Canonical Allele Identifier: CA10257316

Gene: ACO2

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41507848C>T , CM000684.2:g.41507848C>T	GRCh38
NC_000022.10:g.41903852C>T , CM000684.1:g.41903852C>T	GRCh37
NC_000022.9:g.40233798C>T	NCBI36
NG_032143.1:g.43724C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001098.3:c.231C>T MANE Select	NP_001089.1:p.Pro77=
ENST00000216254.9:c.231C>T MANE Select	ENSP00000216254.4:p.Pro77=
NM_001098.2:c.231C>T	NP_001089.1:p.Pro77=
ENST00000216254.8:c.231C>T	ENSP00000216254.4:p.Pro77=
ENST00000396512.3:c.231C>T	ENSP00000379769.3:p.Pro77=
ENST00000466237.2:c.231C>T	ENSP00000504719.1:p.Pro77=
ENST00000471094.1:n.407C>T
ENST00000482208.1:n.11C>T
ENST00000676664.1:c.177C>T	ENSP00000503709.1:p.Pro59=
ENST00000676714.1:c.*149C>T	ENSP00000504699.1:n.*149C>T
ENST00000676748.1:c.132C>T	ENSP00000503371.1:p.Pro44=
ENST00000676792.1:c.66C>T	ENSP00000503590.1:p.Pro22=
ENST00000676822.1:n.479C>T
ENST00000676959.1:c.231C>T	ENSP00000504377.1:p.Pro77=
ENST00000677007.1:c.231C>T	ENSP00000504634.1:p.Pro77=
ENST00000677153.1:c.132C>T	ENSP00000504453.1:p.Pro44=
ENST00000677427.1:n.261C>T
ENST00000677516.1:c.231C>T	ENSP00000503370.1:p.Pro77=
ENST00000677532.1:c.255C>T	ENSP00000503471.1:p.Pro85=
ENST00000677554.1:c.231C>T	ENSP00000504513.1:p.Pro77=
ENST00000677698.1:c.604C>T
ENST00000678269.1:c.231C>T	ENSP00000504150.1:p.Pro77=
ENST00000678394.1:n.408C>T
ENST00000678454.1:n.261C>T
ENST00000678600.1:n.272C>T
ENST00000678688.1:c.231C>T	ENSP00000503990.1:p.Pro77=
ENST00000678788.1:c.231C>T	ENSP00000504684.1:p.Pro77=
ENST00000678819.1:c.*94C>T	ENSP00000503199.1:n.*94C>T
ENST00000679264.1:n.260C>T
ENST00000679311.1:n.261C>T
ENST00000679320.1:c.231C>T	ENSP00000504780.1:p.Pro77=
XM_017028812.1:c.132C>T	XP_016884301.1:p.Pro44=
XM_024452250.1:c.231C>T	XP_024308018.1:p.Pro77=