Canonical Allele Identifier: CA4337422
Community Standard Title: NM_005751.5(AKAP9):c.8150A>G (p.Glu2717Gly)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92082652A>G , CM000669.2:g.92082652A>G GRCh38
NC_000007.13:g.91711966A>G , CM000669.1:g.91711966A>G GRCh37
NC_000007.12:g.91549902A>G NCBI36
NG_011623.1:g.146778A>G , LRG_331:g.146778A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8150A>G MANE Select NP_005742.4:p.Glu2717Gly
ENST00000356239.8:c.8150A>G MANE Select ENSP00000348573.3:p.Glu2717Gly
NM_001379277.1:c.2795A>G NP_001366206.1:p.Glu932Gly
NM_005751.4:c.8150A>G , LRG_331t1:c.8150A>G NP_005742.4:p.Glu2717Gly
NM_147185.2:c.8126A>G NP_671714.1:p.Glu2709Gly
NM_147185.3:c.8126A>G NP_671714.1:p.Glu2709Gly
ENST00000356239.7:c.8150A>G ENSP00000348573.3:p.Glu2717Gly
ENST00000358100.6:c.8009A>G ENSP00000350813.3:p.Glu2670Gly
ENST00000359028.6:c.8183A>G ENSP00000351922.3:p.Glu2728Gly
ENST00000359028.7:c.8222A>G ENSP00000351922.4:p.Glu2741Gly
ENST00000394534.6:c.1688A>G ENSP00000378042.2:p.Glu563Gly
ENST00000394534.7:c.1643A>G ENSP00000378042.3:p.Glu548Gly
ENST00000491695.2:c.2795A>G ENSP00000494626.2:p.Glu932Gly
ENST00000674381.2:c.*7879A>G ENSP00000501536.2:n.*7879A>G
ENST00000679448.1:c.8126A>G ENSP00000505889.1:p.Glu2709Gly
ENST00000679457.1:c.8126A>G ENSP00000505450.1:p.Glu2709Gly
ENST00000679474.1:n.8348A>G
ENST00000679521.1:c.8096A>G ENSP00000505456.1:p.Glu2699Gly
ENST00000679554.1:c.*7935A>G ENSP00000506415.1:n.*7935A>G
ENST00000679722.1:n.8372A>G
ENST00000679821.1:c.7892A>G ENSP00000506040.1:p.Glu2631Gly
ENST00000680047.1:n.8348A>G
ENST00000680072.1:c.7973A>G ENSP00000506581.1:p.Glu2658Gly
ENST00000680181.1:c.8057A>G ENSP00000505548.1:p.Glu2686Gly
ENST00000680365.1:c.1643A>G ENSP00000506019.1:p.Glu548Gly
ENST00000680513.1:c.8009A>G ENSP00000505284.1:p.Glu2670Gly
ENST00000680534.1:c.8189A>G ENSP00000506674.1:p.Glu2730Gly
ENST00000680766.1:c.8126A>G ENSP00000505204.1:p.Glu2709Gly
ENST00000680952.1:c.8126A>G ENSP00000506407.1:p.Glu2709Gly
ENST00000681216.1:c.1643A>G ENSP00000505551.1:p.Glu548Gly
ENST00000681412.1:c.8150A>G ENSP00000506486.1:p.Glu2717Gly
ENST00000681722.1:c.8126A>G ENSP00000506566.1:p.Glu2709Gly
XM_006715827.1:c.8009A>G XP_006715890.1:p.Glu2670Gly
XM_011515709.1:c.8297A>G XP_011514011.1:p.Glu2766Gly
XM_011515710.1:c.8321A>G XP_011514012.1:p.Glu2774Gly
XM_011515711.1:c.8261A>G XP_011514013.1:p.Glu2754Gly
XM_011515712.1:c.8258A>G XP_011514014.1:p.Glu2753Gly
XM_011515713.1:c.8243A>G XP_011514015.1:p.Glu2748Gly
XM_011515714.1:c.8282A>G XP_011514016.1:p.Glu2761Gly
XM_011515716.1:c.8201A>G XP_011514018.1:p.Glu2734Gly
XM_011515717.1:c.8156A>G XP_011514019.1:p.Glu2719Gly
XM_011515718.1:c.8186A>G XP_011514020.1:p.Glu2729Gly
XM_011515719.1:c.8162A>G XP_011514021.1:p.Glu2721Gly
XM_011515720.1:c.8045A>G XP_011514022.1:p.Glu2682Gly
XM_011515721.1:c.2810A>G XP_011514023.1:p.Glu937Gly
XM_011515722.1:c.2771A>G XP_011514024.1:p.Glu924Gly
XM_017011642.2:c.8285A>G XP_016867131.1:p.Glu2762Gly
XM_017011643.2:c.8246A>G XP_016867132.1:p.Glu2749Gly
XM_017011644.2:c.8285A>G XP_016867133.1:p.Glu2762Gly
XM_017011645.2:c.8231A>G XP_016867134.1:p.Glu2744Gly
XM_017011646.2:c.8246A>G XP_016867135.1:p.Glu2749Gly
XM_017011647.2:c.8192A>G XP_016867136.1:p.Glu2731Gly
XM_017011648.2:c.8189A>G XP_016867137.1:p.Glu2730Gly
XM_017011649.2:c.8222A>G XP_016867138.1:p.Glu2741Gly
XM_017011650.2:c.8150A>G XP_016867139.1:p.Glu2717Gly
XM_017011651.2:c.8144A>G XP_016867140.1:p.Glu2715Gly
XM_017011652.2:c.8285A>G XP_016867141.1:p.Glu2762Gly
XM_017011653.2:c.8057A>G XP_016867142.1:p.Glu2686Gly
XM_017011654.2:c.8009A>G XP_016867143.1:p.Glu2670Gly
XM_017011655.2:c.7913A>G XP_016867144.1:p.Glu2638Gly
XM_017011656.2:c.7913A>G XP_016867145.1:p.Glu2638Gly
XM_017011657.2:c.3950A>G XP_016867146.1:p.Glu1317Gly
XM_017011658.2:c.2834A>G XP_016867147.1:p.Glu945Gly
XM_017011659.2:c.2795A>G XP_016867148.1:p.Glu932Gly
XM_017011660.2:c.2795A>G XP_016867149.1:p.Glu932Gly
XM_024446631.1:c.8048A>G XP_024302399.1:p.Glu2683Gly