Canonical Allele Identifier: CA843822575
Community Standard Title: NM_005751.5(AKAP9):c.6330+7A>G
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92066553A>G , CM000669.2:g.92066553A>G GRCh38
NC_000007.13:g.91695867A>G , CM000669.1:g.91695867A>G GRCh37
NC_000007.12:g.91533803A>G NCBI36
NG_011623.1:g.130679A>G , LRG_331:g.130679A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.6330+7A>G MANE Select NP_005742.4:n.6330+7A>G
ENST00000356239.8:c.6330+7A>G MANE Select ENSP00000348573.3:n.6330+7A>G
NM_001379277.1:c.975+7A>G NP_001366206.1:n.975+7A>G
NM_005751.4:c.6330+7A>G , LRG_331t1:c.6330+7A>G NP_005742.4:n.6330+7A>G
NM_147185.2:c.6330+7A>G NP_671714.1:n.6330+7A>G
NM_147185.3:c.6330+7A>G NP_671714.1:n.6330+7A>G
ENST00000356239.7:c.6330+7A>G ENSP00000348573.3:n.6330+7A>G
ENST00000358100.6:c.6189+7A>G ENSP00000350813.3:n.6189+7A>G
ENST00000359028.6:c.6363+7A>G ENSP00000351922.3:n.6363+7A>G
ENST00000359028.7:c.6426+7A>G ENSP00000351922.4:n.6426+7A>G
ENST00000491695.2:c.975+7A>G ENSP00000494626.2:n.975+7A>G
ENST00000674381.2:c.*6059+7A>G ENSP00000501536.2:n.*6059+7A>G
ENST00000679448.1:c.6330+7A>G ENSP00000505889.1:n.6330+7A>G
ENST00000679457.1:c.6330+7A>G ENSP00000505450.1:n.6330+7A>G
ENST00000679474.1:n.6552+7A>G
ENST00000679521.1:c.6276+7A>G ENSP00000505456.1:n.6276+7A>G
ENST00000679554.1:c.*6115+7A>G ENSP00000506415.1:n.*6115+7A>G
ENST00000679722.1:n.6552+7A>G
ENST00000679821.1:c.6072+7A>G ENSP00000506040.1:n.6072+7A>G
ENST00000680047.1:n.6552+7A>G
ENST00000680072.1:c.6330+7A>G ENSP00000506581.1:n.6330+7A>G
ENST00000680074.1:n.9296+7A>G
ENST00000680181.1:c.6237+7A>G ENSP00000505548.1:n.6237+7A>G
ENST00000680513.1:c.6189+7A>G ENSP00000505284.1:n.6189+7A>G
ENST00000680534.1:c.6369+7A>G ENSP00000506674.1:n.6369+7A>G
ENST00000680766.1:c.6330+7A>G ENSP00000505204.1:n.6330+7A>G
ENST00000680952.1:c.6330+7A>G ENSP00000506407.1:n.6330+7A>G
ENST00000681412.1:c.6330+7A>G ENSP00000506486.1:n.6330+7A>G
ENST00000681722.1:c.6330+7A>G ENSP00000506566.1:n.6330+7A>G
XM_006715827.1:c.6189+7A>G XP_006715890.1:n.6189+7A>G
XM_011515709.1:c.6501+7A>G XP_011514011.1:n.6501+7A>G
XM_011515710.1:c.6501+7A>G XP_011514012.1:n.6501+7A>G
XM_011515711.1:c.6465+7A>G XP_011514013.1:n.6465+7A>G
XM_011515712.1:c.6462+7A>G XP_011514014.1:n.6462+7A>G
XM_011515713.1:c.6447+7A>G XP_011514015.1:n.6447+7A>G
XM_011515714.1:c.6462+7A>G XP_011514016.1:n.6462+7A>G
XM_011515716.1:c.6405+7A>G XP_011514018.1:n.6405+7A>G
XM_011515717.1:c.6360+7A>G XP_011514019.1:n.6360+7A>G
XM_011515718.1:c.6366+7A>G XP_011514020.1:n.6366+7A>G
XM_011515719.1:c.6366+7A>G XP_011514021.1:n.6366+7A>G
XM_011515720.1:c.6225+7A>G XP_011514022.1:n.6225+7A>G
XM_011515721.1:c.1014+7A>G XP_011514023.1:n.1014+7A>G
XM_011515722.1:c.975+7A>G XP_011514024.1:n.975+7A>G
XM_017011642.2:c.6465+7A>G XP_016867131.1:n.6465+7A>G
XM_017011643.2:c.6426+7A>G XP_016867132.1:n.6426+7A>G
XM_017011644.2:c.6465+7A>G XP_016867133.1:n.6465+7A>G
XM_017011645.2:c.6411+7A>G XP_016867134.1:n.6411+7A>G
XM_017011646.2:c.6426+7A>G XP_016867135.1:n.6426+7A>G
XM_017011647.2:c.6372+7A>G XP_016867136.1:n.6372+7A>G
XM_017011648.2:c.6369+7A>G XP_016867137.1:n.6369+7A>G
XM_017011649.2:c.6426+7A>G XP_016867138.1:n.6426+7A>G
XM_017011650.2:c.6330+7A>G XP_016867139.1:n.6330+7A>G
XM_017011651.2:c.6324+7A>G XP_016867140.1:n.6324+7A>G
XM_017011652.2:c.6465+7A>G XP_016867141.1:n.6465+7A>G
XM_017011653.2:c.6237+7A>G XP_016867142.1:n.6237+7A>G
XM_017011654.2:c.6189+7A>G XP_016867143.1:n.6189+7A>G
XM_017011655.2:c.6093+7A>G XP_016867144.1:n.6093+7A>G
XM_017011656.2:c.6093+7A>G XP_016867145.1:n.6093+7A>G
XM_017011657.2:c.2130+7A>G XP_016867146.1:n.2130+7A>G
XM_017011658.2:c.1014+7A>G XP_016867147.1:n.1014+7A>G
XM_017011659.2:c.975+7A>G XP_016867148.1:n.975+7A>G
XM_017011660.2:c.975+7A>G XP_016867149.1:n.975+7A>G
XM_024446631.1:c.6228+7A>G XP_024302399.1:n.6228+7A>G