Canonical Allele Identifier: CA368133630

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707053C>G (hg19) ; chr7:g.92077739C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077739C>G , CM000669.2:g.92077739C>G	GRCh38
NC_000007.13:g.91707053C>G , CM000669.1:g.91707053C>G	GRCh37
NC_000007.12:g.91544989C>G	NCBI36
NG_011623.1:g.141865C>G , LRG_331:g.141865C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6809C>G MANE Select	ENSP00000348573.3:p.Ala2270Gly
ENST00000359028.7:c.6881C>G	ENSP00000351922.4:p.Ala2294Gly
ENST00000394534.7:c.302C>G	ENSP00000378042.3:p.Ala101Gly
ENST00000491695.2:c.1454C>G	ENSP00000494626.2:p.Ala485Gly
ENST00000674381.2:c.*6538C>G	ENSP00000501536.2:n.*6538C>G
ENST00000679448.1:c.6785C>G	ENSP00000505889.1:p.Ala2262Gly
ENST00000679457.1:c.6785C>G	ENSP00000505450.1:p.Ala2262Gly
ENST00000679474.1:n.7007C>G
ENST00000679521.1:c.6755C>G	ENSP00000505456.1:p.Ala2252Gly
ENST00000679554.1:c.*6594C>G	ENSP00000506415.1:n.*6594C>G
ENST00000679722.1:n.7031C>G
ENST00000679821.1:c.6551C>G	ENSP00000506040.1:p.Ala2184Gly
ENST00000680047.1:n.7007C>G
ENST00000680072.1:c.6632C>G	ENSP00000506581.1:p.Ala2211Gly
ENST00000680181.1:c.6716C>G	ENSP00000505548.1:p.Ala2239Gly
ENST00000680365.1:c.302C>G	ENSP00000506019.1:p.Ala101Gly
ENST00000680513.1:c.6668C>G	ENSP00000505284.1:p.Ala2223Gly
ENST00000680534.1:c.6848C>G	ENSP00000506674.1:p.Ala2283Gly
ENST00000680766.1:c.6785C>G	ENSP00000505204.1:p.Ala2262Gly
ENST00000680952.1:c.6785C>G	ENSP00000506407.1:p.Ala2262Gly
ENST00000681216.1:c.302C>G	ENSP00000505551.1:p.Ala101Gly
ENST00000681412.1:c.6809C>G	ENSP00000506486.1:p.Ala2270Gly
ENST00000681722.1:c.6785C>G	ENSP00000506566.1:p.Ala2262Gly
ENST00000356239.7:c.6809C>G	ENSP00000348573.3:p.Ala2270Gly
ENST00000358100.6:c.6668C>G	ENSP00000350813.3:p.Ala2223Gly
ENST00000359028.6:c.6842C>G	ENSP00000351922.3:p.Ala2281Gly
ENST00000394534.6:c.347C>G	ENSP00000378042.2:p.Ala116Gly
NM_005751.4:c.6809C>G , LRG_331t1:c.6809C>G	NP_005742.4:p.Ala2270Gly
NM_147185.2:c.6785C>G	NP_671714.1:p.Ala2262Gly
XM_006715827.1:c.6668C>G	XP_006715890.1:p.Ala2223Gly
XM_011515709.1:c.6956C>G	XP_011514011.1:p.Ala2319Gly
XM_011515710.1:c.6980C>G	XP_011514012.1:p.Ala2327Gly
XM_011515711.1:c.6920C>G	XP_011514013.1:p.Ala2307Gly
XM_011515712.1:c.6917C>G	XP_011514014.1:p.Ala2306Gly
XM_011515713.1:c.6902C>G	XP_011514015.1:p.Ala2301Gly
XM_011515714.1:c.6941C>G	XP_011514016.1:p.Ala2314Gly
XM_011515716.1:c.6860C>G	XP_011514018.1:p.Ala2287Gly
XM_011515717.1:c.6815C>G	XP_011514019.1:p.Ala2272Gly
XM_011515718.1:c.6845C>G	XP_011514020.1:p.Ala2282Gly
XM_011515719.1:c.6821C>G	XP_011514021.1:p.Ala2274Gly
XM_011515720.1:c.6704C>G	XP_011514022.1:p.Ala2235Gly
XM_011515721.1:c.1469C>G	XP_011514023.1:p.Ala490Gly
XM_011515722.1:c.1430C>G	XP_011514024.1:p.Ala477Gly
XM_017011642.2:c.6944C>G	XP_016867131.1:p.Ala2315Gly
XM_017011643.2:c.6905C>G	XP_016867132.1:p.Ala2302Gly
XM_017011644.2:c.6944C>G	XP_016867133.1:p.Ala2315Gly
XM_017011645.2:c.6890C>G	XP_016867134.1:p.Ala2297Gly
XM_017011646.2:c.6905C>G	XP_016867135.1:p.Ala2302Gly
XM_017011647.2:c.6851C>G	XP_016867136.1:p.Ala2284Gly
XM_017011648.2:c.6848C>G	XP_016867137.1:p.Ala2283Gly
XM_017011649.2:c.6881C>G	XP_016867138.1:p.Ala2294Gly
XM_017011650.2:c.6809C>G	XP_016867139.1:p.Ala2270Gly
XM_017011651.2:c.6803C>G	XP_016867140.1:p.Ala2268Gly
XM_017011652.2:c.6944C>G	XP_016867141.1:p.Ala2315Gly
XM_017011653.2:c.6716C>G	XP_016867142.1:p.Ala2239Gly
XM_017011654.2:c.6668C>G	XP_016867143.1:p.Ala2223Gly
XM_017011655.2:c.6572C>G	XP_016867144.1:p.Ala2191Gly
XM_017011656.2:c.6572C>G	XP_016867145.1:p.Ala2191Gly
XM_017011657.2:c.2609C>G	XP_016867146.1:p.Ala870Gly
XM_017011658.2:c.1493C>G	XP_016867147.1:p.Ala498Gly
XM_017011659.2:c.1454C>G	XP_016867148.1:p.Ala485Gly
XM_017011660.2:c.1454C>G	XP_016867149.1:p.Ala485Gly
XM_024446631.1:c.6707C>G	XP_024302399.1:p.Ala2236Gly
NM_147185.3:c.6785C>G	NP_671714.1:p.Ala2262Gly
NM_001379277.1:c.1454C>G	NP_001366206.1:p.Ala485Gly
NM_005751.5:c.6809C>G MANE Select	NP_005742.4:p.Ala2270Gly