Canonical Allele Identifier: CA368133881

Gene: AKAP9

Linked Data

• MyVariant Identifiers: chr7:g.91707162G>C (hg19) ; chr7:g.92077848G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92077848G>C , CM000669.2:g.92077848G>C	GRCh38
NC_000007.13:g.91707162G>C , CM000669.1:g.91707162G>C	GRCh37
NC_000007.12:g.91545098G>C	NCBI36
NG_011623.1:g.141974G>C , LRG_331:g.141974G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6918G>C MANE Select	ENSP00000348573.3:p.Gln2306His
ENST00000359028.7:c.6990G>C	ENSP00000351922.4:p.Gln2330His
ENST00000394534.7:c.411G>C	ENSP00000378042.3:p.Gln137His
ENST00000491695.2:c.1563G>C	ENSP00000494626.2:p.Gln521His
ENST00000674381.2:c.*6647G>C	ENSP00000501536.2:n.*6647G>C
ENST00000679448.1:c.6894G>C	ENSP00000505889.1:p.Gln2298His
ENST00000679457.1:c.6894G>C	ENSP00000505450.1:p.Gln2298His
ENST00000679474.1:n.7116G>C
ENST00000679521.1:c.6864G>C	ENSP00000505456.1:p.Gln2288His
ENST00000679554.1:c.*6703G>C	ENSP00000506415.1:n.*6703G>C
ENST00000679722.1:n.7140G>C
ENST00000679821.1:c.6660G>C	ENSP00000506040.1:p.Gln2220His
ENST00000680047.1:n.7116G>C
ENST00000680072.1:c.6741G>C	ENSP00000506581.1:p.Gln2247His
ENST00000680181.1:c.6825G>C	ENSP00000505548.1:p.Gln2275His
ENST00000680365.1:c.411G>C	ENSP00000506019.1:p.Gln137His
ENST00000680513.1:c.6777G>C	ENSP00000505284.1:p.Gln2259His
ENST00000680534.1:c.6957G>C	ENSP00000506674.1:p.Gln2319His
ENST00000680766.1:c.6894G>C	ENSP00000505204.1:p.Gln2298His
ENST00000680952.1:c.6894G>C	ENSP00000506407.1:p.Gln2298His
ENST00000681216.1:c.411G>C	ENSP00000505551.1:p.Gln137His
ENST00000681412.1:c.6918G>C	ENSP00000506486.1:p.Gln2306His
ENST00000681722.1:c.6894G>C	ENSP00000506566.1:p.Gln2298His
ENST00000356239.7:c.6918G>C	ENSP00000348573.3:p.Gln2306His
ENST00000358100.6:c.6777G>C	ENSP00000350813.3:p.Gln2259His
ENST00000359028.6:c.6951G>C	ENSP00000351922.3:p.Gln2317His
ENST00000394534.6:c.456G>C	ENSP00000378042.2:p.Gln152His
NM_005751.4:c.6918G>C , LRG_331t1:c.6918G>C	NP_005742.4:p.Gln2306His
NM_147185.2:c.6894G>C	NP_671714.1:p.Gln2298His
XM_006715827.1:c.6777G>C	XP_006715890.1:p.Gln2259His
XM_011515709.1:c.7065G>C	XP_011514011.1:p.Gln2355His
XM_011515710.1:c.7089G>C	XP_011514012.1:p.Gln2363His
XM_011515711.1:c.7029G>C	XP_011514013.1:p.Gln2343His
XM_011515712.1:c.7026G>C	XP_011514014.1:p.Gln2342His
XM_011515713.1:c.7011G>C	XP_011514015.1:p.Gln2337His
XM_011515714.1:c.7050G>C	XP_011514016.1:p.Gln2350His
XM_011515716.1:c.6969G>C	XP_011514018.1:p.Gln2323His
XM_011515717.1:c.6924G>C	XP_011514019.1:p.Gln2308His
XM_011515718.1:c.6954G>C	XP_011514020.1:p.Gln2318His
XM_011515719.1:c.6930G>C	XP_011514021.1:p.Gln2310His
XM_011515720.1:c.6813G>C	XP_011514022.1:p.Gln2271His
XM_011515721.1:c.1578G>C	XP_011514023.1:p.Gln526His
XM_011515722.1:c.1539G>C	XP_011514024.1:p.Gln513His
XM_017011642.2:c.7053G>C	XP_016867131.1:p.Gln2351His
XM_017011643.2:c.7014G>C	XP_016867132.1:p.Gln2338His
XM_017011644.2:c.7053G>C	XP_016867133.1:p.Gln2351His
XM_017011645.2:c.6999G>C	XP_016867134.1:p.Gln2333His
XM_017011646.2:c.7014G>C	XP_016867135.1:p.Gln2338His
XM_017011647.2:c.6960G>C	XP_016867136.1:p.Gln2320His
XM_017011648.2:c.6957G>C	XP_016867137.1:p.Gln2319His
XM_017011649.2:c.6990G>C	XP_016867138.1:p.Gln2330His
XM_017011650.2:c.6918G>C	XP_016867139.1:p.Gln2306His
XM_017011651.2:c.6912G>C	XP_016867140.1:p.Gln2304His
XM_017011652.2:c.7053G>C	XP_016867141.1:p.Gln2351His
XM_017011653.2:c.6825G>C	XP_016867142.1:p.Gln2275His
XM_017011654.2:c.6777G>C	XP_016867143.1:p.Gln2259His
XM_017011655.2:c.6681G>C	XP_016867144.1:p.Gln2227His
XM_017011656.2:c.6681G>C	XP_016867145.1:p.Gln2227His
XM_017011657.2:c.2718G>C	XP_016867146.1:p.Gln906His
XM_017011658.2:c.1602G>C	XP_016867147.1:p.Gln534His
XM_017011659.2:c.1563G>C	XP_016867148.1:p.Gln521His
XM_017011660.2:c.1563G>C	XP_016867149.1:p.Gln521His
XM_024446631.1:c.6816G>C	XP_024302399.1:p.Gln2272His
NM_147185.3:c.6894G>C	NP_671714.1:p.Gln2298His
NM_001379277.1:c.1563G>C	NP_001366206.1:p.Gln521His
NM_005751.5:c.6918G>C MANE Select	NP_005742.4:p.Gln2306His