Canonical Allele Identifier: CA368133931

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707185A>G (hg19) ; chr7:g.92077871A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077871A>G , CM000669.2:g.92077871A>G	GRCh38
NC_000007.13:g.91707185A>G , CM000669.1:g.91707185A>G	GRCh37
NC_000007.12:g.91545121A>G	NCBI36
NG_011623.1:g.141997A>G , LRG_331:g.141997A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6941A>G MANE Select	ENSP00000348573.3:p.Asn2314Ser
ENST00000359028.7:c.7013A>G	ENSP00000351922.4:p.Asn2338Ser
ENST00000394534.7:c.434A>G	ENSP00000378042.3:p.Asn145Ser
ENST00000491695.2:c.1586A>G	ENSP00000494626.2:p.Asn529Ser
ENST00000674381.2:c.*6670A>G	ENSP00000501536.2:n.*6670A>G
ENST00000679448.1:c.6917A>G	ENSP00000505889.1:p.Asn2306Ser
ENST00000679457.1:c.6917A>G	ENSP00000505450.1:p.Asn2306Ser
ENST00000679474.1:n.7139A>G
ENST00000679521.1:c.6887A>G	ENSP00000505456.1:p.Asn2296Ser
ENST00000679554.1:c.*6726A>G	ENSP00000506415.1:n.*6726A>G
ENST00000679722.1:n.7163A>G
ENST00000679821.1:c.6683A>G	ENSP00000506040.1:p.Asn2228Ser
ENST00000680047.1:n.7139A>G
ENST00000680072.1:c.6764A>G	ENSP00000506581.1:p.Asn2255Ser
ENST00000680181.1:c.6848A>G	ENSP00000505548.1:p.Asn2283Ser
ENST00000680365.1:c.434A>G	ENSP00000506019.1:p.Asn145Ser
ENST00000680513.1:c.6800A>G	ENSP00000505284.1:p.Asn2267Ser
ENST00000680534.1:c.6980A>G	ENSP00000506674.1:p.Asn2327Ser
ENST00000680766.1:c.6917A>G	ENSP00000505204.1:p.Asn2306Ser
ENST00000680952.1:c.6917A>G	ENSP00000506407.1:p.Asn2306Ser
ENST00000681216.1:c.434A>G	ENSP00000505551.1:p.Asn145Ser
ENST00000681412.1:c.6941A>G	ENSP00000506486.1:p.Asn2314Ser
ENST00000681722.1:c.6917A>G	ENSP00000506566.1:p.Asn2306Ser
ENST00000356239.7:c.6941A>G	ENSP00000348573.3:p.Asn2314Ser
ENST00000358100.6:c.6800A>G	ENSP00000350813.3:p.Asn2267Ser
ENST00000359028.6:c.6974A>G	ENSP00000351922.3:p.Asn2325Ser
ENST00000394534.6:c.479A>G	ENSP00000378042.2:p.Asn160Ser
NM_005751.4:c.6941A>G , LRG_331t1:c.6941A>G	NP_005742.4:p.Asn2314Ser
NM_147185.2:c.6917A>G	NP_671714.1:p.Asn2306Ser
XM_006715827.1:c.6800A>G	XP_006715890.1:p.Asn2267Ser
XM_011515709.1:c.7088A>G	XP_011514011.1:p.Asn2363Ser
XM_011515710.1:c.7112A>G	XP_011514012.1:p.Asn2371Ser
XM_011515711.1:c.7052A>G	XP_011514013.1:p.Asn2351Ser
XM_011515712.1:c.7049A>G	XP_011514014.1:p.Asn2350Ser
XM_011515713.1:c.7034A>G	XP_011514015.1:p.Asn2345Ser
XM_011515714.1:c.7073A>G	XP_011514016.1:p.Asn2358Ser
XM_011515716.1:c.6992A>G	XP_011514018.1:p.Asn2331Ser
XM_011515717.1:c.6947A>G	XP_011514019.1:p.Asn2316Ser
XM_011515718.1:c.6977A>G	XP_011514020.1:p.Asn2326Ser
XM_011515719.1:c.6953A>G	XP_011514021.1:p.Asn2318Ser
XM_011515720.1:c.6836A>G	XP_011514022.1:p.Asn2279Ser
XM_011515721.1:c.1601A>G	XP_011514023.1:p.Asn534Ser
XM_011515722.1:c.1562A>G	XP_011514024.1:p.Asn521Ser
XM_017011642.2:c.7076A>G	XP_016867131.1:p.Asn2359Ser
XM_017011643.2:c.7037A>G	XP_016867132.1:p.Asn2346Ser
XM_017011644.2:c.7076A>G	XP_016867133.1:p.Asn2359Ser
XM_017011645.2:c.7022A>G	XP_016867134.1:p.Asn2341Ser
XM_017011646.2:c.7037A>G	XP_016867135.1:p.Asn2346Ser
XM_017011647.2:c.6983A>G	XP_016867136.1:p.Asn2328Ser
XM_017011648.2:c.6980A>G	XP_016867137.1:p.Asn2327Ser
XM_017011649.2:c.7013A>G	XP_016867138.1:p.Asn2338Ser
XM_017011650.2:c.6941A>G	XP_016867139.1:p.Asn2314Ser
XM_017011651.2:c.6935A>G	XP_016867140.1:p.Asn2312Ser
XM_017011652.2:c.7076A>G	XP_016867141.1:p.Asn2359Ser
XM_017011653.2:c.6848A>G	XP_016867142.1:p.Asn2283Ser
XM_017011654.2:c.6800A>G	XP_016867143.1:p.Asn2267Ser
XM_017011655.2:c.6704A>G	XP_016867144.1:p.Asn2235Ser
XM_017011656.2:c.6704A>G	XP_016867145.1:p.Asn2235Ser
XM_017011657.2:c.2741A>G	XP_016867146.1:p.Asn914Ser
XM_017011658.2:c.1625A>G	XP_016867147.1:p.Asn542Ser
XM_017011659.2:c.1586A>G	XP_016867148.1:p.Asn529Ser
XM_017011660.2:c.1586A>G	XP_016867149.1:p.Asn529Ser
XM_024446631.1:c.6839A>G	XP_024302399.1:p.Asn2280Ser
NM_147185.3:c.6917A>G	NP_671714.1:p.Asn2306Ser
NM_001379277.1:c.1586A>G	NP_001366206.1:p.Asn529Ser
NM_005751.5:c.6941A>G MANE Select	NP_005742.4:p.Asn2314Ser