Canonical Allele Identifier: CA2776933695

Gene: AKAP9

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92040650_92040651insGT , CM000669.2:g.92040650_92040651insGT	GRCh38
NC_000007.13:g.91669964_91669965insGT , CM000669.1:g.91669964_91669965insGT	GRCh37
NC_000007.12:g.91507900_91507901insGT	NCBI36
NG_011623.1:g.104776_104777insGT , LRG_331:g.104776_104777insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.4693-24_4693-23insGT MANE Select	ENSP00000348573.3:n.4693-24_4693-23insGT
ENST00000359028.7:c.4693-24_4693-23insGT	ENSP00000351922.4:n.4693-24_4693-23insGT
ENST00000674381.2:c.*4422-24_*4422-23insGT	ENSP00000501536.2:n.*4422-24_*4422-23insGT
ENST00000679448.1:c.4693-24_4693-23insGT	ENSP00000505889.1:n.4693-24_4693-23insGT
ENST00000679457.1:c.4693-24_4693-23insGT	ENSP00000505450.1:n.4693-24_4693-23insGT
ENST00000679474.1:n.4915-24_4915-23insGT
ENST00000679521.1:c.4639-24_4639-23insGT	ENSP00000505456.1:n.4639-24_4639-23insGT
ENST00000679554.1:c.*4478-24_*4478-23insGT	ENSP00000506415.1:n.*4478-24_*4478-23insGT
ENST00000679722.1:n.4915-24_4915-23insGT
ENST00000679821.1:c.4435-24_4435-23insGT	ENSP00000506040.1:n.4435-24_4435-23insGT
ENST00000680047.1:n.4915-24_4915-23insGT
ENST00000680072.1:c.4693-24_4693-23insGT	ENSP00000506581.1:n.4693-24_4693-23insGT
ENST00000680074.1:n.4915-24_4915-23insGT
ENST00000680181.1:c.4600-24_4600-23insGT	ENSP00000505548.1:n.4600-24_4600-23insGT
ENST00000680513.1:c.4693-24_4693-23insGT	ENSP00000505284.1:n.4693-24_4693-23insGT
ENST00000680534.1:c.4693-24_4693-23insGT	ENSP00000506674.1:n.4693-24_4693-23insGT
ENST00000680766.1:c.4693-24_4693-23insGT	ENSP00000505204.1:n.4693-24_4693-23insGT
ENST00000680952.1:c.4693-24_4693-23insGT	ENSP00000506407.1:n.4693-24_4693-23insGT
ENST00000681412.1:c.4693-24_4693-23insGT	ENSP00000506486.1:n.4693-24_4693-23insGT
ENST00000681722.1:c.4693-24_4693-23insGT	ENSP00000506566.1:n.4693-24_4693-23insGT
ENST00000356239.7:c.4693-24_4693-23insGT	ENSP00000348573.3:n.4693-24_4693-23insGT
ENST00000358100.6:c.4693-24_4693-23insGT	ENSP00000350813.3:n.4693-24_4693-23insGT
ENST00000359028.6:c.4726-24_4726-23insGT	ENSP00000351922.3:n.4726-24_4726-23insGT
ENST00000493453.1:n.4913-24_4913-23insGT
ENST00000619023.4:c.4717-24_4717-23insGT	ENSP00000480807.1:n.4717-24_4717-23insGT
NM_005751.4:c.4693-24_4693-23insGT , LRG_331t1:c.4693-24_4693-23insGT	NP_005742.4:n.4693-24_4693-23insGT
NM_147185.2:c.4693-24_4693-23insGT	NP_671714.1:n.4693-24_4693-23insGT
XM_006715827.1:c.4693-24_4693-23insGT	XP_006715890.1:n.4693-24_4693-23insGT
XM_011515709.1:c.4729-24_4729-23insGT	XP_011514011.1:n.4729-24_4729-23insGT
XM_011515710.1:c.4729-24_4729-23insGT	XP_011514012.1:n.4729-24_4729-23insGT
XM_011515711.1:c.4693-24_4693-23insGT	XP_011514013.1:n.4693-24_4693-23insGT
XM_011515712.1:c.4729-24_4729-23insGT	XP_011514014.1:n.4729-24_4729-23insGT
XM_011515713.1:c.4675-24_4675-23insGT	XP_011514015.1:n.4675-24_4675-23insGT
XM_011515714.1:c.4729-24_4729-23insGT	XP_011514016.1:n.4729-24_4729-23insGT
XM_011515716.1:c.4729-24_4729-23insGT	XP_011514018.1:n.4729-24_4729-23insGT
XM_011515717.1:c.4729-24_4729-23insGT	XP_011514019.1:n.4729-24_4729-23insGT
XM_011515718.1:c.4729-24_4729-23insGT	XP_011514020.1:n.4729-24_4729-23insGT
XM_011515719.1:c.4729-24_4729-23insGT	XP_011514021.1:n.4729-24_4729-23insGT
XM_011515720.1:c.4729-24_4729-23insGT	XP_011514022.1:n.4729-24_4729-23insGT
XM_017011642.2:c.4693-24_4693-23insGT	XP_016867131.1:n.4693-24_4693-23insGT
XM_017011643.2:c.4693-24_4693-23insGT	XP_016867132.1:n.4693-24_4693-23insGT
XM_017011644.2:c.4693-24_4693-23insGT	XP_016867133.1:n.4693-24_4693-23insGT
XM_017011645.2:c.4639-24_4639-23insGT	XP_016867134.1:n.4639-24_4639-23insGT
XM_017011646.2:c.4693-24_4693-23insGT	XP_016867135.1:n.4693-24_4693-23insGT
XM_017011647.2:c.4600-24_4600-23insGT	XP_016867136.1:n.4600-24_4600-23insGT
XM_017011648.2:c.4693-24_4693-23insGT	XP_016867137.1:n.4693-24_4693-23insGT
XM_017011649.2:c.4693-24_4693-23insGT	XP_016867138.1:n.4693-24_4693-23insGT
XM_017011650.2:c.4693-24_4693-23insGT	XP_016867139.1:n.4693-24_4693-23insGT
XM_017011651.2:c.4693-24_4693-23insGT	XP_016867140.1:n.4693-24_4693-23insGT
XM_017011652.2:c.4693-24_4693-23insGT	XP_016867141.1:n.4693-24_4693-23insGT
XM_017011653.2:c.4600-24_4600-23insGT	XP_016867142.1:n.4600-24_4600-23insGT
XM_017011654.2:c.4693-24_4693-23insGT	XP_016867143.1:n.4693-24_4693-23insGT
XM_017011655.2:c.4321-24_4321-23insGT	XP_016867144.1:n.4321-24_4321-23insGT
XM_017011656.2:c.4321-24_4321-23insGT	XP_016867145.1:n.4321-24_4321-23insGT
XM_017011657.2:c.358-24_358-23insGT	XP_016867146.1:n.358-24_358-23insGT
XM_024446631.1:c.4693-24_4693-23insGT	XP_024302399.1:n.4693-24_4693-23insGT
NM_147185.3:c.4693-24_4693-23insGT	NP_671714.1:n.4693-24_4693-23insGT
NM_005751.5:c.4693-24_4693-23insGT MANE Select	NP_005742.4:n.4693-24_4693-23insGT