Canonical Allele Identifier: CA456450481

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707144A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077830A>G , CM000669.2:g.92077830A>G	GRCh38
NC_000007.13:g.91707144A>G , CM000669.1:g.91707144A>G	GRCh37
NC_000007.12:g.91545080A>G	NCBI36
NG_011623.1:g.141956A>G , LRG_331:g.141956A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6900A>G MANE Select	ENSP00000348573.3:p.Gln2300=
ENST00000359028.7:c.6972A>G	ENSP00000351922.4:p.Gln2324=
ENST00000394534.7:c.393A>G	ENSP00000378042.3:p.Gln131=
ENST00000491695.2:c.1545A>G	ENSP00000494626.2:p.Gln515=
ENST00000674381.2:c.*6629A>G	ENSP00000501536.2:n.*6629A>G
ENST00000679448.1:c.6876A>G	ENSP00000505889.1:p.Gln2292=
ENST00000679457.1:c.6876A>G	ENSP00000505450.1:p.Gln2292=
ENST00000679474.1:n.7098A>G
ENST00000679521.1:c.6846A>G	ENSP00000505456.1:p.Gln2282=
ENST00000679554.1:c.*6685A>G	ENSP00000506415.1:n.*6685A>G
ENST00000679722.1:n.7122A>G
ENST00000679821.1:c.6642A>G	ENSP00000506040.1:p.Gln2214=
ENST00000680047.1:n.7098A>G
ENST00000680072.1:c.6723A>G	ENSP00000506581.1:p.Gln2241=
ENST00000680181.1:c.6807A>G	ENSP00000505548.1:p.Gln2269=
ENST00000680365.1:c.393A>G	ENSP00000506019.1:p.Gln131=
ENST00000680513.1:c.6759A>G	ENSP00000505284.1:p.Gln2253=
ENST00000680534.1:c.6939A>G	ENSP00000506674.1:p.Gln2313=
ENST00000680766.1:c.6876A>G	ENSP00000505204.1:p.Gln2292=
ENST00000680952.1:c.6876A>G	ENSP00000506407.1:p.Gln2292=
ENST00000681216.1:c.393A>G	ENSP00000505551.1:p.Gln131=
ENST00000681412.1:c.6900A>G	ENSP00000506486.1:p.Gln2300=
ENST00000681722.1:c.6876A>G	ENSP00000506566.1:p.Gln2292=
ENST00000356239.7:c.6900A>G	ENSP00000348573.3:p.Gln2300=
ENST00000358100.6:c.6759A>G	ENSP00000350813.3:p.Gln2253=
ENST00000359028.6:c.6933A>G	ENSP00000351922.3:p.Gln2311=
ENST00000394534.6:c.438A>G	ENSP00000378042.2:p.Gln146=
NM_005751.4:c.6900A>G , LRG_331t1:c.6900A>G	NP_005742.4:p.Gln2300=
NM_147185.2:c.6876A>G	NP_671714.1:p.Gln2292=
XM_006715827.1:c.6759A>G	XP_006715890.1:p.Gln2253=
XM_011515709.1:c.7047A>G	XP_011514011.1:p.Gln2349=
XM_011515710.1:c.7071A>G	XP_011514012.1:p.Gln2357=
XM_011515711.1:c.7011A>G	XP_011514013.1:p.Gln2337=
XM_011515712.1:c.7008A>G	XP_011514014.1:p.Gln2336=
XM_011515713.1:c.6993A>G	XP_011514015.1:p.Gln2331=
XM_011515714.1:c.7032A>G	XP_011514016.1:p.Gln2344=
XM_011515716.1:c.6951A>G	XP_011514018.1:p.Gln2317=
XM_011515717.1:c.6906A>G	XP_011514019.1:p.Gln2302=
XM_011515718.1:c.6936A>G	XP_011514020.1:p.Gln2312=
XM_011515719.1:c.6912A>G	XP_011514021.1:p.Gln2304=
XM_011515720.1:c.6795A>G	XP_011514022.1:p.Gln2265=
XM_011515721.1:c.1560A>G	XP_011514023.1:p.Gln520=
XM_011515722.1:c.1521A>G	XP_011514024.1:p.Gln507=
XM_017011642.2:c.7035A>G	XP_016867131.1:p.Gln2345=
XM_017011643.2:c.6996A>G	XP_016867132.1:p.Gln2332=
XM_017011644.2:c.7035A>G	XP_016867133.1:p.Gln2345=
XM_017011645.2:c.6981A>G	XP_016867134.1:p.Gln2327=
XM_017011646.2:c.6996A>G	XP_016867135.1:p.Gln2332=
XM_017011647.2:c.6942A>G	XP_016867136.1:p.Gln2314=
XM_017011648.2:c.6939A>G	XP_016867137.1:p.Gln2313=
XM_017011649.2:c.6972A>G	XP_016867138.1:p.Gln2324=
XM_017011650.2:c.6900A>G	XP_016867139.1:p.Gln2300=
XM_017011651.2:c.6894A>G	XP_016867140.1:p.Gln2298=
XM_017011652.2:c.7035A>G	XP_016867141.1:p.Gln2345=
XM_017011653.2:c.6807A>G	XP_016867142.1:p.Gln2269=
XM_017011654.2:c.6759A>G	XP_016867143.1:p.Gln2253=
XM_017011655.2:c.6663A>G	XP_016867144.1:p.Gln2221=
XM_017011656.2:c.6663A>G	XP_016867145.1:p.Gln2221=
XM_017011657.2:c.2700A>G	XP_016867146.1:p.Gln900=
XM_017011658.2:c.1584A>G	XP_016867147.1:p.Gln528=
XM_017011659.2:c.1545A>G	XP_016867148.1:p.Gln515=
XM_017011660.2:c.1545A>G	XP_016867149.1:p.Gln515=
XM_024446631.1:c.6798A>G	XP_024302399.1:p.Gln2266=
NM_147185.3:c.6876A>G	NP_671714.1:p.Gln2292=
NM_001379277.1:c.1545A>G	NP_001366206.1:p.Gln515=
NM_005751.5:c.6900A>G MANE Select	NP_005742.4:p.Gln2300=