Canonical Allele Identifier: CA368138806
Community Standard Title: NM_005751.5(AKAP9):c.8402A>G (p.Asn2801Ser)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92083411A>G , CM000669.2:g.92083411A>G GRCh38
NC_000007.13:g.91712725A>G , CM000669.1:g.91712725A>G GRCh37
NC_000007.12:g.91550661A>G NCBI36
NG_011623.1:g.147537A>G , LRG_331:g.147537A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8402A>G MANE Select NP_005742.4:p.Asn2801Ser
ENST00000356239.8:c.8402A>G MANE Select ENSP00000348573.3:p.Asn2801Ser
NM_001379277.1:c.3047A>G NP_001366206.1:p.Asn1016Ser
NM_005751.4:c.8402A>G , LRG_331t1:c.8402A>G NP_005742.4:p.Asn2801Ser
NM_147185.2:c.8378A>G NP_671714.1:p.Asn2793Ser
NM_147185.3:c.8378A>G NP_671714.1:p.Asn2793Ser
ENST00000356239.7:c.8402A>G ENSP00000348573.3:p.Asn2801Ser
ENST00000358100.6:c.8261A>G ENSP00000350813.3:p.Asn2754Ser
ENST00000359028.6:c.8435A>G ENSP00000351922.3:p.Asn2812Ser
ENST00000359028.7:c.8474A>G ENSP00000351922.4:p.Asn2825Ser
ENST00000394534.6:c.1940A>G ENSP00000378042.2:p.Asn647Ser
ENST00000394534.7:c.1895A>G ENSP00000378042.3:p.Asn632Ser
ENST00000435423.2:n.242A>G
ENST00000491695.2:c.3047A>G ENSP00000494626.2:p.Asn1016Ser
ENST00000679448.1:c.8378A>G ENSP00000505889.1:p.Asn2793Ser
ENST00000679457.1:c.8378A>G ENSP00000505450.1:p.Asn2793Ser
ENST00000679474.1:n.8600A>G
ENST00000679521.1:c.8348A>G ENSP00000505456.1:p.Asn2783Ser
ENST00000679722.1:n.8624A>G
ENST00000679821.1:c.8144A>G ENSP00000506040.1:p.Asn2715Ser
ENST00000680047.1:n.8600A>G
ENST00000680072.1:c.8225A>G ENSP00000506581.1:p.Asn2742Ser
ENST00000680181.1:c.8309A>G ENSP00000505548.1:p.Asn2770Ser
ENST00000680365.1:c.1895A>G ENSP00000506019.1:p.Asn632Ser
ENST00000680513.1:c.8261A>G ENSP00000505284.1:p.Asn2754Ser
ENST00000680534.1:c.8441A>G ENSP00000506674.1:p.Asn2814Ser
ENST00000680766.1:c.8378A>G ENSP00000505204.1:p.Asn2793Ser
ENST00000680952.1:c.8378A>G ENSP00000506407.1:p.Asn2793Ser
ENST00000681216.1:c.1765-26A>G ENSP00000505551.1:n.1765-26A>G
ENST00000681412.1:c.8402A>G ENSP00000506486.1:p.Asn2801Ser
ENST00000681722.1:c.8378A>G ENSP00000506566.1:p.Asn2793Ser
XM_006715827.1:c.8261A>G XP_006715890.1:p.Asn2754Ser
XM_011515709.1:c.8549A>G XP_011514011.1:p.Asn2850Ser
XM_011515710.1:c.8573A>G XP_011514012.1:p.Asn2858Ser
XM_011515711.1:c.8513A>G XP_011514013.1:p.Asn2838Ser
XM_011515712.1:c.8510A>G XP_011514014.1:p.Asn2837Ser
XM_011515713.1:c.8495A>G XP_011514015.1:p.Asn2832Ser
XM_011515714.1:c.8534A>G XP_011514016.1:p.Asn2845Ser
XM_011515716.1:c.8453A>G XP_011514018.1:p.Asn2818Ser
XM_011515717.1:c.8408A>G XP_011514019.1:p.Asn2803Ser
XM_011515718.1:c.8438A>G XP_011514020.1:p.Asn2813Ser
XM_011515719.1:c.8414A>G XP_011514021.1:p.Asn2805Ser
XM_011515720.1:c.8297A>G XP_011514022.1:p.Asn2766Ser
XM_011515721.1:c.3062A>G XP_011514023.1:p.Asn1021Ser
XM_011515722.1:c.3023A>G XP_011514024.1:p.Asn1008Ser
XM_017011642.2:c.8537A>G XP_016867131.1:p.Asn2846Ser
XM_017011643.2:c.8498A>G XP_016867132.1:p.Asn2833Ser
XM_017011644.2:c.8537A>G XP_016867133.1:p.Asn2846Ser
XM_017011645.2:c.8483A>G XP_016867134.1:p.Asn2828Ser
XM_017011646.2:c.8498A>G XP_016867135.1:p.Asn2833Ser
XM_017011647.2:c.8444A>G XP_016867136.1:p.Asn2815Ser
XM_017011648.2:c.8441A>G XP_016867137.1:p.Asn2814Ser
XM_017011649.2:c.8474A>G XP_016867138.1:p.Asn2825Ser
XM_017011650.2:c.8402A>G XP_016867139.1:p.Asn2801Ser
XM_017011651.2:c.8396A>G XP_016867140.1:p.Asn2799Ser
XM_017011652.2:c.8537A>G XP_016867141.1:p.Asn2846Ser
XM_017011653.2:c.8309A>G XP_016867142.1:p.Asn2770Ser
XM_017011654.2:c.8261A>G XP_016867143.1:p.Asn2754Ser
XM_017011655.2:c.8165A>G XP_016867144.1:p.Asn2722Ser
XM_017011656.2:c.8165A>G XP_016867145.1:p.Asn2722Ser
XM_017011657.2:c.4202A>G XP_016867146.1:p.Asn1401Ser
XM_017011658.2:c.3086A>G XP_016867147.1:p.Asn1029Ser
XM_017011659.2:c.3047A>G XP_016867148.1:p.Asn1016Ser
XM_017011660.2:c.3047A>G XP_016867149.1:p.Asn1016Ser
XM_024446631.1:c.8300A>G XP_024302399.1:p.Asn2767Ser