Canonical Allele Identifier: CA456450496

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707156C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077842C>G , CM000669.2:g.92077842C>G	GRCh38
NC_000007.13:g.91707156C>G , CM000669.1:g.91707156C>G	GRCh37
NC_000007.12:g.91545092C>G	NCBI36
NG_011623.1:g.141968C>G , LRG_331:g.141968C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6912C>G MANE Select	ENSP00000348573.3:p.Leu2304=
ENST00000359028.7:c.6984C>G	ENSP00000351922.4:p.Leu2328=
ENST00000394534.7:c.405C>G	ENSP00000378042.3:p.Leu135=
ENST00000491695.2:c.1557C>G	ENSP00000494626.2:p.Leu519=
ENST00000674381.2:c.*6641C>G	ENSP00000501536.2:n.*6641C>G
ENST00000679448.1:c.6888C>G	ENSP00000505889.1:p.Leu2296=
ENST00000679457.1:c.6888C>G	ENSP00000505450.1:p.Leu2296=
ENST00000679474.1:n.7110C>G
ENST00000679521.1:c.6858C>G	ENSP00000505456.1:p.Leu2286=
ENST00000679554.1:c.*6697C>G	ENSP00000506415.1:n.*6697C>G
ENST00000679722.1:n.7134C>G
ENST00000679821.1:c.6654C>G	ENSP00000506040.1:p.Leu2218=
ENST00000680047.1:n.7110C>G
ENST00000680072.1:c.6735C>G	ENSP00000506581.1:p.Leu2245=
ENST00000680181.1:c.6819C>G	ENSP00000505548.1:p.Leu2273=
ENST00000680365.1:c.405C>G	ENSP00000506019.1:p.Leu135=
ENST00000680513.1:c.6771C>G	ENSP00000505284.1:p.Leu2257=
ENST00000680534.1:c.6951C>G	ENSP00000506674.1:p.Leu2317=
ENST00000680766.1:c.6888C>G	ENSP00000505204.1:p.Leu2296=
ENST00000680952.1:c.6888C>G	ENSP00000506407.1:p.Leu2296=
ENST00000681216.1:c.405C>G	ENSP00000505551.1:p.Leu135=
ENST00000681412.1:c.6912C>G	ENSP00000506486.1:p.Leu2304=
ENST00000681722.1:c.6888C>G	ENSP00000506566.1:p.Leu2296=
ENST00000356239.7:c.6912C>G	ENSP00000348573.3:p.Leu2304=
ENST00000358100.6:c.6771C>G	ENSP00000350813.3:p.Leu2257=
ENST00000359028.6:c.6945C>G	ENSP00000351922.3:p.Leu2315=
ENST00000394534.6:c.450C>G	ENSP00000378042.2:p.Leu150=
NM_005751.4:c.6912C>G , LRG_331t1:c.6912C>G	NP_005742.4:p.Leu2304=
NM_147185.2:c.6888C>G	NP_671714.1:p.Leu2296=
XM_006715827.1:c.6771C>G	XP_006715890.1:p.Leu2257=
XM_011515709.1:c.7059C>G	XP_011514011.1:p.Leu2353=
XM_011515710.1:c.7083C>G	XP_011514012.1:p.Leu2361=
XM_011515711.1:c.7023C>G	XP_011514013.1:p.Leu2341=
XM_011515712.1:c.7020C>G	XP_011514014.1:p.Leu2340=
XM_011515713.1:c.7005C>G	XP_011514015.1:p.Leu2335=
XM_011515714.1:c.7044C>G	XP_011514016.1:p.Leu2348=
XM_011515716.1:c.6963C>G	XP_011514018.1:p.Leu2321=
XM_011515717.1:c.6918C>G	XP_011514019.1:p.Leu2306=
XM_011515718.1:c.6948C>G	XP_011514020.1:p.Leu2316=
XM_011515719.1:c.6924C>G	XP_011514021.1:p.Leu2308=
XM_011515720.1:c.6807C>G	XP_011514022.1:p.Leu2269=
XM_011515721.1:c.1572C>G	XP_011514023.1:p.Leu524=
XM_011515722.1:c.1533C>G	XP_011514024.1:p.Leu511=
XM_017011642.2:c.7047C>G	XP_016867131.1:p.Leu2349=
XM_017011643.2:c.7008C>G	XP_016867132.1:p.Leu2336=
XM_017011644.2:c.7047C>G	XP_016867133.1:p.Leu2349=
XM_017011645.2:c.6993C>G	XP_016867134.1:p.Leu2331=
XM_017011646.2:c.7008C>G	XP_016867135.1:p.Leu2336=
XM_017011647.2:c.6954C>G	XP_016867136.1:p.Leu2318=
XM_017011648.2:c.6951C>G	XP_016867137.1:p.Leu2317=
XM_017011649.2:c.6984C>G	XP_016867138.1:p.Leu2328=
XM_017011650.2:c.6912C>G	XP_016867139.1:p.Leu2304=
XM_017011651.2:c.6906C>G	XP_016867140.1:p.Leu2302=
XM_017011652.2:c.7047C>G	XP_016867141.1:p.Leu2349=
XM_017011653.2:c.6819C>G	XP_016867142.1:p.Leu2273=
XM_017011654.2:c.6771C>G	XP_016867143.1:p.Leu2257=
XM_017011655.2:c.6675C>G	XP_016867144.1:p.Leu2225=
XM_017011656.2:c.6675C>G	XP_016867145.1:p.Leu2225=
XM_017011657.2:c.2712C>G	XP_016867146.1:p.Leu904=
XM_017011658.2:c.1596C>G	XP_016867147.1:p.Leu532=
XM_017011659.2:c.1557C>G	XP_016867148.1:p.Leu519=
XM_017011660.2:c.1557C>G	XP_016867149.1:p.Leu519=
XM_024446631.1:c.6810C>G	XP_024302399.1:p.Leu2270=
NM_147185.3:c.6888C>G	NP_671714.1:p.Leu2296=
NM_001379277.1:c.1557C>G	NP_001366206.1:p.Leu519=
NM_005751.5:c.6912C>G MANE Select	NP_005742.4:p.Leu2304=