Canonical Allele Identifier: CA411711676

Gene: ACO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41499775G>C , CM000684.2:g.41499775G>C	GRCh38
NC_000022.10:g.41895779G>C , CM000684.1:g.41895779G>C	GRCh37
NC_000022.9:g.40225725G>C	NCBI36
NG_032143.1:g.35651G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001098.3:c.86G>C MANE Select	NP_001089.1:p.Arg29Pro
ENST00000216254.9:c.86G>C MANE Select	ENSP00000216254.4:p.Arg29Pro
NM_001098.2:c.86G>C	NP_001089.1:p.Arg29Pro
ENST00000216254.8:c.86G>C	ENSP00000216254.4:p.Arg29Pro
ENST00000396512.3:c.86G>C	ENSP00000379769.3:p.Arg29Pro
ENST00000466237.2:c.86G>C	ENSP00000504719.1:p.Arg29Pro
ENST00000471094.1:n.350-8016G>C
ENST00000676664.1:c.32G>C	ENSP00000503709.1:p.Arg11Pro
ENST00000676714.1:c.86G>C	ENSP00000504699.1:p.Arg29Pro
ENST00000676748.1:c.-14G>C	ENSP00000503371.1:n.-14G>C
ENST00000676792.1:c.-222G>C	ENSP00000503590.1:n.-222G>C
ENST00000676822.1:n.334G>C
ENST00000676959.1:c.86G>C	ENSP00000504377.1:p.Arg29Pro
ENST00000677007.1:c.86G>C	ENSP00000504634.1:p.Arg29Pro
ENST00000677153.1:c.-14G>C	ENSP00000504453.1:n.-14G>C
ENST00000677427.1:n.116G>C
ENST00000677516.1:c.86G>C	ENSP00000503370.1:p.Arg29Pro
ENST00000677532.1:c.198-8016G>C	ENSP00000503471.1:n.198-8016G>C
ENST00000677554.1:c.86G>C	ENSP00000504513.1:p.Arg29Pro
ENST00000677698.1:c.192G>C
ENST00000678269.1:c.86G>C	ENSP00000504150.1:p.Arg29Pro
ENST00000678394.1:n.121G>C
ENST00000678454.1:n.116G>C
ENST00000678600.1:n.127G>C
ENST00000678688.1:c.86G>C	ENSP00000503990.1:p.Arg29Pro
ENST00000678788.1:c.86G>C	ENSP00000504684.1:p.Arg29Pro
ENST00000678819.1:c.86G>C	ENSP00000503199.1:p.Arg29Pro
ENST00000679264.1:n.203-8016G>C
ENST00000679311.1:n.116G>C
ENST00000679320.1:c.86G>C	ENSP00000504780.1:p.Arg29Pro
XM_017028812.1:c.-14G>C	XP_016884301.1:n.-14G>C
XM_024452250.1:c.86G>C	XP_024308018.1:p.Arg29Pro