Canonical Allele Identifier: CA4337199

Gene: AKAP9

Linked Data

• dbSNP Id: rs372381497
• ExAC: 7:91707177 A / G
• gnomAD v4: 7-92077863-A-G
• MyVariant Identifiers: chr7:g.91707177A>G (hg19) ; chr7:g.92077863A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077863A>G , CM000669.2:g.92077863A>G	GRCh38
NC_000007.13:g.91707177A>G , CM000669.1:g.91707177A>G	GRCh37
NC_000007.12:g.91545113A>G	NCBI36
NG_011623.1:g.141989A>G , LRG_331:g.141989A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6933A>G MANE Select	ENSP00000348573.3:p.Thr2311=
ENST00000359028.7:c.7005A>G	ENSP00000351922.4:p.Thr2335=
ENST00000394534.7:c.426A>G	ENSP00000378042.3:p.Thr142=
ENST00000491695.2:c.1578A>G	ENSP00000494626.2:p.Thr526=
ENST00000674381.2:c.*6662A>G	ENSP00000501536.2:n.*6662A>G
ENST00000679448.1:c.6909A>G	ENSP00000505889.1:p.Thr2303=
ENST00000679457.1:c.6909A>G	ENSP00000505450.1:p.Thr2303=
ENST00000679474.1:n.7131A>G
ENST00000679521.1:c.6879A>G	ENSP00000505456.1:p.Thr2293=
ENST00000679554.1:c.*6718A>G	ENSP00000506415.1:n.*6718A>G
ENST00000679722.1:n.7155A>G
ENST00000679821.1:c.6675A>G	ENSP00000506040.1:p.Thr2225=
ENST00000680047.1:n.7131A>G
ENST00000680072.1:c.6756A>G	ENSP00000506581.1:p.Thr2252=
ENST00000680181.1:c.6840A>G	ENSP00000505548.1:p.Thr2280=
ENST00000680365.1:c.426A>G	ENSP00000506019.1:p.Thr142=
ENST00000680513.1:c.6792A>G	ENSP00000505284.1:p.Thr2264=
ENST00000680534.1:c.6972A>G	ENSP00000506674.1:p.Thr2324=
ENST00000680766.1:c.6909A>G	ENSP00000505204.1:p.Thr2303=
ENST00000680952.1:c.6909A>G	ENSP00000506407.1:p.Thr2303=
ENST00000681216.1:c.426A>G	ENSP00000505551.1:p.Thr142=
ENST00000681412.1:c.6933A>G	ENSP00000506486.1:p.Thr2311=
ENST00000681722.1:c.6909A>G	ENSP00000506566.1:p.Thr2303=
ENST00000356239.7:c.6933A>G	ENSP00000348573.3:p.Thr2311=
ENST00000358100.6:c.6792A>G	ENSP00000350813.3:p.Thr2264=
ENST00000359028.6:c.6966A>G	ENSP00000351922.3:p.Thr2322=
ENST00000394534.6:c.471A>G	ENSP00000378042.2:p.Thr157=
NM_005751.4:c.6933A>G , LRG_331t1:c.6933A>G	NP_005742.4:p.Thr2311=
NM_147185.2:c.6909A>G	NP_671714.1:p.Thr2303=
XM_006715827.1:c.6792A>G	XP_006715890.1:p.Thr2264=
XM_011515709.1:c.7080A>G	XP_011514011.1:p.Thr2360=
XM_011515710.1:c.7104A>G	XP_011514012.1:p.Thr2368=
XM_011515711.1:c.7044A>G	XP_011514013.1:p.Thr2348=
XM_011515712.1:c.7041A>G	XP_011514014.1:p.Thr2347=
XM_011515713.1:c.7026A>G	XP_011514015.1:p.Thr2342=
XM_011515714.1:c.7065A>G	XP_011514016.1:p.Thr2355=
XM_011515716.1:c.6984A>G	XP_011514018.1:p.Thr2328=
XM_011515717.1:c.6939A>G	XP_011514019.1:p.Thr2313=
XM_011515718.1:c.6969A>G	XP_011514020.1:p.Thr2323=
XM_011515719.1:c.6945A>G	XP_011514021.1:p.Thr2315=
XM_011515720.1:c.6828A>G	XP_011514022.1:p.Thr2276=
XM_011515721.1:c.1593A>G	XP_011514023.1:p.Thr531=
XM_011515722.1:c.1554A>G	XP_011514024.1:p.Thr518=
XM_017011642.2:c.7068A>G	XP_016867131.1:p.Thr2356=
XM_017011643.2:c.7029A>G	XP_016867132.1:p.Thr2343=
XM_017011644.2:c.7068A>G	XP_016867133.1:p.Thr2356=
XM_017011645.2:c.7014A>G	XP_016867134.1:p.Thr2338=
XM_017011646.2:c.7029A>G	XP_016867135.1:p.Thr2343=
XM_017011647.2:c.6975A>G	XP_016867136.1:p.Thr2325=
XM_017011648.2:c.6972A>G	XP_016867137.1:p.Thr2324=
XM_017011649.2:c.7005A>G	XP_016867138.1:p.Thr2335=
XM_017011650.2:c.6933A>G	XP_016867139.1:p.Thr2311=
XM_017011651.2:c.6927A>G	XP_016867140.1:p.Thr2309=
XM_017011652.2:c.7068A>G	XP_016867141.1:p.Thr2356=
XM_017011653.2:c.6840A>G	XP_016867142.1:p.Thr2280=
XM_017011654.2:c.6792A>G	XP_016867143.1:p.Thr2264=
XM_017011655.2:c.6696A>G	XP_016867144.1:p.Thr2232=
XM_017011656.2:c.6696A>G	XP_016867145.1:p.Thr2232=
XM_017011657.2:c.2733A>G	XP_016867146.1:p.Thr911=
XM_017011658.2:c.1617A>G	XP_016867147.1:p.Thr539=
XM_017011659.2:c.1578A>G	XP_016867148.1:p.Thr526=
XM_017011660.2:c.1578A>G	XP_016867149.1:p.Thr526=
XM_024446631.1:c.6831A>G	XP_024302399.1:p.Thr2277=
NM_147185.3:c.6909A>G	NP_671714.1:p.Thr2303=
NM_001379277.1:c.1578A>G	NP_001366206.1:p.Thr526=
NM_005751.5:c.6933A>G MANE Select	NP_005742.4:p.Thr2311=