Canonical Allele Identifier: CA368133852

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707148A>T (hg19) ; chr7:g.92077834A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077834A>T , CM000669.2:g.92077834A>T	GRCh38
NC_000007.13:g.91707148A>T , CM000669.1:g.91707148A>T	GRCh37
NC_000007.12:g.91545084A>T	NCBI36
NG_011623.1:g.141960A>T , LRG_331:g.141960A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6904A>T MANE Select	ENSP00000348573.3:p.Thr2302Ser
ENST00000359028.7:c.6976A>T	ENSP00000351922.4:p.Thr2326Ser
ENST00000394534.7:c.397A>T	ENSP00000378042.3:p.Thr133Ser
ENST00000491695.2:c.1549A>T	ENSP00000494626.2:p.Thr517Ser
ENST00000674381.2:c.*6633A>T	ENSP00000501536.2:n.*6633A>T
ENST00000679448.1:c.6880A>T	ENSP00000505889.1:p.Thr2294Ser
ENST00000679457.1:c.6880A>T	ENSP00000505450.1:p.Thr2294Ser
ENST00000679474.1:n.7102A>T
ENST00000679521.1:c.6850A>T	ENSP00000505456.1:p.Thr2284Ser
ENST00000679554.1:c.*6689A>T	ENSP00000506415.1:n.*6689A>T
ENST00000679722.1:n.7126A>T
ENST00000679821.1:c.6646A>T	ENSP00000506040.1:p.Thr2216Ser
ENST00000680047.1:n.7102A>T
ENST00000680072.1:c.6727A>T	ENSP00000506581.1:p.Thr2243Ser
ENST00000680181.1:c.6811A>T	ENSP00000505548.1:p.Thr2271Ser
ENST00000680365.1:c.397A>T	ENSP00000506019.1:p.Thr133Ser
ENST00000680513.1:c.6763A>T	ENSP00000505284.1:p.Thr2255Ser
ENST00000680534.1:c.6943A>T	ENSP00000506674.1:p.Thr2315Ser
ENST00000680766.1:c.6880A>T	ENSP00000505204.1:p.Thr2294Ser
ENST00000680952.1:c.6880A>T	ENSP00000506407.1:p.Thr2294Ser
ENST00000681216.1:c.397A>T	ENSP00000505551.1:p.Thr133Ser
ENST00000681412.1:c.6904A>T	ENSP00000506486.1:p.Thr2302Ser
ENST00000681722.1:c.6880A>T	ENSP00000506566.1:p.Thr2294Ser
ENST00000356239.7:c.6904A>T	ENSP00000348573.3:p.Thr2302Ser
ENST00000358100.6:c.6763A>T	ENSP00000350813.3:p.Thr2255Ser
ENST00000359028.6:c.6937A>T	ENSP00000351922.3:p.Thr2313Ser
ENST00000394534.6:c.442A>T	ENSP00000378042.2:p.Thr148Ser
NM_005751.4:c.6904A>T , LRG_331t1:c.6904A>T	NP_005742.4:p.Thr2302Ser
NM_147185.2:c.6880A>T	NP_671714.1:p.Thr2294Ser
XM_006715827.1:c.6763A>T	XP_006715890.1:p.Thr2255Ser
XM_011515709.1:c.7051A>T	XP_011514011.1:p.Thr2351Ser
XM_011515710.1:c.7075A>T	XP_011514012.1:p.Thr2359Ser
XM_011515711.1:c.7015A>T	XP_011514013.1:p.Thr2339Ser
XM_011515712.1:c.7012A>T	XP_011514014.1:p.Thr2338Ser
XM_011515713.1:c.6997A>T	XP_011514015.1:p.Thr2333Ser
XM_011515714.1:c.7036A>T	XP_011514016.1:p.Thr2346Ser
XM_011515716.1:c.6955A>T	XP_011514018.1:p.Thr2319Ser
XM_011515717.1:c.6910A>T	XP_011514019.1:p.Thr2304Ser
XM_011515718.1:c.6940A>T	XP_011514020.1:p.Thr2314Ser
XM_011515719.1:c.6916A>T	XP_011514021.1:p.Thr2306Ser
XM_011515720.1:c.6799A>T	XP_011514022.1:p.Thr2267Ser
XM_011515721.1:c.1564A>T	XP_011514023.1:p.Thr522Ser
XM_011515722.1:c.1525A>T	XP_011514024.1:p.Thr509Ser
XM_017011642.2:c.7039A>T	XP_016867131.1:p.Thr2347Ser
XM_017011643.2:c.7000A>T	XP_016867132.1:p.Thr2334Ser
XM_017011644.2:c.7039A>T	XP_016867133.1:p.Thr2347Ser
XM_017011645.2:c.6985A>T	XP_016867134.1:p.Thr2329Ser
XM_017011646.2:c.7000A>T	XP_016867135.1:p.Thr2334Ser
XM_017011647.2:c.6946A>T	XP_016867136.1:p.Thr2316Ser
XM_017011648.2:c.6943A>T	XP_016867137.1:p.Thr2315Ser
XM_017011649.2:c.6976A>T	XP_016867138.1:p.Thr2326Ser
XM_017011650.2:c.6904A>T	XP_016867139.1:p.Thr2302Ser
XM_017011651.2:c.6898A>T	XP_016867140.1:p.Thr2300Ser
XM_017011652.2:c.7039A>T	XP_016867141.1:p.Thr2347Ser
XM_017011653.2:c.6811A>T	XP_016867142.1:p.Thr2271Ser
XM_017011654.2:c.6763A>T	XP_016867143.1:p.Thr2255Ser
XM_017011655.2:c.6667A>T	XP_016867144.1:p.Thr2223Ser
XM_017011656.2:c.6667A>T	XP_016867145.1:p.Thr2223Ser
XM_017011657.2:c.2704A>T	XP_016867146.1:p.Thr902Ser
XM_017011658.2:c.1588A>T	XP_016867147.1:p.Thr530Ser
XM_017011659.2:c.1549A>T	XP_016867148.1:p.Thr517Ser
XM_017011660.2:c.1549A>T	XP_016867149.1:p.Thr517Ser
XM_024446631.1:c.6802A>T	XP_024302399.1:p.Thr2268Ser
NM_147185.3:c.6880A>T	NP_671714.1:p.Thr2294Ser
NM_001379277.1:c.1549A>T	NP_001366206.1:p.Thr517Ser
NM_005751.5:c.6904A>T MANE Select	NP_005742.4:p.Thr2302Ser