Canonical Allele Identifier: CA4337485
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92083477A>G , CM000669.2:g.92083477A>G GRCh38
NC_000007.13:g.91712791A>G , CM000669.1:g.91712791A>G GRCh37
NC_000007.12:g.91550727A>G NCBI36
NG_011623.1:g.147603A>G , LRG_331:g.147603A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000356239.8:c.8468A>G MANE Select ENSP00000348573.3:p.Gln2823Arg
ENST00000359028.7:c.8540A>G ENSP00000351922.4:p.Gln2847Arg
ENST00000394534.7:c.1961A>G ENSP00000378042.3:p.Gln654Arg
ENST00000435423.2:n.308A>G
ENST00000491695.2:c.3113A>G ENSP00000494626.2:p.Gln1038Arg
ENST00000679448.1:c.8444A>G ENSP00000505889.1:p.Gln2815Arg
ENST00000679457.1:c.8444A>G ENSP00000505450.1:p.Gln2815Arg
ENST00000679474.1:n.8666A>G
ENST00000679521.1:c.8414A>G ENSP00000505456.1:p.Gln2805Arg
ENST00000679722.1:n.8690A>G
ENST00000679821.1:c.8210A>G ENSP00000506040.1:p.Gln2737Arg
ENST00000680047.1:n.8666A>G
ENST00000680072.1:c.8291A>G ENSP00000506581.1:p.Gln2764Arg
ENST00000680181.1:c.8375A>G ENSP00000505548.1:p.Gln2792Arg
ENST00000680365.1:c.1961A>G ENSP00000506019.1:p.Gln654Arg
ENST00000680513.1:c.8327A>G ENSP00000505284.1:p.Gln2776Arg
ENST00000680534.1:c.8507A>G ENSP00000506674.1:p.Gln2836Arg
ENST00000680766.1:c.8444A>G ENSP00000505204.1:p.Gln2815Arg
ENST00000680952.1:c.8444A>G ENSP00000506407.1:p.Gln2815Arg
ENST00000681216.1:c.1805A>G ENSP00000505551.1:p.Gln602Arg
ENST00000681412.1:c.8468A>G ENSP00000506486.1:p.Gln2823Arg
ENST00000681722.1:c.8444A>G ENSP00000506566.1:p.Gln2815Arg
ENST00000356239.7:c.8468A>G ENSP00000348573.3:p.Gln2823Arg
ENST00000358100.6:c.8327A>G ENSP00000350813.3:p.Gln2776Arg
ENST00000359028.6:c.8501A>G ENSP00000351922.3:p.Gln2834Arg
ENST00000394534.6:c.2006A>G ENSP00000378042.2:p.Gln669Arg
NM_005751.4:c.8468A>G , LRG_331t1:c.8468A>G NP_005742.4:p.Gln2823Arg
NM_147185.2:c.8444A>G NP_671714.1:p.Gln2815Arg
XM_006715827.1:c.8327A>G XP_006715890.1:p.Gln2776Arg
XM_011515709.1:c.8615A>G XP_011514011.1:p.Gln2872Arg
XM_011515710.1:c.8639A>G XP_011514012.1:p.Gln2880Arg
XM_011515711.1:c.8579A>G XP_011514013.1:p.Gln2860Arg
XM_011515712.1:c.8576A>G XP_011514014.1:p.Gln2859Arg
XM_011515713.1:c.8561A>G XP_011514015.1:p.Gln2854Arg
XM_011515714.1:c.8600A>G XP_011514016.1:p.Gln2867Arg
XM_011515716.1:c.8519A>G XP_011514018.1:p.Gln2840Arg
XM_011515717.1:c.8474A>G XP_011514019.1:p.Gln2825Arg
XM_011515718.1:c.8504A>G XP_011514020.1:p.Gln2835Arg
XM_011515719.1:c.8480A>G XP_011514021.1:p.Gln2827Arg
XM_011515720.1:c.8363A>G XP_011514022.1:p.Gln2788Arg
XM_011515721.1:c.3128A>G XP_011514023.1:p.Gln1043Arg
XM_011515722.1:c.3089A>G XP_011514024.1:p.Gln1030Arg
XM_017011642.2:c.8603A>G XP_016867131.1:p.Gln2868Arg
XM_017011643.2:c.8564A>G XP_016867132.1:p.Gln2855Arg
XM_017011644.2:c.8603A>G XP_016867133.1:p.Gln2868Arg
XM_017011645.2:c.8549A>G XP_016867134.1:p.Gln2850Arg
XM_017011646.2:c.8564A>G XP_016867135.1:p.Gln2855Arg
XM_017011647.2:c.8510A>G XP_016867136.1:p.Gln2837Arg
XM_017011648.2:c.8507A>G XP_016867137.1:p.Gln2836Arg
XM_017011649.2:c.8540A>G XP_016867138.1:p.Gln2847Arg
XM_017011650.2:c.8468A>G XP_016867139.1:p.Gln2823Arg
XM_017011651.2:c.8462A>G XP_016867140.1:p.Gln2821Arg
XM_017011652.2:c.8603A>G XP_016867141.1:p.Gln2868Arg
XM_017011653.2:c.8375A>G XP_016867142.1:p.Gln2792Arg
XM_017011654.2:c.8327A>G XP_016867143.1:p.Gln2776Arg
XM_017011655.2:c.8231A>G XP_016867144.1:p.Gln2744Arg
XM_017011656.2:c.8231A>G XP_016867145.1:p.Gln2744Arg
XM_017011657.2:c.4268A>G XP_016867146.1:p.Gln1423Arg
XM_017011658.2:c.3152A>G XP_016867147.1:p.Gln1051Arg
XM_017011659.2:c.3113A>G XP_016867148.1:p.Gln1038Arg
XM_017011660.2:c.3113A>G XP_016867149.1:p.Gln1038Arg
XM_024446631.1:c.8366A>G XP_024302399.1:p.Gln2789Arg
NM_147185.3:c.8444A>G NP_671714.1:p.Gln2815Arg
NM_001379277.1:c.3113A>G NP_001366206.1:p.Gln1038Arg
NM_005751.5:c.8468A>G MANE Select NP_005742.4:p.Gln2823Arg