Canonical Allele Identifier: CA368133843

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707144A>C (hg19) ; chr7:g.92077830A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077830A>C , CM000669.2:g.92077830A>C	GRCh38
NC_000007.13:g.91707144A>C , CM000669.1:g.91707144A>C	GRCh37
NC_000007.12:g.91545080A>C	NCBI36
NG_011623.1:g.141956A>C , LRG_331:g.141956A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6900A>C MANE Select	ENSP00000348573.3:p.Gln2300His
ENST00000359028.7:c.6972A>C	ENSP00000351922.4:p.Gln2324His
ENST00000394534.7:c.393A>C	ENSP00000378042.3:p.Gln131His
ENST00000491695.2:c.1545A>C	ENSP00000494626.2:p.Gln515His
ENST00000674381.2:c.*6629A>C	ENSP00000501536.2:n.*6629A>C
ENST00000679448.1:c.6876A>C	ENSP00000505889.1:p.Gln2292His
ENST00000679457.1:c.6876A>C	ENSP00000505450.1:p.Gln2292His
ENST00000679474.1:n.7098A>C
ENST00000679521.1:c.6846A>C	ENSP00000505456.1:p.Gln2282His
ENST00000679554.1:c.*6685A>C	ENSP00000506415.1:n.*6685A>C
ENST00000679722.1:n.7122A>C
ENST00000679821.1:c.6642A>C	ENSP00000506040.1:p.Gln2214His
ENST00000680047.1:n.7098A>C
ENST00000680072.1:c.6723A>C	ENSP00000506581.1:p.Gln2241His
ENST00000680181.1:c.6807A>C	ENSP00000505548.1:p.Gln2269His
ENST00000680365.1:c.393A>C	ENSP00000506019.1:p.Gln131His
ENST00000680513.1:c.6759A>C	ENSP00000505284.1:p.Gln2253His
ENST00000680534.1:c.6939A>C	ENSP00000506674.1:p.Gln2313His
ENST00000680766.1:c.6876A>C	ENSP00000505204.1:p.Gln2292His
ENST00000680952.1:c.6876A>C	ENSP00000506407.1:p.Gln2292His
ENST00000681216.1:c.393A>C	ENSP00000505551.1:p.Gln131His
ENST00000681412.1:c.6900A>C	ENSP00000506486.1:p.Gln2300His
ENST00000681722.1:c.6876A>C	ENSP00000506566.1:p.Gln2292His
ENST00000356239.7:c.6900A>C	ENSP00000348573.3:p.Gln2300His
ENST00000358100.6:c.6759A>C	ENSP00000350813.3:p.Gln2253His
ENST00000359028.6:c.6933A>C	ENSP00000351922.3:p.Gln2311His
ENST00000394534.6:c.438A>C	ENSP00000378042.2:p.Gln146His
NM_005751.4:c.6900A>C , LRG_331t1:c.6900A>C	NP_005742.4:p.Gln2300His
NM_147185.2:c.6876A>C	NP_671714.1:p.Gln2292His
XM_006715827.1:c.6759A>C	XP_006715890.1:p.Gln2253His
XM_011515709.1:c.7047A>C	XP_011514011.1:p.Gln2349His
XM_011515710.1:c.7071A>C	XP_011514012.1:p.Gln2357His
XM_011515711.1:c.7011A>C	XP_011514013.1:p.Gln2337His
XM_011515712.1:c.7008A>C	XP_011514014.1:p.Gln2336His
XM_011515713.1:c.6993A>C	XP_011514015.1:p.Gln2331His
XM_011515714.1:c.7032A>C	XP_011514016.1:p.Gln2344His
XM_011515716.1:c.6951A>C	XP_011514018.1:p.Gln2317His
XM_011515717.1:c.6906A>C	XP_011514019.1:p.Gln2302His
XM_011515718.1:c.6936A>C	XP_011514020.1:p.Gln2312His
XM_011515719.1:c.6912A>C	XP_011514021.1:p.Gln2304His
XM_011515720.1:c.6795A>C	XP_011514022.1:p.Gln2265His
XM_011515721.1:c.1560A>C	XP_011514023.1:p.Gln520His
XM_011515722.1:c.1521A>C	XP_011514024.1:p.Gln507His
XM_017011642.2:c.7035A>C	XP_016867131.1:p.Gln2345His
XM_017011643.2:c.6996A>C	XP_016867132.1:p.Gln2332His
XM_017011644.2:c.7035A>C	XP_016867133.1:p.Gln2345His
XM_017011645.2:c.6981A>C	XP_016867134.1:p.Gln2327His
XM_017011646.2:c.6996A>C	XP_016867135.1:p.Gln2332His
XM_017011647.2:c.6942A>C	XP_016867136.1:p.Gln2314His
XM_017011648.2:c.6939A>C	XP_016867137.1:p.Gln2313His
XM_017011649.2:c.6972A>C	XP_016867138.1:p.Gln2324His
XM_017011650.2:c.6900A>C	XP_016867139.1:p.Gln2300His
XM_017011651.2:c.6894A>C	XP_016867140.1:p.Gln2298His
XM_017011652.2:c.7035A>C	XP_016867141.1:p.Gln2345His
XM_017011653.2:c.6807A>C	XP_016867142.1:p.Gln2269His
XM_017011654.2:c.6759A>C	XP_016867143.1:p.Gln2253His
XM_017011655.2:c.6663A>C	XP_016867144.1:p.Gln2221His
XM_017011656.2:c.6663A>C	XP_016867145.1:p.Gln2221His
XM_017011657.2:c.2700A>C	XP_016867146.1:p.Gln900His
XM_017011658.2:c.1584A>C	XP_016867147.1:p.Gln528His
XM_017011659.2:c.1545A>C	XP_016867148.1:p.Gln515His
XM_017011660.2:c.1545A>C	XP_016867149.1:p.Gln515His
XM_024446631.1:c.6798A>C	XP_024302399.1:p.Gln2266His
NM_147185.3:c.6876A>C	NP_671714.1:p.Gln2292His
NM_001379277.1:c.1545A>C	NP_001366206.1:p.Gln515His
NM_005751.5:c.6900A>C MANE Select	NP_005742.4:p.Gln2300His