Canonical Allele Identifier: CA368133878

Gene: AKAP9

Linked Data

• gnomAD v4: 7-92077847-A-G
• MyVariant Identifiers: chr7:g.91707161A>G (hg19) ; chr7:g.92077847A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077847A>G , CM000669.2:g.92077847A>G	GRCh38
NC_000007.13:g.91707161A>G , CM000669.1:g.91707161A>G	GRCh37
NC_000007.12:g.91545097A>G	NCBI36
NG_011623.1:g.141973A>G , LRG_331:g.141973A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6917A>G MANE Select	ENSP00000348573.3:p.Gln2306Arg
ENST00000359028.7:c.6989A>G	ENSP00000351922.4:p.Gln2330Arg
ENST00000394534.7:c.410A>G	ENSP00000378042.3:p.Gln137Arg
ENST00000491695.2:c.1562A>G	ENSP00000494626.2:p.Gln521Arg
ENST00000674381.2:c.*6646A>G	ENSP00000501536.2:n.*6646A>G
ENST00000679448.1:c.6893A>G	ENSP00000505889.1:p.Gln2298Arg
ENST00000679457.1:c.6893A>G	ENSP00000505450.1:p.Gln2298Arg
ENST00000679474.1:n.7115A>G
ENST00000679521.1:c.6863A>G	ENSP00000505456.1:p.Gln2288Arg
ENST00000679554.1:c.*6702A>G	ENSP00000506415.1:n.*6702A>G
ENST00000679722.1:n.7139A>G
ENST00000679821.1:c.6659A>G	ENSP00000506040.1:p.Gln2220Arg
ENST00000680047.1:n.7115A>G
ENST00000680072.1:c.6740A>G	ENSP00000506581.1:p.Gln2247Arg
ENST00000680181.1:c.6824A>G	ENSP00000505548.1:p.Gln2275Arg
ENST00000680365.1:c.410A>G	ENSP00000506019.1:p.Gln137Arg
ENST00000680513.1:c.6776A>G	ENSP00000505284.1:p.Gln2259Arg
ENST00000680534.1:c.6956A>G	ENSP00000506674.1:p.Gln2319Arg
ENST00000680766.1:c.6893A>G	ENSP00000505204.1:p.Gln2298Arg
ENST00000680952.1:c.6893A>G	ENSP00000506407.1:p.Gln2298Arg
ENST00000681216.1:c.410A>G	ENSP00000505551.1:p.Gln137Arg
ENST00000681412.1:c.6917A>G	ENSP00000506486.1:p.Gln2306Arg
ENST00000681722.1:c.6893A>G	ENSP00000506566.1:p.Gln2298Arg
ENST00000356239.7:c.6917A>G	ENSP00000348573.3:p.Gln2306Arg
ENST00000358100.6:c.6776A>G	ENSP00000350813.3:p.Gln2259Arg
ENST00000359028.6:c.6950A>G	ENSP00000351922.3:p.Gln2317Arg
ENST00000394534.6:c.455A>G	ENSP00000378042.2:p.Gln152Arg
NM_005751.4:c.6917A>G , LRG_331t1:c.6917A>G	NP_005742.4:p.Gln2306Arg
NM_147185.2:c.6893A>G	NP_671714.1:p.Gln2298Arg
XM_006715827.1:c.6776A>G	XP_006715890.1:p.Gln2259Arg
XM_011515709.1:c.7064A>G	XP_011514011.1:p.Gln2355Arg
XM_011515710.1:c.7088A>G	XP_011514012.1:p.Gln2363Arg
XM_011515711.1:c.7028A>G	XP_011514013.1:p.Gln2343Arg
XM_011515712.1:c.7025A>G	XP_011514014.1:p.Gln2342Arg
XM_011515713.1:c.7010A>G	XP_011514015.1:p.Gln2337Arg
XM_011515714.1:c.7049A>G	XP_011514016.1:p.Gln2350Arg
XM_011515716.1:c.6968A>G	XP_011514018.1:p.Gln2323Arg
XM_011515717.1:c.6923A>G	XP_011514019.1:p.Gln2308Arg
XM_011515718.1:c.6953A>G	XP_011514020.1:p.Gln2318Arg
XM_011515719.1:c.6929A>G	XP_011514021.1:p.Gln2310Arg
XM_011515720.1:c.6812A>G	XP_011514022.1:p.Gln2271Arg
XM_011515721.1:c.1577A>G	XP_011514023.1:p.Gln526Arg
XM_011515722.1:c.1538A>G	XP_011514024.1:p.Gln513Arg
XM_017011642.2:c.7052A>G	XP_016867131.1:p.Gln2351Arg
XM_017011643.2:c.7013A>G	XP_016867132.1:p.Gln2338Arg
XM_017011644.2:c.7052A>G	XP_016867133.1:p.Gln2351Arg
XM_017011645.2:c.6998A>G	XP_016867134.1:p.Gln2333Arg
XM_017011646.2:c.7013A>G	XP_016867135.1:p.Gln2338Arg
XM_017011647.2:c.6959A>G	XP_016867136.1:p.Gln2320Arg
XM_017011648.2:c.6956A>G	XP_016867137.1:p.Gln2319Arg
XM_017011649.2:c.6989A>G	XP_016867138.1:p.Gln2330Arg
XM_017011650.2:c.6917A>G	XP_016867139.1:p.Gln2306Arg
XM_017011651.2:c.6911A>G	XP_016867140.1:p.Gln2304Arg
XM_017011652.2:c.7052A>G	XP_016867141.1:p.Gln2351Arg
XM_017011653.2:c.6824A>G	XP_016867142.1:p.Gln2275Arg
XM_017011654.2:c.6776A>G	XP_016867143.1:p.Gln2259Arg
XM_017011655.2:c.6680A>G	XP_016867144.1:p.Gln2227Arg
XM_017011656.2:c.6680A>G	XP_016867145.1:p.Gln2227Arg
XM_017011657.2:c.2717A>G	XP_016867146.1:p.Gln906Arg
XM_017011658.2:c.1601A>G	XP_016867147.1:p.Gln534Arg
XM_017011659.2:c.1562A>G	XP_016867148.1:p.Gln521Arg
XM_017011660.2:c.1562A>G	XP_016867149.1:p.Gln521Arg
XM_024446631.1:c.6815A>G	XP_024302399.1:p.Gln2272Arg
NM_147185.3:c.6893A>G	NP_671714.1:p.Gln2298Arg
NM_001379277.1:c.1562A>G	NP_001366206.1:p.Gln521Arg
NM_005751.5:c.6917A>G MANE Select	NP_005742.4:p.Gln2306Arg