Canonical Allele Identifier: CA368133879

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707161A>T (hg19) ; chr7:g.92077847A>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6917A>T MANE Select	ENSP00000348573.3:p.Gln2306Leu
ENST00000359028.7:c.6989A>T	ENSP00000351922.4:p.Gln2330Leu
ENST00000394534.7:c.410A>T	ENSP00000378042.3:p.Gln137Leu
ENST00000491695.2:c.1562A>T	ENSP00000494626.2:p.Gln521Leu
ENST00000674381.2:c.*6646A>T	ENSP00000501536.2:n.*6646A>T
ENST00000679448.1:c.6893A>T	ENSP00000505889.1:p.Gln2298Leu
ENST00000679457.1:c.6893A>T	ENSP00000505450.1:p.Gln2298Leu
ENST00000679474.1:n.7115A>T
ENST00000679521.1:c.6863A>T	ENSP00000505456.1:p.Gln2288Leu
ENST00000679554.1:c.*6702A>T	ENSP00000506415.1:n.*6702A>T
ENST00000679722.1:n.7139A>T
ENST00000679821.1:c.6659A>T	ENSP00000506040.1:p.Gln2220Leu
ENST00000680047.1:n.7115A>T
ENST00000680072.1:c.6740A>T	ENSP00000506581.1:p.Gln2247Leu
ENST00000680181.1:c.6824A>T	ENSP00000505548.1:p.Gln2275Leu
ENST00000680365.1:c.410A>T	ENSP00000506019.1:p.Gln137Leu
ENST00000680513.1:c.6776A>T	ENSP00000505284.1:p.Gln2259Leu
ENST00000680534.1:c.6956A>T	ENSP00000506674.1:p.Gln2319Leu
ENST00000680766.1:c.6893A>T	ENSP00000505204.1:p.Gln2298Leu
ENST00000680952.1:c.6893A>T	ENSP00000506407.1:p.Gln2298Leu
ENST00000681216.1:c.410A>T	ENSP00000505551.1:p.Gln137Leu
ENST00000681412.1:c.6917A>T	ENSP00000506486.1:p.Gln2306Leu
ENST00000681722.1:c.6893A>T	ENSP00000506566.1:p.Gln2298Leu
ENST00000356239.7:c.6917A>T	ENSP00000348573.3:p.Gln2306Leu
ENST00000358100.6:c.6776A>T	ENSP00000350813.3:p.Gln2259Leu
ENST00000359028.6:c.6950A>T	ENSP00000351922.3:p.Gln2317Leu
ENST00000394534.6:c.455A>T	ENSP00000378042.2:p.Gln152Leu
NM_005751.4:c.6917A>T , LRG_331t1:c.6917A>T	NP_005742.4:p.Gln2306Leu
NM_147185.2:c.6893A>T	NP_671714.1:p.Gln2298Leu
XM_006715827.1:c.6776A>T	XP_006715890.1:p.Gln2259Leu
XM_011515709.1:c.7064A>T	XP_011514011.1:p.Gln2355Leu
XM_011515710.1:c.7088A>T	XP_011514012.1:p.Gln2363Leu
XM_011515711.1:c.7028A>T	XP_011514013.1:p.Gln2343Leu
XM_011515712.1:c.7025A>T	XP_011514014.1:p.Gln2342Leu
XM_011515713.1:c.7010A>T	XP_011514015.1:p.Gln2337Leu
XM_011515714.1:c.7049A>T	XP_011514016.1:p.Gln2350Leu
XM_011515716.1:c.6968A>T	XP_011514018.1:p.Gln2323Leu
XM_011515717.1:c.6923A>T	XP_011514019.1:p.Gln2308Leu
XM_011515718.1:c.6953A>T	XP_011514020.1:p.Gln2318Leu
XM_011515719.1:c.6929A>T	XP_011514021.1:p.Gln2310Leu
XM_011515720.1:c.6812A>T	XP_011514022.1:p.Gln2271Leu
XM_011515721.1:c.1577A>T	XP_011514023.1:p.Gln526Leu
XM_011515722.1:c.1538A>T	XP_011514024.1:p.Gln513Leu
XM_017011642.2:c.7052A>T	XP_016867131.1:p.Gln2351Leu
XM_017011643.2:c.7013A>T	XP_016867132.1:p.Gln2338Leu
XM_017011644.2:c.7052A>T	XP_016867133.1:p.Gln2351Leu
XM_017011645.2:c.6998A>T	XP_016867134.1:p.Gln2333Leu
XM_017011646.2:c.7013A>T	XP_016867135.1:p.Gln2338Leu
XM_017011647.2:c.6959A>T	XP_016867136.1:p.Gln2320Leu
XM_017011648.2:c.6956A>T	XP_016867137.1:p.Gln2319Leu
XM_017011649.2:c.6989A>T	XP_016867138.1:p.Gln2330Leu
XM_017011650.2:c.6917A>T	XP_016867139.1:p.Gln2306Leu
XM_017011651.2:c.6911A>T	XP_016867140.1:p.Gln2304Leu
XM_017011652.2:c.7052A>T	XP_016867141.1:p.Gln2351Leu
XM_017011653.2:c.6824A>T	XP_016867142.1:p.Gln2275Leu
XM_017011654.2:c.6776A>T	XP_016867143.1:p.Gln2259Leu
XM_017011655.2:c.6680A>T	XP_016867144.1:p.Gln2227Leu
XM_017011656.2:c.6680A>T	XP_016867145.1:p.Gln2227Leu
XM_017011657.2:c.2717A>T	XP_016867146.1:p.Gln906Leu
XM_017011658.2:c.1601A>T	XP_016867147.1:p.Gln534Leu
XM_017011659.2:c.1562A>T	XP_016867148.1:p.Gln521Leu
XM_017011660.2:c.1562A>T	XP_016867149.1:p.Gln521Leu
XM_024446631.1:c.6815A>T	XP_024302399.1:p.Gln2272Leu
NM_147185.3:c.6893A>T	NP_671714.1:p.Gln2298Leu
NM_001379277.1:c.1562A>T	NP_001366206.1:p.Gln521Leu
NM_005751.5:c.6917A>T MANE Select	NP_005742.4:p.Gln2306Leu