Canonical Allele Identifier: CA368133871

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707158A>G (hg19) ; chr7:g.92077844A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077844A>G , CM000669.2:g.92077844A>G	GRCh38
NC_000007.13:g.91707158A>G , CM000669.1:g.91707158A>G	GRCh37
NC_000007.12:g.91545094A>G	NCBI36
NG_011623.1:g.141970A>G , LRG_331:g.141970A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6914A>G MANE Select	ENSP00000348573.3:p.Gln2305Arg
ENST00000359028.7:c.6986A>G	ENSP00000351922.4:p.Gln2329Arg
ENST00000394534.7:c.407A>G	ENSP00000378042.3:p.Gln136Arg
ENST00000491695.2:c.1559A>G	ENSP00000494626.2:p.Gln520Arg
ENST00000674381.2:c.*6643A>G	ENSP00000501536.2:n.*6643A>G
ENST00000679448.1:c.6890A>G	ENSP00000505889.1:p.Gln2297Arg
ENST00000679457.1:c.6890A>G	ENSP00000505450.1:p.Gln2297Arg
ENST00000679474.1:n.7112A>G
ENST00000679521.1:c.6860A>G	ENSP00000505456.1:p.Gln2287Arg
ENST00000679554.1:c.*6699A>G	ENSP00000506415.1:n.*6699A>G
ENST00000679722.1:n.7136A>G
ENST00000679821.1:c.6656A>G	ENSP00000506040.1:p.Gln2219Arg
ENST00000680047.1:n.7112A>G
ENST00000680072.1:c.6737A>G	ENSP00000506581.1:p.Gln2246Arg
ENST00000680181.1:c.6821A>G	ENSP00000505548.1:p.Gln2274Arg
ENST00000680365.1:c.407A>G	ENSP00000506019.1:p.Gln136Arg
ENST00000680513.1:c.6773A>G	ENSP00000505284.1:p.Gln2258Arg
ENST00000680534.1:c.6953A>G	ENSP00000506674.1:p.Gln2318Arg
ENST00000680766.1:c.6890A>G	ENSP00000505204.1:p.Gln2297Arg
ENST00000680952.1:c.6890A>G	ENSP00000506407.1:p.Gln2297Arg
ENST00000681216.1:c.407A>G	ENSP00000505551.1:p.Gln136Arg
ENST00000681412.1:c.6914A>G	ENSP00000506486.1:p.Gln2305Arg
ENST00000681722.1:c.6890A>G	ENSP00000506566.1:p.Gln2297Arg
ENST00000356239.7:c.6914A>G	ENSP00000348573.3:p.Gln2305Arg
ENST00000358100.6:c.6773A>G	ENSP00000350813.3:p.Gln2258Arg
ENST00000359028.6:c.6947A>G	ENSP00000351922.3:p.Gln2316Arg
ENST00000394534.6:c.452A>G	ENSP00000378042.2:p.Gln151Arg
NM_005751.4:c.6914A>G , LRG_331t1:c.6914A>G	NP_005742.4:p.Gln2305Arg
NM_147185.2:c.6890A>G	NP_671714.1:p.Gln2297Arg
XM_006715827.1:c.6773A>G	XP_006715890.1:p.Gln2258Arg
XM_011515709.1:c.7061A>G	XP_011514011.1:p.Gln2354Arg
XM_011515710.1:c.7085A>G	XP_011514012.1:p.Gln2362Arg
XM_011515711.1:c.7025A>G	XP_011514013.1:p.Gln2342Arg
XM_011515712.1:c.7022A>G	XP_011514014.1:p.Gln2341Arg
XM_011515713.1:c.7007A>G	XP_011514015.1:p.Gln2336Arg
XM_011515714.1:c.7046A>G	XP_011514016.1:p.Gln2349Arg
XM_011515716.1:c.6965A>G	XP_011514018.1:p.Gln2322Arg
XM_011515717.1:c.6920A>G	XP_011514019.1:p.Gln2307Arg
XM_011515718.1:c.6950A>G	XP_011514020.1:p.Gln2317Arg
XM_011515719.1:c.6926A>G	XP_011514021.1:p.Gln2309Arg
XM_011515720.1:c.6809A>G	XP_011514022.1:p.Gln2270Arg
XM_011515721.1:c.1574A>G	XP_011514023.1:p.Gln525Arg
XM_011515722.1:c.1535A>G	XP_011514024.1:p.Gln512Arg
XM_017011642.2:c.7049A>G	XP_016867131.1:p.Gln2350Arg
XM_017011643.2:c.7010A>G	XP_016867132.1:p.Gln2337Arg
XM_017011644.2:c.7049A>G	XP_016867133.1:p.Gln2350Arg
XM_017011645.2:c.6995A>G	XP_016867134.1:p.Gln2332Arg
XM_017011646.2:c.7010A>G	XP_016867135.1:p.Gln2337Arg
XM_017011647.2:c.6956A>G	XP_016867136.1:p.Gln2319Arg
XM_017011648.2:c.6953A>G	XP_016867137.1:p.Gln2318Arg
XM_017011649.2:c.6986A>G	XP_016867138.1:p.Gln2329Arg
XM_017011650.2:c.6914A>G	XP_016867139.1:p.Gln2305Arg
XM_017011651.2:c.6908A>G	XP_016867140.1:p.Gln2303Arg
XM_017011652.2:c.7049A>G	XP_016867141.1:p.Gln2350Arg
XM_017011653.2:c.6821A>G	XP_016867142.1:p.Gln2274Arg
XM_017011654.2:c.6773A>G	XP_016867143.1:p.Gln2258Arg
XM_017011655.2:c.6677A>G	XP_016867144.1:p.Gln2226Arg
XM_017011656.2:c.6677A>G	XP_016867145.1:p.Gln2226Arg
XM_017011657.2:c.2714A>G	XP_016867146.1:p.Gln905Arg
XM_017011658.2:c.1598A>G	XP_016867147.1:p.Gln533Arg
XM_017011659.2:c.1559A>G	XP_016867148.1:p.Gln520Arg
XM_017011660.2:c.1559A>G	XP_016867149.1:p.Gln520Arg
XM_024446631.1:c.6812A>G	XP_024302399.1:p.Gln2271Arg
NM_147185.3:c.6890A>G	NP_671714.1:p.Gln2297Arg
NM_001379277.1:c.1559A>G	NP_001366206.1:p.Gln520Arg
NM_005751.5:c.6914A>G MANE Select	NP_005742.4:p.Gln2305Arg