Canonical Allele Identifier: CA368133841

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707143A>G (hg19) ; chr7:g.92077829A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077829A>G , CM000669.2:g.92077829A>G	GRCh38
NC_000007.13:g.91707143A>G , CM000669.1:g.91707143A>G	GRCh37
NC_000007.12:g.91545079A>G	NCBI36
NG_011623.1:g.141955A>G , LRG_331:g.141955A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6899A>G MANE Select	ENSP00000348573.3:p.Gln2300Arg
ENST00000359028.7:c.6971A>G	ENSP00000351922.4:p.Gln2324Arg
ENST00000394534.7:c.392A>G	ENSP00000378042.3:p.Gln131Arg
ENST00000491695.2:c.1544A>G	ENSP00000494626.2:p.Gln515Arg
ENST00000674381.2:c.*6628A>G	ENSP00000501536.2:n.*6628A>G
ENST00000679448.1:c.6875A>G	ENSP00000505889.1:p.Gln2292Arg
ENST00000679457.1:c.6875A>G	ENSP00000505450.1:p.Gln2292Arg
ENST00000679474.1:n.7097A>G
ENST00000679521.1:c.6845A>G	ENSP00000505456.1:p.Gln2282Arg
ENST00000679554.1:c.*6684A>G	ENSP00000506415.1:n.*6684A>G
ENST00000679722.1:n.7121A>G
ENST00000679821.1:c.6641A>G	ENSP00000506040.1:p.Gln2214Arg
ENST00000680047.1:n.7097A>G
ENST00000680072.1:c.6722A>G	ENSP00000506581.1:p.Gln2241Arg
ENST00000680181.1:c.6806A>G	ENSP00000505548.1:p.Gln2269Arg
ENST00000680365.1:c.392A>G	ENSP00000506019.1:p.Gln131Arg
ENST00000680513.1:c.6758A>G	ENSP00000505284.1:p.Gln2253Arg
ENST00000680534.1:c.6938A>G	ENSP00000506674.1:p.Gln2313Arg
ENST00000680766.1:c.6875A>G	ENSP00000505204.1:p.Gln2292Arg
ENST00000680952.1:c.6875A>G	ENSP00000506407.1:p.Gln2292Arg
ENST00000681216.1:c.392A>G	ENSP00000505551.1:p.Gln131Arg
ENST00000681412.1:c.6899A>G	ENSP00000506486.1:p.Gln2300Arg
ENST00000681722.1:c.6875A>G	ENSP00000506566.1:p.Gln2292Arg
ENST00000356239.7:c.6899A>G	ENSP00000348573.3:p.Gln2300Arg
ENST00000358100.6:c.6758A>G	ENSP00000350813.3:p.Gln2253Arg
ENST00000359028.6:c.6932A>G	ENSP00000351922.3:p.Gln2311Arg
ENST00000394534.6:c.437A>G	ENSP00000378042.2:p.Gln146Arg
NM_005751.4:c.6899A>G , LRG_331t1:c.6899A>G	NP_005742.4:p.Gln2300Arg
NM_147185.2:c.6875A>G	NP_671714.1:p.Gln2292Arg
XM_006715827.1:c.6758A>G	XP_006715890.1:p.Gln2253Arg
XM_011515709.1:c.7046A>G	XP_011514011.1:p.Gln2349Arg
XM_011515710.1:c.7070A>G	XP_011514012.1:p.Gln2357Arg
XM_011515711.1:c.7010A>G	XP_011514013.1:p.Gln2337Arg
XM_011515712.1:c.7007A>G	XP_011514014.1:p.Gln2336Arg
XM_011515713.1:c.6992A>G	XP_011514015.1:p.Gln2331Arg
XM_011515714.1:c.7031A>G	XP_011514016.1:p.Gln2344Arg
XM_011515716.1:c.6950A>G	XP_011514018.1:p.Gln2317Arg
XM_011515717.1:c.6905A>G	XP_011514019.1:p.Gln2302Arg
XM_011515718.1:c.6935A>G	XP_011514020.1:p.Gln2312Arg
XM_011515719.1:c.6911A>G	XP_011514021.1:p.Gln2304Arg
XM_011515720.1:c.6794A>G	XP_011514022.1:p.Gln2265Arg
XM_011515721.1:c.1559A>G	XP_011514023.1:p.Gln520Arg
XM_011515722.1:c.1520A>G	XP_011514024.1:p.Gln507Arg
XM_017011642.2:c.7034A>G	XP_016867131.1:p.Gln2345Arg
XM_017011643.2:c.6995A>G	XP_016867132.1:p.Gln2332Arg
XM_017011644.2:c.7034A>G	XP_016867133.1:p.Gln2345Arg
XM_017011645.2:c.6980A>G	XP_016867134.1:p.Gln2327Arg
XM_017011646.2:c.6995A>G	XP_016867135.1:p.Gln2332Arg
XM_017011647.2:c.6941A>G	XP_016867136.1:p.Gln2314Arg
XM_017011648.2:c.6938A>G	XP_016867137.1:p.Gln2313Arg
XM_017011649.2:c.6971A>G	XP_016867138.1:p.Gln2324Arg
XM_017011650.2:c.6899A>G	XP_016867139.1:p.Gln2300Arg
XM_017011651.2:c.6893A>G	XP_016867140.1:p.Gln2298Arg
XM_017011652.2:c.7034A>G	XP_016867141.1:p.Gln2345Arg
XM_017011653.2:c.6806A>G	XP_016867142.1:p.Gln2269Arg
XM_017011654.2:c.6758A>G	XP_016867143.1:p.Gln2253Arg
XM_017011655.2:c.6662A>G	XP_016867144.1:p.Gln2221Arg
XM_017011656.2:c.6662A>G	XP_016867145.1:p.Gln2221Arg
XM_017011657.2:c.2699A>G	XP_016867146.1:p.Gln900Arg
XM_017011658.2:c.1583A>G	XP_016867147.1:p.Gln528Arg
XM_017011659.2:c.1544A>G	XP_016867148.1:p.Gln515Arg
XM_017011660.2:c.1544A>G	XP_016867149.1:p.Gln515Arg
XM_024446631.1:c.6797A>G	XP_024302399.1:p.Gln2266Arg
NM_147185.3:c.6875A>G	NP_671714.1:p.Gln2292Arg
NM_001379277.1:c.1544A>G	NP_001366206.1:p.Gln515Arg
NM_005751.5:c.6899A>G MANE Select	NP_005742.4:p.Gln2300Arg