Canonical Allele Identifier: CA456450503
Gene: AKAP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.91707174T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92077860T>C , CM000669.2:g.92077860T>C GRCh38
NC_000007.13:g.91707174T>C , CM000669.1:g.91707174T>C GRCh37
NC_000007.12:g.91545110T>C NCBI36
NG_011623.1:g.141986T>C , LRG_331:g.141986T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000356239.8:c.6930T>C MANE Select ENSP00000348573.3:p.Ile2310=
ENST00000359028.7:c.7002T>C ENSP00000351922.4:p.Ile2334=
ENST00000394534.7:c.423T>C ENSP00000378042.3:p.Ile141=
ENST00000491695.2:c.1575T>C ENSP00000494626.2:p.Ile525=
ENST00000674381.2:c.*6659T>C ENSP00000501536.2:n.*6659T>C
ENST00000679448.1:c.6906T>C ENSP00000505889.1:p.Ile2302=
ENST00000679457.1:c.6906T>C ENSP00000505450.1:p.Ile2302=
ENST00000679474.1:n.7128T>C
ENST00000679521.1:c.6876T>C ENSP00000505456.1:p.Ile2292=
ENST00000679554.1:c.*6715T>C ENSP00000506415.1:n.*6715T>C
ENST00000679722.1:n.7152T>C
ENST00000679821.1:c.6672T>C ENSP00000506040.1:p.Ile2224=
ENST00000680047.1:n.7128T>C
ENST00000680072.1:c.6753T>C ENSP00000506581.1:p.Ile2251=
ENST00000680181.1:c.6837T>C ENSP00000505548.1:p.Ile2279=
ENST00000680365.1:c.423T>C ENSP00000506019.1:p.Ile141=
ENST00000680513.1:c.6789T>C ENSP00000505284.1:p.Ile2263=
ENST00000680534.1:c.6969T>C ENSP00000506674.1:p.Ile2323=
ENST00000680766.1:c.6906T>C ENSP00000505204.1:p.Ile2302=
ENST00000680952.1:c.6906T>C ENSP00000506407.1:p.Ile2302=
ENST00000681216.1:c.423T>C ENSP00000505551.1:p.Ile141=
ENST00000681412.1:c.6930T>C ENSP00000506486.1:p.Ile2310=
ENST00000681722.1:c.6906T>C ENSP00000506566.1:p.Ile2302=
ENST00000356239.7:c.6930T>C ENSP00000348573.3:p.Ile2310=
ENST00000358100.6:c.6789T>C ENSP00000350813.3:p.Ile2263=
ENST00000359028.6:c.6963T>C ENSP00000351922.3:p.Ile2321=
ENST00000394534.6:c.468T>C ENSP00000378042.2:p.Ile156=
NM_005751.4:c.6930T>C , LRG_331t1:c.6930T>C NP_005742.4:p.Ile2310=
NM_147185.2:c.6906T>C NP_671714.1:p.Ile2302=
XM_006715827.1:c.6789T>C XP_006715890.1:p.Ile2263=
XM_011515709.1:c.7077T>C XP_011514011.1:p.Ile2359=
XM_011515710.1:c.7101T>C XP_011514012.1:p.Ile2367=
XM_011515711.1:c.7041T>C XP_011514013.1:p.Ile2347=
XM_011515712.1:c.7038T>C XP_011514014.1:p.Ile2346=
XM_011515713.1:c.7023T>C XP_011514015.1:p.Ile2341=
XM_011515714.1:c.7062T>C XP_011514016.1:p.Ile2354=
XM_011515716.1:c.6981T>C XP_011514018.1:p.Ile2327=
XM_011515717.1:c.6936T>C XP_011514019.1:p.Ile2312=
XM_011515718.1:c.6966T>C XP_011514020.1:p.Ile2322=
XM_011515719.1:c.6942T>C XP_011514021.1:p.Ile2314=
XM_011515720.1:c.6825T>C XP_011514022.1:p.Ile2275=
XM_011515721.1:c.1590T>C XP_011514023.1:p.Ile530=
XM_011515722.1:c.1551T>C XP_011514024.1:p.Ile517=
XM_017011642.2:c.7065T>C XP_016867131.1:p.Ile2355=
XM_017011643.2:c.7026T>C XP_016867132.1:p.Ile2342=
XM_017011644.2:c.7065T>C XP_016867133.1:p.Ile2355=
XM_017011645.2:c.7011T>C XP_016867134.1:p.Ile2337=
XM_017011646.2:c.7026T>C XP_016867135.1:p.Ile2342=
XM_017011647.2:c.6972T>C XP_016867136.1:p.Ile2324=
XM_017011648.2:c.6969T>C XP_016867137.1:p.Ile2323=
XM_017011649.2:c.7002T>C XP_016867138.1:p.Ile2334=
XM_017011650.2:c.6930T>C XP_016867139.1:p.Ile2310=
XM_017011651.2:c.6924T>C XP_016867140.1:p.Ile2308=
XM_017011652.2:c.7065T>C XP_016867141.1:p.Ile2355=
XM_017011653.2:c.6837T>C XP_016867142.1:p.Ile2279=
XM_017011654.2:c.6789T>C XP_016867143.1:p.Ile2263=
XM_017011655.2:c.6693T>C XP_016867144.1:p.Ile2231=
XM_017011656.2:c.6693T>C XP_016867145.1:p.Ile2231=
XM_017011657.2:c.2730T>C XP_016867146.1:p.Ile910=
XM_017011658.2:c.1614T>C XP_016867147.1:p.Ile538=
XM_017011659.2:c.1575T>C XP_016867148.1:p.Ile525=
XM_017011660.2:c.1575T>C XP_016867149.1:p.Ile525=
XM_024446631.1:c.6828T>C XP_024302399.1:p.Ile2276=
NM_147185.3:c.6906T>C NP_671714.1:p.Ile2302=
NM_001379277.1:c.1575T>C NP_001366206.1:p.Ile525=
NM_005751.5:c.6930T>C MANE Select NP_005742.4:p.Ile2310=