Canonical Allele Identifier: CA368133606

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707043G>A (hg19) ; chr7:g.92077729G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077729G>A , CM000669.2:g.92077729G>A	GRCh38
NC_000007.13:g.91707043G>A , CM000669.1:g.91707043G>A	GRCh37
NC_000007.12:g.91544979G>A	NCBI36
NG_011623.1:g.141855G>A , LRG_331:g.141855G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6799G>A MANE Select	ENSP00000348573.3:p.Glu2267Lys
ENST00000359028.7:c.6871G>A	ENSP00000351922.4:p.Glu2291Lys
ENST00000394534.7:c.292G>A	ENSP00000378042.3:p.Glu98Lys
ENST00000491695.2:c.1444G>A	ENSP00000494626.2:p.Glu482Lys
ENST00000674381.2:c.*6528G>A	ENSP00000501536.2:n.*6528G>A
ENST00000679448.1:c.6775G>A	ENSP00000505889.1:p.Glu2259Lys
ENST00000679457.1:c.6775G>A	ENSP00000505450.1:p.Glu2259Lys
ENST00000679474.1:n.6997G>A
ENST00000679521.1:c.6745G>A	ENSP00000505456.1:p.Glu2249Lys
ENST00000679554.1:c.*6584G>A	ENSP00000506415.1:n.*6584G>A
ENST00000679722.1:n.7021G>A
ENST00000679821.1:c.6541G>A	ENSP00000506040.1:p.Glu2181Lys
ENST00000680047.1:n.6997G>A
ENST00000680072.1:c.6622G>A	ENSP00000506581.1:p.Glu2208Lys
ENST00000680181.1:c.6706G>A	ENSP00000505548.1:p.Glu2236Lys
ENST00000680365.1:c.292G>A	ENSP00000506019.1:p.Glu98Lys
ENST00000680513.1:c.6658G>A	ENSP00000505284.1:p.Glu2220Lys
ENST00000680534.1:c.6838G>A	ENSP00000506674.1:p.Glu2280Lys
ENST00000680766.1:c.6775G>A	ENSP00000505204.1:p.Glu2259Lys
ENST00000680952.1:c.6775G>A	ENSP00000506407.1:p.Glu2259Lys
ENST00000681216.1:c.292G>A	ENSP00000505551.1:p.Glu98Lys
ENST00000681412.1:c.6799G>A	ENSP00000506486.1:p.Glu2267Lys
ENST00000681722.1:c.6775G>A	ENSP00000506566.1:p.Glu2259Lys
ENST00000356239.7:c.6799G>A	ENSP00000348573.3:p.Glu2267Lys
ENST00000358100.6:c.6658G>A	ENSP00000350813.3:p.Glu2220Lys
ENST00000359028.6:c.6832G>A	ENSP00000351922.3:p.Glu2278Lys
ENST00000394534.6:c.337G>A	ENSP00000378042.2:p.Glu113Lys
NM_005751.4:c.6799G>A , LRG_331t1:c.6799G>A	NP_005742.4:p.Glu2267Lys
NM_147185.2:c.6775G>A	NP_671714.1:p.Glu2259Lys
XM_006715827.1:c.6658G>A	XP_006715890.1:p.Glu2220Lys
XM_011515709.1:c.6946G>A	XP_011514011.1:p.Glu2316Lys
XM_011515710.1:c.6970G>A	XP_011514012.1:p.Glu2324Lys
XM_011515711.1:c.6910G>A	XP_011514013.1:p.Glu2304Lys
XM_011515712.1:c.6907G>A	XP_011514014.1:p.Glu2303Lys
XM_011515713.1:c.6892G>A	XP_011514015.1:p.Glu2298Lys
XM_011515714.1:c.6931G>A	XP_011514016.1:p.Glu2311Lys
XM_011515716.1:c.6850G>A	XP_011514018.1:p.Glu2284Lys
XM_011515717.1:c.6805G>A	XP_011514019.1:p.Glu2269Lys
XM_011515718.1:c.6835G>A	XP_011514020.1:p.Glu2279Lys
XM_011515719.1:c.6811G>A	XP_011514021.1:p.Glu2271Lys
XM_011515720.1:c.6694G>A	XP_011514022.1:p.Glu2232Lys
XM_011515721.1:c.1459G>A	XP_011514023.1:p.Glu487Lys
XM_011515722.1:c.1420G>A	XP_011514024.1:p.Glu474Lys
XM_017011642.2:c.6934G>A	XP_016867131.1:p.Glu2312Lys
XM_017011643.2:c.6895G>A	XP_016867132.1:p.Glu2299Lys
XM_017011644.2:c.6934G>A	XP_016867133.1:p.Glu2312Lys
XM_017011645.2:c.6880G>A	XP_016867134.1:p.Glu2294Lys
XM_017011646.2:c.6895G>A	XP_016867135.1:p.Glu2299Lys
XM_017011647.2:c.6841G>A	XP_016867136.1:p.Glu2281Lys
XM_017011648.2:c.6838G>A	XP_016867137.1:p.Glu2280Lys
XM_017011649.2:c.6871G>A	XP_016867138.1:p.Glu2291Lys
XM_017011650.2:c.6799G>A	XP_016867139.1:p.Glu2267Lys
XM_017011651.2:c.6793G>A	XP_016867140.1:p.Glu2265Lys
XM_017011652.2:c.6934G>A	XP_016867141.1:p.Glu2312Lys
XM_017011653.2:c.6706G>A	XP_016867142.1:p.Glu2236Lys
XM_017011654.2:c.6658G>A	XP_016867143.1:p.Glu2220Lys
XM_017011655.2:c.6562G>A	XP_016867144.1:p.Glu2188Lys
XM_017011656.2:c.6562G>A	XP_016867145.1:p.Glu2188Lys
XM_017011657.2:c.2599G>A	XP_016867146.1:p.Glu867Lys
XM_017011658.2:c.1483G>A	XP_016867147.1:p.Glu495Lys
XM_017011659.2:c.1444G>A	XP_016867148.1:p.Glu482Lys
XM_017011660.2:c.1444G>A	XP_016867149.1:p.Glu482Lys
XM_024446631.1:c.6697G>A	XP_024302399.1:p.Glu2233Lys
NM_147185.3:c.6775G>A	NP_671714.1:p.Glu2259Lys
NM_001379277.1:c.1444G>A	NP_001366206.1:p.Glu482Lys
NM_005751.5:c.6799G>A MANE Select	NP_005742.4:p.Glu2267Lys