Canonical Allele Identifier: CA4337502

Gene: AKAP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92083594A>G , CM000669.2:g.92083594A>G	GRCh38
NC_000007.13:g.91712908A>G , CM000669.1:g.91712908A>G	GRCh37
NC_000007.12:g.91550844A>G	NCBI36
NG_011623.1:g.147720A>G , LRG_331:g.147720A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.8585A>G MANE Select	ENSP00000348573.3:p.Gln2862Arg
ENST00000359028.7:c.8657A>G	ENSP00000351922.4:p.Gln2886Arg
ENST00000394534.7:c.2078A>G	ENSP00000378042.3:p.Gln693Arg
ENST00000435423.2:n.425A>G
ENST00000491695.2:c.3230A>G	ENSP00000494626.2:p.Gln1077Arg
ENST00000679448.1:c.8561A>G	ENSP00000505889.1:p.Gln2854Arg
ENST00000679457.1:c.8561A>G	ENSP00000505450.1:p.Gln2854Arg
ENST00000679474.1:n.8783A>G
ENST00000679521.1:c.8531A>G	ENSP00000505456.1:p.Gln2844Arg
ENST00000679722.1:n.8807A>G
ENST00000679821.1:c.8327A>G	ENSP00000506040.1:p.Gln2776Arg
ENST00000680047.1:n.8783A>G
ENST00000680072.1:c.8408A>G	ENSP00000506581.1:p.Gln2803Arg
ENST00000680181.1:c.8492A>G	ENSP00000505548.1:p.Gln2831Arg
ENST00000680365.1:c.2078A>G	ENSP00000506019.1:p.Gln693Arg
ENST00000680513.1:c.8444A>G	ENSP00000505284.1:p.Gln2815Arg
ENST00000680534.1:c.8624A>G	ENSP00000506674.1:p.Gln2875Arg
ENST00000680766.1:c.8561A>G	ENSP00000505204.1:p.Gln2854Arg
ENST00000680952.1:c.8561A>G	ENSP00000506407.1:p.Gln2854Arg
ENST00000681216.1:c.1922A>G	ENSP00000505551.1:p.Gln641Arg
ENST00000681412.1:c.8585A>G	ENSP00000506486.1:p.Gln2862Arg
ENST00000681722.1:c.8561A>G	ENSP00000506566.1:p.Gln2854Arg
ENST00000356239.7:c.8585A>G	ENSP00000348573.3:p.Gln2862Arg
ENST00000358100.6:c.8444A>G	ENSP00000350813.3:p.Gln2815Arg
ENST00000359028.6:c.8618A>G	ENSP00000351922.3:p.Gln2873Arg
ENST00000394534.6:c.2123A>G	ENSP00000378042.2:p.Gln708Arg
ENST00000435423.1:c.19A>G
NM_005751.4:c.8585A>G , LRG_331t1:c.8585A>G	NP_005742.4:p.Gln2862Arg
NM_147185.2:c.8561A>G	NP_671714.1:p.Gln2854Arg
XM_006715827.1:c.8444A>G	XP_006715890.1:p.Gln2815Arg
XM_011515709.1:c.8732A>G	XP_011514011.1:p.Gln2911Arg
XM_011515710.1:c.8756A>G	XP_011514012.1:p.Gln2919Arg
XM_011515711.1:c.8696A>G	XP_011514013.1:p.Gln2899Arg
XM_011515712.1:c.8693A>G	XP_011514014.1:p.Gln2898Arg
XM_011515713.1:c.8678A>G	XP_011514015.1:p.Gln2893Arg
XM_011515714.1:c.8717A>G	XP_011514016.1:p.Gln2906Arg
XM_011515716.1:c.8636A>G	XP_011514018.1:p.Gln2879Arg
XM_011515717.1:c.8591A>G	XP_011514019.1:p.Gln2864Arg
XM_011515718.1:c.8621A>G	XP_011514020.1:p.Gln2874Arg
XM_011515719.1:c.8597A>G	XP_011514021.1:p.Gln2866Arg
XM_011515720.1:c.8480A>G	XP_011514022.1:p.Gln2827Arg
XM_011515721.1:c.3245A>G	XP_011514023.1:p.Gln1082Arg
XM_011515722.1:c.3206A>G	XP_011514024.1:p.Gln1069Arg
XM_017011642.2:c.8720A>G	XP_016867131.1:p.Gln2907Arg
XM_017011643.2:c.8681A>G	XP_016867132.1:p.Gln2894Arg
XM_017011644.2:c.8720A>G	XP_016867133.1:p.Gln2907Arg
XM_017011645.2:c.8666A>G	XP_016867134.1:p.Gln2889Arg
XM_017011646.2:c.8681A>G	XP_016867135.1:p.Gln2894Arg
XM_017011647.2:c.8627A>G	XP_016867136.1:p.Gln2876Arg
XM_017011648.2:c.8624A>G	XP_016867137.1:p.Gln2875Arg
XM_017011649.2:c.8657A>G	XP_016867138.1:p.Gln2886Arg
XM_017011650.2:c.8585A>G	XP_016867139.1:p.Gln2862Arg
XM_017011651.2:c.8579A>G	XP_016867140.1:p.Gln2860Arg
XM_017011652.2:c.8720A>G	XP_016867141.1:p.Gln2907Arg
XM_017011653.2:c.8492A>G	XP_016867142.1:p.Gln2831Arg
XM_017011654.2:c.8444A>G	XP_016867143.1:p.Gln2815Arg
XM_017011655.2:c.8348A>G	XP_016867144.1:p.Gln2783Arg
XM_017011656.2:c.8348A>G	XP_016867145.1:p.Gln2783Arg
XM_017011657.2:c.4385A>G	XP_016867146.1:p.Gln1462Arg
XM_017011658.2:c.3269A>G	XP_016867147.1:p.Gln1090Arg
XM_017011659.2:c.3230A>G	XP_016867148.1:p.Gln1077Arg
XM_017011660.2:c.3230A>G	XP_016867149.1:p.Gln1077Arg
XM_024446631.1:c.8483A>G	XP_024302399.1:p.Gln2828Arg
NM_147185.3:c.8561A>G	NP_671714.1:p.Gln2854Arg
NM_001379277.1:c.3230A>G	NP_001366206.1:p.Gln1077Arg
NM_005751.5:c.8585A>G MANE Select	NP_005742.4:p.Gln2862Arg