Canonical Allele Identifier: CA368133854

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707151A>C (hg19) ; chr7:g.92077837A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077837A>C , CM000669.2:g.92077837A>C	GRCh38
NC_000007.13:g.91707151A>C , CM000669.1:g.91707151A>C	GRCh37
NC_000007.12:g.91545087A>C	NCBI36
NG_011623.1:g.141963A>C , LRG_331:g.141963A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6907A>C MANE Select	ENSP00000348573.3:p.Lys2303Gln
ENST00000359028.7:c.6979A>C	ENSP00000351922.4:p.Lys2327Gln
ENST00000394534.7:c.400A>C	ENSP00000378042.3:p.Lys134Gln
ENST00000491695.2:c.1552A>C	ENSP00000494626.2:p.Lys518Gln
ENST00000674381.2:c.*6636A>C	ENSP00000501536.2:n.*6636A>C
ENST00000679448.1:c.6883A>C	ENSP00000505889.1:p.Lys2295Gln
ENST00000679457.1:c.6883A>C	ENSP00000505450.1:p.Lys2295Gln
ENST00000679474.1:n.7105A>C
ENST00000679521.1:c.6853A>C	ENSP00000505456.1:p.Lys2285Gln
ENST00000679554.1:c.*6692A>C	ENSP00000506415.1:n.*6692A>C
ENST00000679722.1:n.7129A>C
ENST00000679821.1:c.6649A>C	ENSP00000506040.1:p.Lys2217Gln
ENST00000680047.1:n.7105A>C
ENST00000680072.1:c.6730A>C	ENSP00000506581.1:p.Lys2244Gln
ENST00000680181.1:c.6814A>C	ENSP00000505548.1:p.Lys2272Gln
ENST00000680365.1:c.400A>C	ENSP00000506019.1:p.Lys134Gln
ENST00000680513.1:c.6766A>C	ENSP00000505284.1:p.Lys2256Gln
ENST00000680534.1:c.6946A>C	ENSP00000506674.1:p.Lys2316Gln
ENST00000680766.1:c.6883A>C	ENSP00000505204.1:p.Lys2295Gln
ENST00000680952.1:c.6883A>C	ENSP00000506407.1:p.Lys2295Gln
ENST00000681216.1:c.400A>C	ENSP00000505551.1:p.Lys134Gln
ENST00000681412.1:c.6907A>C	ENSP00000506486.1:p.Lys2303Gln
ENST00000681722.1:c.6883A>C	ENSP00000506566.1:p.Lys2295Gln
ENST00000356239.7:c.6907A>C	ENSP00000348573.3:p.Lys2303Gln
ENST00000358100.6:c.6766A>C	ENSP00000350813.3:p.Lys2256Gln
ENST00000359028.6:c.6940A>C	ENSP00000351922.3:p.Lys2314Gln
ENST00000394534.6:c.445A>C	ENSP00000378042.2:p.Lys149Gln
NM_005751.4:c.6907A>C , LRG_331t1:c.6907A>C	NP_005742.4:p.Lys2303Gln
NM_147185.2:c.6883A>C	NP_671714.1:p.Lys2295Gln
XM_006715827.1:c.6766A>C	XP_006715890.1:p.Lys2256Gln
XM_011515709.1:c.7054A>C	XP_011514011.1:p.Lys2352Gln
XM_011515710.1:c.7078A>C	XP_011514012.1:p.Lys2360Gln
XM_011515711.1:c.7018A>C	XP_011514013.1:p.Lys2340Gln
XM_011515712.1:c.7015A>C	XP_011514014.1:p.Lys2339Gln
XM_011515713.1:c.7000A>C	XP_011514015.1:p.Lys2334Gln
XM_011515714.1:c.7039A>C	XP_011514016.1:p.Lys2347Gln
XM_011515716.1:c.6958A>C	XP_011514018.1:p.Lys2320Gln
XM_011515717.1:c.6913A>C	XP_011514019.1:p.Lys2305Gln
XM_011515718.1:c.6943A>C	XP_011514020.1:p.Lys2315Gln
XM_011515719.1:c.6919A>C	XP_011514021.1:p.Lys2307Gln
XM_011515720.1:c.6802A>C	XP_011514022.1:p.Lys2268Gln
XM_011515721.1:c.1567A>C	XP_011514023.1:p.Lys523Gln
XM_011515722.1:c.1528A>C	XP_011514024.1:p.Lys510Gln
XM_017011642.2:c.7042A>C	XP_016867131.1:p.Lys2348Gln
XM_017011643.2:c.7003A>C	XP_016867132.1:p.Lys2335Gln
XM_017011644.2:c.7042A>C	XP_016867133.1:p.Lys2348Gln
XM_017011645.2:c.6988A>C	XP_016867134.1:p.Lys2330Gln
XM_017011646.2:c.7003A>C	XP_016867135.1:p.Lys2335Gln
XM_017011647.2:c.6949A>C	XP_016867136.1:p.Lys2317Gln
XM_017011648.2:c.6946A>C	XP_016867137.1:p.Lys2316Gln
XM_017011649.2:c.6979A>C	XP_016867138.1:p.Lys2327Gln
XM_017011650.2:c.6907A>C	XP_016867139.1:p.Lys2303Gln
XM_017011651.2:c.6901A>C	XP_016867140.1:p.Lys2301Gln
XM_017011652.2:c.7042A>C	XP_016867141.1:p.Lys2348Gln
XM_017011653.2:c.6814A>C	XP_016867142.1:p.Lys2272Gln
XM_017011654.2:c.6766A>C	XP_016867143.1:p.Lys2256Gln
XM_017011655.2:c.6670A>C	XP_016867144.1:p.Lys2224Gln
XM_017011656.2:c.6670A>C	XP_016867145.1:p.Lys2224Gln
XM_017011657.2:c.2707A>C	XP_016867146.1:p.Lys903Gln
XM_017011658.2:c.1591A>C	XP_016867147.1:p.Lys531Gln
XM_017011659.2:c.1552A>C	XP_016867148.1:p.Lys518Gln
XM_017011660.2:c.1552A>C	XP_016867149.1:p.Lys518Gln
XM_024446631.1:c.6805A>C	XP_024302399.1:p.Lys2269Gln
NM_147185.3:c.6883A>C	NP_671714.1:p.Lys2295Gln
NM_001379277.1:c.1552A>C	NP_001366206.1:p.Lys518Gln
NM_005751.5:c.6907A>C MANE Select	NP_005742.4:p.Lys2303Gln