Canonical Allele Identifier: CA1725747784

Gene: AKAP9

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6897A= MANE Select	ENSP00000348573.3:p.Glu2299=
ENST00000359028.7:c.6969A=	ENSP00000351922.4:p.Glu2323=
ENST00000394534.7:c.390A=	ENSP00000378042.3:p.Glu130=
ENST00000491695.2:c.1542A=	ENSP00000494626.2:p.Glu514=
ENST00000674381.2:c.*6626A=	ENSP00000501536.2:n.*6626A=
ENST00000679448.1:c.6873A=	ENSP00000505889.1:p.Glu2291=
ENST00000679457.1:c.6873A=	ENSP00000505450.1:p.Glu2291=
ENST00000679474.1:n.7095A=
ENST00000679521.1:c.6843A=	ENSP00000505456.1:p.Glu2281=
ENST00000679554.1:c.*6682A=	ENSP00000506415.1:n.*6682A=
ENST00000679722.1:n.7119A=
ENST00000679821.1:c.6639A=	ENSP00000506040.1:p.Glu2213=
ENST00000680047.1:n.7095A=
ENST00000680072.1:c.6720A=	ENSP00000506581.1:p.Glu2240=
ENST00000680181.1:c.6804A=	ENSP00000505548.1:p.Glu2268=
ENST00000680365.1:c.390A=	ENSP00000506019.1:p.Glu130=
ENST00000680513.1:c.6756A=	ENSP00000505284.1:p.Glu2252=
ENST00000680534.1:c.6936A=	ENSP00000506674.1:p.Glu2312=
ENST00000680766.1:c.6873A=	ENSP00000505204.1:p.Glu2291=
ENST00000680952.1:c.6873A=	ENSP00000506407.1:p.Glu2291=
ENST00000681216.1:c.390A=	ENSP00000505551.1:p.Glu130=
ENST00000681412.1:c.6897A=	ENSP00000506486.1:p.Glu2299=
ENST00000681722.1:c.6873A=	ENSP00000506566.1:p.Glu2291=
ENST00000356239.7:c.6897A=	ENSP00000348573.3:p.Glu2299=
ENST00000358100.6:c.6756A=	ENSP00000350813.3:p.Glu2252=
ENST00000359028.6:c.6930A=	ENSP00000351922.3:p.Glu2310=
ENST00000394534.6:c.435A=	ENSP00000378042.2:p.Glu145=
NM_005751.4:c.6897A= , LRG_331t1:c.6897A=	NP_005742.4:p.Glu2299=
NM_147185.2:c.6873A=	NP_671714.1:p.Glu2291=
XM_006715827.1:c.6756A=	XP_006715890.1:p.Glu2252=
XM_011515709.1:c.7044A=	XP_011514011.1:p.Glu2348=
XM_011515710.1:c.7068A=	XP_011514012.1:p.Glu2356=
XM_011515711.1:c.7008A=	XP_011514013.1:p.Glu2336=
XM_011515712.1:c.7005A=	XP_011514014.1:p.Glu2335=
XM_011515713.1:c.6990A=	XP_011514015.1:p.Glu2330=
XM_011515714.1:c.7029A=	XP_011514016.1:p.Glu2343=
XM_011515716.1:c.6948A=	XP_011514018.1:p.Glu2316=
XM_011515717.1:c.6903A=	XP_011514019.1:p.Glu2301=
XM_011515718.1:c.6933A=	XP_011514020.1:p.Glu2311=
XM_011515719.1:c.6909A=	XP_011514021.1:p.Glu2303=
XM_011515720.1:c.6792A=	XP_011514022.1:p.Glu2264=
XM_011515721.1:c.1557A=	XP_011514023.1:p.Glu519=
XM_011515722.1:c.1518A=	XP_011514024.1:p.Glu506=
XM_017011642.2:c.7032A=	XP_016867131.1:p.Glu2344=
XM_017011643.2:c.6993A=	XP_016867132.1:p.Glu2331=
XM_017011644.2:c.7032A=	XP_016867133.1:p.Glu2344=
XM_017011645.2:c.6978A=	XP_016867134.1:p.Glu2326=
XM_017011646.2:c.6993A=	XP_016867135.1:p.Glu2331=
XM_017011647.2:c.6939A=	XP_016867136.1:p.Glu2313=
XM_017011648.2:c.6936A=	XP_016867137.1:p.Glu2312=
XM_017011649.2:c.6969A=	XP_016867138.1:p.Glu2323=
XM_017011650.2:c.6897A=	XP_016867139.1:p.Glu2299=
XM_017011651.2:c.6891A=	XP_016867140.1:p.Glu2297=
XM_017011652.2:c.7032A=	XP_016867141.1:p.Glu2344=
XM_017011653.2:c.6804A=	XP_016867142.1:p.Glu2268=
XM_017011654.2:c.6756A=	XP_016867143.1:p.Glu2252=
XM_017011655.2:c.6660A=	XP_016867144.1:p.Glu2220=
XM_017011656.2:c.6660A=	XP_016867145.1:p.Glu2220=
XM_017011657.2:c.2697A=	XP_016867146.1:p.Glu899=
XM_017011658.2:c.1581A=	XP_016867147.1:p.Glu527=
XM_017011659.2:c.1542A=	XP_016867148.1:p.Glu514=
XM_017011660.2:c.1542A=	XP_016867149.1:p.Glu514=
XM_024446631.1:c.6795A=	XP_024302399.1:p.Glu2265=
NM_147185.3:c.6873A=	NP_671714.1:p.Glu2291=
NM_001379277.1:c.1542A=	NP_001366206.1:p.Glu514=
NM_005751.5:c.6897A= MANE Select	NP_005742.4:p.Glu2299=