Canonical Allele Identifier: CA456450486
Gene: AKAP9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.91707147T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92077833T>A , CM000669.2:g.92077833T>A GRCh38
NC_000007.13:g.91707147T>A , CM000669.1:g.91707147T>A GRCh37
NC_000007.12:g.91545083T>A NCBI36
NG_011623.1:g.141959T>A , LRG_331:g.141959T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000356239.8:c.6903T>A MANE Select ENSP00000348573.3:p.Val2301=
ENST00000359028.7:c.6975T>A ENSP00000351922.4:p.Val2325=
ENST00000394534.7:c.396T>A ENSP00000378042.3:p.Val132=
ENST00000491695.2:c.1548T>A ENSP00000494626.2:p.Val516=
ENST00000674381.2:c.*6632T>A ENSP00000501536.2:n.*6632T>A
ENST00000679448.1:c.6879T>A ENSP00000505889.1:p.Val2293=
ENST00000679457.1:c.6879T>A ENSP00000505450.1:p.Val2293=
ENST00000679474.1:n.7101T>A
ENST00000679521.1:c.6849T>A ENSP00000505456.1:p.Val2283=
ENST00000679554.1:c.*6688T>A ENSP00000506415.1:n.*6688T>A
ENST00000679722.1:n.7125T>A
ENST00000679821.1:c.6645T>A ENSP00000506040.1:p.Val2215=
ENST00000680047.1:n.7101T>A
ENST00000680072.1:c.6726T>A ENSP00000506581.1:p.Val2242=
ENST00000680181.1:c.6810T>A ENSP00000505548.1:p.Val2270=
ENST00000680365.1:c.396T>A ENSP00000506019.1:p.Val132=
ENST00000680513.1:c.6762T>A ENSP00000505284.1:p.Val2254=
ENST00000680534.1:c.6942T>A ENSP00000506674.1:p.Val2314=
ENST00000680766.1:c.6879T>A ENSP00000505204.1:p.Val2293=
ENST00000680952.1:c.6879T>A ENSP00000506407.1:p.Val2293=
ENST00000681216.1:c.396T>A ENSP00000505551.1:p.Val132=
ENST00000681412.1:c.6903T>A ENSP00000506486.1:p.Val2301=
ENST00000681722.1:c.6879T>A ENSP00000506566.1:p.Val2293=
ENST00000356239.7:c.6903T>A ENSP00000348573.3:p.Val2301=
ENST00000358100.6:c.6762T>A ENSP00000350813.3:p.Val2254=
ENST00000359028.6:c.6936T>A ENSP00000351922.3:p.Val2312=
ENST00000394534.6:c.441T>A ENSP00000378042.2:p.Val147=
NM_005751.4:c.6903T>A , LRG_331t1:c.6903T>A NP_005742.4:p.Val2301=
NM_147185.2:c.6879T>A NP_671714.1:p.Val2293=
XM_006715827.1:c.6762T>A XP_006715890.1:p.Val2254=
XM_011515709.1:c.7050T>A XP_011514011.1:p.Val2350=
XM_011515710.1:c.7074T>A XP_011514012.1:p.Val2358=
XM_011515711.1:c.7014T>A XP_011514013.1:p.Val2338=
XM_011515712.1:c.7011T>A XP_011514014.1:p.Val2337=
XM_011515713.1:c.6996T>A XP_011514015.1:p.Val2332=
XM_011515714.1:c.7035T>A XP_011514016.1:p.Val2345=
XM_011515716.1:c.6954T>A XP_011514018.1:p.Val2318=
XM_011515717.1:c.6909T>A XP_011514019.1:p.Val2303=
XM_011515718.1:c.6939T>A XP_011514020.1:p.Val2313=
XM_011515719.1:c.6915T>A XP_011514021.1:p.Val2305=
XM_011515720.1:c.6798T>A XP_011514022.1:p.Val2266=
XM_011515721.1:c.1563T>A XP_011514023.1:p.Val521=
XM_011515722.1:c.1524T>A XP_011514024.1:p.Val508=
XM_017011642.2:c.7038T>A XP_016867131.1:p.Val2346=
XM_017011643.2:c.6999T>A XP_016867132.1:p.Val2333=
XM_017011644.2:c.7038T>A XP_016867133.1:p.Val2346=
XM_017011645.2:c.6984T>A XP_016867134.1:p.Val2328=
XM_017011646.2:c.6999T>A XP_016867135.1:p.Val2333=
XM_017011647.2:c.6945T>A XP_016867136.1:p.Val2315=
XM_017011648.2:c.6942T>A XP_016867137.1:p.Val2314=
XM_017011649.2:c.6975T>A XP_016867138.1:p.Val2325=
XM_017011650.2:c.6903T>A XP_016867139.1:p.Val2301=
XM_017011651.2:c.6897T>A XP_016867140.1:p.Val2299=
XM_017011652.2:c.7038T>A XP_016867141.1:p.Val2346=
XM_017011653.2:c.6810T>A XP_016867142.1:p.Val2270=
XM_017011654.2:c.6762T>A XP_016867143.1:p.Val2254=
XM_017011655.2:c.6666T>A XP_016867144.1:p.Val2222=
XM_017011656.2:c.6666T>A XP_016867145.1:p.Val2222=
XM_017011657.2:c.2703T>A XP_016867146.1:p.Val901=
XM_017011658.2:c.1587T>A XP_016867147.1:p.Val529=
XM_017011659.2:c.1548T>A XP_016867148.1:p.Val516=
XM_017011660.2:c.1548T>A XP_016867149.1:p.Val516=
XM_024446631.1:c.6801T>A XP_024302399.1:p.Val2267=
NM_147185.3:c.6879T>A NP_671714.1:p.Val2293=
NM_001379277.1:c.1548T>A NP_001366206.1:p.Val516=
NM_005751.5:c.6903T>A MANE Select NP_005742.4:p.Val2301=