Canonical Allele Identifier: CA368133934

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707186C>G (hg19) ; chr7:g.92077872C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077872C>G , CM000669.2:g.92077872C>G	GRCh38
NC_000007.13:g.91707186C>G , CM000669.1:g.91707186C>G	GRCh37
NC_000007.12:g.91545122C>G	NCBI36
NG_011623.1:g.141998C>G , LRG_331:g.141998C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6942C>G MANE Select	ENSP00000348573.3:p.Asn2314Lys
ENST00000359028.7:c.7014C>G	ENSP00000351922.4:p.Asn2338Lys
ENST00000394534.7:c.435C>G	ENSP00000378042.3:p.Asn145Lys
ENST00000491695.2:c.1587C>G	ENSP00000494626.2:p.Asn529Lys
ENST00000674381.2:c.*6671C>G	ENSP00000501536.2:n.*6671C>G
ENST00000679448.1:c.6918C>G	ENSP00000505889.1:p.Asn2306Lys
ENST00000679457.1:c.6918C>G	ENSP00000505450.1:p.Asn2306Lys
ENST00000679474.1:n.7140C>G
ENST00000679521.1:c.6888C>G	ENSP00000505456.1:p.Asn2296Lys
ENST00000679554.1:c.*6727C>G	ENSP00000506415.1:n.*6727C>G
ENST00000679722.1:n.7164C>G
ENST00000679821.1:c.6684C>G	ENSP00000506040.1:p.Asn2228Lys
ENST00000680047.1:n.7140C>G
ENST00000680072.1:c.6765C>G	ENSP00000506581.1:p.Asn2255Lys
ENST00000680181.1:c.6849C>G	ENSP00000505548.1:p.Asn2283Lys
ENST00000680365.1:c.435C>G	ENSP00000506019.1:p.Asn145Lys
ENST00000680513.1:c.6801C>G	ENSP00000505284.1:p.Asn2267Lys
ENST00000680534.1:c.6981C>G	ENSP00000506674.1:p.Asn2327Lys
ENST00000680766.1:c.6918C>G	ENSP00000505204.1:p.Asn2306Lys
ENST00000680952.1:c.6918C>G	ENSP00000506407.1:p.Asn2306Lys
ENST00000681216.1:c.435C>G	ENSP00000505551.1:p.Asn145Lys
ENST00000681412.1:c.6942C>G	ENSP00000506486.1:p.Asn2314Lys
ENST00000681722.1:c.6918C>G	ENSP00000506566.1:p.Asn2306Lys
ENST00000356239.7:c.6942C>G	ENSP00000348573.3:p.Asn2314Lys
ENST00000358100.6:c.6801C>G	ENSP00000350813.3:p.Asn2267Lys
ENST00000359028.6:c.6975C>G	ENSP00000351922.3:p.Asn2325Lys
ENST00000394534.6:c.480C>G	ENSP00000378042.2:p.Asn160Lys
NM_005751.4:c.6942C>G , LRG_331t1:c.6942C>G	NP_005742.4:p.Asn2314Lys
NM_147185.2:c.6918C>G	NP_671714.1:p.Asn2306Lys
XM_006715827.1:c.6801C>G	XP_006715890.1:p.Asn2267Lys
XM_011515709.1:c.7089C>G	XP_011514011.1:p.Asn2363Lys
XM_011515710.1:c.7113C>G	XP_011514012.1:p.Asn2371Lys
XM_011515711.1:c.7053C>G	XP_011514013.1:p.Asn2351Lys
XM_011515712.1:c.7050C>G	XP_011514014.1:p.Asn2350Lys
XM_011515713.1:c.7035C>G	XP_011514015.1:p.Asn2345Lys
XM_011515714.1:c.7074C>G	XP_011514016.1:p.Asn2358Lys
XM_011515716.1:c.6993C>G	XP_011514018.1:p.Asn2331Lys
XM_011515717.1:c.6948C>G	XP_011514019.1:p.Asn2316Lys
XM_011515718.1:c.6978C>G	XP_011514020.1:p.Asn2326Lys
XM_011515719.1:c.6954C>G	XP_011514021.1:p.Asn2318Lys
XM_011515720.1:c.6837C>G	XP_011514022.1:p.Asn2279Lys
XM_011515721.1:c.1602C>G	XP_011514023.1:p.Asn534Lys
XM_011515722.1:c.1563C>G	XP_011514024.1:p.Asn521Lys
XM_017011642.2:c.7077C>G	XP_016867131.1:p.Asn2359Lys
XM_017011643.2:c.7038C>G	XP_016867132.1:p.Asn2346Lys
XM_017011644.2:c.7077C>G	XP_016867133.1:p.Asn2359Lys
XM_017011645.2:c.7023C>G	XP_016867134.1:p.Asn2341Lys
XM_017011646.2:c.7038C>G	XP_016867135.1:p.Asn2346Lys
XM_017011647.2:c.6984C>G	XP_016867136.1:p.Asn2328Lys
XM_017011648.2:c.6981C>G	XP_016867137.1:p.Asn2327Lys
XM_017011649.2:c.7014C>G	XP_016867138.1:p.Asn2338Lys
XM_017011650.2:c.6942C>G	XP_016867139.1:p.Asn2314Lys
XM_017011651.2:c.6936C>G	XP_016867140.1:p.Asn2312Lys
XM_017011652.2:c.7077C>G	XP_016867141.1:p.Asn2359Lys
XM_017011653.2:c.6849C>G	XP_016867142.1:p.Asn2283Lys
XM_017011654.2:c.6801C>G	XP_016867143.1:p.Asn2267Lys
XM_017011655.2:c.6705C>G	XP_016867144.1:p.Asn2235Lys
XM_017011656.2:c.6705C>G	XP_016867145.1:p.Asn2235Lys
XM_017011657.2:c.2742C>G	XP_016867146.1:p.Asn914Lys
XM_017011658.2:c.1626C>G	XP_016867147.1:p.Asn542Lys
XM_017011659.2:c.1587C>G	XP_016867148.1:p.Asn529Lys
XM_017011660.2:c.1587C>G	XP_016867149.1:p.Asn529Lys
XM_024446631.1:c.6840C>G	XP_024302399.1:p.Asn2280Lys
NM_147185.3:c.6918C>G	NP_671714.1:p.Asn2306Lys
NM_001379277.1:c.1587C>G	NP_001366206.1:p.Asn529Lys
NM_005751.5:c.6942C>G MANE Select	NP_005742.4:p.Asn2314Lys