Canonical Allele Identifier: CA368133927

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707183T>G (hg19) ; chr7:g.92077869T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077869T>G , CM000669.2:g.92077869T>G	GRCh38
NC_000007.13:g.91707183T>G , CM000669.1:g.91707183T>G	GRCh37
NC_000007.12:g.91545119T>G	NCBI36
NG_011623.1:g.141995T>G , LRG_331:g.141995T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6939T>G MANE Select	ENSP00000348573.3:p.Asp2313Glu
ENST00000359028.7:c.7011T>G	ENSP00000351922.4:p.Asp2337Glu
ENST00000394534.7:c.432T>G	ENSP00000378042.3:p.Asp144Glu
ENST00000491695.2:c.1584T>G	ENSP00000494626.2:p.Asp528Glu
ENST00000674381.2:c.*6668T>G	ENSP00000501536.2:n.*6668T>G
ENST00000679448.1:c.6915T>G	ENSP00000505889.1:p.Asp2305Glu
ENST00000679457.1:c.6915T>G	ENSP00000505450.1:p.Asp2305Glu
ENST00000679474.1:n.7137T>G
ENST00000679521.1:c.6885T>G	ENSP00000505456.1:p.Asp2295Glu
ENST00000679554.1:c.*6724T>G	ENSP00000506415.1:n.*6724T>G
ENST00000679722.1:n.7161T>G
ENST00000679821.1:c.6681T>G	ENSP00000506040.1:p.Asp2227Glu
ENST00000680047.1:n.7137T>G
ENST00000680072.1:c.6762T>G	ENSP00000506581.1:p.Asp2254Glu
ENST00000680181.1:c.6846T>G	ENSP00000505548.1:p.Asp2282Glu
ENST00000680365.1:c.432T>G	ENSP00000506019.1:p.Asp144Glu
ENST00000680513.1:c.6798T>G	ENSP00000505284.1:p.Asp2266Glu
ENST00000680534.1:c.6978T>G	ENSP00000506674.1:p.Asp2326Glu
ENST00000680766.1:c.6915T>G	ENSP00000505204.1:p.Asp2305Glu
ENST00000680952.1:c.6915T>G	ENSP00000506407.1:p.Asp2305Glu
ENST00000681216.1:c.432T>G	ENSP00000505551.1:p.Asp144Glu
ENST00000681412.1:c.6939T>G	ENSP00000506486.1:p.Asp2313Glu
ENST00000681722.1:c.6915T>G	ENSP00000506566.1:p.Asp2305Glu
ENST00000356239.7:c.6939T>G	ENSP00000348573.3:p.Asp2313Glu
ENST00000358100.6:c.6798T>G	ENSP00000350813.3:p.Asp2266Glu
ENST00000359028.6:c.6972T>G	ENSP00000351922.3:p.Asp2324Glu
ENST00000394534.6:c.477T>G	ENSP00000378042.2:p.Asp159Glu
NM_005751.4:c.6939T>G , LRG_331t1:c.6939T>G	NP_005742.4:p.Asp2313Glu
NM_147185.2:c.6915T>G	NP_671714.1:p.Asp2305Glu
XM_006715827.1:c.6798T>G	XP_006715890.1:p.Asp2266Glu
XM_011515709.1:c.7086T>G	XP_011514011.1:p.Asp2362Glu
XM_011515710.1:c.7110T>G	XP_011514012.1:p.Asp2370Glu
XM_011515711.1:c.7050T>G	XP_011514013.1:p.Asp2350Glu
XM_011515712.1:c.7047T>G	XP_011514014.1:p.Asp2349Glu
XM_011515713.1:c.7032T>G	XP_011514015.1:p.Asp2344Glu
XM_011515714.1:c.7071T>G	XP_011514016.1:p.Asp2357Glu
XM_011515716.1:c.6990T>G	XP_011514018.1:p.Asp2330Glu
XM_011515717.1:c.6945T>G	XP_011514019.1:p.Asp2315Glu
XM_011515718.1:c.6975T>G	XP_011514020.1:p.Asp2325Glu
XM_011515719.1:c.6951T>G	XP_011514021.1:p.Asp2317Glu
XM_011515720.1:c.6834T>G	XP_011514022.1:p.Asp2278Glu
XM_011515721.1:c.1599T>G	XP_011514023.1:p.Asp533Glu
XM_011515722.1:c.1560T>G	XP_011514024.1:p.Asp520Glu
XM_017011642.2:c.7074T>G	XP_016867131.1:p.Asp2358Glu
XM_017011643.2:c.7035T>G	XP_016867132.1:p.Asp2345Glu
XM_017011644.2:c.7074T>G	XP_016867133.1:p.Asp2358Glu
XM_017011645.2:c.7020T>G	XP_016867134.1:p.Asp2340Glu
XM_017011646.2:c.7035T>G	XP_016867135.1:p.Asp2345Glu
XM_017011647.2:c.6981T>G	XP_016867136.1:p.Asp2327Glu
XM_017011648.2:c.6978T>G	XP_016867137.1:p.Asp2326Glu
XM_017011649.2:c.7011T>G	XP_016867138.1:p.Asp2337Glu
XM_017011650.2:c.6939T>G	XP_016867139.1:p.Asp2313Glu
XM_017011651.2:c.6933T>G	XP_016867140.1:p.Asp2311Glu
XM_017011652.2:c.7074T>G	XP_016867141.1:p.Asp2358Glu
XM_017011653.2:c.6846T>G	XP_016867142.1:p.Asp2282Glu
XM_017011654.2:c.6798T>G	XP_016867143.1:p.Asp2266Glu
XM_017011655.2:c.6702T>G	XP_016867144.1:p.Asp2234Glu
XM_017011656.2:c.6702T>G	XP_016867145.1:p.Asp2234Glu
XM_017011657.2:c.2739T>G	XP_016867146.1:p.Asp913Glu
XM_017011658.2:c.1623T>G	XP_016867147.1:p.Asp541Glu
XM_017011659.2:c.1584T>G	XP_016867148.1:p.Asp528Glu
XM_017011660.2:c.1584T>G	XP_016867149.1:p.Asp528Glu
XM_024446631.1:c.6837T>G	XP_024302399.1:p.Asp2279Glu
NM_147185.3:c.6915T>G	NP_671714.1:p.Asp2305Glu
NM_001379277.1:c.1584T>G	NP_001366206.1:p.Asp528Glu
NM_005751.5:c.6939T>G MANE Select	NP_005742.4:p.Asp2313Glu