Canonical Allele Identifier: CA2241520537

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89154191A= , CM000678.2:g.89154191A=	GRCh38
NC_000016.9:g.89220599A= , CM000678.1:g.89220599A=	GRCh37
NC_000016.8:g.87748100A=	NCBI36
NG_031961.1:g.65383A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1715A=	ENSP00000320646.4:p.His572=
ENST00000614302.5:c.1715A= MANE Select	ENSP00000479130.1:p.His572=
ENST00000649953.1:c.1925A=	ENSP00000497456.1:p.His642=
ENST00000317447.8:c.1715A=	ENSP00000320646.4:p.His572=
ENST00000378345.8:c.920A=	ENSP00000367596.4:p.His307=
ENST00000393145.5:n.6625A=
ENST00000406948.7:c.1715A=	ENSP00000384627.3:p.His572=
ENST00000537116.5:n.841A=
ENST00000537155.1:n.455A=
ENST00000542688.5:c.*459A=	ENSP00000446281.1:n.*459A=
ENST00000614302.4:c.1715A=	ENSP00000479130.1:p.His572=
NM_001127214.3:c.1715A=	NP_001120686.1:p.His572=
NM_001243279.2:c.1715A=	NP_001230208.1:p.His572=
NM_001284316.1:c.920A=	NP_001271245.1:p.His307=
NM_174917.4:c.1715A=	NP_777577.2:p.His572=
NR_045667.2:n.841A=
NR_104293.1:n.2149A=
XR_933239.1:n.2156A=
XR_933240.1:n.2153A=
XR_933241.1:n.1910A=
NR_147928.1:n.2193A=
NR_147929.1:n.1947A=
XM_017023020.2:c.-3390A=	XP_016878509.1:n.-3390A=
XM_024450187.1:c.920A=	XP_024305955.1:p.His307=
XR_001751864.2:n.1962A=
XR_933240.3:n.2152A=
NM_001127214.4:c.1715A=	NP_001120686.1:p.His572=
NM_001243279.3:c.1715A= MANE Select	NP_001230208.1:p.His572=
NM_001284316.2:c.920A=	NP_001271245.1:p.His307=
NM_174917.5:c.1715A=	NP_777577.2:p.His572=
NR_104293.2:n.2106A=
NR_147928.2:n.2150A=
NR_147929.2:n.1904A=