Canonical Allele Identifier: CA2241520312

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153801_89153803delinsCTG , CM000678.2:g.89153801_89153803delinsCTG	GRCh38
NC_000016.9:g.89220209_89220211delinsCTG , CM000678.1:g.89220209_89220211delinsCTG	GRCh37
NC_000016.8:g.87747710_87747712delinsCTG	NCBI36
NG_031961.1:g.64993_64995delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-289_1614-287delinsCTG	ENSP00000320646.4:n.1614-289_1614-287delinsCTG
ENST00000614302.5:c.1614-289_1614-287delinsCTG MANE Select	ENSP00000479130.1:n.1614-289_1614-287delinsCTG
ENST00000649953.1:c.1824-289_1824-287delinsCTG	ENSP00000497456.1:n.1824-289_1824-287delinsCTG
ENST00000317447.8:c.1614-289_1614-287delinsCTG	ENSP00000320646.4:n.1614-289_1614-287delinsCTG
ENST00000378345.8:c.819-289_819-287delinsCTG	ENSP00000367596.4:n.819-289_819-287delinsCTG
ENST00000393145.5:n.6235_6237delinsCTG
ENST00000406948.7:c.1614-289_1614-287delinsCTG	ENSP00000384627.3:n.1614-289_1614-287delinsCTG
ENST00000537116.5:n.740-289_740-287delinsCTG
ENST00000537155.1:n.354-289_354-287delinsCTG
ENST00000542688.5:c.*358-289_*358-287delinsCTG	ENSP00000446281.1:n.*358-289_*358-287delinsCTG
ENST00000614302.4:c.1614-289_1614-287delinsCTG	ENSP00000479130.1:n.1614-289_1614-287delinsCTG
NM_001127214.3:c.1614-289_1614-287delinsCTG	NP_001120686.1:n.1614-289_1614-287delinsCTG
NM_001243279.2:c.1614-289_1614-287delinsCTG	NP_001230208.1:n.1614-289_1614-287delinsCTG
NM_001284316.1:c.819-289_819-287delinsCTG	NP_001271245.1:n.819-289_819-287delinsCTG
NM_174917.4:c.1614-289_1614-287delinsCTG	NP_777577.2:n.1614-289_1614-287delinsCTG
NR_045667.2:n.740-289_740-287delinsCTG
NR_104293.1:n.2048-289_2048-287delinsCTG
XR_933239.1:n.2055-289_2055-287delinsCTG
XR_933240.1:n.2052-289_2052-287delinsCTG
XR_933241.1:n.1809-289_1809-287delinsCTG
NR_147928.1:n.2092-289_2092-287delinsCTG
NR_147929.1:n.1846-289_1846-287delinsCTG
XM_017023020.2:c.-3491-289_-3491-287delinsCTG	XP_016878509.1:n.-3491-289_-3491-287delinsCTG
XM_024450187.1:c.819-289_819-287delinsCTG	XP_024305955.1:n.819-289_819-287delinsCTG
XR_001751864.2:n.1861-289_1861-287delinsCTG
XR_933240.3:n.2051-289_2051-287delinsCTG
NM_001127214.4:c.1614-289_1614-287delinsCTG	NP_001120686.1:n.1614-289_1614-287delinsCTG
NM_001243279.3:c.1614-289_1614-287delinsCTG MANE Select	NP_001230208.1:n.1614-289_1614-287delinsCTG
NM_001284316.2:c.819-289_819-287delinsCTG	NP_001271245.1:n.819-289_819-287delinsCTG
NM_174917.5:c.1614-289_1614-287delinsCTG	NP_777577.2:n.1614-289_1614-287delinsCTG
NR_104293.2:n.2005-289_2005-287delinsCTG
NR_147928.2:n.2049-289_2049-287delinsCTG
NR_147929.2:n.1803-289_1803-287delinsCTG