Canonical Allele Identifier: CA368133859

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707152A>T (hg19) ; chr7:g.92077838A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077838A>T , CM000669.2:g.92077838A>T	GRCh38
NC_000007.13:g.91707152A>T , CM000669.1:g.91707152A>T	GRCh37
NC_000007.12:g.91545088A>T	NCBI36
NG_011623.1:g.141964A>T , LRG_331:g.141964A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6908A>T MANE Select	ENSP00000348573.3:p.Lys2303Ile
ENST00000359028.7:c.6980A>T	ENSP00000351922.4:p.Lys2327Ile
ENST00000394534.7:c.401A>T	ENSP00000378042.3:p.Lys134Ile
ENST00000491695.2:c.1553A>T	ENSP00000494626.2:p.Lys518Ile
ENST00000674381.2:c.*6637A>T	ENSP00000501536.2:n.*6637A>T
ENST00000679448.1:c.6884A>T	ENSP00000505889.1:p.Lys2295Ile
ENST00000679457.1:c.6884A>T	ENSP00000505450.1:p.Lys2295Ile
ENST00000679474.1:n.7106A>T
ENST00000679521.1:c.6854A>T	ENSP00000505456.1:p.Lys2285Ile
ENST00000679554.1:c.*6693A>T	ENSP00000506415.1:n.*6693A>T
ENST00000679722.1:n.7130A>T
ENST00000679821.1:c.6650A>T	ENSP00000506040.1:p.Lys2217Ile
ENST00000680047.1:n.7106A>T
ENST00000680072.1:c.6731A>T	ENSP00000506581.1:p.Lys2244Ile
ENST00000680181.1:c.6815A>T	ENSP00000505548.1:p.Lys2272Ile
ENST00000680365.1:c.401A>T	ENSP00000506019.1:p.Lys134Ile
ENST00000680513.1:c.6767A>T	ENSP00000505284.1:p.Lys2256Ile
ENST00000680534.1:c.6947A>T	ENSP00000506674.1:p.Lys2316Ile
ENST00000680766.1:c.6884A>T	ENSP00000505204.1:p.Lys2295Ile
ENST00000680952.1:c.6884A>T	ENSP00000506407.1:p.Lys2295Ile
ENST00000681216.1:c.401A>T	ENSP00000505551.1:p.Lys134Ile
ENST00000681412.1:c.6908A>T	ENSP00000506486.1:p.Lys2303Ile
ENST00000681722.1:c.6884A>T	ENSP00000506566.1:p.Lys2295Ile
ENST00000356239.7:c.6908A>T	ENSP00000348573.3:p.Lys2303Ile
ENST00000358100.6:c.6767A>T	ENSP00000350813.3:p.Lys2256Ile
ENST00000359028.6:c.6941A>T	ENSP00000351922.3:p.Lys2314Ile
ENST00000394534.6:c.446A>T	ENSP00000378042.2:p.Lys149Ile
NM_005751.4:c.6908A>T , LRG_331t1:c.6908A>T	NP_005742.4:p.Lys2303Ile
NM_147185.2:c.6884A>T	NP_671714.1:p.Lys2295Ile
XM_006715827.1:c.6767A>T	XP_006715890.1:p.Lys2256Ile
XM_011515709.1:c.7055A>T	XP_011514011.1:p.Lys2352Ile
XM_011515710.1:c.7079A>T	XP_011514012.1:p.Lys2360Ile
XM_011515711.1:c.7019A>T	XP_011514013.1:p.Lys2340Ile
XM_011515712.1:c.7016A>T	XP_011514014.1:p.Lys2339Ile
XM_011515713.1:c.7001A>T	XP_011514015.1:p.Lys2334Ile
XM_011515714.1:c.7040A>T	XP_011514016.1:p.Lys2347Ile
XM_011515716.1:c.6959A>T	XP_011514018.1:p.Lys2320Ile
XM_011515717.1:c.6914A>T	XP_011514019.1:p.Lys2305Ile
XM_011515718.1:c.6944A>T	XP_011514020.1:p.Lys2315Ile
XM_011515719.1:c.6920A>T	XP_011514021.1:p.Lys2307Ile
XM_011515720.1:c.6803A>T	XP_011514022.1:p.Lys2268Ile
XM_011515721.1:c.1568A>T	XP_011514023.1:p.Lys523Ile
XM_011515722.1:c.1529A>T	XP_011514024.1:p.Lys510Ile
XM_017011642.2:c.7043A>T	XP_016867131.1:p.Lys2348Ile
XM_017011643.2:c.7004A>T	XP_016867132.1:p.Lys2335Ile
XM_017011644.2:c.7043A>T	XP_016867133.1:p.Lys2348Ile
XM_017011645.2:c.6989A>T	XP_016867134.1:p.Lys2330Ile
XM_017011646.2:c.7004A>T	XP_016867135.1:p.Lys2335Ile
XM_017011647.2:c.6950A>T	XP_016867136.1:p.Lys2317Ile
XM_017011648.2:c.6947A>T	XP_016867137.1:p.Lys2316Ile
XM_017011649.2:c.6980A>T	XP_016867138.1:p.Lys2327Ile
XM_017011650.2:c.6908A>T	XP_016867139.1:p.Lys2303Ile
XM_017011651.2:c.6902A>T	XP_016867140.1:p.Lys2301Ile
XM_017011652.2:c.7043A>T	XP_016867141.1:p.Lys2348Ile
XM_017011653.2:c.6815A>T	XP_016867142.1:p.Lys2272Ile
XM_017011654.2:c.6767A>T	XP_016867143.1:p.Lys2256Ile
XM_017011655.2:c.6671A>T	XP_016867144.1:p.Lys2224Ile
XM_017011656.2:c.6671A>T	XP_016867145.1:p.Lys2224Ile
XM_017011657.2:c.2708A>T	XP_016867146.1:p.Lys903Ile
XM_017011658.2:c.1592A>T	XP_016867147.1:p.Lys531Ile
XM_017011659.2:c.1553A>T	XP_016867148.1:p.Lys518Ile
XM_017011660.2:c.1553A>T	XP_016867149.1:p.Lys518Ile
XM_024446631.1:c.6806A>T	XP_024302399.1:p.Lys2269Ile
NM_147185.3:c.6884A>T	NP_671714.1:p.Lys2295Ile
NM_001379277.1:c.1553A>T	NP_001366206.1:p.Lys518Ile
NM_005751.5:c.6908A>T MANE Select	NP_005742.4:p.Lys2303Ile