Canonical Allele Identifier: CA368133836

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707140A>T (hg19) ; chr7:g.92077826A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077826A>T , CM000669.2:g.92077826A>T	GRCh38
NC_000007.13:g.91707140A>T , CM000669.1:g.91707140A>T	GRCh37
NC_000007.12:g.91545076A>T	NCBI36
NG_011623.1:g.141952A>T , LRG_331:g.141952A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6896A>T MANE Select	ENSP00000348573.3:p.Glu2299Val
ENST00000359028.7:c.6968A>T	ENSP00000351922.4:p.Glu2323Val
ENST00000394534.7:c.389A>T	ENSP00000378042.3:p.Glu130Val
ENST00000491695.2:c.1541A>T	ENSP00000494626.2:p.Glu514Val
ENST00000674381.2:c.*6625A>T	ENSP00000501536.2:n.*6625A>T
ENST00000679448.1:c.6872A>T	ENSP00000505889.1:p.Glu2291Val
ENST00000679457.1:c.6872A>T	ENSP00000505450.1:p.Glu2291Val
ENST00000679474.1:n.7094A>T
ENST00000679521.1:c.6842A>T	ENSP00000505456.1:p.Glu2281Val
ENST00000679554.1:c.*6681A>T	ENSP00000506415.1:n.*6681A>T
ENST00000679722.1:n.7118A>T
ENST00000679821.1:c.6638A>T	ENSP00000506040.1:p.Glu2213Val
ENST00000680047.1:n.7094A>T
ENST00000680072.1:c.6719A>T	ENSP00000506581.1:p.Glu2240Val
ENST00000680181.1:c.6803A>T	ENSP00000505548.1:p.Glu2268Val
ENST00000680365.1:c.389A>T	ENSP00000506019.1:p.Glu130Val
ENST00000680513.1:c.6755A>T	ENSP00000505284.1:p.Glu2252Val
ENST00000680534.1:c.6935A>T	ENSP00000506674.1:p.Glu2312Val
ENST00000680766.1:c.6872A>T	ENSP00000505204.1:p.Glu2291Val
ENST00000680952.1:c.6872A>T	ENSP00000506407.1:p.Glu2291Val
ENST00000681216.1:c.389A>T	ENSP00000505551.1:p.Glu130Val
ENST00000681412.1:c.6896A>T	ENSP00000506486.1:p.Glu2299Val
ENST00000681722.1:c.6872A>T	ENSP00000506566.1:p.Glu2291Val
ENST00000356239.7:c.6896A>T	ENSP00000348573.3:p.Glu2299Val
ENST00000358100.6:c.6755A>T	ENSP00000350813.3:p.Glu2252Val
ENST00000359028.6:c.6929A>T	ENSP00000351922.3:p.Glu2310Val
ENST00000394534.6:c.434A>T	ENSP00000378042.2:p.Glu145Val
NM_005751.4:c.6896A>T , LRG_331t1:c.6896A>T	NP_005742.4:p.Glu2299Val
NM_147185.2:c.6872A>T	NP_671714.1:p.Glu2291Val
XM_006715827.1:c.6755A>T	XP_006715890.1:p.Glu2252Val
XM_011515709.1:c.7043A>T	XP_011514011.1:p.Glu2348Val
XM_011515710.1:c.7067A>T	XP_011514012.1:p.Glu2356Val
XM_011515711.1:c.7007A>T	XP_011514013.1:p.Glu2336Val
XM_011515712.1:c.7004A>T	XP_011514014.1:p.Glu2335Val
XM_011515713.1:c.6989A>T	XP_011514015.1:p.Glu2330Val
XM_011515714.1:c.7028A>T	XP_011514016.1:p.Glu2343Val
XM_011515716.1:c.6947A>T	XP_011514018.1:p.Glu2316Val
XM_011515717.1:c.6902A>T	XP_011514019.1:p.Glu2301Val
XM_011515718.1:c.6932A>T	XP_011514020.1:p.Glu2311Val
XM_011515719.1:c.6908A>T	XP_011514021.1:p.Glu2303Val
XM_011515720.1:c.6791A>T	XP_011514022.1:p.Glu2264Val
XM_011515721.1:c.1556A>T	XP_011514023.1:p.Glu519Val
XM_011515722.1:c.1517A>T	XP_011514024.1:p.Glu506Val
XM_017011642.2:c.7031A>T	XP_016867131.1:p.Glu2344Val
XM_017011643.2:c.6992A>T	XP_016867132.1:p.Glu2331Val
XM_017011644.2:c.7031A>T	XP_016867133.1:p.Glu2344Val
XM_017011645.2:c.6977A>T	XP_016867134.1:p.Glu2326Val
XM_017011646.2:c.6992A>T	XP_016867135.1:p.Glu2331Val
XM_017011647.2:c.6938A>T	XP_016867136.1:p.Glu2313Val
XM_017011648.2:c.6935A>T	XP_016867137.1:p.Glu2312Val
XM_017011649.2:c.6968A>T	XP_016867138.1:p.Glu2323Val
XM_017011650.2:c.6896A>T	XP_016867139.1:p.Glu2299Val
XM_017011651.2:c.6890A>T	XP_016867140.1:p.Glu2297Val
XM_017011652.2:c.7031A>T	XP_016867141.1:p.Glu2344Val
XM_017011653.2:c.6803A>T	XP_016867142.1:p.Glu2268Val
XM_017011654.2:c.6755A>T	XP_016867143.1:p.Glu2252Val
XM_017011655.2:c.6659A>T	XP_016867144.1:p.Glu2220Val
XM_017011656.2:c.6659A>T	XP_016867145.1:p.Glu2220Val
XM_017011657.2:c.2696A>T	XP_016867146.1:p.Glu899Val
XM_017011658.2:c.1580A>T	XP_016867147.1:p.Glu527Val
XM_017011659.2:c.1541A>T	XP_016867148.1:p.Glu514Val
XM_017011660.2:c.1541A>T	XP_016867149.1:p.Glu514Val
XM_024446631.1:c.6794A>T	XP_024302399.1:p.Glu2265Val
NM_147185.3:c.6872A>T	NP_671714.1:p.Glu2291Val
NM_001379277.1:c.1541A>T	NP_001366206.1:p.Glu514Val
NM_005751.5:c.6896A>T MANE Select	NP_005742.4:p.Glu2299Val