Canonical Allele Identifier: CA368133908

Gene: AKAP9

Linked Data

• dbSNP Id: rs1812865171
• MyVariant Identifiers: chr7:g.91707173T>G (hg19) ; chr7:g.92077859T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077859T>G , CM000669.2:g.92077859T>G	GRCh38
NC_000007.13:g.91707173T>G , CM000669.1:g.91707173T>G	GRCh37
NC_000007.12:g.91545109T>G	NCBI36
NG_011623.1:g.141985T>G , LRG_331:g.141985T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6929T>G MANE Select	ENSP00000348573.3:p.Ile2310Ser
ENST00000359028.7:c.7001T>G	ENSP00000351922.4:p.Ile2334Ser
ENST00000394534.7:c.422T>G	ENSP00000378042.3:p.Ile141Ser
ENST00000491695.2:c.1574T>G	ENSP00000494626.2:p.Ile525Ser
ENST00000674381.2:c.*6658T>G	ENSP00000501536.2:n.*6658T>G
ENST00000679448.1:c.6905T>G	ENSP00000505889.1:p.Ile2302Ser
ENST00000679457.1:c.6905T>G	ENSP00000505450.1:p.Ile2302Ser
ENST00000679474.1:n.7127T>G
ENST00000679521.1:c.6875T>G	ENSP00000505456.1:p.Ile2292Ser
ENST00000679554.1:c.*6714T>G	ENSP00000506415.1:n.*6714T>G
ENST00000679722.1:n.7151T>G
ENST00000679821.1:c.6671T>G	ENSP00000506040.1:p.Ile2224Ser
ENST00000680047.1:n.7127T>G
ENST00000680072.1:c.6752T>G	ENSP00000506581.1:p.Ile2251Ser
ENST00000680181.1:c.6836T>G	ENSP00000505548.1:p.Ile2279Ser
ENST00000680365.1:c.422T>G	ENSP00000506019.1:p.Ile141Ser
ENST00000680513.1:c.6788T>G	ENSP00000505284.1:p.Ile2263Ser
ENST00000680534.1:c.6968T>G	ENSP00000506674.1:p.Ile2323Ser
ENST00000680766.1:c.6905T>G	ENSP00000505204.1:p.Ile2302Ser
ENST00000680952.1:c.6905T>G	ENSP00000506407.1:p.Ile2302Ser
ENST00000681216.1:c.422T>G	ENSP00000505551.1:p.Ile141Ser
ENST00000681412.1:c.6929T>G	ENSP00000506486.1:p.Ile2310Ser
ENST00000681722.1:c.6905T>G	ENSP00000506566.1:p.Ile2302Ser
ENST00000356239.7:c.6929T>G	ENSP00000348573.3:p.Ile2310Ser
ENST00000358100.6:c.6788T>G	ENSP00000350813.3:p.Ile2263Ser
ENST00000359028.6:c.6962T>G	ENSP00000351922.3:p.Ile2321Ser
ENST00000394534.6:c.467T>G	ENSP00000378042.2:p.Ile156Ser
NM_005751.4:c.6929T>G , LRG_331t1:c.6929T>G	NP_005742.4:p.Ile2310Ser
NM_147185.2:c.6905T>G	NP_671714.1:p.Ile2302Ser
XM_006715827.1:c.6788T>G	XP_006715890.1:p.Ile2263Ser
XM_011515709.1:c.7076T>G	XP_011514011.1:p.Ile2359Ser
XM_011515710.1:c.7100T>G	XP_011514012.1:p.Ile2367Ser
XM_011515711.1:c.7040T>G	XP_011514013.1:p.Ile2347Ser
XM_011515712.1:c.7037T>G	XP_011514014.1:p.Ile2346Ser
XM_011515713.1:c.7022T>G	XP_011514015.1:p.Ile2341Ser
XM_011515714.1:c.7061T>G	XP_011514016.1:p.Ile2354Ser
XM_011515716.1:c.6980T>G	XP_011514018.1:p.Ile2327Ser
XM_011515717.1:c.6935T>G	XP_011514019.1:p.Ile2312Ser
XM_011515718.1:c.6965T>G	XP_011514020.1:p.Ile2322Ser
XM_011515719.1:c.6941T>G	XP_011514021.1:p.Ile2314Ser
XM_011515720.1:c.6824T>G	XP_011514022.1:p.Ile2275Ser
XM_011515721.1:c.1589T>G	XP_011514023.1:p.Ile530Ser
XM_011515722.1:c.1550T>G	XP_011514024.1:p.Ile517Ser
XM_017011642.2:c.7064T>G	XP_016867131.1:p.Ile2355Ser
XM_017011643.2:c.7025T>G	XP_016867132.1:p.Ile2342Ser
XM_017011644.2:c.7064T>G	XP_016867133.1:p.Ile2355Ser
XM_017011645.2:c.7010T>G	XP_016867134.1:p.Ile2337Ser
XM_017011646.2:c.7025T>G	XP_016867135.1:p.Ile2342Ser
XM_017011647.2:c.6971T>G	XP_016867136.1:p.Ile2324Ser
XM_017011648.2:c.6968T>G	XP_016867137.1:p.Ile2323Ser
XM_017011649.2:c.7001T>G	XP_016867138.1:p.Ile2334Ser
XM_017011650.2:c.6929T>G	XP_016867139.1:p.Ile2310Ser
XM_017011651.2:c.6923T>G	XP_016867140.1:p.Ile2308Ser
XM_017011652.2:c.7064T>G	XP_016867141.1:p.Ile2355Ser
XM_017011653.2:c.6836T>G	XP_016867142.1:p.Ile2279Ser
XM_017011654.2:c.6788T>G	XP_016867143.1:p.Ile2263Ser
XM_017011655.2:c.6692T>G	XP_016867144.1:p.Ile2231Ser
XM_017011656.2:c.6692T>G	XP_016867145.1:p.Ile2231Ser
XM_017011657.2:c.2729T>G	XP_016867146.1:p.Ile910Ser
XM_017011658.2:c.1613T>G	XP_016867147.1:p.Ile538Ser
XM_017011659.2:c.1574T>G	XP_016867148.1:p.Ile525Ser
XM_017011660.2:c.1574T>G	XP_016867149.1:p.Ile525Ser
XM_024446631.1:c.6827T>G	XP_024302399.1:p.Ile2276Ser
NM_147185.3:c.6905T>G	NP_671714.1:p.Ile2302Ser
NM_001379277.1:c.1574T>G	NP_001366206.1:p.Ile525Ser
NM_005751.5:c.6929T>G MANE Select	NP_005742.4:p.Ile2310Ser