Canonical Allele Identifier: CA368133610

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707044A>G (hg19) ; chr7:g.92077730A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077730A>G , CM000669.2:g.92077730A>G	GRCh38
NC_000007.13:g.91707044A>G , CM000669.1:g.91707044A>G	GRCh37
NC_000007.12:g.91544980A>G	NCBI36
NG_011623.1:g.141856A>G , LRG_331:g.141856A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000356239.8:c.6800A>G MANE Select	ENSP00000348573.3:p.Glu2267Gly
ENST00000359028.7:c.6872A>G	ENSP00000351922.4:p.Glu2291Gly
ENST00000394534.7:c.293A>G	ENSP00000378042.3:p.Glu98Gly
ENST00000491695.2:c.1445A>G	ENSP00000494626.2:p.Glu482Gly
ENST00000674381.2:c.*6529A>G	ENSP00000501536.2:n.*6529A>G
ENST00000679448.1:c.6776A>G	ENSP00000505889.1:p.Glu2259Gly
ENST00000679457.1:c.6776A>G	ENSP00000505450.1:p.Glu2259Gly
ENST00000679474.1:n.6998A>G
ENST00000679521.1:c.6746A>G	ENSP00000505456.1:p.Glu2249Gly
ENST00000679554.1:c.*6585A>G	ENSP00000506415.1:n.*6585A>G
ENST00000679722.1:n.7022A>G
ENST00000679821.1:c.6542A>G	ENSP00000506040.1:p.Glu2181Gly
ENST00000680047.1:n.6998A>G
ENST00000680072.1:c.6623A>G	ENSP00000506581.1:p.Glu2208Gly
ENST00000680181.1:c.6707A>G	ENSP00000505548.1:p.Glu2236Gly
ENST00000680365.1:c.293A>G	ENSP00000506019.1:p.Glu98Gly
ENST00000680513.1:c.6659A>G	ENSP00000505284.1:p.Glu2220Gly
ENST00000680534.1:c.6839A>G	ENSP00000506674.1:p.Glu2280Gly
ENST00000680766.1:c.6776A>G	ENSP00000505204.1:p.Glu2259Gly
ENST00000680952.1:c.6776A>G	ENSP00000506407.1:p.Glu2259Gly
ENST00000681216.1:c.293A>G	ENSP00000505551.1:p.Glu98Gly
ENST00000681412.1:c.6800A>G	ENSP00000506486.1:p.Glu2267Gly
ENST00000681722.1:c.6776A>G	ENSP00000506566.1:p.Glu2259Gly
ENST00000356239.7:c.6800A>G	ENSP00000348573.3:p.Glu2267Gly
ENST00000358100.6:c.6659A>G	ENSP00000350813.3:p.Glu2220Gly
ENST00000359028.6:c.6833A>G	ENSP00000351922.3:p.Glu2278Gly
ENST00000394534.6:c.338A>G	ENSP00000378042.2:p.Glu113Gly
NM_005751.4:c.6800A>G , LRG_331t1:c.6800A>G	NP_005742.4:p.Glu2267Gly
NM_147185.2:c.6776A>G	NP_671714.1:p.Glu2259Gly
XM_006715827.1:c.6659A>G	XP_006715890.1:p.Glu2220Gly
XM_011515709.1:c.6947A>G	XP_011514011.1:p.Glu2316Gly
XM_011515710.1:c.6971A>G	XP_011514012.1:p.Glu2324Gly
XM_011515711.1:c.6911A>G	XP_011514013.1:p.Glu2304Gly
XM_011515712.1:c.6908A>G	XP_011514014.1:p.Glu2303Gly
XM_011515713.1:c.6893A>G	XP_011514015.1:p.Glu2298Gly
XM_011515714.1:c.6932A>G	XP_011514016.1:p.Glu2311Gly
XM_011515716.1:c.6851A>G	XP_011514018.1:p.Glu2284Gly
XM_011515717.1:c.6806A>G	XP_011514019.1:p.Glu2269Gly
XM_011515718.1:c.6836A>G	XP_011514020.1:p.Glu2279Gly
XM_011515719.1:c.6812A>G	XP_011514021.1:p.Glu2271Gly
XM_011515720.1:c.6695A>G	XP_011514022.1:p.Glu2232Gly
XM_011515721.1:c.1460A>G	XP_011514023.1:p.Glu487Gly
XM_011515722.1:c.1421A>G	XP_011514024.1:p.Glu474Gly
XM_017011642.2:c.6935A>G	XP_016867131.1:p.Glu2312Gly
XM_017011643.2:c.6896A>G	XP_016867132.1:p.Glu2299Gly
XM_017011644.2:c.6935A>G	XP_016867133.1:p.Glu2312Gly
XM_017011645.2:c.6881A>G	XP_016867134.1:p.Glu2294Gly
XM_017011646.2:c.6896A>G	XP_016867135.1:p.Glu2299Gly
XM_017011647.2:c.6842A>G	XP_016867136.1:p.Glu2281Gly
XM_017011648.2:c.6839A>G	XP_016867137.1:p.Glu2280Gly
XM_017011649.2:c.6872A>G	XP_016867138.1:p.Glu2291Gly
XM_017011650.2:c.6800A>G	XP_016867139.1:p.Glu2267Gly
XM_017011651.2:c.6794A>G	XP_016867140.1:p.Glu2265Gly
XM_017011652.2:c.6935A>G	XP_016867141.1:p.Glu2312Gly
XM_017011653.2:c.6707A>G	XP_016867142.1:p.Glu2236Gly
XM_017011654.2:c.6659A>G	XP_016867143.1:p.Glu2220Gly
XM_017011655.2:c.6563A>G	XP_016867144.1:p.Glu2188Gly
XM_017011656.2:c.6563A>G	XP_016867145.1:p.Glu2188Gly
XM_017011657.2:c.2600A>G	XP_016867146.1:p.Glu867Gly
XM_017011658.2:c.1484A>G	XP_016867147.1:p.Glu495Gly
XM_017011659.2:c.1445A>G	XP_016867148.1:p.Glu482Gly
XM_017011660.2:c.1445A>G	XP_016867149.1:p.Glu482Gly
XM_024446631.1:c.6698A>G	XP_024302399.1:p.Glu2233Gly
NM_147185.3:c.6776A>G	NP_671714.1:p.Glu2259Gly
NM_001379277.1:c.1445A>G	NP_001366206.1:p.Glu482Gly
NM_005751.5:c.6800A>G MANE Select	NP_005742.4:p.Glu2267Gly