Canonical Allele Identifier: CA368133837

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707141A>C (hg19) ; chr7:g.92077827A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077827A>C , CM000669.2:g.92077827A>C	GRCh38
NC_000007.13:g.91707141A>C , CM000669.1:g.91707141A>C	GRCh37
NC_000007.12:g.91545077A>C	NCBI36
NG_011623.1:g.141953A>C , LRG_331:g.141953A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6897A>C MANE Select	ENSP00000348573.3:p.Glu2299Asp
ENST00000359028.7:c.6969A>C	ENSP00000351922.4:p.Glu2323Asp
ENST00000394534.7:c.390A>C	ENSP00000378042.3:p.Glu130Asp
ENST00000491695.2:c.1542A>C	ENSP00000494626.2:p.Glu514Asp
ENST00000674381.2:c.*6626A>C	ENSP00000501536.2:n.*6626A>C
ENST00000679448.1:c.6873A>C	ENSP00000505889.1:p.Glu2291Asp
ENST00000679457.1:c.6873A>C	ENSP00000505450.1:p.Glu2291Asp
ENST00000679474.1:n.7095A>C
ENST00000679521.1:c.6843A>C	ENSP00000505456.1:p.Glu2281Asp
ENST00000679554.1:c.*6682A>C	ENSP00000506415.1:n.*6682A>C
ENST00000679722.1:n.7119A>C
ENST00000679821.1:c.6639A>C	ENSP00000506040.1:p.Glu2213Asp
ENST00000680047.1:n.7095A>C
ENST00000680072.1:c.6720A>C	ENSP00000506581.1:p.Glu2240Asp
ENST00000680181.1:c.6804A>C	ENSP00000505548.1:p.Glu2268Asp
ENST00000680365.1:c.390A>C	ENSP00000506019.1:p.Glu130Asp
ENST00000680513.1:c.6756A>C	ENSP00000505284.1:p.Glu2252Asp
ENST00000680534.1:c.6936A>C	ENSP00000506674.1:p.Glu2312Asp
ENST00000680766.1:c.6873A>C	ENSP00000505204.1:p.Glu2291Asp
ENST00000680952.1:c.6873A>C	ENSP00000506407.1:p.Glu2291Asp
ENST00000681216.1:c.390A>C	ENSP00000505551.1:p.Glu130Asp
ENST00000681412.1:c.6897A>C	ENSP00000506486.1:p.Glu2299Asp
ENST00000681722.1:c.6873A>C	ENSP00000506566.1:p.Glu2291Asp
ENST00000356239.7:c.6897A>C	ENSP00000348573.3:p.Glu2299Asp
ENST00000358100.6:c.6756A>C	ENSP00000350813.3:p.Glu2252Asp
ENST00000359028.6:c.6930A>C	ENSP00000351922.3:p.Glu2310Asp
ENST00000394534.6:c.435A>C	ENSP00000378042.2:p.Glu145Asp
NM_005751.4:c.6897A>C , LRG_331t1:c.6897A>C	NP_005742.4:p.Glu2299Asp
NM_147185.2:c.6873A>C	NP_671714.1:p.Glu2291Asp
XM_006715827.1:c.6756A>C	XP_006715890.1:p.Glu2252Asp
XM_011515709.1:c.7044A>C	XP_011514011.1:p.Glu2348Asp
XM_011515710.1:c.7068A>C	XP_011514012.1:p.Glu2356Asp
XM_011515711.1:c.7008A>C	XP_011514013.1:p.Glu2336Asp
XM_011515712.1:c.7005A>C	XP_011514014.1:p.Glu2335Asp
XM_011515713.1:c.6990A>C	XP_011514015.1:p.Glu2330Asp
XM_011515714.1:c.7029A>C	XP_011514016.1:p.Glu2343Asp
XM_011515716.1:c.6948A>C	XP_011514018.1:p.Glu2316Asp
XM_011515717.1:c.6903A>C	XP_011514019.1:p.Glu2301Asp
XM_011515718.1:c.6933A>C	XP_011514020.1:p.Glu2311Asp
XM_011515719.1:c.6909A>C	XP_011514021.1:p.Glu2303Asp
XM_011515720.1:c.6792A>C	XP_011514022.1:p.Glu2264Asp
XM_011515721.1:c.1557A>C	XP_011514023.1:p.Glu519Asp
XM_011515722.1:c.1518A>C	XP_011514024.1:p.Glu506Asp
XM_017011642.2:c.7032A>C	XP_016867131.1:p.Glu2344Asp
XM_017011643.2:c.6993A>C	XP_016867132.1:p.Glu2331Asp
XM_017011644.2:c.7032A>C	XP_016867133.1:p.Glu2344Asp
XM_017011645.2:c.6978A>C	XP_016867134.1:p.Glu2326Asp
XM_017011646.2:c.6993A>C	XP_016867135.1:p.Glu2331Asp
XM_017011647.2:c.6939A>C	XP_016867136.1:p.Glu2313Asp
XM_017011648.2:c.6936A>C	XP_016867137.1:p.Glu2312Asp
XM_017011649.2:c.6969A>C	XP_016867138.1:p.Glu2323Asp
XM_017011650.2:c.6897A>C	XP_016867139.1:p.Glu2299Asp
XM_017011651.2:c.6891A>C	XP_016867140.1:p.Glu2297Asp
XM_017011652.2:c.7032A>C	XP_016867141.1:p.Glu2344Asp
XM_017011653.2:c.6804A>C	XP_016867142.1:p.Glu2268Asp
XM_017011654.2:c.6756A>C	XP_016867143.1:p.Glu2252Asp
XM_017011655.2:c.6660A>C	XP_016867144.1:p.Glu2220Asp
XM_017011656.2:c.6660A>C	XP_016867145.1:p.Glu2220Asp
XM_017011657.2:c.2697A>C	XP_016867146.1:p.Glu899Asp
XM_017011658.2:c.1581A>C	XP_016867147.1:p.Glu527Asp
XM_017011659.2:c.1542A>C	XP_016867148.1:p.Glu514Asp
XM_017011660.2:c.1542A>C	XP_016867149.1:p.Glu514Asp
XM_024446631.1:c.6795A>C	XP_024302399.1:p.Glu2265Asp
NM_147185.3:c.6873A>C	NP_671714.1:p.Glu2291Asp
NM_001379277.1:c.1542A>C	NP_001366206.1:p.Glu514Asp
NM_005751.5:c.6897A>C MANE Select	NP_005742.4:p.Glu2299Asp