Canonical Allele Identifier: CA236882

Gene: AKAP9

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92070953T>C , CM000669.2:g.92070953T>C	GRCh38
NC_000007.13:g.91700267T>C , CM000669.1:g.91700267T>C	GRCh37
NC_000007.12:g.91538203T>C	NCBI36
NG_011623.1:g.135079T>C , LRG_331:g.135079T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000356239.8:c.6556T>C MANE Select	ENSP00000348573.3:p.Ser2186Pro
ENST00000359028.7:c.6628T>C	ENSP00000351922.4:p.Ser2210Pro
ENST00000394534.7:c.49T>C	ENSP00000378042.3:p.Ser17Pro
ENST00000491695.2:c.1201T>C	ENSP00000494626.2:p.Ser401Pro
ENST00000674381.2:c.*6285T>C	ENSP00000501536.2:n.*6285T>C
ENST00000679448.1:c.6532T>C	ENSP00000505889.1:p.Ser2178Pro
ENST00000679457.1:c.6532T>C	ENSP00000505450.1:p.Ser2178Pro
ENST00000679474.1:n.6754T>C
ENST00000679521.1:c.6502T>C	ENSP00000505456.1:p.Ser2168Pro
ENST00000679554.1:c.*6341T>C	ENSP00000506415.1:n.*6341T>C
ENST00000679722.1:n.6778T>C
ENST00000679821.1:c.6298T>C	ENSP00000506040.1:p.Ser2100Pro
ENST00000680047.1:n.6754T>C
ENST00000680072.1:c.6379T>C	ENSP00000506581.1:p.Ser2127Pro
ENST00000680181.1:c.6463T>C	ENSP00000505548.1:p.Ser2155Pro
ENST00000680365.1:c.49T>C	ENSP00000506019.1:p.Ser17Pro
ENST00000680513.1:c.6415T>C	ENSP00000505284.1:p.Ser2139Pro
ENST00000680534.1:c.6595T>C	ENSP00000506674.1:p.Ser2199Pro
ENST00000680766.1:c.6532T>C	ENSP00000505204.1:p.Ser2178Pro
ENST00000680952.1:c.6532T>C	ENSP00000506407.1:p.Ser2178Pro
ENST00000681216.1:c.49T>C	ENSP00000505551.1:p.Ser17Pro
ENST00000681412.1:c.6556T>C	ENSP00000506486.1:p.Ser2186Pro
ENST00000681722.1:c.6532T>C	ENSP00000506566.1:p.Ser2178Pro
ENST00000356239.7:c.6556T>C	ENSP00000348573.3:p.Ser2186Pro
ENST00000358100.6:c.6415T>C	ENSP00000350813.3:p.Ser2139Pro
ENST00000359028.6:c.6589T>C	ENSP00000351922.3:p.Ser2197Pro
ENST00000394534.6:c.94T>C	ENSP00000378042.2:p.Ser32Pro
NM_005751.4:c.6556T>C , LRG_331t1:c.6556T>C	NP_005742.4:p.Ser2186Pro
NM_147185.2:c.6532T>C	NP_671714.1:p.Ser2178Pro
XM_006715827.1:c.6415T>C	XP_006715890.1:p.Ser2139Pro
XM_011515709.1:c.6703T>C	XP_011514011.1:p.Ser2235Pro
XM_011515710.1:c.6727T>C	XP_011514012.1:p.Ser2243Pro
XM_011515711.1:c.6667T>C	XP_011514013.1:p.Ser2223Pro
XM_011515712.1:c.6664T>C	XP_011514014.1:p.Ser2222Pro
XM_011515713.1:c.6649T>C	XP_011514015.1:p.Ser2217Pro
XM_011515714.1:c.6688T>C	XP_011514016.1:p.Ser2230Pro
XM_011515716.1:c.6607T>C	XP_011514018.1:p.Ser2203Pro
XM_011515717.1:c.6562T>C	XP_011514019.1:p.Ser2188Pro
XM_011515718.1:c.6592T>C	XP_011514020.1:p.Ser2198Pro
XM_011515719.1:c.6568T>C	XP_011514021.1:p.Ser2190Pro
XM_011515720.1:c.6451T>C	XP_011514022.1:p.Ser2151Pro
XM_011515721.1:c.1216T>C	XP_011514023.1:p.Ser406Pro
XM_011515722.1:c.1177T>C	XP_011514024.1:p.Ser393Pro
XM_017011642.2:c.6691T>C	XP_016867131.1:p.Ser2231Pro
XM_017011643.2:c.6652T>C	XP_016867132.1:p.Ser2218Pro
XM_017011644.2:c.6691T>C	XP_016867133.1:p.Ser2231Pro
XM_017011645.2:c.6637T>C	XP_016867134.1:p.Ser2213Pro
XM_017011646.2:c.6652T>C	XP_016867135.1:p.Ser2218Pro
XM_017011647.2:c.6598T>C	XP_016867136.1:p.Ser2200Pro
XM_017011648.2:c.6595T>C	XP_016867137.1:p.Ser2199Pro
XM_017011649.2:c.6628T>C	XP_016867138.1:p.Ser2210Pro
XM_017011650.2:c.6556T>C	XP_016867139.1:p.Ser2186Pro
XM_017011651.2:c.6550T>C	XP_016867140.1:p.Ser2184Pro
XM_017011652.2:c.6691T>C	XP_016867141.1:p.Ser2231Pro
XM_017011653.2:c.6463T>C	XP_016867142.1:p.Ser2155Pro
XM_017011654.2:c.6415T>C	XP_016867143.1:p.Ser2139Pro
XM_017011655.2:c.6319T>C	XP_016867144.1:p.Ser2107Pro
XM_017011656.2:c.6319T>C	XP_016867145.1:p.Ser2107Pro
XM_017011657.2:c.2356T>C	XP_016867146.1:p.Ser786Pro
XM_017011658.2:c.1240T>C	XP_016867147.1:p.Ser414Pro
XM_017011659.2:c.1201T>C	XP_016867148.1:p.Ser401Pro
XM_017011660.2:c.1201T>C	XP_016867149.1:p.Ser401Pro
XM_024446631.1:c.6454T>C	XP_024302399.1:p.Ser2152Pro
NM_147185.3:c.6532T>C	NP_671714.1:p.Ser2178Pro
NM_001379277.1:c.1201T>C	NP_001366206.1:p.Ser401Pro
NM_005751.5:c.6556T>C MANE Select	NP_005742.4:p.Ser2186Pro