Canonical Allele Identifier: CA368133939

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707188A>G (hg19) ; chr7:g.92077874A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077874A>G , CM000669.2:g.92077874A>G	GRCh38
NC_000007.13:g.91707188A>G , CM000669.1:g.91707188A>G	GRCh37
NC_000007.12:g.91545124A>G	NCBI36
NG_011623.1:g.142000A>G , LRG_331:g.142000A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6944A>G MANE Select	ENSP00000348573.3:p.Lys2315Arg
ENST00000359028.7:c.7016A>G	ENSP00000351922.4:p.Lys2339Arg
ENST00000394534.7:c.437A>G	ENSP00000378042.3:p.Lys146Arg
ENST00000491695.2:c.1589A>G	ENSP00000494626.2:p.Lys530Arg
ENST00000674381.2:c.*6673A>G	ENSP00000501536.2:n.*6673A>G
ENST00000679448.1:c.6920A>G	ENSP00000505889.1:p.Lys2307Arg
ENST00000679457.1:c.6920A>G	ENSP00000505450.1:p.Lys2307Arg
ENST00000679474.1:n.7142A>G
ENST00000679521.1:c.6890A>G	ENSP00000505456.1:p.Lys2297Arg
ENST00000679554.1:c.*6729A>G	ENSP00000506415.1:n.*6729A>G
ENST00000679722.1:n.7166A>G
ENST00000679821.1:c.6686A>G	ENSP00000506040.1:p.Lys2229Arg
ENST00000680047.1:n.7142A>G
ENST00000680072.1:c.6767A>G	ENSP00000506581.1:p.Lys2256Arg
ENST00000680181.1:c.6851A>G	ENSP00000505548.1:p.Lys2284Arg
ENST00000680365.1:c.437A>G	ENSP00000506019.1:p.Lys146Arg
ENST00000680513.1:c.6803A>G	ENSP00000505284.1:p.Lys2268Arg
ENST00000680534.1:c.6983A>G	ENSP00000506674.1:p.Lys2328Arg
ENST00000680766.1:c.6920A>G	ENSP00000505204.1:p.Lys2307Arg
ENST00000680952.1:c.6920A>G	ENSP00000506407.1:p.Lys2307Arg
ENST00000681216.1:c.437A>G	ENSP00000505551.1:p.Lys146Arg
ENST00000681412.1:c.6944A>G	ENSP00000506486.1:p.Lys2315Arg
ENST00000681722.1:c.6920A>G	ENSP00000506566.1:p.Lys2307Arg
ENST00000356239.7:c.6944A>G	ENSP00000348573.3:p.Lys2315Arg
ENST00000358100.6:c.6803A>G	ENSP00000350813.3:p.Lys2268Arg
ENST00000359028.6:c.6977A>G	ENSP00000351922.3:p.Lys2326Arg
ENST00000394534.6:c.482A>G	ENSP00000378042.2:p.Lys161Arg
NM_005751.4:c.6944A>G , LRG_331t1:c.6944A>G	NP_005742.4:p.Lys2315Arg
NM_147185.2:c.6920A>G	NP_671714.1:p.Lys2307Arg
XM_006715827.1:c.6803A>G	XP_006715890.1:p.Lys2268Arg
XM_011515709.1:c.7091A>G	XP_011514011.1:p.Lys2364Arg
XM_011515710.1:c.7115A>G	XP_011514012.1:p.Lys2372Arg
XM_011515711.1:c.7055A>G	XP_011514013.1:p.Lys2352Arg
XM_011515712.1:c.7052A>G	XP_011514014.1:p.Lys2351Arg
XM_011515713.1:c.7037A>G	XP_011514015.1:p.Lys2346Arg
XM_011515714.1:c.7076A>G	XP_011514016.1:p.Lys2359Arg
XM_011515716.1:c.6995A>G	XP_011514018.1:p.Lys2332Arg
XM_011515717.1:c.6950A>G	XP_011514019.1:p.Lys2317Arg
XM_011515718.1:c.6980A>G	XP_011514020.1:p.Lys2327Arg
XM_011515719.1:c.6956A>G	XP_011514021.1:p.Lys2319Arg
XM_011515720.1:c.6839A>G	XP_011514022.1:p.Lys2280Arg
XM_011515721.1:c.1604A>G	XP_011514023.1:p.Lys535Arg
XM_011515722.1:c.1565A>G	XP_011514024.1:p.Lys522Arg
XM_017011642.2:c.7079A>G	XP_016867131.1:p.Lys2360Arg
XM_017011643.2:c.7040A>G	XP_016867132.1:p.Lys2347Arg
XM_017011644.2:c.7079A>G	XP_016867133.1:p.Lys2360Arg
XM_017011645.2:c.7025A>G	XP_016867134.1:p.Lys2342Arg
XM_017011646.2:c.7040A>G	XP_016867135.1:p.Lys2347Arg
XM_017011647.2:c.6986A>G	XP_016867136.1:p.Lys2329Arg
XM_017011648.2:c.6983A>G	XP_016867137.1:p.Lys2328Arg
XM_017011649.2:c.7016A>G	XP_016867138.1:p.Lys2339Arg
XM_017011650.2:c.6944A>G	XP_016867139.1:p.Lys2315Arg
XM_017011651.2:c.6938A>G	XP_016867140.1:p.Lys2313Arg
XM_017011652.2:c.7079A>G	XP_016867141.1:p.Lys2360Arg
XM_017011653.2:c.6851A>G	XP_016867142.1:p.Lys2284Arg
XM_017011654.2:c.6803A>G	XP_016867143.1:p.Lys2268Arg
XM_017011655.2:c.6707A>G	XP_016867144.1:p.Lys2236Arg
XM_017011656.2:c.6707A>G	XP_016867145.1:p.Lys2236Arg
XM_017011657.2:c.2744A>G	XP_016867146.1:p.Lys915Arg
XM_017011658.2:c.1628A>G	XP_016867147.1:p.Lys543Arg
XM_017011659.2:c.1589A>G	XP_016867148.1:p.Lys530Arg
XM_017011660.2:c.1589A>G	XP_016867149.1:p.Lys530Arg
XM_024446631.1:c.6842A>G	XP_024302399.1:p.Lys2281Arg
NM_147185.3:c.6920A>G	NP_671714.1:p.Lys2307Arg
NM_001379277.1:c.1589A>G	NP_001366206.1:p.Lys530Arg
NM_005751.5:c.6944A>G MANE Select	NP_005742.4:p.Lys2315Arg