Canonical Allele Identifier: CA4337473
Community Standard Title: NM_005751.5(AKAP9):c.8314A>G (p.Ile2772Val)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92083323A>G , CM000669.2:g.92083323A>G GRCh38
NC_000007.13:g.91712637A>G , CM000669.1:g.91712637A>G GRCh37
NC_000007.12:g.91550573A>G NCBI36
NG_011623.1:g.147449A>G , LRG_331:g.147449A>G

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.8314A>G MANE Select NP_005742.4:p.Ile2772Val
ENST00000356239.8:c.8314A>G MANE Select ENSP00000348573.3:p.Ile2772Val
NM_001379277.1:c.2959A>G NP_001366206.1:p.Ile987Val
NM_005751.4:c.8314A>G , LRG_331t1:c.8314A>G NP_005742.4:p.Ile2772Val
NM_147185.2:c.8290A>G NP_671714.1:p.Ile2764Val
NM_147185.3:c.8290A>G NP_671714.1:p.Ile2764Val
ENST00000356239.7:c.8314A>G ENSP00000348573.3:p.Ile2772Val
ENST00000358100.6:c.8173A>G ENSP00000350813.3:p.Ile2725Val
ENST00000359028.6:c.8347A>G ENSP00000351922.3:p.Ile2783Val
ENST00000359028.7:c.8386A>G ENSP00000351922.4:p.Ile2796Val
ENST00000394534.6:c.1852A>G ENSP00000378042.2:p.Ile618Val
ENST00000394534.7:c.1807A>G ENSP00000378042.3:p.Ile603Val
ENST00000435423.2:n.154A>G
ENST00000491695.2:c.2959A>G ENSP00000494626.2:p.Ile987Val
ENST00000679448.1:c.8290A>G ENSP00000505889.1:p.Ile2764Val
ENST00000679457.1:c.8290A>G ENSP00000505450.1:p.Ile2764Val
ENST00000679474.1:n.8512A>G
ENST00000679521.1:c.8260A>G ENSP00000505456.1:p.Ile2754Val
ENST00000679722.1:n.8536A>G
ENST00000679821.1:c.8056A>G ENSP00000506040.1:p.Ile2686Val
ENST00000680047.1:n.8512A>G
ENST00000680072.1:c.8137A>G ENSP00000506581.1:p.Ile2713Val
ENST00000680181.1:c.8221A>G ENSP00000505548.1:p.Ile2741Val
ENST00000680365.1:c.1807A>G ENSP00000506019.1:p.Ile603Val
ENST00000680513.1:c.8173A>G ENSP00000505284.1:p.Ile2725Val
ENST00000680534.1:c.8353A>G ENSP00000506674.1:p.Ile2785Val
ENST00000680766.1:c.8290A>G ENSP00000505204.1:p.Ile2764Val
ENST00000680952.1:c.8290A>G ENSP00000506407.1:p.Ile2764Val
ENST00000681216.1:c.1764+43A>G ENSP00000505551.1:n.1764+43A>G
ENST00000681412.1:c.8314A>G ENSP00000506486.1:p.Ile2772Val
ENST00000681722.1:c.8290A>G ENSP00000506566.1:p.Ile2764Val
XM_006715827.1:c.8173A>G XP_006715890.1:p.Ile2725Val
XM_011515709.1:c.8461A>G XP_011514011.1:p.Ile2821Val
XM_011515710.1:c.8485A>G XP_011514012.1:p.Ile2829Val
XM_011515711.1:c.8425A>G XP_011514013.1:p.Ile2809Val
XM_011515712.1:c.8422A>G XP_011514014.1:p.Ile2808Val
XM_011515713.1:c.8407A>G XP_011514015.1:p.Ile2803Val
XM_011515714.1:c.8446A>G XP_011514016.1:p.Ile2816Val
XM_011515716.1:c.8365A>G XP_011514018.1:p.Ile2789Val
XM_011515717.1:c.8320A>G XP_011514019.1:p.Ile2774Val
XM_011515718.1:c.8350A>G XP_011514020.1:p.Ile2784Val
XM_011515719.1:c.8326A>G XP_011514021.1:p.Ile2776Val
XM_011515720.1:c.8209A>G XP_011514022.1:p.Ile2737Val
XM_011515721.1:c.2974A>G XP_011514023.1:p.Ile992Val
XM_011515722.1:c.2935A>G XP_011514024.1:p.Ile979Val
XM_017011642.2:c.8449A>G XP_016867131.1:p.Ile2817Val
XM_017011643.2:c.8410A>G XP_016867132.1:p.Ile2804Val
XM_017011644.2:c.8449A>G XP_016867133.1:p.Ile2817Val
XM_017011645.2:c.8395A>G XP_016867134.1:p.Ile2799Val
XM_017011646.2:c.8410A>G XP_016867135.1:p.Ile2804Val
XM_017011647.2:c.8356A>G XP_016867136.1:p.Ile2786Val
XM_017011648.2:c.8353A>G XP_016867137.1:p.Ile2785Val
XM_017011649.2:c.8386A>G XP_016867138.1:p.Ile2796Val
XM_017011650.2:c.8314A>G XP_016867139.1:p.Ile2772Val
XM_017011651.2:c.8308A>G XP_016867140.1:p.Ile2770Val
XM_017011652.2:c.8449A>G XP_016867141.1:p.Ile2817Val
XM_017011653.2:c.8221A>G XP_016867142.1:p.Ile2741Val
XM_017011654.2:c.8173A>G XP_016867143.1:p.Ile2725Val
XM_017011655.2:c.8077A>G XP_016867144.1:p.Ile2693Val
XM_017011656.2:c.8077A>G XP_016867145.1:p.Ile2693Val
XM_017011657.2:c.4114A>G XP_016867146.1:p.Ile1372Val
XM_017011658.2:c.2998A>G XP_016867147.1:p.Ile1000Val
XM_017011659.2:c.2959A>G XP_016867148.1:p.Ile987Val
XM_017011660.2:c.2959A>G XP_016867149.1:p.Ile987Val
XM_024446631.1:c.8212A>G XP_024302399.1:p.Ile2738Val