Canonical Allele Identifier: CA4337034
Community Standard Title: NM_005751.5(AKAP9):c.6302A>C (p.Gln2101Pro)
Gene: AKAP9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92066518A>C , CM000669.2:g.92066518A>C GRCh38
NC_000007.13:g.91695832A>C , CM000669.1:g.91695832A>C GRCh37
NC_000007.12:g.91533768A>C NCBI36
NG_011623.1:g.130644A>C , LRG_331:g.130644A>C

Transcript Alleles

HGVS Amino-acid Change
NM_005751.5:c.6302A>C MANE Select NP_005742.4:p.Gln2101Pro
ENST00000356239.8:c.6302A>C MANE Select ENSP00000348573.3:p.Gln2101Pro
NM_001379277.1:c.947A>C NP_001366206.1:p.Gln316Pro
NM_005751.4:c.6302A>C , LRG_331t1:c.6302A>C NP_005742.4:p.Gln2101Pro
NM_147185.2:c.6302A>C NP_671714.1:p.Gln2101Pro
NM_147185.3:c.6302A>C NP_671714.1:p.Gln2101Pro
ENST00000356239.7:c.6302A>C ENSP00000348573.3:p.Gln2101Pro
ENST00000358100.6:c.6161A>C ENSP00000350813.3:p.Gln2054Pro
ENST00000359028.6:c.6335A>C ENSP00000351922.3:p.Gln2112Pro
ENST00000359028.7:c.6398A>C ENSP00000351922.4:p.Gln2133Pro
ENST00000491695.2:c.947A>C ENSP00000494626.2:p.Gln316Pro
ENST00000674381.2:c.*6031A>C ENSP00000501536.2:n.*6031A>C
ENST00000679448.1:c.6302A>C ENSP00000505889.1:p.Gln2101Pro
ENST00000679457.1:c.6302A>C ENSP00000505450.1:p.Gln2101Pro
ENST00000679474.1:n.6524A>C
ENST00000679521.1:c.6248A>C ENSP00000505456.1:p.Gln2083Pro
ENST00000679554.1:c.*6087A>C ENSP00000506415.1:n.*6087A>C
ENST00000679722.1:n.6524A>C
ENST00000679821.1:c.6044A>C ENSP00000506040.1:p.Gln2015Pro
ENST00000680047.1:n.6524A>C
ENST00000680072.1:c.6302A>C ENSP00000506581.1:p.Gln2101Pro
ENST00000680074.1:n.9268A>C
ENST00000680181.1:c.6209A>C ENSP00000505548.1:p.Gln2070Pro
ENST00000680513.1:c.6161A>C ENSP00000505284.1:p.Gln2054Pro
ENST00000680534.1:c.6341A>C ENSP00000506674.1:p.Gln2114Pro
ENST00000680766.1:c.6302A>C ENSP00000505204.1:p.Gln2101Pro
ENST00000680952.1:c.6302A>C ENSP00000506407.1:p.Gln2101Pro
ENST00000681412.1:c.6302A>C ENSP00000506486.1:p.Gln2101Pro
ENST00000681722.1:c.6302A>C ENSP00000506566.1:p.Gln2101Pro
XM_006715827.1:c.6161A>C XP_006715890.1:p.Gln2054Pro
XM_011515709.1:c.6473A>C XP_011514011.1:p.Gln2158Pro
XM_011515710.1:c.6473A>C XP_011514012.1:p.Gln2158Pro
XM_011515711.1:c.6437A>C XP_011514013.1:p.Gln2146Pro
XM_011515712.1:c.6434A>C XP_011514014.1:p.Gln2145Pro
XM_011515713.1:c.6419A>C XP_011514015.1:p.Gln2140Pro
XM_011515714.1:c.6434A>C XP_011514016.1:p.Gln2145Pro
XM_011515716.1:c.6377A>C XP_011514018.1:p.Gln2126Pro
XM_011515717.1:c.6332A>C XP_011514019.1:p.Gln2111Pro
XM_011515718.1:c.6338A>C XP_011514020.1:p.Gln2113Pro
XM_011515719.1:c.6338A>C XP_011514021.1:p.Gln2113Pro
XM_011515720.1:c.6197A>C XP_011514022.1:p.Gln2066Pro
XM_011515721.1:c.986A>C XP_011514023.1:p.Gln329Pro
XM_011515722.1:c.947A>C XP_011514024.1:p.Gln316Pro
XM_017011642.2:c.6437A>C XP_016867131.1:p.Gln2146Pro
XM_017011643.2:c.6398A>C XP_016867132.1:p.Gln2133Pro
XM_017011644.2:c.6437A>C XP_016867133.1:p.Gln2146Pro
XM_017011645.2:c.6383A>C XP_016867134.1:p.Gln2128Pro
XM_017011646.2:c.6398A>C XP_016867135.1:p.Gln2133Pro
XM_017011647.2:c.6344A>C XP_016867136.1:p.Gln2115Pro
XM_017011648.2:c.6341A>C XP_016867137.1:p.Gln2114Pro
XM_017011649.2:c.6398A>C XP_016867138.1:p.Gln2133Pro
XM_017011650.2:c.6302A>C XP_016867139.1:p.Gln2101Pro
XM_017011651.2:c.6296A>C XP_016867140.1:p.Gln2099Pro
XM_017011652.2:c.6437A>C XP_016867141.1:p.Gln2146Pro
XM_017011653.2:c.6209A>C XP_016867142.1:p.Gln2070Pro
XM_017011654.2:c.6161A>C XP_016867143.1:p.Gln2054Pro
XM_017011655.2:c.6065A>C XP_016867144.1:p.Gln2022Pro
XM_017011656.2:c.6065A>C XP_016867145.1:p.Gln2022Pro
XM_017011657.2:c.2102A>C XP_016867146.1:p.Gln701Pro
XM_017011658.2:c.986A>C XP_016867147.1:p.Gln329Pro
XM_017011659.2:c.947A>C XP_016867148.1:p.Gln316Pro
XM_017011660.2:c.947A>C XP_016867149.1:p.Gln316Pro
XM_024446631.1:c.6200A>C XP_024302399.1:p.Gln2067Pro