Canonical Allele Identifier: CA456450389

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707054C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077740C>A , CM000669.2:g.92077740C>A	GRCh38
NC_000007.13:g.91707054C>A , CM000669.1:g.91707054C>A	GRCh37
NC_000007.12:g.91544990C>A	NCBI36
NG_011623.1:g.141866C>A , LRG_331:g.141866C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6810C>A MANE Select	ENSP00000348573.3:p.Ala2270=
ENST00000359028.7:c.6882C>A	ENSP00000351922.4:p.Ala2294=
ENST00000394534.7:c.303C>A	ENSP00000378042.3:p.Ala101=
ENST00000491695.2:c.1455C>A	ENSP00000494626.2:p.Ala485=
ENST00000674381.2:c.*6539C>A	ENSP00000501536.2:n.*6539C>A
ENST00000679448.1:c.6786C>A	ENSP00000505889.1:p.Ala2262=
ENST00000679457.1:c.6786C>A	ENSP00000505450.1:p.Ala2262=
ENST00000679474.1:n.7008C>A
ENST00000679521.1:c.6756C>A	ENSP00000505456.1:p.Ala2252=
ENST00000679554.1:c.*6595C>A	ENSP00000506415.1:n.*6595C>A
ENST00000679722.1:n.7032C>A
ENST00000679821.1:c.6552C>A	ENSP00000506040.1:p.Ala2184=
ENST00000680047.1:n.7008C>A
ENST00000680072.1:c.6633C>A	ENSP00000506581.1:p.Ala2211=
ENST00000680181.1:c.6717C>A	ENSP00000505548.1:p.Ala2239=
ENST00000680365.1:c.303C>A	ENSP00000506019.1:p.Ala101=
ENST00000680513.1:c.6669C>A	ENSP00000505284.1:p.Ala2223=
ENST00000680534.1:c.6849C>A	ENSP00000506674.1:p.Ala2283=
ENST00000680766.1:c.6786C>A	ENSP00000505204.1:p.Ala2262=
ENST00000680952.1:c.6786C>A	ENSP00000506407.1:p.Ala2262=
ENST00000681216.1:c.303C>A	ENSP00000505551.1:p.Ala101=
ENST00000681412.1:c.6810C>A	ENSP00000506486.1:p.Ala2270=
ENST00000681722.1:c.6786C>A	ENSP00000506566.1:p.Ala2262=
ENST00000356239.7:c.6810C>A	ENSP00000348573.3:p.Ala2270=
ENST00000358100.6:c.6669C>A	ENSP00000350813.3:p.Ala2223=
ENST00000359028.6:c.6843C>A	ENSP00000351922.3:p.Ala2281=
ENST00000394534.6:c.348C>A	ENSP00000378042.2:p.Ala116=
NM_005751.4:c.6810C>A , LRG_331t1:c.6810C>A	NP_005742.4:p.Ala2270=
NM_147185.2:c.6786C>A	NP_671714.1:p.Ala2262=
XM_006715827.1:c.6669C>A	XP_006715890.1:p.Ala2223=
XM_011515709.1:c.6957C>A	XP_011514011.1:p.Ala2319=
XM_011515710.1:c.6981C>A	XP_011514012.1:p.Ala2327=
XM_011515711.1:c.6921C>A	XP_011514013.1:p.Ala2307=
XM_011515712.1:c.6918C>A	XP_011514014.1:p.Ala2306=
XM_011515713.1:c.6903C>A	XP_011514015.1:p.Ala2301=
XM_011515714.1:c.6942C>A	XP_011514016.1:p.Ala2314=
XM_011515716.1:c.6861C>A	XP_011514018.1:p.Ala2287=
XM_011515717.1:c.6816C>A	XP_011514019.1:p.Ala2272=
XM_011515718.1:c.6846C>A	XP_011514020.1:p.Ala2282=
XM_011515719.1:c.6822C>A	XP_011514021.1:p.Ala2274=
XM_011515720.1:c.6705C>A	XP_011514022.1:p.Ala2235=
XM_011515721.1:c.1470C>A	XP_011514023.1:p.Ala490=
XM_011515722.1:c.1431C>A	XP_011514024.1:p.Ala477=
XM_017011642.2:c.6945C>A	XP_016867131.1:p.Ala2315=
XM_017011643.2:c.6906C>A	XP_016867132.1:p.Ala2302=
XM_017011644.2:c.6945C>A	XP_016867133.1:p.Ala2315=
XM_017011645.2:c.6891C>A	XP_016867134.1:p.Ala2297=
XM_017011646.2:c.6906C>A	XP_016867135.1:p.Ala2302=
XM_017011647.2:c.6852C>A	XP_016867136.1:p.Ala2284=
XM_017011648.2:c.6849C>A	XP_016867137.1:p.Ala2283=
XM_017011649.2:c.6882C>A	XP_016867138.1:p.Ala2294=
XM_017011650.2:c.6810C>A	XP_016867139.1:p.Ala2270=
XM_017011651.2:c.6804C>A	XP_016867140.1:p.Ala2268=
XM_017011652.2:c.6945C>A	XP_016867141.1:p.Ala2315=
XM_017011653.2:c.6717C>A	XP_016867142.1:p.Ala2239=
XM_017011654.2:c.6669C>A	XP_016867143.1:p.Ala2223=
XM_017011655.2:c.6573C>A	XP_016867144.1:p.Ala2191=
XM_017011656.2:c.6573C>A	XP_016867145.1:p.Ala2191=
XM_017011657.2:c.2610C>A	XP_016867146.1:p.Ala870=
XM_017011658.2:c.1494C>A	XP_016867147.1:p.Ala498=
XM_017011659.2:c.1455C>A	XP_016867148.1:p.Ala485=
XM_017011660.2:c.1455C>A	XP_016867149.1:p.Ala485=
XM_024446631.1:c.6708C>A	XP_024302399.1:p.Ala2236=
NM_147185.3:c.6786C>A	NP_671714.1:p.Ala2262=
NM_001379277.1:c.1455C>A	NP_001366206.1:p.Ala485=
NM_005751.5:c.6810C>A MANE Select	NP_005742.4:p.Ala2270=