Canonical Allele Identifier: CA368133941

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707189G>C (hg19) ; chr7:g.92077875G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077875G>C , CM000669.2:g.92077875G>C	GRCh38
NC_000007.13:g.91707189G>C , CM000669.1:g.91707189G>C	GRCh37
NC_000007.12:g.91545125G>C	NCBI36
NG_011623.1:g.142001G>C , LRG_331:g.142001G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6945G>C MANE Select	ENSP00000348573.3:p.Lys2315Asn
ENST00000359028.7:c.7017G>C	ENSP00000351922.4:p.Lys2339Asn
ENST00000394534.7:c.438G>C	ENSP00000378042.3:p.Lys146Asn
ENST00000491695.2:c.1590G>C	ENSP00000494626.2:p.Lys530Asn
ENST00000674381.2:c.*6674G>C	ENSP00000501536.2:n.*6674G>C
ENST00000679448.1:c.6921G>C	ENSP00000505889.1:p.Lys2307Asn
ENST00000679457.1:c.6921G>C	ENSP00000505450.1:p.Lys2307Asn
ENST00000679474.1:n.7143G>C
ENST00000679521.1:c.6891G>C	ENSP00000505456.1:p.Lys2297Asn
ENST00000679554.1:c.*6730G>C	ENSP00000506415.1:n.*6730G>C
ENST00000679722.1:n.7167G>C
ENST00000679821.1:c.6687G>C	ENSP00000506040.1:p.Lys2229Asn
ENST00000680047.1:n.7143G>C
ENST00000680072.1:c.6768G>C	ENSP00000506581.1:p.Lys2256Asn
ENST00000680181.1:c.6852G>C	ENSP00000505548.1:p.Lys2284Asn
ENST00000680365.1:c.438G>C	ENSP00000506019.1:p.Lys146Asn
ENST00000680513.1:c.6804G>C	ENSP00000505284.1:p.Lys2268Asn
ENST00000680534.1:c.6984G>C	ENSP00000506674.1:p.Lys2328Asn
ENST00000680766.1:c.6921G>C	ENSP00000505204.1:p.Lys2307Asn
ENST00000680952.1:c.6921G>C	ENSP00000506407.1:p.Lys2307Asn
ENST00000681216.1:c.438G>C	ENSP00000505551.1:p.Lys146Asn
ENST00000681412.1:c.6945G>C	ENSP00000506486.1:p.Lys2315Asn
ENST00000681722.1:c.6921G>C	ENSP00000506566.1:p.Lys2307Asn
ENST00000356239.7:c.6945G>C	ENSP00000348573.3:p.Lys2315Asn
ENST00000358100.6:c.6804G>C	ENSP00000350813.3:p.Lys2268Asn
ENST00000359028.6:c.6978G>C	ENSP00000351922.3:p.Lys2326Asn
ENST00000394534.6:c.483G>C	ENSP00000378042.2:p.Lys161Asn
NM_005751.4:c.6945G>C , LRG_331t1:c.6945G>C	NP_005742.4:p.Lys2315Asn
NM_147185.2:c.6921G>C	NP_671714.1:p.Lys2307Asn
XM_006715827.1:c.6804G>C	XP_006715890.1:p.Lys2268Asn
XM_011515709.1:c.7092G>C	XP_011514011.1:p.Lys2364Asn
XM_011515710.1:c.7116G>C	XP_011514012.1:p.Lys2372Asn
XM_011515711.1:c.7056G>C	XP_011514013.1:p.Lys2352Asn
XM_011515712.1:c.7053G>C	XP_011514014.1:p.Lys2351Asn
XM_011515713.1:c.7038G>C	XP_011514015.1:p.Lys2346Asn
XM_011515714.1:c.7077G>C	XP_011514016.1:p.Lys2359Asn
XM_011515716.1:c.6996G>C	XP_011514018.1:p.Lys2332Asn
XM_011515717.1:c.6951G>C	XP_011514019.1:p.Lys2317Asn
XM_011515718.1:c.6981G>C	XP_011514020.1:p.Lys2327Asn
XM_011515719.1:c.6957G>C	XP_011514021.1:p.Lys2319Asn
XM_011515720.1:c.6840G>C	XP_011514022.1:p.Lys2280Asn
XM_011515721.1:c.1605G>C	XP_011514023.1:p.Lys535Asn
XM_011515722.1:c.1566G>C	XP_011514024.1:p.Lys522Asn
XM_017011642.2:c.7080G>C	XP_016867131.1:p.Lys2360Asn
XM_017011643.2:c.7041G>C	XP_016867132.1:p.Lys2347Asn
XM_017011644.2:c.7080G>C	XP_016867133.1:p.Lys2360Asn
XM_017011645.2:c.7026G>C	XP_016867134.1:p.Lys2342Asn
XM_017011646.2:c.7041G>C	XP_016867135.1:p.Lys2347Asn
XM_017011647.2:c.6987G>C	XP_016867136.1:p.Lys2329Asn
XM_017011648.2:c.6984G>C	XP_016867137.1:p.Lys2328Asn
XM_017011649.2:c.7017G>C	XP_016867138.1:p.Lys2339Asn
XM_017011650.2:c.6945G>C	XP_016867139.1:p.Lys2315Asn
XM_017011651.2:c.6939G>C	XP_016867140.1:p.Lys2313Asn
XM_017011652.2:c.7080G>C	XP_016867141.1:p.Lys2360Asn
XM_017011653.2:c.6852G>C	XP_016867142.1:p.Lys2284Asn
XM_017011654.2:c.6804G>C	XP_016867143.1:p.Lys2268Asn
XM_017011655.2:c.6708G>C	XP_016867144.1:p.Lys2236Asn
XM_017011656.2:c.6708G>C	XP_016867145.1:p.Lys2236Asn
XM_017011657.2:c.2745G>C	XP_016867146.1:p.Lys915Asn
XM_017011658.2:c.1629G>C	XP_016867147.1:p.Lys543Asn
XM_017011659.2:c.1590G>C	XP_016867148.1:p.Lys530Asn
XM_017011660.2:c.1590G>C	XP_016867149.1:p.Lys530Asn
XM_024446631.1:c.6843G>C	XP_024302399.1:p.Lys2281Asn
NM_147185.3:c.6921G>C	NP_671714.1:p.Lys2307Asn
NM_001379277.1:c.1590G>C	NP_001366206.1:p.Lys530Asn
NM_005751.5:c.6945G>C MANE Select	NP_005742.4:p.Lys2315Asn