Canonical Allele Identifier: CA10257334

Gene: ACO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41507956C>T , CM000684.2:g.41507956C>T	GRCh38
NC_000022.10:g.41903960C>T , CM000684.1:g.41903960C>T	GRCh37
NC_000022.9:g.40233906C>T	NCBI36
NG_032143.1:g.43832C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216254.9:c.339C>T MANE Select	ENSP00000216254.4:p.Ser113=
ENST00000466237.2:c.339C>T	ENSP00000504719.1:p.Ser113=
ENST00000676664.1:c.285C>T	ENSP00000503709.1:p.Ser95=
ENST00000676714.1:c.*257C>T	ENSP00000504699.1:n.*257C>T
ENST00000676748.1:c.240C>T	ENSP00000503371.1:p.Ser80=
ENST00000676792.1:c.174C>T	ENSP00000503590.1:p.Ser58=
ENST00000676822.1:n.587C>T
ENST00000676959.1:c.339C>T	ENSP00000504377.1:p.Ser113=
ENST00000677007.1:c.339C>T	ENSP00000504634.1:p.Ser113=
ENST00000677153.1:c.240C>T	ENSP00000504453.1:p.Ser80=
ENST00000677427.1:n.369C>T
ENST00000677516.1:c.339C>T	ENSP00000503370.1:p.Ser113=
ENST00000677532.1:c.363C>T	ENSP00000503471.1:p.Ser121=
ENST00000677554.1:c.339C>T	ENSP00000504513.1:p.Ser113=
ENST00000677698.1:c.712C>T
ENST00000678269.1:c.339C>T	ENSP00000504150.1:p.Ser113=
ENST00000678394.1:n.516C>T
ENST00000678454.1:n.369C>T
ENST00000678600.1:n.380C>T
ENST00000678688.1:c.339C>T	ENSP00000503990.1:p.Ser113=
ENST00000678788.1:c.339C>T	ENSP00000504684.1:p.Ser113=
ENST00000678819.1:c.*202C>T	ENSP00000503199.1:n.*202C>T
ENST00000679264.1:n.368C>T
ENST00000679311.1:n.369C>T
ENST00000679320.1:c.339C>T	ENSP00000504780.1:p.Ser113=
ENST00000216254.8:c.339C>T	ENSP00000216254.4:p.Ser113=
ENST00000396512.3:c.339C>T	ENSP00000379769.3:p.Ser113=
ENST00000471094.1:n.515C>T
ENST00000482208.1:n.119C>T
NM_001098.2:c.339C>T	NP_001089.1:p.Ser113=
XM_017028812.1:c.240C>T	XP_016884301.1:p.Ser80=
XM_024452250.1:c.339C>T	XP_024308018.1:p.Ser113=
NM_001098.3:c.339C>T MANE Select	NP_001089.1:p.Ser113=