.2:c.7893A>T XP_016867138.1:p.Arg2631Ser
XM_017011650.2:c.7821A>T XP_016867139.1:p.Arg2607Ser
XM_017011651.2:c.7815A>T XP_016867140.1:p.Arg2605Ser
XM_017011652.2:c.7956A>T XP_016867141.1:p.Arg2652Ser
XM_017011653.2:c.7728A>T XP_016867142.1:p.Arg2576Ser
XM_017011654.2:c.7680A>T XP_016867143.1:p.Arg2560Ser
XM_017011655.2:c.7584A>T XP_016867144.1:p.Arg2528Ser
XM_017011656.2:c.7584A>T XP_016867145.1:p.Arg2528Ser
XM_017011657.2:c.3621A>T XP_016867146.1:p.Arg1207Ser
XM_017011658.2:c.2505A>T XP_016867147.1:p.Arg835Ser
XM_017011659.2:c.2466A>T XP_016867148.1:p.Arg822Ser
XM_017011660.2:c.2466A>T XP_016867149.1:p.Arg822Ser
XM_024446631.1:c.7719A>T XP_024302399.1:p.Arg2573Ser