Canonical Allele Identifier: CA4337193
Gene: AKAP9 HGNC NCBI

Linked Data

dbSNP Id: rs769336831
gnomAD v3: 7-92077839-A-C
gnomAD v4: 7-92077839-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92077839A>C , CM000669.2:g.92077839A>C GRCh38
NC_000007.13:g.91707153A>C , CM000669.1:g.91707153A>C GRCh37
NC_000007.12:g.91545089A>C NCBI36
NG_011623.1:g.141965A>C , LRG_331:g.141965A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356239.8:c.6909A>C MANE Select ENSP00000348573.3:p.Lys2303Asn
ENST00000359028.7:c.6981A>C ENSP00000351922.4:p.Lys2327Asn
ENST00000394534.7:c.402A>C ENSP00000378042.3:p.Lys134Asn
ENST00000491695.2:c.1554A>C ENSP00000494626.2:p.Lys518Asn
ENST00000674381.2:c.*6638A>C ENSP00000501536.2:n.*6638A>C
ENST00000679448.1:c.6885A>C ENSP00000505889.1:p.Lys2295Asn
ENST00000679457.1:c.6885A>C ENSP00000505450.1:p.Lys2295Asn
ENST00000679474.1:n.7107A>C
ENST00000679521.1:c.6855A>C ENSP00000505456.1:p.Lys2285Asn
ENST00000679554.1:c.*6694A>C ENSP00000506415.1:n.*6694A>C
ENST00000679722.1:n.7131A>C
ENST00000679821.1:c.6651A>C ENSP00000506040.1:p.Lys2217Asn
ENST00000680047.1:n.7107A>C
ENST00000680072.1:c.6732A>C ENSP00000506581.1:p.Lys2244Asn
ENST00000680181.1:c.6816A>C ENSP00000505548.1:p.Lys2272Asn
ENST00000680365.1:c.402A>C ENSP00000506019.1:p.Lys134Asn
ENST00000680513.1:c.6768A>C ENSP00000505284.1:p.Lys2256Asn
ENST00000680534.1:c.6948A>C ENSP00000506674.1:p.Lys2316Asn
ENST00000680766.1:c.6885A>C ENSP00000505204.1:p.Lys2295Asn
ENST00000680952.1:c.6885A>C ENSP00000506407.1:p.Lys2295Asn
ENST00000681216.1:c.402A>C ENSP00000505551.1:p.Lys134Asn
ENST00000681412.1:c.6909A>C ENSP00000506486.1:p.Lys2303Asn
ENST00000681722.1:c.6885A>C ENSP00000506566.1:p.Lys2295Asn
ENST00000356239.7:c.6909A>C ENSP00000348573.3:p.Lys2303Asn
ENST00000358100.6:c.6768A>C ENSP00000350813.3:p.Lys2256Asn
ENST00000359028.6:c.6942A>C ENSP00000351922.3:p.Lys2314Asn
ENST00000394534.6:c.447A>C ENSP00000378042.2:p.Lys149Asn
NM_005751.4:c.6909A>C , LRG_331t1:c.6909A>C NP_005742.4:p.Lys2303Asn
NM_147185.2:c.6885A>C NP_671714.1:p.Lys2295Asn
XM_006715827.1:c.6768A>C XP_006715890.1:p.Lys2256Asn
XM_011515709.1:c.7056A>C XP_011514011.1:p.Lys2352Asn
XM_011515710.1:c.7080A>C XP_011514012.1:p.Lys2360Asn
XM_011515711.1:c.7020A>C XP_011514013.1:p.Lys2340Asn
XM_011515712.1:c.7017A>C XP_011514014.1:p.Lys2339Asn
XM_011515713.1:c.7002A>C XP_011514015.1:p.Lys2334Asn
XM_011515714.1:c.7041A>C XP_011514016.1:p.Lys2347Asn
XM_011515716.1:c.6960A>C XP_011514018.1:p.Lys2320Asn
XM_011515717.1:c.6915A>C XP_011514019.1:p.Lys2305Asn
XM_011515718.1:c.6945A>C XP_011514020.1:p.Lys2315Asn
XM_011515719.1:c.6921A>C XP_011514021.1:p.Lys2307Asn
XM_011515720.1:c.6804A>C XP_011514022.1:p.Lys2268Asn
XM_011515721.1:c.1569A>C XP_011514023.1:p.Lys523Asn
XM_011515722.1:c.1530A>C XP_011514024.1:p.Lys510Asn
XM_017011642.2:c.7044A>C XP_016867131.1:p.Lys2348Asn
XM_017011643.2:c.7005A>C XP_016867132.1:p.Lys2335Asn
XM_017011644.2:c.7044A>C XP_016867133.1:p.Lys2348Asn
XM_017011645.2:c.6990A>C XP_016867134.1:p.Lys2330Asn
XM_017011646.2:c.7005A>C XP_016867135.1:p.Lys2335Asn
XM_017011647.2:c.6951A>C XP_016867136.1:p.Lys2317Asn
XM_017011648.2:c.6948A>C XP_016867137.1:p.Lys2316Asn
XM_017011649.2:c.6981A>C XP_016867138.1:p.Lys2327Asn
XM_017011650.2:c.6909A>C XP_016867139.1:p.Lys2303Asn
XM_017011651.2:c.6903A>C XP_016867140.1:p.Lys2301Asn
XM_017011652.2:c.7044A>C XP_016867141.1:p.Lys2348Asn
XM_017011653.2:c.6816A>C XP_016867142.1:p.Lys2272Asn
XM_017011654.2:c.6768A>C XP_016867143.1:p.Lys2256Asn
XM_017011655.2:c.6672A>C XP_016867144.1:p.Lys2224Asn
XM_017011656.2:c.6672A>C XP_016867145.1:p.Lys2224Asn
XM_017011657.2:c.2709A>C XP_016867146.1:p.Lys903Asn
XM_017011658.2:c.1593A>C XP_016867147.1:p.Lys531Asn
XM_017011659.2:c.1554A>C XP_016867148.1:p.Lys518Asn
XM_017011660.2:c.1554A>C XP_016867149.1:p.Lys518Asn
XM_024446631.1:c.6807A>C XP_024302399.1:p.Lys2269Asn
NM_147185.3:c.6885A>C NP_671714.1:p.Lys2295Asn
NM_001379277.1:c.1554A>C NP_001366206.1:p.Lys518Asn
NM_005751.5:c.6909A>C MANE Select NP_005742.4:p.Lys2303Asn