Canonical Allele Identifier: CA2241515430

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89145369A= , CM000678.2:g.89145369A=	GRCh38
NC_000016.9:g.89211777A= , CM000678.1:g.89211777A=	GRCh37
NC_000016.8:g.87739278A=	NCBI36
NG_031961.1:g.56561A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1469A=	ENSP00000320646.4:p.Glu490=
ENST00000614302.5:c.1469A= MANE Select	ENSP00000479130.1:p.Glu490=
ENST00000649953.1:c.1679A=	ENSP00000497456.1:p.Glu560=
ENST00000317447.8:c.1469A=	ENSP00000320646.4:p.Glu490=
ENST00000378345.8:c.674A=	ENSP00000367596.4:p.Glu225=
ENST00000406948.7:c.1469A=	ENSP00000384627.3:p.Glu490=
ENST00000537116.5:n.595A=
ENST00000537155.1:n.209A=
ENST00000542688.5:c.*213A=	ENSP00000446281.1:n.*213A=
ENST00000544543.5:c.674A=	ENSP00000442781.1:p.Glu225=
ENST00000562204.1:n.442A=
ENST00000614302.4:c.1469A=	ENSP00000479130.1:p.Glu490=
NM_001127214.3:c.1469A=	NP_001120686.1:p.Glu490=
NM_001243279.2:c.1469A=	NP_001230208.1:p.Glu490=
NM_001284316.1:c.674A=	NP_001271245.1:p.Glu225=
NM_174917.4:c.1469A=	NP_777577.2:p.Glu490=
NR_045667.2:n.595A=
NR_104293.1:n.1903A=
XM_005256293.1:c.1469A=	XP_005256350.1:p.Glu490=
XM_011522942.1:c.1469A=	XP_011521244.1:p.Glu490=
XM_011522943.1:c.1469A=	XP_011521245.1:p.Glu490=
XR_933239.1:n.1910A=
XR_933240.1:n.1907A=
XR_933241.1:n.1664A=
NR_147928.1:n.1947A=
NR_147929.1:n.1701A=
XM_005256293.2:c.1469A=	XP_005256350.1:p.Glu490=
XM_017023018.1:c.1469A=	XP_016878507.1:p.Glu490=
XM_017023019.1:c.1469A=	XP_016878508.1:p.Glu490=
XM_017023020.2:c.-3636A=	XP_016878509.1:n.-3636A=
XM_017023022.1:c.602A=	XP_016878511.1:p.Glu201=
XM_024450186.1:c.674A=	XP_024305954.1:p.Glu225=
XM_024450187.1:c.674A=	XP_024305955.1:p.Glu225=
XR_001751864.2:n.1716A=
XR_001751865.1:n.1663A=
XR_933240.3:n.1906A=
NM_001127214.4:c.1469A=	NP_001120686.1:p.Glu490=
NM_001243279.3:c.1469A= MANE Select	NP_001230208.1:p.Glu490=
NM_001284316.2:c.674A=	NP_001271245.1:p.Glu225=
NM_174917.5:c.1469A=	NP_777577.2:p.Glu490=
NR_104293.2:n.1860A=
NR_147928.2:n.1904A=
NR_147929.2:n.1658A=