Canonical Allele Identifier: CA4337188

Gene: AKAP9

Linked Data

• dbSNP Id: rs751990585
• ExAC: 7:91707143 A / AT
• MyVariant Identifiers: chr7:g.91707143_91707144insT (hg19) ; chr7:g.92077829_92077830insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077829_92077830insT , CM000669.2:g.92077829_92077830insT	GRCh38
NC_000007.13:g.91707143_91707144insT , CM000669.1:g.91707143_91707144insT	GRCh37
NC_000007.12:g.91545079_91545080insT	NCBI36
NG_011623.1:g.141955_141956insT , LRG_331:g.141955_141956insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6899_6900insT MANE Select	ENSP00000348573.3:p.Gln2300HisfsTer10
ENST00000359028.7:c.6971_6972insT	ENSP00000351922.4:p.Gln2324HisfsTer10
ENST00000394534.7:c.392_393insT	ENSP00000378042.3:p.Gln131HisfsTer10
ENST00000491695.2:c.1544_1545insT	ENSP00000494626.2:p.Gln515HisfsTer10
ENST00000674381.2:c.*6628_*6629insT	ENSP00000501536.2:n.*6628_*6629insT
ENST00000679448.1:c.6875_6876insT	ENSP00000505889.1:p.Gln2292HisfsTer10
ENST00000679457.1:c.6875_6876insT	ENSP00000505450.1:p.Gln2292HisfsTer10
ENST00000679474.1:n.7097_7098insT
ENST00000679521.1:c.6845_6846insT	ENSP00000505456.1:p.Gln2282HisfsTer10
ENST00000679554.1:c.*6684_*6685insT	ENSP00000506415.1:n.*6684_*6685insT
ENST00000679722.1:n.7121_7122insT
ENST00000679821.1:c.6641_6642insT	ENSP00000506040.1:p.Gln2214HisfsTer10
ENST00000680047.1:n.7097_7098insT
ENST00000680072.1:c.6722_6723insT	ENSP00000506581.1:p.Gln2241HisfsTer10
ENST00000680181.1:c.6806_6807insT	ENSP00000505548.1:p.Gln2269HisfsTer10
ENST00000680365.1:c.392_393insT	ENSP00000506019.1:p.Gln131HisfsTer10
ENST00000680513.1:c.6758_6759insT	ENSP00000505284.1:p.Gln2253HisfsTer10
ENST00000680534.1:c.6938_6939insT	ENSP00000506674.1:p.Gln2313HisfsTer10
ENST00000680766.1:c.6875_6876insT	ENSP00000505204.1:p.Gln2292HisfsTer10
ENST00000680952.1:c.6875_6876insT	ENSP00000506407.1:p.Gln2292HisfsTer10
ENST00000681216.1:c.392_393insT	ENSP00000505551.1:p.Gln131HisfsTer10
ENST00000681412.1:c.6899_6900insT	ENSP00000506486.1:p.Gln2300HisfsTer10
ENST00000681722.1:c.6875_6876insT	ENSP00000506566.1:p.Gln2292HisfsTer10
ENST00000356239.7:c.6899_6900insT	ENSP00000348573.3:p.Gln2300HisfsTer10
ENST00000358100.6:c.6758_6759insT	ENSP00000350813.3:p.Gln2253HisfsTer10
ENST00000359028.6:c.6932_6933insT	ENSP00000351922.3:p.Gln2311HisfsTer10
ENST00000394534.6:c.437_438insT	ENSP00000378042.2:p.Gln146HisfsTer10
NM_005751.4:c.6899_6900insT , LRG_331t1:c.6899_6900insT	NP_005742.4:p.Gln2300HisfsTer10
NM_147185.2:c.6875_6876insT	NP_671714.1:p.Gln2292HisfsTer10
XM_006715827.1:c.6758_6759insT	XP_006715890.1:p.Gln2253HisfsTer10
XM_011515709.1:c.7046_7047insT	XP_011514011.1:p.Gln2349HisfsTer10
XM_011515710.1:c.7070_7071insT	XP_011514012.1:p.Gln2357HisfsTer10
XM_011515711.1:c.7010_7011insT	XP_011514013.1:p.Gln2337HisfsTer10
XM_011515712.1:c.7007_7008insT	XP_011514014.1:p.Gln2336HisfsTer10
XM_011515713.1:c.6992_6993insT	XP_011514015.1:p.Gln2331HisfsTer10
XM_011515714.1:c.7031_7032insT	XP_011514016.1:p.Gln2344HisfsTer10
XM_011515716.1:c.6950_6951insT	XP_011514018.1:p.Gln2317HisfsTer10
XM_011515717.1:c.6905_6906insT	XP_011514019.1:p.Gln2302HisfsTer10
XM_011515718.1:c.6935_6936insT	XP_011514020.1:p.Gln2312HisfsTer10
XM_011515719.1:c.6911_6912insT	XP_011514021.1:p.Gln2304HisfsTer10
XM_011515720.1:c.6794_6795insT	XP_011514022.1:p.Gln2265HisfsTer10
XM_011515721.1:c.1559_1560insT	XP_011514023.1:p.Gln520HisfsTer10
XM_011515722.1:c.1520_1521insT	XP_011514024.1:p.Gln507HisfsTer10
XM_017011642.2:c.7034_7035insT	XP_016867131.1:p.Gln2345HisfsTer10
XM_017011643.2:c.6995_6996insT	XP_016867132.1:p.Gln2332HisfsTer10
XM_017011644.2:c.7034_7035insT	XP_016867133.1:p.Gln2345HisfsTer10
XM_017011645.2:c.6980_6981insT	XP_016867134.1:p.Gln2327HisfsTer10
XM_017011646.2:c.6995_6996insT	XP_016867135.1:p.Gln2332HisfsTer10
XM_017011647.2:c.6941_6942insT	XP_016867136.1:p.Gln2314HisfsTer10
XM_017011648.2:c.6938_6939insT	XP_016867137.1:p.Gln2313HisfsTer10
XM_017011649.2:c.6971_6972insT	XP_016867138.1:p.Gln2324HisfsTer10
XM_017011650.2:c.6899_6900insT	XP_016867139.1:p.Gln2300HisfsTer10
XM_017011651.2:c.6893_6894insT	XP_016867140.1:p.Gln2298HisfsTer10
XM_017011652.2:c.7034_7035insT	XP_016867141.1:p.Gln2345HisfsTer10
XM_017011653.2:c.6806_6807insT	XP_016867142.1:p.Gln2269HisfsTer10
XM_017011654.2:c.6758_6759insT	XP_016867143.1:p.Gln2253HisfsTer10
XM_017011655.2:c.6662_6663insT	XP_016867144.1:p.Gln2221HisfsTer10
XM_017011656.2:c.6662_6663insT	XP_016867145.1:p.Gln2221HisfsTer10
XM_017011657.2:c.2699_2700insT	XP_016867146.1:p.Gln900HisfsTer10
XM_017011658.2:c.1583_1584insT	XP_016867147.1:p.Gln528HisfsTer10
XM_017011659.2:c.1544_1545insT	XP_016867148.1:p.Gln515HisfsTer10
XM_017011660.2:c.1544_1545insT	XP_016867149.1:p.Gln515HisfsTer10
XM_024446631.1:c.6797_6798insT	XP_024302399.1:p.Gln2266HisfsTer10
NM_147185.3:c.6875_6876insT	NP_671714.1:p.Gln2292HisfsTer10
NM_001379277.1:c.1544_1545insT	NP_001366206.1:p.Gln515HisfsTer10
NM_005751.5:c.6899_6900insT MANE Select	NP_005742.4:p.Gln2300HisfsTer10