Canonical Allele Identifier: CA2808083846

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153614_89153615insGGTGGTCG , CM000678.2:g.89153614_89153615insGGTGGTCG	GRCh38
NC_000016.9:g.89220022_89220023insGGTGGTCG , CM000678.1:g.89220022_89220023insGGTGGTCG	GRCh37
NC_000016.8:g.87747523_87747524insGGTGGTCG	NCBI36
NG_031961.1:g.64806_64807insGGTGGTCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-476_1614-475insGGTGGTCG	ENSP00000320646.4:n.1614-476_1614-475insGGTGGTCG
ENST00000614302.5:c.1614-476_1614-475insGGTGGTCG MANE Select	ENSP00000479130.1:n.1614-476_1614-475insGGTGGTCG
ENST00000649953.1:c.1824-476_1824-475insGGTGGTCG	ENSP00000497456.1:n.1824-476_1824-475insGGTGGTCG
ENST00000317447.8:c.1614-476_1614-475insGGTGGTCG	ENSP00000320646.4:n.1614-476_1614-475insGGTGGTCG
ENST00000378345.8:c.819-476_819-475insGGTGGTCG	ENSP00000367596.4:n.819-476_819-475insGGTGGTCG
ENST00000393145.5:n.6048_6049insGGTGGTCG
ENST00000406948.7:c.1614-476_1614-475insGGTGGTCG	ENSP00000384627.3:n.1614-476_1614-475insGGTGGTCG
ENST00000537116.5:n.740-476_740-475insGGTGGTCG
ENST00000537155.1:n.354-476_354-475insGGTGGTCG
ENST00000542688.5:c.*358-476_*358-475insGGTGGTCG	ENSP00000446281.1:n.*358-476_*358-475insGGTGGTCG
ENST00000614302.4:c.1614-476_1614-475insGGTGGTCG	ENSP00000479130.1:n.1614-476_1614-475insGGTGGTCG
NM_001127214.3:c.1614-476_1614-475insGGTGGTCG	NP_001120686.1:n.1614-476_1614-475insGGTGGTCG
NM_001243279.2:c.1614-476_1614-475insGGTGGTCG	NP_001230208.1:n.1614-476_1614-475insGGTGGTCG
NM_001284316.1:c.819-476_819-475insGGTGGTCG	NP_001271245.1:n.819-476_819-475insGGTGGTCG
NM_174917.4:c.1614-476_1614-475insGGTGGTCG	NP_777577.2:n.1614-476_1614-475insGGTGGTCG
NR_045667.2:n.740-476_740-475insGGTGGTCG
NR_104293.1:n.2048-476_2048-475insGGTGGTCG
XR_933239.1:n.2055-476_2055-475insGGTGGTCG
XR_933240.1:n.2052-476_2052-475insGGTGGTCG
XR_933241.1:n.1809-476_1809-475insGGTGGTCG
NR_147928.1:n.2092-476_2092-475insGGTGGTCG
NR_147929.1:n.1846-476_1846-475insGGTGGTCG
XM_017023020.2:c.-3491-476_-3491-475insGGTGGTCG	XP_016878509.1:n.-3491-476_-3491-475insGGTGGTCG
XM_024450187.1:c.819-476_819-475insGGTGGTCG	XP_024305955.1:n.819-476_819-475insGGTGGTCG
XR_001751864.2:n.1861-476_1861-475insGGTGGTCG
XR_933240.3:n.2051-476_2051-475insGGTGGTCG
NM_001127214.4:c.1614-476_1614-475insGGTGGTCG	NP_001120686.1:n.1614-476_1614-475insGGTGGTCG
NM_001243279.3:c.1614-476_1614-475insGGTGGTCG MANE Select	NP_001230208.1:n.1614-476_1614-475insGGTGGTCG
NM_001284316.2:c.819-476_819-475insGGTGGTCG	NP_001271245.1:n.819-476_819-475insGGTGGTCG
NM_174917.5:c.1614-476_1614-475insGGTGGTCG	NP_777577.2:n.1614-476_1614-475insGGTGGTCG
NR_104293.2:n.2005-476_2005-475insGGTGGTCG
NR_147928.2:n.2049-476_2049-475insGGTGGTCG
NR_147929.2:n.1803-476_1803-475insGGTGGTCG