Canonical Allele Identifier: CA1844641162

Gene: ACO1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32433444C= , CM000671.2:g.32433444C=	GRCh38
NC_000009.11:g.32433442C= , CM000671.1:g.32433442C=	GRCh37
NC_000009.10:g.32423442C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000309951.8:c.1852-284C= MANE Select	ENSP00000309477.5:n.1852-284C=
ENST00000309951.7:c.1852-284C=	ENSP00000309477.5:n.1852-284C=
ENST00000379923.5:c.1852-284C=	ENSP00000369255.1:n.1852-284C=
ENST00000541043.5:c.1852-284C=	ENSP00000438733.2:n.1852-284C=
NM_001278352.1:c.1852-284C=	NP_001265281.1:n.1852-284C=
NM_002197.2:c.1852-284C=	NP_002188.1:n.1852-284C=
XM_005251476.1:c.1852-284C=	XP_005251533.1:n.1852-284C=
XM_011517888.1:c.1852-284C=	XP_011516190.1:n.1852-284C=
NM_001362840.1:c.1852-284C=	NP_001349769.1:n.1852-284C=
XM_011517888.2:c.1852-284C=	XP_011516190.1:n.1852-284C=
NM_002197.3:c.1852-284C= MANE Select	NP_002188.1:n.1852-284C=
NM_001362840.2:c.1852-284C=	NP_001349769.1:n.1852-284C=
NM_001278352.2:c.1852-284C=	NP_001265281.1:n.1852-284C=