Canonical Allele Identifier: CA368133900

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707170A>G (hg19) ; chr7:g.92077856A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077856A>G , CM000669.2:g.92077856A>G	GRCh38
NC_000007.13:g.91707170A>G , CM000669.1:g.91707170A>G	GRCh37
NC_000007.12:g.91545106A>G	NCBI36
NG_011623.1:g.141982A>G , LRG_331:g.141982A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6926A>G MANE Select	ENSP00000348573.3:p.Lys2309Arg
ENST00000359028.7:c.6998A>G	ENSP00000351922.4:p.Lys2333Arg
ENST00000394534.7:c.419A>G	ENSP00000378042.3:p.Lys140Arg
ENST00000491695.2:c.1571A>G	ENSP00000494626.2:p.Lys524Arg
ENST00000674381.2:c.*6655A>G	ENSP00000501536.2:n.*6655A>G
ENST00000679448.1:c.6902A>G	ENSP00000505889.1:p.Lys2301Arg
ENST00000679457.1:c.6902A>G	ENSP00000505450.1:p.Lys2301Arg
ENST00000679474.1:n.7124A>G
ENST00000679521.1:c.6872A>G	ENSP00000505456.1:p.Lys2291Arg
ENST00000679554.1:c.*6711A>G	ENSP00000506415.1:n.*6711A>G
ENST00000679722.1:n.7148A>G
ENST00000679821.1:c.6668A>G	ENSP00000506040.1:p.Lys2223Arg
ENST00000680047.1:n.7124A>G
ENST00000680072.1:c.6749A>G	ENSP00000506581.1:p.Lys2250Arg
ENST00000680181.1:c.6833A>G	ENSP00000505548.1:p.Lys2278Arg
ENST00000680365.1:c.419A>G	ENSP00000506019.1:p.Lys140Arg
ENST00000680513.1:c.6785A>G	ENSP00000505284.1:p.Lys2262Arg
ENST00000680534.1:c.6965A>G	ENSP00000506674.1:p.Lys2322Arg
ENST00000680766.1:c.6902A>G	ENSP00000505204.1:p.Lys2301Arg
ENST00000680952.1:c.6902A>G	ENSP00000506407.1:p.Lys2301Arg
ENST00000681216.1:c.419A>G	ENSP00000505551.1:p.Lys140Arg
ENST00000681412.1:c.6926A>G	ENSP00000506486.1:p.Lys2309Arg
ENST00000681722.1:c.6902A>G	ENSP00000506566.1:p.Lys2301Arg
ENST00000356239.7:c.6926A>G	ENSP00000348573.3:p.Lys2309Arg
ENST00000358100.6:c.6785A>G	ENSP00000350813.3:p.Lys2262Arg
ENST00000359028.6:c.6959A>G	ENSP00000351922.3:p.Lys2320Arg
ENST00000394534.6:c.464A>G	ENSP00000378042.2:p.Lys155Arg
NM_005751.4:c.6926A>G , LRG_331t1:c.6926A>G	NP_005742.4:p.Lys2309Arg
NM_147185.2:c.6902A>G	NP_671714.1:p.Lys2301Arg
XM_006715827.1:c.6785A>G	XP_006715890.1:p.Lys2262Arg
XM_011515709.1:c.7073A>G	XP_011514011.1:p.Lys2358Arg
XM_011515710.1:c.7097A>G	XP_011514012.1:p.Lys2366Arg
XM_011515711.1:c.7037A>G	XP_011514013.1:p.Lys2346Arg
XM_011515712.1:c.7034A>G	XP_011514014.1:p.Lys2345Arg
XM_011515713.1:c.7019A>G	XP_011514015.1:p.Lys2340Arg
XM_011515714.1:c.7058A>G	XP_011514016.1:p.Lys2353Arg
XM_011515716.1:c.6977A>G	XP_011514018.1:p.Lys2326Arg
XM_011515717.1:c.6932A>G	XP_011514019.1:p.Lys2311Arg
XM_011515718.1:c.6962A>G	XP_011514020.1:p.Lys2321Arg
XM_011515719.1:c.6938A>G	XP_011514021.1:p.Lys2313Arg
XM_011515720.1:c.6821A>G	XP_011514022.1:p.Lys2274Arg
XM_011515721.1:c.1586A>G	XP_011514023.1:p.Lys529Arg
XM_011515722.1:c.1547A>G	XP_011514024.1:p.Lys516Arg
XM_017011642.2:c.7061A>G	XP_016867131.1:p.Lys2354Arg
XM_017011643.2:c.7022A>G	XP_016867132.1:p.Lys2341Arg
XM_017011644.2:c.7061A>G	XP_016867133.1:p.Lys2354Arg
XM_017011645.2:c.7007A>G	XP_016867134.1:p.Lys2336Arg
XM_017011646.2:c.7022A>G	XP_016867135.1:p.Lys2341Arg
XM_017011647.2:c.6968A>G	XP_016867136.1:p.Lys2323Arg
XM_017011648.2:c.6965A>G	XP_016867137.1:p.Lys2322Arg
XM_017011649.2:c.6998A>G	XP_016867138.1:p.Lys2333Arg
XM_017011650.2:c.6926A>G	XP_016867139.1:p.Lys2309Arg
XM_017011651.2:c.6920A>G	XP_016867140.1:p.Lys2307Arg
XM_017011652.2:c.7061A>G	XP_016867141.1:p.Lys2354Arg
XM_017011653.2:c.6833A>G	XP_016867142.1:p.Lys2278Arg
XM_017011654.2:c.6785A>G	XP_016867143.1:p.Lys2262Arg
XM_017011655.2:c.6689A>G	XP_016867144.1:p.Lys2230Arg
XM_017011656.2:c.6689A>G	XP_016867145.1:p.Lys2230Arg
XM_017011657.2:c.2726A>G	XP_016867146.1:p.Lys909Arg
XM_017011658.2:c.1610A>G	XP_016867147.1:p.Lys537Arg
XM_017011659.2:c.1571A>G	XP_016867148.1:p.Lys524Arg
XM_017011660.2:c.1571A>G	XP_016867149.1:p.Lys524Arg
XM_024446631.1:c.6824A>G	XP_024302399.1:p.Lys2275Arg
NM_147185.3:c.6902A>G	NP_671714.1:p.Lys2301Arg
NM_001379277.1:c.1571A>G	NP_001366206.1:p.Lys524Arg
NM_005751.5:c.6926A>G MANE Select	NP_005742.4:p.Lys2309Arg