Canonical Allele Identifier: CA161884631

Gene: AKAP9

Linked Data

• dbSNP Id: rs201490585
• gnomAD v3: 7-92077870-A-G
• gnomAD v4: 7-92077870-A-G
• MyVariant Identifiers: chr7:g.91707184A>G (hg19) ; chr7:g.92077870A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077870A>G , CM000669.2:g.92077870A>G	GRCh38
NC_000007.13:g.91707184A>G , CM000669.1:g.91707184A>G	GRCh37
NC_000007.12:g.91545120A>G	NCBI36
NG_011623.1:g.141996A>G , LRG_331:g.141996A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6940A>G MANE Select	ENSP00000348573.3:p.Asn2314Asp
ENST00000359028.7:c.7012A>G	ENSP00000351922.4:p.Asn2338Asp
ENST00000394534.7:c.433A>G	ENSP00000378042.3:p.Asn145Asp
ENST00000491695.2:c.1585A>G	ENSP00000494626.2:p.Asn529Asp
ENST00000674381.2:c.*6669A>G	ENSP00000501536.2:n.*6669A>G
ENST00000679448.1:c.6916A>G	ENSP00000505889.1:p.Asn2306Asp
ENST00000679457.1:c.6916A>G	ENSP00000505450.1:p.Asn2306Asp
ENST00000679474.1:n.7138A>G
ENST00000679521.1:c.6886A>G	ENSP00000505456.1:p.Asn2296Asp
ENST00000679554.1:c.*6725A>G	ENSP00000506415.1:n.*6725A>G
ENST00000679722.1:n.7162A>G
ENST00000679821.1:c.6682A>G	ENSP00000506040.1:p.Asn2228Asp
ENST00000680047.1:n.7138A>G
ENST00000680072.1:c.6763A>G	ENSP00000506581.1:p.Asn2255Asp
ENST00000680181.1:c.6847A>G	ENSP00000505548.1:p.Asn2283Asp
ENST00000680365.1:c.433A>G	ENSP00000506019.1:p.Asn145Asp
ENST00000680513.1:c.6799A>G	ENSP00000505284.1:p.Asn2267Asp
ENST00000680534.1:c.6979A>G	ENSP00000506674.1:p.Asn2327Asp
ENST00000680766.1:c.6916A>G	ENSP00000505204.1:p.Asn2306Asp
ENST00000680952.1:c.6916A>G	ENSP00000506407.1:p.Asn2306Asp
ENST00000681216.1:c.433A>G	ENSP00000505551.1:p.Asn145Asp
ENST00000681412.1:c.6940A>G	ENSP00000506486.1:p.Asn2314Asp
ENST00000681722.1:c.6916A>G	ENSP00000506566.1:p.Asn2306Asp
ENST00000356239.7:c.6940A>G	ENSP00000348573.3:p.Asn2314Asp
ENST00000358100.6:c.6799A>G	ENSP00000350813.3:p.Asn2267Asp
ENST00000359028.6:c.6973A>G	ENSP00000351922.3:p.Asn2325Asp
ENST00000394534.6:c.478A>G	ENSP00000378042.2:p.Asn160Asp
NM_005751.4:c.6940A>G , LRG_331t1:c.6940A>G	NP_005742.4:p.Asn2314Asp
NM_147185.2:c.6916A>G	NP_671714.1:p.Asn2306Asp
XM_006715827.1:c.6799A>G	XP_006715890.1:p.Asn2267Asp
XM_011515709.1:c.7087A>G	XP_011514011.1:p.Asn2363Asp
XM_011515710.1:c.7111A>G	XP_011514012.1:p.Asn2371Asp
XM_011515711.1:c.7051A>G	XP_011514013.1:p.Asn2351Asp
XM_011515712.1:c.7048A>G	XP_011514014.1:p.Asn2350Asp
XM_011515713.1:c.7033A>G	XP_011514015.1:p.Asn2345Asp
XM_011515714.1:c.7072A>G	XP_011514016.1:p.Asn2358Asp
XM_011515716.1:c.6991A>G	XP_011514018.1:p.Asn2331Asp
XM_011515717.1:c.6946A>G	XP_011514019.1:p.Asn2316Asp
XM_011515718.1:c.6976A>G	XP_011514020.1:p.Asn2326Asp
XM_011515719.1:c.6952A>G	XP_011514021.1:p.Asn2318Asp
XM_011515720.1:c.6835A>G	XP_011514022.1:p.Asn2279Asp
XM_011515721.1:c.1600A>G	XP_011514023.1:p.Asn534Asp
XM_011515722.1:c.1561A>G	XP_011514024.1:p.Asn521Asp
XM_017011642.2:c.7075A>G	XP_016867131.1:p.Asn2359Asp
XM_017011643.2:c.7036A>G	XP_016867132.1:p.Asn2346Asp
XM_017011644.2:c.7075A>G	XP_016867133.1:p.Asn2359Asp
XM_017011645.2:c.7021A>G	XP_016867134.1:p.Asn2341Asp
XM_017011646.2:c.7036A>G	XP_016867135.1:p.Asn2346Asp
XM_017011647.2:c.6982A>G	XP_016867136.1:p.Asn2328Asp
XM_017011648.2:c.6979A>G	XP_016867137.1:p.Asn2327Asp
XM_017011649.2:c.7012A>G	XP_016867138.1:p.Asn2338Asp
XM_017011650.2:c.6940A>G	XP_016867139.1:p.Asn2314Asp
XM_017011651.2:c.6934A>G	XP_016867140.1:p.Asn2312Asp
XM_017011652.2:c.7075A>G	XP_016867141.1:p.Asn2359Asp
XM_017011653.2:c.6847A>G	XP_016867142.1:p.Asn2283Asp
XM_017011654.2:c.6799A>G	XP_016867143.1:p.Asn2267Asp
XM_017011655.2:c.6703A>G	XP_016867144.1:p.Asn2235Asp
XM_017011656.2:c.6703A>G	XP_016867145.1:p.Asn2235Asp
XM_017011657.2:c.2740A>G	XP_016867146.1:p.Asn914Asp
XM_017011658.2:c.1624A>G	XP_016867147.1:p.Asn542Asp
XM_017011659.2:c.1585A>G	XP_016867148.1:p.Asn529Asp
XM_017011660.2:c.1585A>G	XP_016867149.1:p.Asn529Asp
XM_024446631.1:c.6838A>G	XP_024302399.1:p.Asn2280Asp
NM_147185.3:c.6916A>G	NP_671714.1:p.Asn2306Asp
NM_001379277.1:c.1585A>G	NP_001366206.1:p.Asn529Asp
NM_005751.5:c.6940A>G MANE Select	NP_005742.4:p.Asn2314Asp