Canonical Allele Identifier: CA10257322
Gene: ACO2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41507877C>T , CM000684.2:g.41507877C>T GRCh38
NC_000022.10:g.41903881C>T , CM000684.1:g.41903881C>T GRCh37
NC_000022.9:g.40233827C>T NCBI36
NG_032143.1:g.43753C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000216254.9:c.260C>T MANE Select ENSP00000216254.4:p.Ser87Leu
ENST00000466237.2:c.260C>T ENSP00000504719.1:p.Ser87Leu
ENST00000676664.1:c.206C>T ENSP00000503709.1:p.Ser69Leu
ENST00000676714.1:c.*178C>T ENSP00000504699.1:n.*178C>T
ENST00000676748.1:c.161C>T ENSP00000503371.1:p.Ser54Leu
ENST00000676792.1:c.95C>T ENSP00000503590.1:p.Ser32Leu
ENST00000676822.1:n.508C>T
ENST00000676959.1:c.260C>T ENSP00000504377.1:p.Ser87Leu
ENST00000677007.1:c.260C>T ENSP00000504634.1:p.Ser87Leu
ENST00000677153.1:c.161C>T ENSP00000504453.1:p.Ser54Leu
ENST00000677427.1:n.290C>T
ENST00000677516.1:c.260C>T ENSP00000503370.1:p.Ser87Leu
ENST00000677532.1:c.284C>T ENSP00000503471.1:p.Ser95Leu
ENST00000677554.1:c.260C>T ENSP00000504513.1:p.Ser87Leu
ENST00000677698.1:c.633C>T
ENST00000678269.1:c.260C>T ENSP00000504150.1:p.Ser87Leu
ENST00000678394.1:n.437C>T
ENST00000678454.1:n.290C>T
ENST00000678600.1:n.301C>T
ENST00000678688.1:c.260C>T ENSP00000503990.1:p.Ser87Leu
ENST00000678788.1:c.260C>T ENSP00000504684.1:p.Ser87Leu
ENST00000678819.1:c.*123C>T ENSP00000503199.1:n.*123C>T
ENST00000679264.1:n.289C>T
ENST00000679311.1:n.290C>T
ENST00000679320.1:c.260C>T ENSP00000504780.1:p.Ser87Leu
ENST00000216254.8:c.260C>T ENSP00000216254.4:p.Ser87Leu
ENST00000396512.3:c.260C>T ENSP00000379769.3:p.Ser87Leu
ENST00000471094.1:n.436C>T
ENST00000482208.1:n.40C>T
NM_001098.2:c.260C>T NP_001089.1:p.Ser87Leu
XM_017028812.1:c.161C>T XP_016884301.1:p.Ser54Leu
XM_024452250.1:c.260C>T XP_024308018.1:p.Ser87Leu
NM_001098.3:c.260C>T MANE Select NP_001089.1:p.Ser87Leu