Canonical Allele Identifier: CA368133619

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707047C>G (hg19) ; chr7:g.92077733C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077733C>G , CM000669.2:g.92077733C>G	GRCh38
NC_000007.13:g.91707047C>G , CM000669.1:g.91707047C>G	GRCh37
NC_000007.12:g.91544983C>G	NCBI36
NG_011623.1:g.141859C>G , LRG_331:g.141859C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356239.8:c.6803C>G MANE Select	ENSP00000348573.3:p.Ser2268Cys
ENST00000359028.7:c.6875C>G	ENSP00000351922.4:p.Ser2292Cys
ENST00000394534.7:c.296C>G	ENSP00000378042.3:p.Ser99Cys
ENST00000491695.2:c.1448C>G	ENSP00000494626.2:p.Ser483Cys
ENST00000674381.2:c.*6532C>G	ENSP00000501536.2:n.*6532C>G
ENST00000679448.1:c.6779C>G	ENSP00000505889.1:p.Ser2260Cys
ENST00000679457.1:c.6779C>G	ENSP00000505450.1:p.Ser2260Cys
ENST00000679474.1:n.7001C>G
ENST00000679521.1:c.6749C>G	ENSP00000505456.1:p.Ser2250Cys
ENST00000679554.1:c.*6588C>G	ENSP00000506415.1:n.*6588C>G
ENST00000679722.1:n.7025C>G
ENST00000679821.1:c.6545C>G	ENSP00000506040.1:p.Ser2182Cys
ENST00000680047.1:n.7001C>G
ENST00000680072.1:c.6626C>G	ENSP00000506581.1:p.Ser2209Cys
ENST00000680181.1:c.6710C>G	ENSP00000505548.1:p.Ser2237Cys
ENST00000680365.1:c.296C>G	ENSP00000506019.1:p.Ser99Cys
ENST00000680513.1:c.6662C>G	ENSP00000505284.1:p.Ser2221Cys
ENST00000680534.1:c.6842C>G	ENSP00000506674.1:p.Ser2281Cys
ENST00000680766.1:c.6779C>G	ENSP00000505204.1:p.Ser2260Cys
ENST00000680952.1:c.6779C>G	ENSP00000506407.1:p.Ser2260Cys
ENST00000681216.1:c.296C>G	ENSP00000505551.1:p.Ser99Cys
ENST00000681412.1:c.6803C>G	ENSP00000506486.1:p.Ser2268Cys
ENST00000681722.1:c.6779C>G	ENSP00000506566.1:p.Ser2260Cys
ENST00000356239.7:c.6803C>G	ENSP00000348573.3:p.Ser2268Cys
ENST00000358100.6:c.6662C>G	ENSP00000350813.3:p.Ser2221Cys
ENST00000359028.6:c.6836C>G	ENSP00000351922.3:p.Ser2279Cys
ENST00000394534.6:c.341C>G	ENSP00000378042.2:p.Ser114Cys
NM_005751.4:c.6803C>G , LRG_331t1:c.6803C>G	NP_005742.4:p.Ser2268Cys
NM_147185.2:c.6779C>G	NP_671714.1:p.Ser2260Cys
XM_006715827.1:c.6662C>G	XP_006715890.1:p.Ser2221Cys
XM_011515709.1:c.6950C>G	XP_011514011.1:p.Ser2317Cys
XM_011515710.1:c.6974C>G	XP_011514012.1:p.Ser2325Cys
XM_011515711.1:c.6914C>G	XP_011514013.1:p.Ser2305Cys
XM_011515712.1:c.6911C>G	XP_011514014.1:p.Ser2304Cys
XM_011515713.1:c.6896C>G	XP_011514015.1:p.Ser2299Cys
XM_011515714.1:c.6935C>G	XP_011514016.1:p.Ser2312Cys
XM_011515716.1:c.6854C>G	XP_011514018.1:p.Ser2285Cys
XM_011515717.1:c.6809C>G	XP_011514019.1:p.Ser2270Cys
XM_011515718.1:c.6839C>G	XP_011514020.1:p.Ser2280Cys
XM_011515719.1:c.6815C>G	XP_011514021.1:p.Ser2272Cys
XM_011515720.1:c.6698C>G	XP_011514022.1:p.Ser2233Cys
XM_011515721.1:c.1463C>G	XP_011514023.1:p.Ser488Cys
XM_011515722.1:c.1424C>G	XP_011514024.1:p.Ser475Cys
XM_017011642.2:c.6938C>G	XP_016867131.1:p.Ser2313Cys
XM_017011643.2:c.6899C>G	XP_016867132.1:p.Ser2300Cys
XM_017011644.2:c.6938C>G	XP_016867133.1:p.Ser2313Cys
XM_017011645.2:c.6884C>G	XP_016867134.1:p.Ser2295Cys
XM_017011646.2:c.6899C>G	XP_016867135.1:p.Ser2300Cys
XM_017011647.2:c.6845C>G	XP_016867136.1:p.Ser2282Cys
XM_017011648.2:c.6842C>G	XP_016867137.1:p.Ser2281Cys
XM_017011649.2:c.6875C>G	XP_016867138.1:p.Ser2292Cys
XM_017011650.2:c.6803C>G	XP_016867139.1:p.Ser2268Cys
XM_017011651.2:c.6797C>G	XP_016867140.1:p.Ser2266Cys
XM_017011652.2:c.6938C>G	XP_016867141.1:p.Ser2313Cys
XM_017011653.2:c.6710C>G	XP_016867142.1:p.Ser2237Cys
XM_017011654.2:c.6662C>G	XP_016867143.1:p.Ser2221Cys
XM_017011655.2:c.6566C>G	XP_016867144.1:p.Ser2189Cys
XM_017011656.2:c.6566C>G	XP_016867145.1:p.Ser2189Cys
XM_017011657.2:c.2603C>G	XP_016867146.1:p.Ser868Cys
XM_017011658.2:c.1487C>G	XP_016867147.1:p.Ser496Cys
XM_017011659.2:c.1448C>G	XP_016867148.1:p.Ser483Cys
XM_017011660.2:c.1448C>G	XP_016867149.1:p.Ser483Cys
XM_024446631.1:c.6701C>G	XP_024302399.1:p.Ser2234Cys
NM_147185.3:c.6779C>G	NP_671714.1:p.Ser2260Cys
NM_001379277.1:c.1448C>G	NP_001366206.1:p.Ser483Cys
NM_005751.5:c.6803C>G MANE Select	NP_005742.4:p.Ser2268Cys