Canonical Allele Identifier: CA368135459

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91708761A>C (hg19) ; chr7:g.92079447A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92079447A>C , CM000669.2:g.92079447A>C	GRCh38
NC_000007.13:g.91708761A>C , CM000669.1:g.91708761A>C	GRCh37
NC_000007.12:g.91546697A>C	NCBI36
NG_011623.1:g.143573A>C , LRG_331:g.143573A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.7314A>C MANE Select	ENSP00000348573.3:p.Glu2438Asp
ENST00000359028.7:c.7386A>C	ENSP00000351922.4:p.Glu2462Asp
ENST00000394534.7:c.807A>C	ENSP00000378042.3:p.Glu269Asp
ENST00000491695.2:c.1959A>C	ENSP00000494626.2:p.Glu653Asp
ENST00000674381.2:c.*7043A>C	ENSP00000501536.2:n.*7043A>C
ENST00000679448.1:c.7290A>C	ENSP00000505889.1:p.Glu2430Asp
ENST00000679457.1:c.7290A>C	ENSP00000505450.1:p.Glu2430Asp
ENST00000679474.1:n.7512A>C
ENST00000679521.1:c.7260A>C	ENSP00000505456.1:p.Glu2420Asp
ENST00000679554.1:c.*7099A>C	ENSP00000506415.1:n.*7099A>C
ENST00000679722.1:n.7536A>C
ENST00000679821.1:c.7056A>C	ENSP00000506040.1:p.Glu2352Asp
ENST00000680047.1:n.7512A>C
ENST00000680072.1:c.7137A>C	ENSP00000506581.1:p.Glu2379Asp
ENST00000680181.1:c.7221A>C	ENSP00000505548.1:p.Glu2407Asp
ENST00000680365.1:c.807A>C	ENSP00000506019.1:p.Glu269Asp
ENST00000680513.1:c.7173A>C	ENSP00000505284.1:p.Glu2391Asp
ENST00000680534.1:c.7353A>C	ENSP00000506674.1:p.Glu2451Asp
ENST00000680766.1:c.7290A>C	ENSP00000505204.1:p.Glu2430Asp
ENST00000680952.1:c.7290A>C	ENSP00000506407.1:p.Glu2430Asp
ENST00000681216.1:c.807A>C	ENSP00000505551.1:p.Glu269Asp
ENST00000681412.1:c.7314A>C	ENSP00000506486.1:p.Glu2438Asp
ENST00000681722.1:c.7290A>C	ENSP00000506566.1:p.Glu2430Asp
ENST00000356239.7:c.7314A>C	ENSP00000348573.3:p.Glu2438Asp
ENST00000358100.6:c.7173A>C	ENSP00000350813.3:p.Glu2391Asp
ENST00000359028.6:c.7347A>C	ENSP00000351922.3:p.Glu2449Asp
ENST00000394534.6:c.852A>C	ENSP00000378042.2:p.Glu284Asp
NM_005751.4:c.7314A>C , LRG_331t1:c.7314A>C	NP_005742.4:p.Glu2438Asp
NM_147185.2:c.7290A>C	NP_671714.1:p.Glu2430Asp
XM_006715827.1:c.7173A>C	XP_006715890.1:p.Glu2391Asp
XM_011515709.1:c.7461A>C	XP_011514011.1:p.Glu2487Asp
XM_011515710.1:c.7485A>C	XP_011514012.1:p.Glu2495Asp
XM_011515711.1:c.7425A>C	XP_011514013.1:p.Glu2475Asp
XM_011515712.1:c.7422A>C	XP_011514014.1:p.Glu2474Asp
XM_011515713.1:c.7407A>C	XP_011514015.1:p.Glu2469Asp
XM_011515714.1:c.7446A>C	XP_011514016.1:p.Glu2482Asp
XM_011515716.1:c.7365A>C	XP_011514018.1:p.Glu2455Asp
XM_011515717.1:c.7320A>C	XP_011514019.1:p.Glu2440Asp
XM_011515718.1:c.7350A>C	XP_011514020.1:p.Glu2450Asp
XM_011515719.1:c.7326A>C	XP_011514021.1:p.Glu2442Asp
XM_011515720.1:c.7209A>C	XP_011514022.1:p.Glu2403Asp
XM_011515721.1:c.1974A>C	XP_011514023.1:p.Glu658Asp
XM_011515722.1:c.1935A>C	XP_011514024.1:p.Glu645Asp
XM_017011642.2:c.7449A>C	XP_016867131.1:p.Glu2483Asp
XM_017011643.2:c.7410A>C	XP_016867132.1:p.Glu2470Asp
XM_017011644.2:c.7449A>C	XP_016867133.1:p.Glu2483Asp
XM_017011645.2:c.7395A>C	XP_016867134.1:p.Glu2465Asp
XM_017011646.2:c.7410A>C	XP_016867135.1:p.Glu2470Asp
XM_017011647.2:c.7356A>C	XP_016867136.1:p.Glu2452Asp
XM_017011648.2:c.7353A>C	XP_016867137.1:p.Glu2451Asp
XM_017011649.2:c.7386A>C	XP_016867138.1:p.Glu2462Asp
XM_017011650.2:c.7314A>C	XP_016867139.1:p.Glu2438Asp
XM_017011651.2:c.7308A>C	XP_016867140.1:p.Glu2436Asp
XM_017011652.2:c.7449A>C	XP_016867141.1:p.Glu2483Asp
XM_017011653.2:c.7221A>C	XP_016867142.1:p.Glu2407Asp
XM_017011654.2:c.7173A>C	XP_016867143.1:p.Glu2391Asp
XM_017011655.2:c.7077A>C	XP_016867144.1:p.Glu2359Asp
XM_017011656.2:c.7077A>C	XP_016867145.1:p.Glu2359Asp
XM_017011657.2:c.3114A>C	XP_016867146.1:p.Glu1038Asp
XM_017011658.2:c.1998A>C	XP_016867147.1:p.Glu666Asp
XM_017011659.2:c.1959A>C	XP_016867148.1:p.Glu653Asp
XM_017011660.2:c.1959A>C	XP_016867149.1:p.Glu653Asp
XM_024446631.1:c.7212A>C	XP_024302399.1:p.Glu2404Asp
NM_147185.3:c.7290A>C	NP_671714.1:p.Glu2430Asp
NM_001379277.1:c.1959A>C	NP_001366206.1:p.Glu653Asp
NM_005751.5:c.7314A>C MANE Select	NP_005742.4:p.Glu2438Asp