Canonical Allele Identifier: CA4336890
Community Standard Title: NM_005751.5(AKAP9):c.5668A>T (p.Thr1890Ser)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92061326A>T , CM000669.2:g.92061326A>T GRCh38
NC_000007.13:g.91690640A>T , CM000669.1:g.91690640A>T GRCh37
NC_000007.12:g.91528576A>T NCBI36
NG_011623.1:g.125452A>T , LRG_331:g.125452A>T

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.5668A>T MANE Select NP_005742.4:p.Thr1890Ser
ENST00000356239.8:c.5668A>T MANE Select ENSP00000348573.3:p.Thr1890Ser
NM_001379277.1:c.313A>T NP_001366206.1:p.Thr105Ser
NM_005751.4:c.5668A>T , LRG_331t1:c.5668A>T NP_005742.4:p.Thr1890Ser
NM_147185.2:c.5668A>T NP_671714.1:p.Thr1890Ser
NM_147185.3:c.5668A>T NP_671714.1:p.Thr1890Ser
ENST00000356239.7:c.5668A>T ENSP00000348573.3:p.Thr1890Ser
ENST00000358100.6:c.5527A>T ENSP00000350813.3:p.Thr1843Ser
ENST00000359028.6:c.5701A>T ENSP00000351922.3:p.Thr1901Ser
ENST00000359028.7:c.5764A>T ENSP00000351922.4:p.Thr1922Ser
ENST00000491695.1:n.856A>T
ENST00000491695.2:c.313A>T ENSP00000494626.2:p.Thr105Ser
ENST00000674381.2:c.*5397A>T ENSP00000501536.2:n.*5397A>T
ENST00000679448.1:c.5668A>T ENSP00000505889.1:p.Thr1890Ser
ENST00000679457.1:c.5668A>T ENSP00000505450.1:p.Thr1890Ser
ENST00000679474.1:n.5890A>T
ENST00000679521.1:c.5614A>T ENSP00000505456.1:p.Thr1872Ser
ENST00000679554.1:c.*5453A>T ENSP00000506415.1:n.*5453A>T
ENST00000679722.1:n.5890A>T
ENST00000679821.1:c.5410A>T ENSP00000506040.1:p.Thr1804Ser
ENST00000680047.1:n.5890A>T
ENST00000680072.1:c.5668A>T ENSP00000506581.1:p.Thr1890Ser
ENST00000680074.1:n.5890A>T
ENST00000680181.1:c.5575A>T ENSP00000505548.1:p.Thr1859Ser
ENST00000680513.1:c.5527A>T ENSP00000505284.1:p.Thr1843Ser
ENST00000680534.1:c.5668A>T ENSP00000506674.1:p.Thr1890Ser
ENST00000680766.1:c.5668A>T ENSP00000505204.1:p.Thr1890Ser
ENST00000680952.1:c.5668A>T ENSP00000506407.1:p.Thr1890Ser
ENST00000681412.1:c.5668A>T ENSP00000506486.1:p.Thr1890Ser
ENST00000681722.1:c.5668A>T ENSP00000506566.1:p.Thr1890Ser
XM_006715827.1:c.5527A>T XP_006715890.1:p.Thr1843Ser
XM_011515709.1:c.5800A>T XP_011514011.1:p.Thr1934Ser
XM_011515710.1:c.5800A>T XP_011514012.1:p.Thr1934Ser
XM_011515711.1:c.5764A>T XP_011514013.1:p.Thr1922Ser
XM_011515712.1:c.5800A>T XP_011514014.1:p.Thr1934Ser
XM_011515713.1:c.5746A>T XP_011514015.1:p.Thr1916Ser
XM_011515714.1:c.5800A>T XP_011514016.1:p.Thr1934Ser
XM_011515716.1:c.5704A>T XP_011514018.1:p.Thr1902Ser
XM_011515717.1:c.5659A>T XP_011514019.1:p.Thr1887Ser
XM_011515718.1:c.5704A>T XP_011514020.1:p.Thr1902Ser
XM_011515719.1:c.5704A>T XP_011514021.1:p.Thr1902Ser
XM_011515720.1:c.5563A>T XP_011514022.1:p.Thr1855Ser
XM_011515721.1:c.313A>T XP_011514023.1:p.Thr105Ser
XM_011515722.1:c.313A>T XP_011514024.1:p.Thr105Ser
XM_017011642.2:c.5764A>T XP_016867131.1:p.Thr1922Ser
XM_017011643.2:c.5764A>T XP_016867132.1:p.Thr1922Ser
XM_017011644.2:c.5764A>T XP_016867133.1:p.Thr1922Ser
XM_017011645.2:c.5710A>T XP_016867134.1:p.Thr1904Ser
XM_017011646.2:c.5764A>T XP_016867135.1:p.Thr1922Ser
XM_017011647.2:c.5671A>T XP_016867136.1:p.Thr1891Ser
XM_017011648.2:c.5668A>T XP_016867137.1:p.Thr1890Ser
XM_017011649.2:c.5764A>T XP_016867138.1:p.Thr1922Ser
XM_017011650.2:c.5668A>T XP_016867139.1:p.Thr1890Ser
XM_017011651.2:c.5623A>T XP_016867140.1:p.Thr1875Ser
XM_017011652.2:c.5764A>T XP_016867141.1:p.Thr1922Ser
XM_017011653.2:c.5575A>T XP_016867142.1:p.Thr1859Ser
XM_017011654.2:c.5527A>T XP_016867143.1:p.Thr1843Ser
XM_017011655.2:c.5392A>T XP_016867144.1:p.Thr1798Ser
XM_017011656.2:c.5392A>T XP_016867145.1:p.Thr1798Ser
XM_017011657.2:c.1429A>T XP_016867146.1:p.Thr477Ser
XM_017011658.2:c.313A>T XP_016867147.1:p.Thr105Ser
XM_017011659.2:c.313A>T XP_016867148.1:p.Thr105Ser
XM_017011660.2:c.313A>T XP_016867149.1:p.Thr105Ser
XM_024446631.1:c.5527A>T XP_024302399.1:p.Thr1843Ser