Canonical Allele Identifier: CA368133922

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707181G>T (hg19) ; chr7:g.92077867G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077867G>T , CM000669.2:g.92077867G>T	GRCh38
NC_000007.13:g.91707181G>T , CM000669.1:g.91707181G>T	GRCh37
NC_000007.12:g.91545117G>T	NCBI36
NG_011623.1:g.141993G>T , LRG_331:g.141993G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6937G>T MANE Select	ENSP00000348573.3:p.Asp2313Tyr
ENST00000359028.7:c.7009G>T	ENSP00000351922.4:p.Asp2337Tyr
ENST00000394534.7:c.430G>T	ENSP00000378042.3:p.Asp144Tyr
ENST00000491695.2:c.1582G>T	ENSP00000494626.2:p.Asp528Tyr
ENST00000674381.2:c.*6666G>T	ENSP00000501536.2:n.*6666G>T
ENST00000679448.1:c.6913G>T	ENSP00000505889.1:p.Asp2305Tyr
ENST00000679457.1:c.6913G>T	ENSP00000505450.1:p.Asp2305Tyr
ENST00000679474.1:n.7135G>T
ENST00000679521.1:c.6883G>T	ENSP00000505456.1:p.Asp2295Tyr
ENST00000679554.1:c.*6722G>T	ENSP00000506415.1:n.*6722G>T
ENST00000679722.1:n.7159G>T
ENST00000679821.1:c.6679G>T	ENSP00000506040.1:p.Asp2227Tyr
ENST00000680047.1:n.7135G>T
ENST00000680072.1:c.6760G>T	ENSP00000506581.1:p.Asp2254Tyr
ENST00000680181.1:c.6844G>T	ENSP00000505548.1:p.Asp2282Tyr
ENST00000680365.1:c.430G>T	ENSP00000506019.1:p.Asp144Tyr
ENST00000680513.1:c.6796G>T	ENSP00000505284.1:p.Asp2266Tyr
ENST00000680534.1:c.6976G>T	ENSP00000506674.1:p.Asp2326Tyr
ENST00000680766.1:c.6913G>T	ENSP00000505204.1:p.Asp2305Tyr
ENST00000680952.1:c.6913G>T	ENSP00000506407.1:p.Asp2305Tyr
ENST00000681216.1:c.430G>T	ENSP00000505551.1:p.Asp144Tyr
ENST00000681412.1:c.6937G>T	ENSP00000506486.1:p.Asp2313Tyr
ENST00000681722.1:c.6913G>T	ENSP00000506566.1:p.Asp2305Tyr
ENST00000356239.7:c.6937G>T	ENSP00000348573.3:p.Asp2313Tyr
ENST00000358100.6:c.6796G>T	ENSP00000350813.3:p.Asp2266Tyr
ENST00000359028.6:c.6970G>T	ENSP00000351922.3:p.Asp2324Tyr
ENST00000394534.6:c.475G>T	ENSP00000378042.2:p.Asp159Tyr
NM_005751.4:c.6937G>T , LRG_331t1:c.6937G>T	NP_005742.4:p.Asp2313Tyr
NM_147185.2:c.6913G>T	NP_671714.1:p.Asp2305Tyr
XM_006715827.1:c.6796G>T	XP_006715890.1:p.Asp2266Tyr
XM_011515709.1:c.7084G>T	XP_011514011.1:p.Asp2362Tyr
XM_011515710.1:c.7108G>T	XP_011514012.1:p.Asp2370Tyr
XM_011515711.1:c.7048G>T	XP_011514013.1:p.Asp2350Tyr
XM_011515712.1:c.7045G>T	XP_011514014.1:p.Asp2349Tyr
XM_011515713.1:c.7030G>T	XP_011514015.1:p.Asp2344Tyr
XM_011515714.1:c.7069G>T	XP_011514016.1:p.Asp2357Tyr
XM_011515716.1:c.6988G>T	XP_011514018.1:p.Asp2330Tyr
XM_011515717.1:c.6943G>T	XP_011514019.1:p.Asp2315Tyr
XM_011515718.1:c.6973G>T	XP_011514020.1:p.Asp2325Tyr
XM_011515719.1:c.6949G>T	XP_011514021.1:p.Asp2317Tyr
XM_011515720.1:c.6832G>T	XP_011514022.1:p.Asp2278Tyr
XM_011515721.1:c.1597G>T	XP_011514023.1:p.Asp533Tyr
XM_011515722.1:c.1558G>T	XP_011514024.1:p.Asp520Tyr
XM_017011642.2:c.7072G>T	XP_016867131.1:p.Asp2358Tyr
XM_017011643.2:c.7033G>T	XP_016867132.1:p.Asp2345Tyr
XM_017011644.2:c.7072G>T	XP_016867133.1:p.Asp2358Tyr
XM_017011645.2:c.7018G>T	XP_016867134.1:p.Asp2340Tyr
XM_017011646.2:c.7033G>T	XP_016867135.1:p.Asp2345Tyr
XM_017011647.2:c.6979G>T	XP_016867136.1:p.Asp2327Tyr
XM_017011648.2:c.6976G>T	XP_016867137.1:p.Asp2326Tyr
XM_017011649.2:c.7009G>T	XP_016867138.1:p.Asp2337Tyr
XM_017011650.2:c.6937G>T	XP_016867139.1:p.Asp2313Tyr
XM_017011651.2:c.6931G>T	XP_016867140.1:p.Asp2311Tyr
XM_017011652.2:c.7072G>T	XP_016867141.1:p.Asp2358Tyr
XM_017011653.2:c.6844G>T	XP_016867142.1:p.Asp2282Tyr
XM_017011654.2:c.6796G>T	XP_016867143.1:p.Asp2266Tyr
XM_017011655.2:c.6700G>T	XP_016867144.1:p.Asp2234Tyr
XM_017011656.2:c.6700G>T	XP_016867145.1:p.Asp2234Tyr
XM_017011657.2:c.2737G>T	XP_016867146.1:p.Asp913Tyr
XM_017011658.2:c.1621G>T	XP_016867147.1:p.Asp541Tyr
XM_017011659.2:c.1582G>T	XP_016867148.1:p.Asp528Tyr
XM_017011660.2:c.1582G>T	XP_016867149.1:p.Asp528Tyr
XM_024446631.1:c.6835G>T	XP_024302399.1:p.Asp2279Tyr
NM_147185.3:c.6913G>T	NP_671714.1:p.Asp2305Tyr
NM_001379277.1:c.1582G>T	NP_001366206.1:p.Asp528Tyr
NM_005751.5:c.6937G>T MANE Select	NP_005742.4:p.Asp2313Tyr