Canonical Allele Identifier: CA368133849

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707146T>G (hg19) ; chr7:g.92077832T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077832T>G , CM000669.2:g.92077832T>G	GRCh38
NC_000007.13:g.91707146T>G , CM000669.1:g.91707146T>G	GRCh37
NC_000007.12:g.91545082T>G	NCBI36
NG_011623.1:g.141958T>G , LRG_331:g.141958T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6902T>G MANE Select	ENSP00000348573.3:p.Val2301Gly
ENST00000359028.7:c.6974T>G	ENSP00000351922.4:p.Val2325Gly
ENST00000394534.7:c.395T>G	ENSP00000378042.3:p.Val132Gly
ENST00000491695.2:c.1547T>G	ENSP00000494626.2:p.Val516Gly
ENST00000674381.2:c.*6631T>G	ENSP00000501536.2:n.*6631T>G
ENST00000679448.1:c.6878T>G	ENSP00000505889.1:p.Val2293Gly
ENST00000679457.1:c.6878T>G	ENSP00000505450.1:p.Val2293Gly
ENST00000679474.1:n.7100T>G
ENST00000679521.1:c.6848T>G	ENSP00000505456.1:p.Val2283Gly
ENST00000679554.1:c.*6687T>G	ENSP00000506415.1:n.*6687T>G
ENST00000679722.1:n.7124T>G
ENST00000679821.1:c.6644T>G	ENSP00000506040.1:p.Val2215Gly
ENST00000680047.1:n.7100T>G
ENST00000680072.1:c.6725T>G	ENSP00000506581.1:p.Val2242Gly
ENST00000680181.1:c.6809T>G	ENSP00000505548.1:p.Val2270Gly
ENST00000680365.1:c.395T>G	ENSP00000506019.1:p.Val132Gly
ENST00000680513.1:c.6761T>G	ENSP00000505284.1:p.Val2254Gly
ENST00000680534.1:c.6941T>G	ENSP00000506674.1:p.Val2314Gly
ENST00000680766.1:c.6878T>G	ENSP00000505204.1:p.Val2293Gly
ENST00000680952.1:c.6878T>G	ENSP00000506407.1:p.Val2293Gly
ENST00000681216.1:c.395T>G	ENSP00000505551.1:p.Val132Gly
ENST00000681412.1:c.6902T>G	ENSP00000506486.1:p.Val2301Gly
ENST00000681722.1:c.6878T>G	ENSP00000506566.1:p.Val2293Gly
ENST00000356239.7:c.6902T>G	ENSP00000348573.3:p.Val2301Gly
ENST00000358100.6:c.6761T>G	ENSP00000350813.3:p.Val2254Gly
ENST00000359028.6:c.6935T>G	ENSP00000351922.3:p.Val2312Gly
ENST00000394534.6:c.440T>G	ENSP00000378042.2:p.Val147Gly
NM_005751.4:c.6902T>G , LRG_331t1:c.6902T>G	NP_005742.4:p.Val2301Gly
NM_147185.2:c.6878T>G	NP_671714.1:p.Val2293Gly
XM_006715827.1:c.6761T>G	XP_006715890.1:p.Val2254Gly
XM_011515709.1:c.7049T>G	XP_011514011.1:p.Val2350Gly
XM_011515710.1:c.7073T>G	XP_011514012.1:p.Val2358Gly
XM_011515711.1:c.7013T>G	XP_011514013.1:p.Val2338Gly
XM_011515712.1:c.7010T>G	XP_011514014.1:p.Val2337Gly
XM_011515713.1:c.6995T>G	XP_011514015.1:p.Val2332Gly
XM_011515714.1:c.7034T>G	XP_011514016.1:p.Val2345Gly
XM_011515716.1:c.6953T>G	XP_011514018.1:p.Val2318Gly
XM_011515717.1:c.6908T>G	XP_011514019.1:p.Val2303Gly
XM_011515718.1:c.6938T>G	XP_011514020.1:p.Val2313Gly
XM_011515719.1:c.6914T>G	XP_011514021.1:p.Val2305Gly
XM_011515720.1:c.6797T>G	XP_011514022.1:p.Val2266Gly
XM_011515721.1:c.1562T>G	XP_011514023.1:p.Val521Gly
XM_011515722.1:c.1523T>G	XP_011514024.1:p.Val508Gly
XM_017011642.2:c.7037T>G	XP_016867131.1:p.Val2346Gly
XM_017011643.2:c.6998T>G	XP_016867132.1:p.Val2333Gly
XM_017011644.2:c.7037T>G	XP_016867133.1:p.Val2346Gly
XM_017011645.2:c.6983T>G	XP_016867134.1:p.Val2328Gly
XM_017011646.2:c.6998T>G	XP_016867135.1:p.Val2333Gly
XM_017011647.2:c.6944T>G	XP_016867136.1:p.Val2315Gly
XM_017011648.2:c.6941T>G	XP_016867137.1:p.Val2314Gly
XM_017011649.2:c.6974T>G	XP_016867138.1:p.Val2325Gly
XM_017011650.2:c.6902T>G	XP_016867139.1:p.Val2301Gly
XM_017011651.2:c.6896T>G	XP_016867140.1:p.Val2299Gly
XM_017011652.2:c.7037T>G	XP_016867141.1:p.Val2346Gly
XM_017011653.2:c.6809T>G	XP_016867142.1:p.Val2270Gly
XM_017011654.2:c.6761T>G	XP_016867143.1:p.Val2254Gly
XM_017011655.2:c.6665T>G	XP_016867144.1:p.Val2222Gly
XM_017011656.2:c.6665T>G	XP_016867145.1:p.Val2222Gly
XM_017011657.2:c.2702T>G	XP_016867146.1:p.Val901Gly
XM_017011658.2:c.1586T>G	XP_016867147.1:p.Val529Gly
XM_017011659.2:c.1547T>G	XP_016867148.1:p.Val516Gly
XM_017011660.2:c.1547T>G	XP_016867149.1:p.Val516Gly
XM_024446631.1:c.6800T>G	XP_024302399.1:p.Val2267Gly
NM_147185.3:c.6878T>G	NP_671714.1:p.Val2293Gly
NM_001379277.1:c.1547T>G	NP_001366206.1:p.Val516Gly
NM_005751.5:c.6902T>G MANE Select	NP_005742.4:p.Val2301Gly