Canonical Allele Identifier: CA2241520494

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154122A= , CM000678.2:g.89154122A=	GRCh38
NC_000016.9:g.89220530A= , CM000678.1:g.89220530A=	GRCh37
NC_000016.8:g.87748031A=	NCBI36
NG_031961.1:g.65314A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1646A=	ENSP00000320646.4:p.Glu549=
ENST00000614302.5:c.1646A= MANE Select	ENSP00000479130.1:p.Glu549=
ENST00000649953.1:c.1856A=	ENSP00000497456.1:p.Glu619=
ENST00000317447.8:c.1646A=	ENSP00000320646.4:p.Glu549=
ENST00000378345.8:c.851A=	ENSP00000367596.4:p.Glu284=
ENST00000393145.5:n.6556A=
ENST00000406948.7:c.1646A=	ENSP00000384627.3:p.Glu549=
ENST00000537116.5:n.772A=
ENST00000537155.1:n.386A=
ENST00000542688.5:c.*390A=	ENSP00000446281.1:n.*390A=
ENST00000614302.4:c.1646A=	ENSP00000479130.1:p.Glu549=
NM_001127214.3:c.1646A=	NP_001120686.1:p.Glu549=
NM_001243279.2:c.1646A=	NP_001230208.1:p.Glu549=
NM_001284316.1:c.851A=	NP_001271245.1:p.Glu284=
NM_174917.4:c.1646A=	NP_777577.2:p.Glu549=
NR_045667.2:n.772A=
NR_104293.1:n.2080A=
XR_933239.1:n.2087A=
XR_933240.1:n.2084A=
XR_933241.1:n.1841A=
NR_147928.1:n.2124A=
NR_147929.1:n.1878A=
XM_017023020.2:c.-3459A=	XP_016878509.1:n.-3459A=
XM_024450187.1:c.851A=	XP_024305955.1:p.Glu284=
XR_001751864.2:n.1893A=
XR_933240.3:n.2083A=
NM_001127214.4:c.1646A=	NP_001120686.1:p.Glu549=
NM_001243279.3:c.1646A= MANE Select	NP_001230208.1:p.Glu549=
NM_001284316.2:c.851A=	NP_001271245.1:p.Glu284=
NM_174917.5:c.1646A=	NP_777577.2:p.Glu549=
NR_104293.2:n.2037A=
NR_147928.2:n.2081A=
NR_147929.2:n.1835A=