Canonical Allele Identifier: CA2241515791

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145971G= , CM000678.2:g.89145971G=	GRCh38
NC_000016.9:g.89212379G= , CM000678.1:g.89212379G=	GRCh37
NC_000016.8:g.87739880G=	NCBI36
NG_031961.1:g.57163G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1535G=	ENSP00000320646.4:p.Trp512=
ENST00000614302.5:c.1535G= MANE Select	ENSP00000479130.1:p.Trp512=
ENST00000649953.1:c.1745G=	ENSP00000497456.1:p.Trp582=
ENST00000317447.8:c.1535G=	ENSP00000320646.4:p.Trp512=
ENST00000378345.8:c.740G=	ENSP00000367596.4:p.Trp247=
ENST00000406948.7:c.1535G=	ENSP00000384627.3:p.Trp512=
ENST00000535176.1:c.22G=
ENST00000537116.5:n.661G=
ENST00000537155.1:n.275G=
ENST00000542688.5:c.*279G=	ENSP00000446281.1:n.*279G=
ENST00000562204.1:n.508G=
ENST00000614302.4:c.1535G=	ENSP00000479130.1:p.Trp512=
NM_001127214.3:c.1535G=	NP_001120686.1:p.Trp512=
NM_001243279.2:c.1535G=	NP_001230208.1:p.Trp512=
NM_001284316.1:c.740G=	NP_001271245.1:p.Trp247=
NM_174917.4:c.1535G=	NP_777577.2:p.Trp512=
NR_045667.2:n.661G=
NR_104293.1:n.1969G=
XM_005256293.1:c.1535G=	XP_005256350.1:p.Trp512=
XM_011522942.1:c.1535G=	XP_011521244.1:p.Trp512=
XM_011522943.1:c.1535G=	XP_011521245.1:p.Trp512=
XR_933239.1:n.1976G=
XR_933240.1:n.1973G=
XR_933241.1:n.1730G=
NR_147928.1:n.2013G=
NR_147929.1:n.1767G=
XM_005256293.2:c.1535G=	XP_005256350.1:p.Trp512=
XM_017023018.1:c.1535G=	XP_016878507.1:p.Trp512=
XM_017023019.1:c.1535G=	XP_016878508.1:p.Trp512=
XM_017023020.2:c.-3570G=	XP_016878509.1:n.-3570G=
XM_017023022.1:c.668G=	XP_016878511.1:p.Trp223=
XM_024450186.1:c.740G=	XP_024305954.1:p.Trp247=
XM_024450187.1:c.740G=	XP_024305955.1:p.Trp247=
XR_001751864.2:n.1782G=
XR_001751865.1:n.1729G=
XR_933240.3:n.1972G=
NM_001127214.4:c.1535G=	NP_001120686.1:p.Trp512=
NM_001243279.3:c.1535G= MANE Select	NP_001230208.1:p.Trp512=
NM_001284316.2:c.740G=	NP_001271245.1:p.Trp247=
NM_174917.5:c.1535G=	NP_777577.2:p.Trp512=
NR_104293.2:n.1926G=
NR_147928.2:n.1970G=
NR_147929.2:n.1724G=