Canonical Allele Identifier: CA368133603

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707041A>C (hg19) ; chr7:g.92077727A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077727A>C , CM000669.2:g.92077727A>C	GRCh38
NC_000007.13:g.91707041A>C , CM000669.1:g.91707041A>C	GRCh37
NC_000007.12:g.91544977A>C	NCBI36
NG_011623.1:g.141853A>C , LRG_331:g.141853A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6797A>C MANE Select	ENSP00000348573.3:p.Lys2266Thr
ENST00000359028.7:c.6869A>C	ENSP00000351922.4:p.Lys2290Thr
ENST00000394534.7:c.290A>C	ENSP00000378042.3:p.Lys97Thr
ENST00000491695.2:c.1442A>C	ENSP00000494626.2:p.Lys481Thr
ENST00000674381.2:c.*6526A>C	ENSP00000501536.2:n.*6526A>C
ENST00000679448.1:c.6773A>C	ENSP00000505889.1:p.Lys2258Thr
ENST00000679457.1:c.6773A>C	ENSP00000505450.1:p.Lys2258Thr
ENST00000679474.1:n.6995A>C
ENST00000679521.1:c.6743A>C	ENSP00000505456.1:p.Lys2248Thr
ENST00000679554.1:c.*6582A>C	ENSP00000506415.1:n.*6582A>C
ENST00000679722.1:n.7019A>C
ENST00000679821.1:c.6539A>C	ENSP00000506040.1:p.Lys2180Thr
ENST00000680047.1:n.6995A>C
ENST00000680072.1:c.6620A>C	ENSP00000506581.1:p.Lys2207Thr
ENST00000680181.1:c.6704A>C	ENSP00000505548.1:p.Lys2235Thr
ENST00000680365.1:c.290A>C	ENSP00000506019.1:p.Lys97Thr
ENST00000680513.1:c.6656A>C	ENSP00000505284.1:p.Lys2219Thr
ENST00000680534.1:c.6836A>C	ENSP00000506674.1:p.Lys2279Thr
ENST00000680766.1:c.6773A>C	ENSP00000505204.1:p.Lys2258Thr
ENST00000680952.1:c.6773A>C	ENSP00000506407.1:p.Lys2258Thr
ENST00000681216.1:c.290A>C	ENSP00000505551.1:p.Lys97Thr
ENST00000681412.1:c.6797A>C	ENSP00000506486.1:p.Lys2266Thr
ENST00000681722.1:c.6773A>C	ENSP00000506566.1:p.Lys2258Thr
ENST00000356239.7:c.6797A>C	ENSP00000348573.3:p.Lys2266Thr
ENST00000358100.6:c.6656A>C	ENSP00000350813.3:p.Lys2219Thr
ENST00000359028.6:c.6830A>C	ENSP00000351922.3:p.Lys2277Thr
ENST00000394534.6:c.335A>C	ENSP00000378042.2:p.Lys112Thr
NM_005751.4:c.6797A>C , LRG_331t1:c.6797A>C	NP_005742.4:p.Lys2266Thr
NM_147185.2:c.6773A>C	NP_671714.1:p.Lys2258Thr
XM_006715827.1:c.6656A>C	XP_006715890.1:p.Lys2219Thr
XM_011515709.1:c.6944A>C	XP_011514011.1:p.Lys2315Thr
XM_011515710.1:c.6968A>C	XP_011514012.1:p.Lys2323Thr
XM_011515711.1:c.6908A>C	XP_011514013.1:p.Lys2303Thr
XM_011515712.1:c.6905A>C	XP_011514014.1:p.Lys2302Thr
XM_011515713.1:c.6890A>C	XP_011514015.1:p.Lys2297Thr
XM_011515714.1:c.6929A>C	XP_011514016.1:p.Lys2310Thr
XM_011515716.1:c.6848A>C	XP_011514018.1:p.Lys2283Thr
XM_011515717.1:c.6803A>C	XP_011514019.1:p.Lys2268Thr
XM_011515718.1:c.6833A>C	XP_011514020.1:p.Lys2278Thr
XM_011515719.1:c.6809A>C	XP_011514021.1:p.Lys2270Thr
XM_011515720.1:c.6692A>C	XP_011514022.1:p.Lys2231Thr
XM_011515721.1:c.1457A>C	XP_011514023.1:p.Lys486Thr
XM_011515722.1:c.1418A>C	XP_011514024.1:p.Lys473Thr
XM_017011642.2:c.6932A>C	XP_016867131.1:p.Lys2311Thr
XM_017011643.2:c.6893A>C	XP_016867132.1:p.Lys2298Thr
XM_017011644.2:c.6932A>C	XP_016867133.1:p.Lys2311Thr
XM_017011645.2:c.6878A>C	XP_016867134.1:p.Lys2293Thr
XM_017011646.2:c.6893A>C	XP_016867135.1:p.Lys2298Thr
XM_017011647.2:c.6839A>C	XP_016867136.1:p.Lys2280Thr
XM_017011648.2:c.6836A>C	XP_016867137.1:p.Lys2279Thr
XM_017011649.2:c.6869A>C	XP_016867138.1:p.Lys2290Thr
XM_017011650.2:c.6797A>C	XP_016867139.1:p.Lys2266Thr
XM_017011651.2:c.6791A>C	XP_016867140.1:p.Lys2264Thr
XM_017011652.2:c.6932A>C	XP_016867141.1:p.Lys2311Thr
XM_017011653.2:c.6704A>C	XP_016867142.1:p.Lys2235Thr
XM_017011654.2:c.6656A>C	XP_016867143.1:p.Lys2219Thr
XM_017011655.2:c.6560A>C	XP_016867144.1:p.Lys2187Thr
XM_017011656.2:c.6560A>C	XP_016867145.1:p.Lys2187Thr
XM_017011657.2:c.2597A>C	XP_016867146.1:p.Lys866Thr
XM_017011658.2:c.1481A>C	XP_016867147.1:p.Lys494Thr
XM_017011659.2:c.1442A>C	XP_016867148.1:p.Lys481Thr
XM_017011660.2:c.1442A>C	XP_016867149.1:p.Lys481Thr
XM_024446631.1:c.6695A>C	XP_024302399.1:p.Lys2232Thr
NM_147185.3:c.6773A>C	NP_671714.1:p.Lys2258Thr
NM_001379277.1:c.1442A>C	NP_001366206.1:p.Lys481Thr
NM_005751.5:c.6797A>C MANE Select	NP_005742.4:p.Lys2266Thr