Canonical Allele Identifier: CA2241520532

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154180G= , CM000678.2:g.89154180G=	GRCh38
NC_000016.9:g.89220588G= , CM000678.1:g.89220588G=	GRCh37
NC_000016.8:g.87748089G=	NCBI36
NG_031961.1:g.65372G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1704G=	ENSP00000320646.4:p.Ala568=
ENST00000614302.5:c.1704G= MANE Select	ENSP00000479130.1:p.Ala568=
ENST00000649953.1:c.1914G=	ENSP00000497456.1:p.Ala638=
ENST00000317447.8:c.1704G=	ENSP00000320646.4:p.Ala568=
ENST00000378345.8:c.909G=	ENSP00000367596.4:p.Ala303=
ENST00000393145.5:n.6614G=
ENST00000406948.7:c.1704G=	ENSP00000384627.3:p.Ala568=
ENST00000537116.5:n.830G=
ENST00000537155.1:n.444G=
ENST00000542688.5:c.*448G=	ENSP00000446281.1:n.*448G=
ENST00000614302.4:c.1704G=	ENSP00000479130.1:p.Ala568=
NM_001127214.3:c.1704G=	NP_001120686.1:p.Ala568=
NM_001243279.2:c.1704G=	NP_001230208.1:p.Ala568=
NM_001284316.1:c.909G=	NP_001271245.1:p.Ala303=
NM_174917.4:c.1704G=	NP_777577.2:p.Ala568=
NR_045667.2:n.830G=
NR_104293.1:n.2138G=
XR_933239.1:n.2145G=
XR_933240.1:n.2142G=
XR_933241.1:n.1899G=
NR_147928.1:n.2182G=
NR_147929.1:n.1936G=
XM_017023020.2:c.-3401G=	XP_016878509.1:n.-3401G=
XM_024450187.1:c.909G=	XP_024305955.1:p.Ala303=
XR_001751864.2:n.1951G=
XR_933240.3:n.2141G=
NM_001127214.4:c.1704G=	NP_001120686.1:p.Ala568=
NM_001243279.3:c.1704G= MANE Select	NP_001230208.1:p.Ala568=
NM_001284316.2:c.909G=	NP_001271245.1:p.Ala303=
NM_174917.5:c.1704G=	NP_777577.2:p.Ala568=
NR_104293.2:n.2095G=
NR_147928.2:n.2139G=
NR_147929.2:n.1893G=