Canonical Allele Identifier: CA368133621

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707049G>C (hg19) ; chr7:g.92077735G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077735G>C , CM000669.2:g.92077735G>C	GRCh38
NC_000007.13:g.91707049G>C , CM000669.1:g.91707049G>C	GRCh37
NC_000007.12:g.91544985G>C	NCBI36
NG_011623.1:g.141861G>C , LRG_331:g.141861G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6805G>C MANE Select	ENSP00000348573.3:p.Asp2269His
ENST00000359028.7:c.6877G>C	ENSP00000351922.4:p.Asp2293His
ENST00000394534.7:c.298G>C	ENSP00000378042.3:p.Asp100His
ENST00000491695.2:c.1450G>C	ENSP00000494626.2:p.Asp484His
ENST00000674381.2:c.*6534G>C	ENSP00000501536.2:n.*6534G>C
ENST00000679448.1:c.6781G>C	ENSP00000505889.1:p.Asp2261His
ENST00000679457.1:c.6781G>C	ENSP00000505450.1:p.Asp2261His
ENST00000679474.1:n.7003G>C
ENST00000679521.1:c.6751G>C	ENSP00000505456.1:p.Asp2251His
ENST00000679554.1:c.*6590G>C	ENSP00000506415.1:n.*6590G>C
ENST00000679722.1:n.7027G>C
ENST00000679821.1:c.6547G>C	ENSP00000506040.1:p.Asp2183His
ENST00000680047.1:n.7003G>C
ENST00000680072.1:c.6628G>C	ENSP00000506581.1:p.Asp2210His
ENST00000680181.1:c.6712G>C	ENSP00000505548.1:p.Asp2238His
ENST00000680365.1:c.298G>C	ENSP00000506019.1:p.Asp100His
ENST00000680513.1:c.6664G>C	ENSP00000505284.1:p.Asp2222His
ENST00000680534.1:c.6844G>C	ENSP00000506674.1:p.Asp2282His
ENST00000680766.1:c.6781G>C	ENSP00000505204.1:p.Asp2261His
ENST00000680952.1:c.6781G>C	ENSP00000506407.1:p.Asp2261His
ENST00000681216.1:c.298G>C	ENSP00000505551.1:p.Asp100His
ENST00000681412.1:c.6805G>C	ENSP00000506486.1:p.Asp2269His
ENST00000681722.1:c.6781G>C	ENSP00000506566.1:p.Asp2261His
ENST00000356239.7:c.6805G>C	ENSP00000348573.3:p.Asp2269His
ENST00000358100.6:c.6664G>C	ENSP00000350813.3:p.Asp2222His
ENST00000359028.6:c.6838G>C	ENSP00000351922.3:p.Asp2280His
ENST00000394534.6:c.343G>C	ENSP00000378042.2:p.Asp115His
NM_005751.4:c.6805G>C , LRG_331t1:c.6805G>C	NP_005742.4:p.Asp2269His
NM_147185.2:c.6781G>C	NP_671714.1:p.Asp2261His
XM_006715827.1:c.6664G>C	XP_006715890.1:p.Asp2222His
XM_011515709.1:c.6952G>C	XP_011514011.1:p.Asp2318His
XM_011515710.1:c.6976G>C	XP_011514012.1:p.Asp2326His
XM_011515711.1:c.6916G>C	XP_011514013.1:p.Asp2306His
XM_011515712.1:c.6913G>C	XP_011514014.1:p.Asp2305His
XM_011515713.1:c.6898G>C	XP_011514015.1:p.Asp2300His
XM_011515714.1:c.6937G>C	XP_011514016.1:p.Asp2313His
XM_011515716.1:c.6856G>C	XP_011514018.1:p.Asp2286His
XM_011515717.1:c.6811G>C	XP_011514019.1:p.Asp2271His
XM_011515718.1:c.6841G>C	XP_011514020.1:p.Asp2281His
XM_011515719.1:c.6817G>C	XP_011514021.1:p.Asp2273His
XM_011515720.1:c.6700G>C	XP_011514022.1:p.Asp2234His
XM_011515721.1:c.1465G>C	XP_011514023.1:p.Asp489His
XM_011515722.1:c.1426G>C	XP_011514024.1:p.Asp476His
XM_017011642.2:c.6940G>C	XP_016867131.1:p.Asp2314His
XM_017011643.2:c.6901G>C	XP_016867132.1:p.Asp2301His
XM_017011644.2:c.6940G>C	XP_016867133.1:p.Asp2314His
XM_017011645.2:c.6886G>C	XP_016867134.1:p.Asp2296His
XM_017011646.2:c.6901G>C	XP_016867135.1:p.Asp2301His
XM_017011647.2:c.6847G>C	XP_016867136.1:p.Asp2283His
XM_017011648.2:c.6844G>C	XP_016867137.1:p.Asp2282His
XM_017011649.2:c.6877G>C	XP_016867138.1:p.Asp2293His
XM_017011650.2:c.6805G>C	XP_016867139.1:p.Asp2269His
XM_017011651.2:c.6799G>C	XP_016867140.1:p.Asp2267His
XM_017011652.2:c.6940G>C	XP_016867141.1:p.Asp2314His
XM_017011653.2:c.6712G>C	XP_016867142.1:p.Asp2238His
XM_017011654.2:c.6664G>C	XP_016867143.1:p.Asp2222His
XM_017011655.2:c.6568G>C	XP_016867144.1:p.Asp2190His
XM_017011656.2:c.6568G>C	XP_016867145.1:p.Asp2190His
XM_017011657.2:c.2605G>C	XP_016867146.1:p.Asp869His
XM_017011658.2:c.1489G>C	XP_016867147.1:p.Asp497His
XM_017011659.2:c.1450G>C	XP_016867148.1:p.Asp484His
XM_017011660.2:c.1450G>C	XP_016867149.1:p.Asp484His
XM_024446631.1:c.6703G>C	XP_024302399.1:p.Asp2235His
NM_147185.3:c.6781G>C	NP_671714.1:p.Asp2261His
NM_001379277.1:c.1450G>C	NP_001366206.1:p.Asp484His
NM_005751.5:c.6805G>C MANE Select	NP_005742.4:p.Asp2269His