Canonical Allele Identifier: CA456450492

Gene: AKAP9

Linked Data

• dbSNP Id: rs746485312
• gnomAD v2: 7-91707150-G-T
• gnomAD v3: 7-92077836-G-T
• gnomAD v4: 7-92077836-G-T
• COSMIC: COSM5815897 ; COSM5815898
• MyVariant Identifiers: chr7:g.91707150G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077836G>T , CM000669.2:g.92077836G>T	GRCh38
NC_000007.13:g.91707150G>T , CM000669.1:g.91707150G>T	GRCh37
NC_000007.12:g.91545086G>T	NCBI36
NG_011623.1:g.141962G>T , LRG_331:g.141962G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6906G>T MANE Select	ENSP00000348573.3:p.Thr2302=
ENST00000359028.7:c.6978G>T	ENSP00000351922.4:p.Thr2326=
ENST00000394534.7:c.399G>T	ENSP00000378042.3:p.Thr133=
ENST00000491695.2:c.1551G>T	ENSP00000494626.2:p.Thr517=
ENST00000674381.2:c.*6635G>T	ENSP00000501536.2:n.*6635G>T
ENST00000679448.1:c.6882G>T	ENSP00000505889.1:p.Thr2294=
ENST00000679457.1:c.6882G>T	ENSP00000505450.1:p.Thr2294=
ENST00000679474.1:n.7104G>T
ENST00000679521.1:c.6852G>T	ENSP00000505456.1:p.Thr2284=
ENST00000679554.1:c.*6691G>T	ENSP00000506415.1:n.*6691G>T
ENST00000679722.1:n.7128G>T
ENST00000679821.1:c.6648G>T	ENSP00000506040.1:p.Thr2216=
ENST00000680047.1:n.7104G>T
ENST00000680072.1:c.6729G>T	ENSP00000506581.1:p.Thr2243=
ENST00000680181.1:c.6813G>T	ENSP00000505548.1:p.Thr2271=
ENST00000680365.1:c.399G>T	ENSP00000506019.1:p.Thr133=
ENST00000680513.1:c.6765G>T	ENSP00000505284.1:p.Thr2255=
ENST00000680534.1:c.6945G>T	ENSP00000506674.1:p.Thr2315=
ENST00000680766.1:c.6882G>T	ENSP00000505204.1:p.Thr2294=
ENST00000680952.1:c.6882G>T	ENSP00000506407.1:p.Thr2294=
ENST00000681216.1:c.399G>T	ENSP00000505551.1:p.Thr133=
ENST00000681412.1:c.6906G>T	ENSP00000506486.1:p.Thr2302=
ENST00000681722.1:c.6882G>T	ENSP00000506566.1:p.Thr2294=
ENST00000356239.7:c.6906G>T	ENSP00000348573.3:p.Thr2302=
ENST00000358100.6:c.6765G>T	ENSP00000350813.3:p.Thr2255=
ENST00000359028.6:c.6939G>T	ENSP00000351922.3:p.Thr2313=
ENST00000394534.6:c.444G>T	ENSP00000378042.2:p.Thr148=
NM_005751.4:c.6906G>T , LRG_331t1:c.6906G>T	NP_005742.4:p.Thr2302=
NM_147185.2:c.6882G>T	NP_671714.1:p.Thr2294=
XM_006715827.1:c.6765G>T	XP_006715890.1:p.Thr2255=
XM_011515709.1:c.7053G>T	XP_011514011.1:p.Thr2351=
XM_011515710.1:c.7077G>T	XP_011514012.1:p.Thr2359=
XM_011515711.1:c.7017G>T	XP_011514013.1:p.Thr2339=
XM_011515712.1:c.7014G>T	XP_011514014.1:p.Thr2338=
XM_011515713.1:c.6999G>T	XP_011514015.1:p.Thr2333=
XM_011515714.1:c.7038G>T	XP_011514016.1:p.Thr2346=
XM_011515716.1:c.6957G>T	XP_011514018.1:p.Thr2319=
XM_011515717.1:c.6912G>T	XP_011514019.1:p.Thr2304=
XM_011515718.1:c.6942G>T	XP_011514020.1:p.Thr2314=
XM_011515719.1:c.6918G>T	XP_011514021.1:p.Thr2306=
XM_011515720.1:c.6801G>T	XP_011514022.1:p.Thr2267=
XM_011515721.1:c.1566G>T	XP_011514023.1:p.Thr522=
XM_011515722.1:c.1527G>T	XP_011514024.1:p.Thr509=
XM_017011642.2:c.7041G>T	XP_016867131.1:p.Thr2347=
XM_017011643.2:c.7002G>T	XP_016867132.1:p.Thr2334=
XM_017011644.2:c.7041G>T	XP_016867133.1:p.Thr2347=
XM_017011645.2:c.6987G>T	XP_016867134.1:p.Thr2329=
XM_017011646.2:c.7002G>T	XP_016867135.1:p.Thr2334=
XM_017011647.2:c.6948G>T	XP_016867136.1:p.Thr2316=
XM_017011648.2:c.6945G>T	XP_016867137.1:p.Thr2315=
XM_017011649.2:c.6978G>T	XP_016867138.1:p.Thr2326=
XM_017011650.2:c.6906G>T	XP_016867139.1:p.Thr2302=
XM_017011651.2:c.6900G>T	XP_016867140.1:p.Thr2300=
XM_017011652.2:c.7041G>T	XP_016867141.1:p.Thr2347=
XM_017011653.2:c.6813G>T	XP_016867142.1:p.Thr2271=
XM_017011654.2:c.6765G>T	XP_016867143.1:p.Thr2255=
XM_017011655.2:c.6669G>T	XP_016867144.1:p.Thr2223=
XM_017011656.2:c.6669G>T	XP_016867145.1:p.Thr2223=
XM_017011657.2:c.2706G>T	XP_016867146.1:p.Thr902=
XM_017011658.2:c.1590G>T	XP_016867147.1:p.Thr530=
XM_017011659.2:c.1551G>T	XP_016867148.1:p.Thr517=
XM_017011660.2:c.1551G>T	XP_016867149.1:p.Thr517=
XM_024446631.1:c.6804G>T	XP_024302399.1:p.Thr2268=
NM_147185.3:c.6882G>T	NP_671714.1:p.Thr2294=
NM_001379277.1:c.1551G>T	NP_001366206.1:p.Thr517=
NM_005751.5:c.6906G>T MANE Select	NP_005742.4:p.Thr2302=