Canonical Allele Identifier: CA4336938
Community Standard Title: NM_005751.5(AKAP9):c.5870A>G (p.Asn1957Ser)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92062379A>G , CM000669.2:g.92062379A>G GRCh38
NC_000007.13:g.91691693A>G , CM000669.1:g.91691693A>G GRCh37
NC_000007.12:g.91529629A>G NCBI36
NG_011623.1:g.126505A>G , LRG_331:g.126505A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.5870A>G MANE Select NP_005742.4:p.Asn1957Ser
ENST00000356239.8:c.5870A>G MANE Select ENSP00000348573.3:p.Asn1957Ser
NM_001379277.1:c.515A>G NP_001366206.1:p.Asn172Ser
NM_005751.4:c.5870A>G , LRG_331t1:c.5870A>G NP_005742.4:p.Asn1957Ser
NM_147185.2:c.5870A>G NP_671714.1:p.Asn1957Ser
NM_147185.3:c.5870A>G NP_671714.1:p.Asn1957Ser
ENST00000356239.7:c.5870A>G ENSP00000348573.3:p.Asn1957Ser
ENST00000358100.6:c.5729A>G ENSP00000350813.3:p.Asn1910Ser
ENST00000359028.6:c.5903A>G ENSP00000351922.3:p.Asn1968Ser
ENST00000359028.7:c.5966A>G ENSP00000351922.4:p.Asn1989Ser
ENST00000491695.1:n.1058A>G
ENST00000491695.2:c.515A>G ENSP00000494626.2:p.Asn172Ser
ENST00000674381.2:c.*5599A>G ENSP00000501536.2:n.*5599A>G
ENST00000679448.1:c.5870A>G ENSP00000505889.1:p.Asn1957Ser
ENST00000679457.1:c.5870A>G ENSP00000505450.1:p.Asn1957Ser
ENST00000679474.1:n.6092A>G
ENST00000679521.1:c.5816A>G ENSP00000505456.1:p.Asn1939Ser
ENST00000679554.1:c.*5655A>G ENSP00000506415.1:n.*5655A>G
ENST00000679722.1:n.6092A>G
ENST00000679821.1:c.5612A>G ENSP00000506040.1:p.Asn1871Ser
ENST00000680047.1:n.6092A>G
ENST00000680072.1:c.5870A>G ENSP00000506581.1:p.Asn1957Ser
ENST00000680074.1:n.6092A>G
ENST00000680181.1:c.5777A>G ENSP00000505548.1:p.Asn1926Ser
ENST00000680513.1:c.5729A>G ENSP00000505284.1:p.Asn1910Ser
ENST00000680534.1:c.5870A>G ENSP00000506674.1:p.Asn1957Ser
ENST00000680766.1:c.5870A>G ENSP00000505204.1:p.Asn1957Ser
ENST00000680952.1:c.5870A>G ENSP00000506407.1:p.Asn1957Ser
ENST00000681412.1:c.5870A>G ENSP00000506486.1:p.Asn1957Ser
ENST00000681722.1:c.5870A>G ENSP00000506566.1:p.Asn1957Ser
XM_006715827.1:c.5729A>G XP_006715890.1:p.Asn1910Ser
XM_011515709.1:c.6002A>G XP_011514011.1:p.Asn2001Ser
XM_011515710.1:c.6002A>G XP_011514012.1:p.Asn2001Ser
XM_011515711.1:c.5966A>G XP_011514013.1:p.Asn1989Ser
XM_011515712.1:c.6002A>G XP_011514014.1:p.Asn2001Ser
XM_011515713.1:c.5948A>G XP_011514015.1:p.Asn1983Ser
XM_011515714.1:c.6002A>G XP_011514016.1:p.Asn2001Ser
XM_011515716.1:c.5906A>G XP_011514018.1:p.Asn1969Ser
XM_011515717.1:c.5861A>G XP_011514019.1:p.Asn1954Ser
XM_011515718.1:c.5906A>G XP_011514020.1:p.Asn1969Ser
XM_011515719.1:c.5906A>G XP_011514021.1:p.Asn1969Ser
XM_011515720.1:c.5765A>G XP_011514022.1:p.Asn1922Ser
XM_011515721.1:c.515A>G XP_011514023.1:p.Asn172Ser
XM_011515722.1:c.515A>G XP_011514024.1:p.Asn172Ser
XM_017011642.2:c.5966A>G XP_016867131.1:p.Asn1989Ser
XM_017011643.2:c.5966A>G XP_016867132.1:p.Asn1989Ser
XM_017011644.2:c.5966A>G XP_016867133.1:p.Asn1989Ser
XM_017011645.2:c.5912A>G XP_016867134.1:p.Asn1971Ser
XM_017011646.2:c.5966A>G XP_016867135.1:p.Asn1989Ser
XM_017011647.2:c.5873A>G XP_016867136.1:p.Asn1958Ser
XM_017011648.2:c.5870A>G XP_016867137.1:p.Asn1957Ser
XM_017011649.2:c.5966A>G XP_016867138.1:p.Asn1989Ser
XM_017011650.2:c.5870A>G XP_016867139.1:p.Asn1957Ser
XM_017011651.2:c.5825A>G XP_016867140.1:p.Asn1942Ser
XM_017011652.2:c.5966A>G XP_016867141.1:p.Asn1989Ser
XM_017011653.2:c.5777A>G XP_016867142.1:p.Asn1926Ser
XM_017011654.2:c.5729A>G XP_016867143.1:p.Asn1910Ser
XM_017011655.2:c.5594A>G XP_016867144.1:p.Asn1865Ser
XM_017011656.2:c.5594A>G XP_016867145.1:p.Asn1865Ser
XM_017011657.2:c.1631A>G XP_016867146.1:p.Asn544Ser
XM_017011658.2:c.515A>G XP_016867147.1:p.Asn172Ser
XM_017011659.2:c.515A>G XP_016867148.1:p.Asn172Ser
XM_017011660.2:c.515A>G XP_016867149.1:p.Asn172Ser
XM_024446631.1:c.5729A>G XP_024302399.1:p.Asn1910Ser