Canonical Allele Identifier: CA368133838

Gene: AKAP9

Linked Data

• dbSNP Id: rs778698845
• gnomAD v3: 7-92077828-C-A
• gnomAD v4: 7-92077828-C-A
• MyVariant Identifiers: chr7:g.91707142C>A (hg19) ; chr7:g.92077828C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077828C>A , CM000669.2:g.92077828C>A	GRCh38
NC_000007.13:g.91707142C>A , CM000669.1:g.91707142C>A	GRCh37
NC_000007.12:g.91545078C>A	NCBI36
NG_011623.1:g.141954C>A , LRG_331:g.141954C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6898C>A MANE Select	ENSP00000348573.3:p.Gln2300Lys
ENST00000359028.7:c.6970C>A	ENSP00000351922.4:p.Gln2324Lys
ENST00000394534.7:c.391C>A	ENSP00000378042.3:p.Gln131Lys
ENST00000491695.2:c.1543C>A	ENSP00000494626.2:p.Gln515Lys
ENST00000674381.2:c.*6627C>A	ENSP00000501536.2:n.*6627C>A
ENST00000679448.1:c.6874C>A	ENSP00000505889.1:p.Gln2292Lys
ENST00000679457.1:c.6874C>A	ENSP00000505450.1:p.Gln2292Lys
ENST00000679474.1:n.7096C>A
ENST00000679521.1:c.6844C>A	ENSP00000505456.1:p.Gln2282Lys
ENST00000679554.1:c.*6683C>A	ENSP00000506415.1:n.*6683C>A
ENST00000679722.1:n.7120C>A
ENST00000679821.1:c.6640C>A	ENSP00000506040.1:p.Gln2214Lys
ENST00000680047.1:n.7096C>A
ENST00000680072.1:c.6721C>A	ENSP00000506581.1:p.Gln2241Lys
ENST00000680181.1:c.6805C>A	ENSP00000505548.1:p.Gln2269Lys
ENST00000680365.1:c.391C>A	ENSP00000506019.1:p.Gln131Lys
ENST00000680513.1:c.6757C>A	ENSP00000505284.1:p.Gln2253Lys
ENST00000680534.1:c.6937C>A	ENSP00000506674.1:p.Gln2313Lys
ENST00000680766.1:c.6874C>A	ENSP00000505204.1:p.Gln2292Lys
ENST00000680952.1:c.6874C>A	ENSP00000506407.1:p.Gln2292Lys
ENST00000681216.1:c.391C>A	ENSP00000505551.1:p.Gln131Lys
ENST00000681412.1:c.6898C>A	ENSP00000506486.1:p.Gln2300Lys
ENST00000681722.1:c.6874C>A	ENSP00000506566.1:p.Gln2292Lys
ENST00000356239.7:c.6898C>A	ENSP00000348573.3:p.Gln2300Lys
ENST00000358100.6:c.6757C>A	ENSP00000350813.3:p.Gln2253Lys
ENST00000359028.6:c.6931C>A	ENSP00000351922.3:p.Gln2311Lys
ENST00000394534.6:c.436C>A	ENSP00000378042.2:p.Gln146Lys
NM_005751.4:c.6898C>A , LRG_331t1:c.6898C>A	NP_005742.4:p.Gln2300Lys
NM_147185.2:c.6874C>A	NP_671714.1:p.Gln2292Lys
XM_006715827.1:c.6757C>A	XP_006715890.1:p.Gln2253Lys
XM_011515709.1:c.7045C>A	XP_011514011.1:p.Gln2349Lys
XM_011515710.1:c.7069C>A	XP_011514012.1:p.Gln2357Lys
XM_011515711.1:c.7009C>A	XP_011514013.1:p.Gln2337Lys
XM_011515712.1:c.7006C>A	XP_011514014.1:p.Gln2336Lys
XM_011515713.1:c.6991C>A	XP_011514015.1:p.Gln2331Lys
XM_011515714.1:c.7030C>A	XP_011514016.1:p.Gln2344Lys
XM_011515716.1:c.6949C>A	XP_011514018.1:p.Gln2317Lys
XM_011515717.1:c.6904C>A	XP_011514019.1:p.Gln2302Lys
XM_011515718.1:c.6934C>A	XP_011514020.1:p.Gln2312Lys
XM_011515719.1:c.6910C>A	XP_011514021.1:p.Gln2304Lys
XM_011515720.1:c.6793C>A	XP_011514022.1:p.Gln2265Lys
XM_011515721.1:c.1558C>A	XP_011514023.1:p.Gln520Lys
XM_011515722.1:c.1519C>A	XP_011514024.1:p.Gln507Lys
XM_017011642.2:c.7033C>A	XP_016867131.1:p.Gln2345Lys
XM_017011643.2:c.6994C>A	XP_016867132.1:p.Gln2332Lys
XM_017011644.2:c.7033C>A	XP_016867133.1:p.Gln2345Lys
XM_017011645.2:c.6979C>A	XP_016867134.1:p.Gln2327Lys
XM_017011646.2:c.6994C>A	XP_016867135.1:p.Gln2332Lys
XM_017011647.2:c.6940C>A	XP_016867136.1:p.Gln2314Lys
XM_017011648.2:c.6937C>A	XP_016867137.1:p.Gln2313Lys
XM_017011649.2:c.6970C>A	XP_016867138.1:p.Gln2324Lys
XM_017011650.2:c.6898C>A	XP_016867139.1:p.Gln2300Lys
XM_017011651.2:c.6892C>A	XP_016867140.1:p.Gln2298Lys
XM_017011652.2:c.7033C>A	XP_016867141.1:p.Gln2345Lys
XM_017011653.2:c.6805C>A	XP_016867142.1:p.Gln2269Lys
XM_017011654.2:c.6757C>A	XP_016867143.1:p.Gln2253Lys
XM_017011655.2:c.6661C>A	XP_016867144.1:p.Gln2221Lys
XM_017011656.2:c.6661C>A	XP_016867145.1:p.Gln2221Lys
XM_017011657.2:c.2698C>A	XP_016867146.1:p.Gln900Lys
XM_017011658.2:c.1582C>A	XP_016867147.1:p.Gln528Lys
XM_017011659.2:c.1543C>A	XP_016867148.1:p.Gln515Lys
XM_017011660.2:c.1543C>A	XP_016867149.1:p.Gln515Lys
XM_024446631.1:c.6796C>A	XP_024302399.1:p.Gln2266Lys
NM_147185.3:c.6874C>A	NP_671714.1:p.Gln2292Lys
NM_001379277.1:c.1543C>A	NP_001366206.1:p.Gln515Lys
NM_005751.5:c.6898C>A MANE Select	NP_005742.4:p.Gln2300Lys