Canonical Allele Identifier: CA368129355

Gene: AKAP9

Linked Data

• gnomAD v4: 7-92040674-A-G
• MyVariant Identifiers: chr7:g.91669988A>G (hg19) ; chr7:g.92040674A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92040674A>G , CM000669.2:g.92040674A>G	GRCh38
NC_000007.13:g.91669988A>G , CM000669.1:g.91669988A>G	GRCh37
NC_000007.12:g.91507924A>G	NCBI36
NG_011623.1:g.104800A>G , LRG_331:g.104800A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.4693A>G MANE Select	ENSP00000348573.3:p.Ile1565Val
ENST00000359028.7:c.4693A>G	ENSP00000351922.4:p.Ile1565Val
ENST00000674381.2:c.*4422A>G	ENSP00000501536.2:n.*4422A>G
ENST00000679448.1:c.4693A>G	ENSP00000505889.1:p.Ile1565Val
ENST00000679457.1:c.4693A>G	ENSP00000505450.1:p.Ile1565Val
ENST00000679474.1:n.4915A>G
ENST00000679521.1:c.4639A>G	ENSP00000505456.1:p.Ile1547Val
ENST00000679554.1:c.*4478A>G	ENSP00000506415.1:n.*4478A>G
ENST00000679722.1:n.4915A>G
ENST00000679821.1:c.4435A>G	ENSP00000506040.1:p.Ile1479Val
ENST00000680047.1:n.4915A>G
ENST00000680072.1:c.4693A>G	ENSP00000506581.1:p.Ile1565Val
ENST00000680074.1:n.4915A>G
ENST00000680181.1:c.4600A>G	ENSP00000505548.1:p.Ile1534Val
ENST00000680513.1:c.4693A>G	ENSP00000505284.1:p.Ile1565Val
ENST00000680534.1:c.4693A>G	ENSP00000506674.1:p.Ile1565Val
ENST00000680766.1:c.4693A>G	ENSP00000505204.1:p.Ile1565Val
ENST00000680952.1:c.4693A>G	ENSP00000506407.1:p.Ile1565Val
ENST00000681412.1:c.4693A>G	ENSP00000506486.1:p.Ile1565Val
ENST00000681722.1:c.4693A>G	ENSP00000506566.1:p.Ile1565Val
ENST00000356239.7:c.4693A>G	ENSP00000348573.3:p.Ile1565Val
ENST00000358100.6:c.4693A>G	ENSP00000350813.3:p.Ile1565Val
ENST00000359028.6:c.4726A>G	ENSP00000351922.3:p.Ile1576Val
ENST00000493453.1:n.4913A>G
ENST00000619023.4:c.4717A>G	ENSP00000480807.1:p.Ile1573Val
NM_005751.4:c.4693A>G , LRG_331t1:c.4693A>G	NP_005742.4:p.Ile1565Val
NM_147185.2:c.4693A>G	NP_671714.1:p.Ile1565Val
XM_006715827.1:c.4693A>G	XP_006715890.1:p.Ile1565Val
XM_011515709.1:c.4729A>G	XP_011514011.1:p.Ile1577Val
XM_011515710.1:c.4729A>G	XP_011514012.1:p.Ile1577Val
XM_011515711.1:c.4693A>G	XP_011514013.1:p.Ile1565Val
XM_011515712.1:c.4729A>G	XP_011514014.1:p.Ile1577Val
XM_011515713.1:c.4675A>G	XP_011514015.1:p.Ile1559Val
XM_011515714.1:c.4729A>G	XP_011514016.1:p.Ile1577Val
XM_011515716.1:c.4729A>G	XP_011514018.1:p.Ile1577Val
XM_011515717.1:c.4729A>G	XP_011514019.1:p.Ile1577Val
XM_011515718.1:c.4729A>G	XP_011514020.1:p.Ile1577Val
XM_011515719.1:c.4729A>G	XP_011514021.1:p.Ile1577Val
XM_011515720.1:c.4729A>G	XP_011514022.1:p.Ile1577Val
XM_017011642.2:c.4693A>G	XP_016867131.1:p.Ile1565Val
XM_017011643.2:c.4693A>G	XP_016867132.1:p.Ile1565Val
XM_017011644.2:c.4693A>G	XP_016867133.1:p.Ile1565Val
XM_017011645.2:c.4639A>G	XP_016867134.1:p.Ile1547Val
XM_017011646.2:c.4693A>G	XP_016867135.1:p.Ile1565Val
XM_017011647.2:c.4600A>G	XP_016867136.1:p.Ile1534Val
XM_017011648.2:c.4693A>G	XP_016867137.1:p.Ile1565Val
XM_017011649.2:c.4693A>G	XP_016867138.1:p.Ile1565Val
XM_017011650.2:c.4693A>G	XP_016867139.1:p.Ile1565Val
XM_017011651.2:c.4693A>G	XP_016867140.1:p.Ile1565Val
XM_017011652.2:c.4693A>G	XP_016867141.1:p.Ile1565Val
XM_017011653.2:c.4600A>G	XP_016867142.1:p.Ile1534Val
XM_017011654.2:c.4693A>G	XP_016867143.1:p.Ile1565Val
XM_017011655.2:c.4321A>G	XP_016867144.1:p.Ile1441Val
XM_017011656.2:c.4321A>G	XP_016867145.1:p.Ile1441Val
XM_017011657.2:c.358A>G	XP_016867146.1:p.Ile120Val
XM_024446631.1:c.4693A>G	XP_024302399.1:p.Ile1565Val
NM_147185.3:c.4693A>G	NP_671714.1:p.Ile1565Val
NM_005751.5:c.4693A>G MANE Select	NP_005742.4:p.Ile1565Val