Canonical Allele Identifier: CA2241520470

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154093T= , CM000678.2:g.89154093T=	GRCh38
NC_000016.9:g.89220501T= , CM000678.1:g.89220501T=	GRCh37
NC_000016.8:g.87748002T=	NCBI36
NG_031961.1:g.65285T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1617T=	ENSP00000320646.4:p.Asn539=
ENST00000614302.5:c.1617T= MANE Select	ENSP00000479130.1:p.Asn539=
ENST00000649953.1:c.1827T=	ENSP00000497456.1:p.Asn609=
ENST00000317447.8:c.1617T=	ENSP00000320646.4:p.Asn539=
ENST00000378345.8:c.822T=	ENSP00000367596.4:p.Asn274=
ENST00000393145.5:n.6527T=
ENST00000406948.7:c.1617T=	ENSP00000384627.3:p.Asn539=
ENST00000537116.5:n.743T=
ENST00000537155.1:n.357T=
ENST00000542688.5:c.*361T=	ENSP00000446281.1:n.*361T=
ENST00000614302.4:c.1617T=	ENSP00000479130.1:p.Asn539=
NM_001127214.3:c.1617T=	NP_001120686.1:p.Asn539=
NM_001243279.2:c.1617T=	NP_001230208.1:p.Asn539=
NM_001284316.1:c.822T=	NP_001271245.1:p.Asn274=
NM_174917.4:c.1617T=	NP_777577.2:p.Asn539=
NR_045667.2:n.743T=
NR_104293.1:n.2051T=
XR_933239.1:n.2058T=
XR_933240.1:n.2055T=
XR_933241.1:n.1812T=
NR_147928.1:n.2095T=
NR_147929.1:n.1849T=
XM_017023020.2:c.-3488T=	XP_016878509.1:n.-3488T=
XM_024450187.1:c.822T=	XP_024305955.1:p.Asn274=
XR_001751864.2:n.1864T=
XR_933240.3:n.2054T=
NM_001127214.4:c.1617T=	NP_001120686.1:p.Asn539=
NM_001243279.3:c.1617T= MANE Select	NP_001230208.1:p.Asn539=
NM_001284316.2:c.822T=	NP_001271245.1:p.Asn274=
NM_174917.5:c.1617T=	NP_777577.2:p.Asn539=
NR_104293.2:n.2008T=
NR_147928.2:n.2052T=
NR_147929.2:n.1806T=