Canonical Allele Identifier: CA2241520199

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153638G= , CM000678.2:g.89153638G=	GRCh38
NC_000016.9:g.89220046G= , CM000678.1:g.89220046G=	GRCh37
NC_000016.8:g.87747547G=	NCBI36
NG_031961.1:g.64830G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-452G=	ENSP00000320646.4:n.1614-452G=
ENST00000614302.5:c.1614-452G= MANE Select	ENSP00000479130.1:n.1614-452G=
ENST00000649953.1:c.1824-452G=	ENSP00000497456.1:n.1824-452G=
ENST00000317447.8:c.1614-452G=	ENSP00000320646.4:n.1614-452G=
ENST00000378345.8:c.819-452G=	ENSP00000367596.4:n.819-452G=
ENST00000393145.5:n.6072G=
ENST00000406948.7:c.1614-452G=	ENSP00000384627.3:n.1614-452G=
ENST00000537116.5:n.740-452G=
ENST00000537155.1:n.354-452G=
ENST00000542688.5:c.*358-452G=	ENSP00000446281.1:n.*358-452G=
ENST00000614302.4:c.1614-452G=	ENSP00000479130.1:n.1614-452G=
NM_001127214.3:c.1614-452G=	NP_001120686.1:n.1614-452G=
NM_001243279.2:c.1614-452G=	NP_001230208.1:n.1614-452G=
NM_001284316.1:c.819-452G=	NP_001271245.1:n.819-452G=
NM_174917.4:c.1614-452G=	NP_777577.2:n.1614-452G=
NR_045667.2:n.740-452G=
NR_104293.1:n.2048-452G=
XR_933239.1:n.2055-452G=
XR_933240.1:n.2052-452G=
XR_933241.1:n.1809-452G=
NR_147928.1:n.2092-452G=
NR_147929.1:n.1846-452G=
XM_017023020.2:c.-3491-452G=	XP_016878509.1:n.-3491-452G=
XM_024450187.1:c.819-452G=	XP_024305955.1:n.819-452G=
XR_001751864.2:n.1861-452G=
XR_933240.3:n.2051-452G=
NM_001127214.4:c.1614-452G=	NP_001120686.1:n.1614-452G=
NM_001243279.3:c.1614-452G= MANE Select	NP_001230208.1:n.1614-452G=
NM_001284316.2:c.819-452G=	NP_001271245.1:n.819-452G=
NM_174917.5:c.1614-452G=	NP_777577.2:n.1614-452G=
NR_104293.2:n.2005-452G=
NR_147928.2:n.2049-452G=
NR_147929.2:n.1803-452G=