Canonical Allele Identifier: CA4337370
Community Standard Title: NM_005751.5(AKAP9):c.7980A>C (p.Lys2660Asn)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92080113A>C , CM000669.2:g.92080113A>C GRCh38
NC_000007.13:g.91709427A>C , CM000669.1:g.91709427A>C GRCh37
NC_000007.12:g.91547363A>C NCBI36
NG_011623.1:g.144239A>C , LRG_331:g.144239A>C

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.7980A>C MANE Select NP_005742.4:p.Lys2660Asn
ENST00000356239.8:c.7980A>C MANE Select ENSP00000348573.3:p.Lys2660Asn
NM_001379277.1:c.2625A>C NP_001366206.1:p.Lys875Asn
NM_005751.4:c.7980A>C , LRG_331t1:c.7980A>C NP_005742.4:p.Lys2660Asn
NM_147185.2:c.7956A>C NP_671714.1:p.Lys2652Asn
NM_147185.3:c.7956A>C NP_671714.1:p.Lys2652Asn
ENST00000356239.7:c.7980A>C ENSP00000348573.3:p.Lys2660Asn
ENST00000358100.6:c.7839A>C ENSP00000350813.3:p.Lys2613Asn
ENST00000359028.6:c.8013A>C ENSP00000351922.3:p.Lys2671Asn
ENST00000359028.7:c.8052A>C ENSP00000351922.4:p.Lys2684Asn
ENST00000394534.6:c.1518A>C ENSP00000378042.2:p.Lys506Asn
ENST00000394534.7:c.1473A>C ENSP00000378042.3:p.Lys491Asn
ENST00000491695.2:c.2625A>C ENSP00000494626.2:p.Lys875Asn
ENST00000674381.2:c.*7709A>C ENSP00000501536.2:n.*7709A>C
ENST00000679448.1:c.7956A>C ENSP00000505889.1:p.Lys2652Asn
ENST00000679457.1:c.7956A>C ENSP00000505450.1:p.Lys2652Asn
ENST00000679474.1:n.8178A>C
ENST00000679521.1:c.7926A>C ENSP00000505456.1:p.Lys2642Asn
ENST00000679554.1:c.*7765A>C ENSP00000506415.1:n.*7765A>C
ENST00000679722.1:n.8202A>C
ENST00000679821.1:c.7722A>C ENSP00000506040.1:p.Lys2574Asn
ENST00000680047.1:n.8178A>C
ENST00000680072.1:c.7803A>C ENSP00000506581.1:p.Lys2601Asn
ENST00000680181.1:c.7887A>C ENSP00000505548.1:p.Lys2629Asn
ENST00000680365.1:c.1473A>C ENSP00000506019.1:p.Lys491Asn
ENST00000680513.1:c.7839A>C ENSP00000505284.1:p.Lys2613Asn
ENST00000680534.1:c.8019A>C ENSP00000506674.1:p.Lys2673Asn
ENST00000680766.1:c.7956A>C ENSP00000505204.1:p.Lys2652Asn
ENST00000680952.1:c.7956A>C ENSP00000506407.1:p.Lys2652Asn
ENST00000681216.1:c.1473A>C ENSP00000505551.1:p.Lys491Asn
ENST00000681412.1:c.7980A>C ENSP00000506486.1:p.Lys2660Asn
ENST00000681722.1:c.7956A>C ENSP00000506566.1:p.Lys2652Asn
XM_006715827.1:c.7839A>C XP_006715890.1:p.Lys2613Asn
XM_011515709.1:c.8127A>C XP_011514011.1:p.Lys2709Asn
XM_011515710.1:c.8151A>C XP_011514012.1:p.Lys2717Asn
XM_011515711.1:c.8091A>C XP_011514013.1:p.Lys2697Asn
XM_011515712.1:c.8088A>C XP_011514014.1:p.Lys2696Asn
XM_011515713.1:c.8073A>C XP_011514015.1:p.Lys2691Asn
XM_011515714.1:c.8112A>C XP_011514016.1:p.Lys2704Asn
XM_011515716.1:c.8031A>C XP_011514018.1:p.Lys2677Asn
XM_011515717.1:c.7986A>C XP_011514019.1:p.Lys2662Asn
XM_011515718.1:c.8016A>C XP_011514020.1:p.Lys2672Asn
XM_011515719.1:c.7992A>C XP_011514021.1:p.Lys2664Asn
XM_011515720.1:c.7875A>C XP_011514022.1:p.Lys2625Asn
XM_011515721.1:c.2640A>C XP_011514023.1:p.Lys880Asn
XM_011515722.1:c.2601A>C XP_011514024.1:p.Lys867Asn
XM_017011642.2:c.8115A>C XP_016867131.1:p.Lys2705Asn
XM_017011643.2:c.8076A>C XP_016867132.1:p.Lys2692Asn
XM_017011644.2:c.8115A>C XP_016867133.1:p.Lys2705Asn
XM_017011645.2:c.8061A>C XP_016867134.1:p.Lys2687Asn
XM_017011646.2:c.8076A>C XP_016867135.1:p.Lys2692Asn
XM_017011647.2:c.8022A>C XP_016867136.1:p.Lys2674Asn
XM_017011648.2:c.8019A>C XP_016867137.1:p.Lys2673Asn
XM_017011649.2:c.8052A>C XP_016867138.1:p.Lys2684Asn
XM_017011650.2:c.7980A>C XP_016867139.1:p.Lys2660Asn
XM_017011651.2:c.7974A>C XP_016867140.1:p.Lys2658Asn
XM_017011652.2:c.8115A>C XP_016867141.1:p.Lys2705Asn
XM_017011653.2:c.7887A>C XP_016867142.1:p.Lys2629Asn
XM_017011654.2:c.7839A>C XP_016867143.1:p.Lys2613Asn
XM_017011655.2:c.7743A>C XP_016867144.1:p.Lys2581Asn
XM_017011656.2:c.7743A>C XP_016867145.1:p.Lys2581Asn
XM_017011657.2:c.3780A>C XP_016867146.1:p.Lys1260Asn
XM_017011658.2:c.2664A>C XP_016867147.1:p.Lys888Asn
XM_017011659.2:c.2625A>C XP_016867148.1:p.Lys875Asn
XM_017011660.2:c.2625A>C XP_016867149.1:p.Lys875Asn
XM_024446631.1:c.7878A>C XP_024302399.1:p.Lys2626Asn