Canonical Allele Identifier: CA368133872

Gene: AKAP9

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6914A>T MANE Select	ENSP00000348573.3:p.Gln2305Leu
ENST00000359028.7:c.6986A>T	ENSP00000351922.4:p.Gln2329Leu
ENST00000394534.7:c.407A>T	ENSP00000378042.3:p.Gln136Leu
ENST00000491695.2:c.1559A>T	ENSP00000494626.2:p.Gln520Leu
ENST00000674381.2:c.*6643A>T	ENSP00000501536.2:n.*6643A>T
ENST00000679448.1:c.6890A>T	ENSP00000505889.1:p.Gln2297Leu
ENST00000679457.1:c.6890A>T	ENSP00000505450.1:p.Gln2297Leu
ENST00000679474.1:n.7112A>T
ENST00000679521.1:c.6860A>T	ENSP00000505456.1:p.Gln2287Leu
ENST00000679554.1:c.*6699A>T	ENSP00000506415.1:n.*6699A>T
ENST00000679722.1:n.7136A>T
ENST00000679821.1:c.6656A>T	ENSP00000506040.1:p.Gln2219Leu
ENST00000680047.1:n.7112A>T
ENST00000680072.1:c.6737A>T	ENSP00000506581.1:p.Gln2246Leu
ENST00000680181.1:c.6821A>T	ENSP00000505548.1:p.Gln2274Leu
ENST00000680365.1:c.407A>T	ENSP00000506019.1:p.Gln136Leu
ENST00000680513.1:c.6773A>T	ENSP00000505284.1:p.Gln2258Leu
ENST00000680534.1:c.6953A>T	ENSP00000506674.1:p.Gln2318Leu
ENST00000680766.1:c.6890A>T	ENSP00000505204.1:p.Gln2297Leu
ENST00000680952.1:c.6890A>T	ENSP00000506407.1:p.Gln2297Leu
ENST00000681216.1:c.407A>T	ENSP00000505551.1:p.Gln136Leu
ENST00000681412.1:c.6914A>T	ENSP00000506486.1:p.Gln2305Leu
ENST00000681722.1:c.6890A>T	ENSP00000506566.1:p.Gln2297Leu
ENST00000356239.7:c.6914A>T	ENSP00000348573.3:p.Gln2305Leu
ENST00000358100.6:c.6773A>T	ENSP00000350813.3:p.Gln2258Leu
ENST00000359028.6:c.6947A>T	ENSP00000351922.3:p.Gln2316Leu
ENST00000394534.6:c.452A>T	ENSP00000378042.2:p.Gln151Leu
NM_005751.4:c.6914A>T , LRG_331t1:c.6914A>T	NP_005742.4:p.Gln2305Leu
NM_147185.2:c.6890A>T	NP_671714.1:p.Gln2297Leu
XM_006715827.1:c.6773A>T	XP_006715890.1:p.Gln2258Leu
XM_011515709.1:c.7061A>T	XP_011514011.1:p.Gln2354Leu
XM_011515710.1:c.7085A>T	XP_011514012.1:p.Gln2362Leu
XM_011515711.1:c.7025A>T	XP_011514013.1:p.Gln2342Leu
XM_011515712.1:c.7022A>T	XP_011514014.1:p.Gln2341Leu
XM_011515713.1:c.7007A>T	XP_011514015.1:p.Gln2336Leu
XM_011515714.1:c.7046A>T	XP_011514016.1:p.Gln2349Leu
XM_011515716.1:c.6965A>T	XP_011514018.1:p.Gln2322Leu
XM_011515717.1:c.6920A>T	XP_011514019.1:p.Gln2307Leu
XM_011515718.1:c.6950A>T	XP_011514020.1:p.Gln2317Leu
XM_011515719.1:c.6926A>T	XP_011514021.1:p.Gln2309Leu
XM_011515720.1:c.6809A>T	XP_011514022.1:p.Gln2270Leu
XM_011515721.1:c.1574A>T	XP_011514023.1:p.Gln525Leu
XM_011515722.1:c.1535A>T	XP_011514024.1:p.Gln512Leu
XM_017011642.2:c.7049A>T	XP_016867131.1:p.Gln2350Leu
XM_017011643.2:c.7010A>T	XP_016867132.1:p.Gln2337Leu
XM_017011644.2:c.7049A>T	XP_016867133.1:p.Gln2350Leu
XM_017011645.2:c.6995A>T	XP_016867134.1:p.Gln2332Leu
XM_017011646.2:c.7010A>T	XP_016867135.1:p.Gln2337Leu
XM_017011647.2:c.6956A>T	XP_016867136.1:p.Gln2319Leu
XM_017011648.2:c.6953A>T	XP_016867137.1:p.Gln2318Leu
XM_017011649.2:c.6986A>T	XP_016867138.1:p.Gln2329Leu
XM_017011650.2:c.6914A>T	XP_016867139.1:p.Gln2305Leu
XM_017011651.2:c.6908A>T	XP_016867140.1:p.Gln2303Leu
XM_017011652.2:c.7049A>T	XP_016867141.1:p.Gln2350Leu
XM_017011653.2:c.6821A>T	XP_016867142.1:p.Gln2274Leu
XM_017011654.2:c.6773A>T	XP_016867143.1:p.Gln2258Leu
XM_017011655.2:c.6677A>T	XP_016867144.1:p.Gln2226Leu
XM_017011656.2:c.6677A>T	XP_016867145.1:p.Gln2226Leu
XM_017011657.2:c.2714A>T	XP_016867146.1:p.Gln905Leu
XM_017011658.2:c.1598A>T	XP_016867147.1:p.Gln533Leu
XM_017011659.2:c.1559A>T	XP_016867148.1:p.Gln520Leu
XM_017011660.2:c.1559A>T	XP_016867149.1:p.Gln520Leu
XM_024446631.1:c.6812A>T	XP_024302399.1:p.Gln2271Leu
NM_147185.3:c.6890A>T	NP_671714.1:p.Gln2297Leu
NM_001379277.1:c.1559A>T	NP_001366206.1:p.Gln520Leu
NM_005751.5:c.6914A>T MANE Select	NP_005742.4:p.Gln2305Leu