Canonical Allele Identifier: CA456450494

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707153A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077839A>G , CM000669.2:g.92077839A>G	GRCh38
NC_000007.13:g.91707153A>G , CM000669.1:g.91707153A>G	GRCh37
NC_000007.12:g.91545089A>G	NCBI36
NG_011623.1:g.141965A>G , LRG_331:g.141965A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6909A>G MANE Select	ENSP00000348573.3:p.Lys2303=
ENST00000359028.7:c.6981A>G	ENSP00000351922.4:p.Lys2327=
ENST00000394534.7:c.402A>G	ENSP00000378042.3:p.Lys134=
ENST00000491695.2:c.1554A>G	ENSP00000494626.2:p.Lys518=
ENST00000674381.2:c.*6638A>G	ENSP00000501536.2:n.*6638A>G
ENST00000679448.1:c.6885A>G	ENSP00000505889.1:p.Lys2295=
ENST00000679457.1:c.6885A>G	ENSP00000505450.1:p.Lys2295=
ENST00000679474.1:n.7107A>G
ENST00000679521.1:c.6855A>G	ENSP00000505456.1:p.Lys2285=
ENST00000679554.1:c.*6694A>G	ENSP00000506415.1:n.*6694A>G
ENST00000679722.1:n.7131A>G
ENST00000679821.1:c.6651A>G	ENSP00000506040.1:p.Lys2217=
ENST00000680047.1:n.7107A>G
ENST00000680072.1:c.6732A>G	ENSP00000506581.1:p.Lys2244=
ENST00000680181.1:c.6816A>G	ENSP00000505548.1:p.Lys2272=
ENST00000680365.1:c.402A>G	ENSP00000506019.1:p.Lys134=
ENST00000680513.1:c.6768A>G	ENSP00000505284.1:p.Lys2256=
ENST00000680534.1:c.6948A>G	ENSP00000506674.1:p.Lys2316=
ENST00000680766.1:c.6885A>G	ENSP00000505204.1:p.Lys2295=
ENST00000680952.1:c.6885A>G	ENSP00000506407.1:p.Lys2295=
ENST00000681216.1:c.402A>G	ENSP00000505551.1:p.Lys134=
ENST00000681412.1:c.6909A>G	ENSP00000506486.1:p.Lys2303=
ENST00000681722.1:c.6885A>G	ENSP00000506566.1:p.Lys2295=
ENST00000356239.7:c.6909A>G	ENSP00000348573.3:p.Lys2303=
ENST00000358100.6:c.6768A>G	ENSP00000350813.3:p.Lys2256=
ENST00000359028.6:c.6942A>G	ENSP00000351922.3:p.Lys2314=
ENST00000394534.6:c.447A>G	ENSP00000378042.2:p.Lys149=
NM_005751.4:c.6909A>G , LRG_331t1:c.6909A>G	NP_005742.4:p.Lys2303=
NM_147185.2:c.6885A>G	NP_671714.1:p.Lys2295=
XM_006715827.1:c.6768A>G	XP_006715890.1:p.Lys2256=
XM_011515709.1:c.7056A>G	XP_011514011.1:p.Lys2352=
XM_011515710.1:c.7080A>G	XP_011514012.1:p.Lys2360=
XM_011515711.1:c.7020A>G	XP_011514013.1:p.Lys2340=
XM_011515712.1:c.7017A>G	XP_011514014.1:p.Lys2339=
XM_011515713.1:c.7002A>G	XP_011514015.1:p.Lys2334=
XM_011515714.1:c.7041A>G	XP_011514016.1:p.Lys2347=
XM_011515716.1:c.6960A>G	XP_011514018.1:p.Lys2320=
XM_011515717.1:c.6915A>G	XP_011514019.1:p.Lys2305=
XM_011515718.1:c.6945A>G	XP_011514020.1:p.Lys2315=
XM_011515719.1:c.6921A>G	XP_011514021.1:p.Lys2307=
XM_011515720.1:c.6804A>G	XP_011514022.1:p.Lys2268=
XM_011515721.1:c.1569A>G	XP_011514023.1:p.Lys523=
XM_011515722.1:c.1530A>G	XP_011514024.1:p.Lys510=
XM_017011642.2:c.7044A>G	XP_016867131.1:p.Lys2348=
XM_017011643.2:c.7005A>G	XP_016867132.1:p.Lys2335=
XM_017011644.2:c.7044A>G	XP_016867133.1:p.Lys2348=
XM_017011645.2:c.6990A>G	XP_016867134.1:p.Lys2330=
XM_017011646.2:c.7005A>G	XP_016867135.1:p.Lys2335=
XM_017011647.2:c.6951A>G	XP_016867136.1:p.Lys2317=
XM_017011648.2:c.6948A>G	XP_016867137.1:p.Lys2316=
XM_017011649.2:c.6981A>G	XP_016867138.1:p.Lys2327=
XM_017011650.2:c.6909A>G	XP_016867139.1:p.Lys2303=
XM_017011651.2:c.6903A>G	XP_016867140.1:p.Lys2301=
XM_017011652.2:c.7044A>G	XP_016867141.1:p.Lys2348=
XM_017011653.2:c.6816A>G	XP_016867142.1:p.Lys2272=
XM_017011654.2:c.6768A>G	XP_016867143.1:p.Lys2256=
XM_017011655.2:c.6672A>G	XP_016867144.1:p.Lys2224=
XM_017011656.2:c.6672A>G	XP_016867145.1:p.Lys2224=
XM_017011657.2:c.2709A>G	XP_016867146.1:p.Lys903=
XM_017011658.2:c.1593A>G	XP_016867147.1:p.Lys531=
XM_017011659.2:c.1554A>G	XP_016867148.1:p.Lys518=
XM_017011660.2:c.1554A>G	XP_016867149.1:p.Lys518=
XM_024446631.1:c.6807A>G	XP_024302399.1:p.Lys2269=
NM_147185.3:c.6885A>G	NP_671714.1:p.Lys2295=
NM_001379277.1:c.1554A>G	NP_001366206.1:p.Lys518=
NM_005751.5:c.6909A>G MANE Select	NP_005742.4:p.Lys2303=