Canonical Allele Identifier: CA10257281

Gene: ACO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41499788G>A , CM000684.2:g.41499788G>A	GRCh38
NC_000022.10:g.41895792G>A , CM000684.1:g.41895792G>A	GRCh37
NC_000022.9:g.40225738G>A	NCBI36
NG_032143.1:g.35664G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000216254.9:c.99G>A MANE Select	ENSP00000216254.4:p.Ala33=
ENST00000466237.2:c.99G>A	ENSP00000504719.1:p.Ala33=
ENST00000676664.1:c.45G>A	ENSP00000503709.1:p.Ala15=
ENST00000676714.1:c.99G>A	ENSP00000504699.1:p.Ala33=
ENST00000676748.1:c.-1G>A	ENSP00000503371.1:n.-1G>A
ENST00000676792.1:c.-209G>A	ENSP00000503590.1:n.-209G>A
ENST00000676822.1:n.347G>A
ENST00000676959.1:c.99G>A	ENSP00000504377.1:p.Ala33=
ENST00000677007.1:c.99G>A	ENSP00000504634.1:p.Ala33=
ENST00000677153.1:c.-1G>A	ENSP00000504453.1:n.-1G>A
ENST00000677427.1:n.129G>A
ENST00000677516.1:c.99G>A	ENSP00000503370.1:p.Ala33=
ENST00000677532.1:c.198-8003G>A	ENSP00000503471.1:n.198-8003G>A
ENST00000677554.1:c.99G>A	ENSP00000504513.1:p.Ala33=
ENST00000677698.1:c.205G>A
ENST00000678269.1:c.99G>A	ENSP00000504150.1:p.Ala33=
ENST00000678394.1:n.134G>A
ENST00000678454.1:n.129G>A
ENST00000678600.1:n.140G>A
ENST00000678688.1:c.99G>A	ENSP00000503990.1:p.Ala33=
ENST00000678788.1:c.99G>A	ENSP00000504684.1:p.Ala33=
ENST00000678819.1:c.99G>A	ENSP00000503199.1:p.Ala33=
ENST00000679264.1:n.203-8003G>A
ENST00000679311.1:n.129G>A
ENST00000679320.1:c.99G>A	ENSP00000504780.1:p.Ala33=
ENST00000216254.8:c.99G>A	ENSP00000216254.4:p.Ala33=
ENST00000396512.3:c.99G>A	ENSP00000379769.3:p.Ala33=
ENST00000471094.1:n.350-8003G>A
NM_001098.2:c.99G>A	NP_001089.1:p.Ala33=
XM_017028812.1:c.-1G>A	XP_016884301.1:n.-1G>A
XM_024452250.1:c.99G>A	XP_024308018.1:p.Ala33=
NM_001098.3:c.99G>A MANE Select	NP_001089.1:p.Ala33=