Canonical Allele Identifier: CA368133882

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707163C>G (hg19) ; chr7:g.92077849C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077849C>G , CM000669.2:g.92077849C>G	GRCh38
NC_000007.13:g.91707163C>G , CM000669.1:g.91707163C>G	GRCh37
NC_000007.12:g.91545099C>G	NCBI36
NG_011623.1:g.141975C>G , LRG_331:g.141975C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6919C>G MANE Select	ENSP00000348573.3:p.Gln2307Glu
ENST00000359028.7:c.6991C>G	ENSP00000351922.4:p.Gln2331Glu
ENST00000394534.7:c.412C>G	ENSP00000378042.3:p.Gln138Glu
ENST00000491695.2:c.1564C>G	ENSP00000494626.2:p.Gln522Glu
ENST00000674381.2:c.*6648C>G	ENSP00000501536.2:n.*6648C>G
ENST00000679448.1:c.6895C>G	ENSP00000505889.1:p.Gln2299Glu
ENST00000679457.1:c.6895C>G	ENSP00000505450.1:p.Gln2299Glu
ENST00000679474.1:n.7117C>G
ENST00000679521.1:c.6865C>G	ENSP00000505456.1:p.Gln2289Glu
ENST00000679554.1:c.*6704C>G	ENSP00000506415.1:n.*6704C>G
ENST00000679722.1:n.7141C>G
ENST00000679821.1:c.6661C>G	ENSP00000506040.1:p.Gln2221Glu
ENST00000680047.1:n.7117C>G
ENST00000680072.1:c.6742C>G	ENSP00000506581.1:p.Gln2248Glu
ENST00000680181.1:c.6826C>G	ENSP00000505548.1:p.Gln2276Glu
ENST00000680365.1:c.412C>G	ENSP00000506019.1:p.Gln138Glu
ENST00000680513.1:c.6778C>G	ENSP00000505284.1:p.Gln2260Glu
ENST00000680534.1:c.6958C>G	ENSP00000506674.1:p.Gln2320Glu
ENST00000680766.1:c.6895C>G	ENSP00000505204.1:p.Gln2299Glu
ENST00000680952.1:c.6895C>G	ENSP00000506407.1:p.Gln2299Glu
ENST00000681216.1:c.412C>G	ENSP00000505551.1:p.Gln138Glu
ENST00000681412.1:c.6919C>G	ENSP00000506486.1:p.Gln2307Glu
ENST00000681722.1:c.6895C>G	ENSP00000506566.1:p.Gln2299Glu
ENST00000356239.7:c.6919C>G	ENSP00000348573.3:p.Gln2307Glu
ENST00000358100.6:c.6778C>G	ENSP00000350813.3:p.Gln2260Glu
ENST00000359028.6:c.6952C>G	ENSP00000351922.3:p.Gln2318Glu
ENST00000394534.6:c.457C>G	ENSP00000378042.2:p.Gln153Glu
NM_005751.4:c.6919C>G , LRG_331t1:c.6919C>G	NP_005742.4:p.Gln2307Glu
NM_147185.2:c.6895C>G	NP_671714.1:p.Gln2299Glu
XM_006715827.1:c.6778C>G	XP_006715890.1:p.Gln2260Glu
XM_011515709.1:c.7066C>G	XP_011514011.1:p.Gln2356Glu
XM_011515710.1:c.7090C>G	XP_011514012.1:p.Gln2364Glu
XM_011515711.1:c.7030C>G	XP_011514013.1:p.Gln2344Glu
XM_011515712.1:c.7027C>G	XP_011514014.1:p.Gln2343Glu
XM_011515713.1:c.7012C>G	XP_011514015.1:p.Gln2338Glu
XM_011515714.1:c.7051C>G	XP_011514016.1:p.Gln2351Glu
XM_011515716.1:c.6970C>G	XP_011514018.1:p.Gln2324Glu
XM_011515717.1:c.6925C>G	XP_011514019.1:p.Gln2309Glu
XM_011515718.1:c.6955C>G	XP_011514020.1:p.Gln2319Glu
XM_011515719.1:c.6931C>G	XP_011514021.1:p.Gln2311Glu
XM_011515720.1:c.6814C>G	XP_011514022.1:p.Gln2272Glu
XM_011515721.1:c.1579C>G	XP_011514023.1:p.Gln527Glu
XM_011515722.1:c.1540C>G	XP_011514024.1:p.Gln514Glu
XM_017011642.2:c.7054C>G	XP_016867131.1:p.Gln2352Glu
XM_017011643.2:c.7015C>G	XP_016867132.1:p.Gln2339Glu
XM_017011644.2:c.7054C>G	XP_016867133.1:p.Gln2352Glu
XM_017011645.2:c.7000C>G	XP_016867134.1:p.Gln2334Glu
XM_017011646.2:c.7015C>G	XP_016867135.1:p.Gln2339Glu
XM_017011647.2:c.6961C>G	XP_016867136.1:p.Gln2321Glu
XM_017011648.2:c.6958C>G	XP_016867137.1:p.Gln2320Glu
XM_017011649.2:c.6991C>G	XP_016867138.1:p.Gln2331Glu
XM_017011650.2:c.6919C>G	XP_016867139.1:p.Gln2307Glu
XM_017011651.2:c.6913C>G	XP_016867140.1:p.Gln2305Glu
XM_017011652.2:c.7054C>G	XP_016867141.1:p.Gln2352Glu
XM_017011653.2:c.6826C>G	XP_016867142.1:p.Gln2276Glu
XM_017011654.2:c.6778C>G	XP_016867143.1:p.Gln2260Glu
XM_017011655.2:c.6682C>G	XP_016867144.1:p.Gln2228Glu
XM_017011656.2:c.6682C>G	XP_016867145.1:p.Gln2228Glu
XM_017011657.2:c.2719C>G	XP_016867146.1:p.Gln907Glu
XM_017011658.2:c.1603C>G	XP_016867147.1:p.Gln535Glu
XM_017011659.2:c.1564C>G	XP_016867148.1:p.Gln522Glu
XM_017011660.2:c.1564C>G	XP_016867149.1:p.Gln522Glu
XM_024446631.1:c.6817C>G	XP_024302399.1:p.Gln2273Glu
NM_147185.3:c.6895C>G	NP_671714.1:p.Gln2299Glu
NM_001379277.1:c.1564C>G	NP_001366206.1:p.Gln522Glu
NM_005751.5:c.6919C>G MANE Select	NP_005742.4:p.Gln2307Glu