Canonical Allele Identifier: CA4337448

Gene: AKAP9

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92083198A>G , CM000669.2:g.92083198A>G	GRCh38
NC_000007.13:g.91712512A>G , CM000669.1:g.91712512A>G	GRCh37
NC_000007.12:g.91550448A>G	NCBI36
NG_011623.1:g.147324A>G , LRG_331:g.147324A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.8189A>G MANE Select	ENSP00000348573.3:p.Gln2730Arg
ENST00000359028.7:c.8261A>G	ENSP00000351922.4:p.Gln2754Arg
ENST00000394534.7:c.1682A>G	ENSP00000378042.3:p.Gln561Arg
ENST00000435423.2:n.29A>G
ENST00000491695.2:c.2834A>G	ENSP00000494626.2:p.Gln945Arg
ENST00000674381.2:c.*7918A>G	ENSP00000501536.2:n.*7918A>G
ENST00000679448.1:c.8165A>G	ENSP00000505889.1:p.Gln2722Arg
ENST00000679457.1:c.8165A>G	ENSP00000505450.1:p.Gln2722Arg
ENST00000679474.1:n.8387A>G
ENST00000679521.1:c.8135A>G	ENSP00000505456.1:p.Gln2712Arg
ENST00000679554.1:c.*7974A>G	ENSP00000506415.1:n.*7974A>G
ENST00000679722.1:n.8411A>G
ENST00000679821.1:c.7931A>G	ENSP00000506040.1:p.Gln2644Arg
ENST00000680047.1:n.8387A>G
ENST00000680072.1:c.8012A>G	ENSP00000506581.1:p.Gln2671Arg
ENST00000680181.1:c.8096A>G	ENSP00000505548.1:p.Gln2699Arg
ENST00000680365.1:c.1682A>G	ENSP00000506019.1:p.Gln561Arg
ENST00000680513.1:c.8048A>G	ENSP00000505284.1:p.Gln2683Arg
ENST00000680534.1:c.8228A>G	ENSP00000506674.1:p.Gln2743Arg
ENST00000680766.1:c.8165A>G	ENSP00000505204.1:p.Gln2722Arg
ENST00000680952.1:c.8165A>G	ENSP00000506407.1:p.Gln2722Arg
ENST00000681216.1:c.1682A>G	ENSP00000505551.1:p.Gln561Arg
ENST00000681412.1:c.8189A>G	ENSP00000506486.1:p.Gln2730Arg
ENST00000681722.1:c.8165A>G	ENSP00000506566.1:p.Gln2722Arg
ENST00000356239.7:c.8189A>G	ENSP00000348573.3:p.Gln2730Arg
ENST00000358100.6:c.8048A>G	ENSP00000350813.3:p.Gln2683Arg
ENST00000359028.6:c.8222A>G	ENSP00000351922.3:p.Gln2741Arg
ENST00000394534.6:c.1727A>G	ENSP00000378042.2:p.Gln576Arg
NM_005751.4:c.8189A>G , LRG_331t1:c.8189A>G	NP_005742.4:p.Gln2730Arg
NM_147185.2:c.8165A>G	NP_671714.1:p.Gln2722Arg
XM_006715827.1:c.8048A>G	XP_006715890.1:p.Gln2683Arg
XM_011515709.1:c.8336A>G	XP_011514011.1:p.Gln2779Arg
XM_011515710.1:c.8360A>G	XP_011514012.1:p.Gln2787Arg
XM_011515711.1:c.8300A>G	XP_011514013.1:p.Gln2767Arg
XM_011515712.1:c.8297A>G	XP_011514014.1:p.Gln2766Arg
XM_011515713.1:c.8282A>G	XP_011514015.1:p.Gln2761Arg
XM_011515714.1:c.8321A>G	XP_011514016.1:p.Gln2774Arg
XM_011515716.1:c.8240A>G	XP_011514018.1:p.Gln2747Arg
XM_011515717.1:c.8195A>G	XP_011514019.1:p.Gln2732Arg
XM_011515718.1:c.8225A>G	XP_011514020.1:p.Gln2742Arg
XM_011515719.1:c.8201A>G	XP_011514021.1:p.Gln2734Arg
XM_011515720.1:c.8084A>G	XP_011514022.1:p.Gln2695Arg
XM_011515721.1:c.2849A>G	XP_011514023.1:p.Gln950Arg
XM_011515722.1:c.2810A>G	XP_011514024.1:p.Gln937Arg
XM_017011642.2:c.8324A>G	XP_016867131.1:p.Gln2775Arg
XM_017011643.2:c.8285A>G	XP_016867132.1:p.Gln2762Arg
XM_017011644.2:c.8324A>G	XP_016867133.1:p.Gln2775Arg
XM_017011645.2:c.8270A>G	XP_016867134.1:p.Gln2757Arg
XM_017011646.2:c.8285A>G	XP_016867135.1:p.Gln2762Arg
XM_017011647.2:c.8231A>G	XP_016867136.1:p.Gln2744Arg
XM_017011648.2:c.8228A>G	XP_016867137.1:p.Gln2743Arg
XM_017011649.2:c.8261A>G	XP_016867138.1:p.Gln2754Arg
XM_017011650.2:c.8189A>G	XP_016867139.1:p.Gln2730Arg
XM_017011651.2:c.8183A>G	XP_016867140.1:p.Gln2728Arg
XM_017011652.2:c.8324A>G	XP_016867141.1:p.Gln2775Arg
XM_017011653.2:c.8096A>G	XP_016867142.1:p.Gln2699Arg
XM_017011654.2:c.8048A>G	XP_016867143.1:p.Gln2683Arg
XM_017011655.2:c.7952A>G	XP_016867144.1:p.Gln2651Arg
XM_017011656.2:c.7952A>G	XP_016867145.1:p.Gln2651Arg
XM_017011657.2:c.3989A>G	XP_016867146.1:p.Gln1330Arg
XM_017011658.2:c.2873A>G	XP_016867147.1:p.Gln958Arg
XM_017011659.2:c.2834A>G	XP_016867148.1:p.Gln945Arg
XM_017011660.2:c.2834A>G	XP_016867149.1:p.Gln945Arg
XM_024446631.1:c.8087A>G	XP_024302399.1:p.Gln2696Arg
NM_147185.3:c.8165A>G	NP_671714.1:p.Gln2722Arg
NM_001379277.1:c.2834A>G	NP_001366206.1:p.Gln945Arg
NM_005751.5:c.8189A>G MANE Select	NP_005742.4:p.Gln2730Arg