Canonical Allele Identifier: CA2241496007

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89114436G= , CM000678.2:g.89114436G=	GRCh38
NC_000016.9:g.89180844G= , CM000678.1:g.89180844G=	GRCh37
NC_000016.8:g.87708345G=	NCBI36
NG_031961.1:g.25628G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1075G=	ENSP00000320646.4:p.Glu359=
ENST00000614302.5:c.1075G= MANE Select	ENSP00000479130.1:p.Glu359=
ENST00000649953.1:c.1075G=	ENSP00000497456.1:p.Glu359=
ENST00000317447.8:c.1075G=	ENSP00000320646.4:p.Glu359=
ENST00000378345.8:c.280G=	ENSP00000367596.4:p.Glu94=
ENST00000406948.7:c.1075G=	ENSP00000384627.3:p.Glu359=
ENST00000537895.5:c.280G=	ENSP00000439201.1:p.Glu94=
ENST00000538340.5:c.302+2190G=	ENSP00000445870.1:n.302+2190G=
ENST00000540697.5:c.280G=	ENSP00000445397.1:p.Glu94=
ENST00000542688.5:c.977+2190G=	ENSP00000446281.1:n.977+2190G=
ENST00000543676.1:c.317G=
ENST00000544543.5:c.280G=	ENSP00000442781.1:p.Glu94=
ENST00000562204.1:n.46+2190G=
ENST00000614302.4:c.1075G=	ENSP00000479130.1:p.Glu359=
NM_001127214.3:c.1075G=	NP_001120686.1:p.Glu359=
NM_001243279.2:c.1075G=	NP_001230208.1:p.Glu359=
NM_001284316.1:c.280G=	NP_001271245.1:p.Glu94=
NM_174917.4:c.1075G=	NP_777577.2:p.Glu359=
NR_104293.1:n.1456G=
XM_005256293.1:c.1075G=	XP_005256350.1:p.Glu359=
XM_011522942.1:c.1075G=	XP_011521244.1:p.Glu359=
XM_011522943.1:c.1075G=	XP_011521245.1:p.Glu359=
XM_011522944.1:c.1075G=	XP_011521246.1:p.Glu359=
XR_933238.1:n.1419G=
XR_933239.1:n.1419G=
XR_933240.1:n.1419G=
XR_933241.1:n.1321+2190G=
NR_147928.1:n.1456G=
NR_147929.1:n.1358+2190G=
XM_005256293.2:c.1075G=	XP_005256350.1:p.Glu359=
XM_017023018.1:c.1075G=	XP_016878507.1:p.Glu359=
XM_017023019.1:c.1075G=	XP_016878508.1:p.Glu359=
XM_017023020.2:c.-4032+2190G=	XP_016878509.1:n.-4032+2190G=
XM_017023021.1:c.1075G=	XP_016878510.1:p.Glu359=
XM_024450186.1:c.280G=	XP_024305954.1:p.Glu94=
XM_024450187.1:c.280G=	XP_024305955.1:p.Glu94=
XR_001751864.2:n.1320+2190G=
XR_001751865.1:n.1320+2190G=
XR_933238.2:n.1418G=
XR_933240.3:n.1418G=
NM_001127214.4:c.1075G=	NP_001120686.1:p.Glu359=
NM_001243279.3:c.1075G= MANE Select	NP_001230208.1:p.Glu359=
NM_001284316.2:c.280G=	NP_001271245.1:p.Glu94=
NM_174917.5:c.1075G=	NP_777577.2:p.Glu359=
NR_104293.2:n.1413G=
NR_147928.2:n.1413G=
NR_147929.2:n.1315+2190G=