Canonical Allele Identifier: CA368133888

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707165A>C (hg19) ; chr7:g.92077851A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077851A>C , CM000669.2:g.92077851A>C	GRCh38
NC_000007.13:g.91707165A>C , CM000669.1:g.91707165A>C	GRCh37
NC_000007.12:g.91545101A>C	NCBI36
NG_011623.1:g.141977A>C , LRG_331:g.141977A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6921A>C MANE Select	ENSP00000348573.3:p.Gln2307His
ENST00000359028.7:c.6993A>C	ENSP00000351922.4:p.Gln2331His
ENST00000394534.7:c.414A>C	ENSP00000378042.3:p.Gln138His
ENST00000491695.2:c.1566A>C	ENSP00000494626.2:p.Gln522His
ENST00000674381.2:c.*6650A>C	ENSP00000501536.2:n.*6650A>C
ENST00000679448.1:c.6897A>C	ENSP00000505889.1:p.Gln2299His
ENST00000679457.1:c.6897A>C	ENSP00000505450.1:p.Gln2299His
ENST00000679474.1:n.7119A>C
ENST00000679521.1:c.6867A>C	ENSP00000505456.1:p.Gln2289His
ENST00000679554.1:c.*6706A>C	ENSP00000506415.1:n.*6706A>C
ENST00000679722.1:n.7143A>C
ENST00000679821.1:c.6663A>C	ENSP00000506040.1:p.Gln2221His
ENST00000680047.1:n.7119A>C
ENST00000680072.1:c.6744A>C	ENSP00000506581.1:p.Gln2248His
ENST00000680181.1:c.6828A>C	ENSP00000505548.1:p.Gln2276His
ENST00000680365.1:c.414A>C	ENSP00000506019.1:p.Gln138His
ENST00000680513.1:c.6780A>C	ENSP00000505284.1:p.Gln2260His
ENST00000680534.1:c.6960A>C	ENSP00000506674.1:p.Gln2320His
ENST00000680766.1:c.6897A>C	ENSP00000505204.1:p.Gln2299His
ENST00000680952.1:c.6897A>C	ENSP00000506407.1:p.Gln2299His
ENST00000681216.1:c.414A>C	ENSP00000505551.1:p.Gln138His
ENST00000681412.1:c.6921A>C	ENSP00000506486.1:p.Gln2307His
ENST00000681722.1:c.6897A>C	ENSP00000506566.1:p.Gln2299His
ENST00000356239.7:c.6921A>C	ENSP00000348573.3:p.Gln2307His
ENST00000358100.6:c.6780A>C	ENSP00000350813.3:p.Gln2260His
ENST00000359028.6:c.6954A>C	ENSP00000351922.3:p.Gln2318His
ENST00000394534.6:c.459A>C	ENSP00000378042.2:p.Gln153His
NM_005751.4:c.6921A>C , LRG_331t1:c.6921A>C	NP_005742.4:p.Gln2307His
NM_147185.2:c.6897A>C	NP_671714.1:p.Gln2299His
XM_006715827.1:c.6780A>C	XP_006715890.1:p.Gln2260His
XM_011515709.1:c.7068A>C	XP_011514011.1:p.Gln2356His
XM_011515710.1:c.7092A>C	XP_011514012.1:p.Gln2364His
XM_011515711.1:c.7032A>C	XP_011514013.1:p.Gln2344His
XM_011515712.1:c.7029A>C	XP_011514014.1:p.Gln2343His
XM_011515713.1:c.7014A>C	XP_011514015.1:p.Gln2338His
XM_011515714.1:c.7053A>C	XP_011514016.1:p.Gln2351His
XM_011515716.1:c.6972A>C	XP_011514018.1:p.Gln2324His
XM_011515717.1:c.6927A>C	XP_011514019.1:p.Gln2309His
XM_011515718.1:c.6957A>C	XP_011514020.1:p.Gln2319His
XM_011515719.1:c.6933A>C	XP_011514021.1:p.Gln2311His
XM_011515720.1:c.6816A>C	XP_011514022.1:p.Gln2272His
XM_011515721.1:c.1581A>C	XP_011514023.1:p.Gln527His
XM_011515722.1:c.1542A>C	XP_011514024.1:p.Gln514His
XM_017011642.2:c.7056A>C	XP_016867131.1:p.Gln2352His
XM_017011643.2:c.7017A>C	XP_016867132.1:p.Gln2339His
XM_017011644.2:c.7056A>C	XP_016867133.1:p.Gln2352His
XM_017011645.2:c.7002A>C	XP_016867134.1:p.Gln2334His
XM_017011646.2:c.7017A>C	XP_016867135.1:p.Gln2339His
XM_017011647.2:c.6963A>C	XP_016867136.1:p.Gln2321His
XM_017011648.2:c.6960A>C	XP_016867137.1:p.Gln2320His
XM_017011649.2:c.6993A>C	XP_016867138.1:p.Gln2331His
XM_017011650.2:c.6921A>C	XP_016867139.1:p.Gln2307His
XM_017011651.2:c.6915A>C	XP_016867140.1:p.Gln2305His
XM_017011652.2:c.7056A>C	XP_016867141.1:p.Gln2352His
XM_017011653.2:c.6828A>C	XP_016867142.1:p.Gln2276His
XM_017011654.2:c.6780A>C	XP_016867143.1:p.Gln2260His
XM_017011655.2:c.6684A>C	XP_016867144.1:p.Gln2228His
XM_017011656.2:c.6684A>C	XP_016867145.1:p.Gln2228His
XM_017011657.2:c.2721A>C	XP_016867146.1:p.Gln907His
XM_017011658.2:c.1605A>C	XP_016867147.1:p.Gln535His
XM_017011659.2:c.1566A>C	XP_016867148.1:p.Gln522His
XM_017011660.2:c.1566A>C	XP_016867149.1:p.Gln522His
XM_024446631.1:c.6819A>C	XP_024302399.1:p.Gln2273His
NM_147185.3:c.6897A>C	NP_671714.1:p.Gln2299His
NM_001379277.1:c.1566A>C	NP_001366206.1:p.Gln522His
NM_005751.5:c.6921A>C MANE Select	NP_005742.4:p.Gln2307His