Canonical Allele Identifier: CA2808083859

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153795G>T , CM000678.2:g.89153795G>T	GRCh38
NC_000016.9:g.89220203G>T , CM000678.1:g.89220203G>T	GRCh37
NC_000016.8:g.87747704G>T	NCBI36
NG_031961.1:g.64987G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-295G>T	ENSP00000320646.4:n.1614-295G>T
ENST00000614302.5:c.1614-295G>T MANE Select	ENSP00000479130.1:n.1614-295G>T
ENST00000649953.1:c.1824-295G>T	ENSP00000497456.1:n.1824-295G>T
ENST00000317447.8:c.1614-295G>T	ENSP00000320646.4:n.1614-295G>T
ENST00000378345.8:c.819-295G>T	ENSP00000367596.4:n.819-295G>T
ENST00000393145.5:n.6229G>T
ENST00000406948.7:c.1614-295G>T	ENSP00000384627.3:n.1614-295G>T
ENST00000537116.5:n.740-295G>T
ENST00000537155.1:n.354-295G>T
ENST00000542688.5:c.*358-295G>T	ENSP00000446281.1:n.*358-295G>T
ENST00000614302.4:c.1614-295G>T	ENSP00000479130.1:n.1614-295G>T
NM_001127214.3:c.1614-295G>T	NP_001120686.1:n.1614-295G>T
NM_001243279.2:c.1614-295G>T	NP_001230208.1:n.1614-295G>T
NM_001284316.1:c.819-295G>T	NP_001271245.1:n.819-295G>T
NM_174917.4:c.1614-295G>T	NP_777577.2:n.1614-295G>T
NR_045667.2:n.740-295G>T
NR_104293.1:n.2048-295G>T
XR_933239.1:n.2055-295G>T
XR_933240.1:n.2052-295G>T
XR_933241.1:n.1809-295G>T
NR_147928.1:n.2092-295G>T
NR_147929.1:n.1846-295G>T
XM_017023020.2:c.-3491-295G>T	XP_016878509.1:n.-3491-295G>T
XM_024450187.1:c.819-295G>T	XP_024305955.1:n.819-295G>T
XR_001751864.2:n.1861-295G>T
XR_933240.3:n.2051-295G>T
NM_001127214.4:c.1614-295G>T	NP_001120686.1:n.1614-295G>T
NM_001243279.3:c.1614-295G>T MANE Select	NP_001230208.1:n.1614-295G>T
NM_001284316.2:c.819-295G>T	NP_001271245.1:n.819-295G>T
NM_174917.5:c.1614-295G>T	NP_777577.2:n.1614-295G>T
NR_104293.2:n.2005-295G>T
NR_147928.2:n.2049-295G>T
NR_147929.2:n.1803-295G>T