Canonical Allele Identifier: CA368133839

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707142C>T (hg19) ; chr7:g.92077828C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6898C>T MANE Select	ENSP00000348573.3:p.Gln2300Ter
ENST00000359028.7:c.6970C>T	ENSP00000351922.4:p.Gln2324Ter
ENST00000394534.7:c.391C>T	ENSP00000378042.3:p.Gln131Ter
ENST00000491695.2:c.1543C>T	ENSP00000494626.2:p.Gln515Ter
ENST00000674381.2:c.*6627C>T	ENSP00000501536.2:n.*6627C>T
ENST00000679448.1:c.6874C>T	ENSP00000505889.1:p.Gln2292Ter
ENST00000679457.1:c.6874C>T	ENSP00000505450.1:p.Gln2292Ter
ENST00000679474.1:n.7096C>T
ENST00000679521.1:c.6844C>T	ENSP00000505456.1:p.Gln2282Ter
ENST00000679554.1:c.*6683C>T	ENSP00000506415.1:n.*6683C>T
ENST00000679722.1:n.7120C>T
ENST00000679821.1:c.6640C>T	ENSP00000506040.1:p.Gln2214Ter
ENST00000680047.1:n.7096C>T
ENST00000680072.1:c.6721C>T	ENSP00000506581.1:p.Gln2241Ter
ENST00000680181.1:c.6805C>T	ENSP00000505548.1:p.Gln2269Ter
ENST00000680365.1:c.391C>T	ENSP00000506019.1:p.Gln131Ter
ENST00000680513.1:c.6757C>T	ENSP00000505284.1:p.Gln2253Ter
ENST00000680534.1:c.6937C>T	ENSP00000506674.1:p.Gln2313Ter
ENST00000680766.1:c.6874C>T	ENSP00000505204.1:p.Gln2292Ter
ENST00000680952.1:c.6874C>T	ENSP00000506407.1:p.Gln2292Ter
ENST00000681216.1:c.391C>T	ENSP00000505551.1:p.Gln131Ter
ENST00000681412.1:c.6898C>T	ENSP00000506486.1:p.Gln2300Ter
ENST00000681722.1:c.6874C>T	ENSP00000506566.1:p.Gln2292Ter
ENST00000356239.7:c.6898C>T	ENSP00000348573.3:p.Gln2300Ter
ENST00000358100.6:c.6757C>T	ENSP00000350813.3:p.Gln2253Ter
ENST00000359028.6:c.6931C>T	ENSP00000351922.3:p.Gln2311Ter
ENST00000394534.6:c.436C>T	ENSP00000378042.2:p.Gln146Ter
NM_005751.4:c.6898C>T , LRG_331t1:c.6898C>T	NP_005742.4:p.Gln2300Ter
NM_147185.2:c.6874C>T	NP_671714.1:p.Gln2292Ter
XM_006715827.1:c.6757C>T	XP_006715890.1:p.Gln2253Ter
XM_011515709.1:c.7045C>T	XP_011514011.1:p.Gln2349Ter
XM_011515710.1:c.7069C>T	XP_011514012.1:p.Gln2357Ter
XM_011515711.1:c.7009C>T	XP_011514013.1:p.Gln2337Ter
XM_011515712.1:c.7006C>T	XP_011514014.1:p.Gln2336Ter
XM_011515713.1:c.6991C>T	XP_011514015.1:p.Gln2331Ter
XM_011515714.1:c.7030C>T	XP_011514016.1:p.Gln2344Ter
XM_011515716.1:c.6949C>T	XP_011514018.1:p.Gln2317Ter
XM_011515717.1:c.6904C>T	XP_011514019.1:p.Gln2302Ter
XM_011515718.1:c.6934C>T	XP_011514020.1:p.Gln2312Ter
XM_011515719.1:c.6910C>T	XP_011514021.1:p.Gln2304Ter
XM_011515720.1:c.6793C>T	XP_011514022.1:p.Gln2265Ter
XM_011515721.1:c.1558C>T	XP_011514023.1:p.Gln520Ter
XM_011515722.1:c.1519C>T	XP_011514024.1:p.Gln507Ter
XM_017011642.2:c.7033C>T	XP_016867131.1:p.Gln2345Ter
XM_017011643.2:c.6994C>T	XP_016867132.1:p.Gln2332Ter
XM_017011644.2:c.7033C>T	XP_016867133.1:p.Gln2345Ter
XM_017011645.2:c.6979C>T	XP_016867134.1:p.Gln2327Ter
XM_017011646.2:c.6994C>T	XP_016867135.1:p.Gln2332Ter
XM_017011647.2:c.6940C>T	XP_016867136.1:p.Gln2314Ter
XM_017011648.2:c.6937C>T	XP_016867137.1:p.Gln2313Ter
XM_017011649.2:c.6970C>T	XP_016867138.1:p.Gln2324Ter
XM_017011650.2:c.6898C>T	XP_016867139.1:p.Gln2300Ter
XM_017011651.2:c.6892C>T	XP_016867140.1:p.Gln2298Ter
XM_017011652.2:c.7033C>T	XP_016867141.1:p.Gln2345Ter
XM_017011653.2:c.6805C>T	XP_016867142.1:p.Gln2269Ter
XM_017011654.2:c.6757C>T	XP_016867143.1:p.Gln2253Ter
XM_017011655.2:c.6661C>T	XP_016867144.1:p.Gln2221Ter
XM_017011656.2:c.6661C>T	XP_016867145.1:p.Gln2221Ter
XM_017011657.2:c.2698C>T	XP_016867146.1:p.Gln900Ter
XM_017011658.2:c.1582C>T	XP_016867147.1:p.Gln528Ter
XM_017011659.2:c.1543C>T	XP_016867148.1:p.Gln515Ter
XM_017011660.2:c.1543C>T	XP_016867149.1:p.Gln515Ter
XM_024446631.1:c.6796C>T	XP_024302399.1:p.Gln2266Ter
NM_147185.3:c.6874C>T	NP_671714.1:p.Gln2292Ter
NM_001379277.1:c.1543C>T	NP_001366206.1:p.Gln515Ter
NM_005751.5:c.6898C>T MANE Select	NP_005742.4:p.Gln2300Ter