Canonical Allele Identifier: CA2634928183

Gene: ACSF3

Linked Data

• gnomAD v4: 16-89153687-A-AGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153687_89153688insGCT , CM000678.2:g.89153687_89153688insGCT	GRCh38
NC_000016.9:g.89220095_89220096insGCT , CM000678.1:g.89220095_89220096insGCT	GRCh37
NC_000016.8:g.87747596_87747597insGCT	NCBI36
NG_031961.1:g.64879_64880insGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-403_1614-402insGCT	ENSP00000320646.4:n.1614-403_1614-402insGCT
ENST00000614302.5:c.1614-403_1614-402insGCT MANE Select	ENSP00000479130.1:n.1614-403_1614-402insGCT
ENST00000649953.1:c.1824-403_1824-402insGCT	ENSP00000497456.1:n.1824-403_1824-402insGCT
ENST00000317447.8:c.1614-403_1614-402insGCT	ENSP00000320646.4:n.1614-403_1614-402insGCT
ENST00000378345.8:c.819-403_819-402insGCT	ENSP00000367596.4:n.819-403_819-402insGCT
ENST00000393145.5:n.6121_6122insGCT
ENST00000406948.7:c.1614-403_1614-402insGCT	ENSP00000384627.3:n.1614-403_1614-402insGCT
ENST00000537116.5:n.740-403_740-402insGCT
ENST00000537155.1:n.354-403_354-402insGCT
ENST00000542688.5:c.*358-403_*358-402insGCT	ENSP00000446281.1:n.*358-403_*358-402insGCT
ENST00000614302.4:c.1614-403_1614-402insGCT	ENSP00000479130.1:n.1614-403_1614-402insGCT
NM_001127214.3:c.1614-403_1614-402insGCT	NP_001120686.1:n.1614-403_1614-402insGCT
NM_001243279.2:c.1614-403_1614-402insGCT	NP_001230208.1:n.1614-403_1614-402insGCT
NM_001284316.1:c.819-403_819-402insGCT	NP_001271245.1:n.819-403_819-402insGCT
NM_174917.4:c.1614-403_1614-402insGCT	NP_777577.2:n.1614-403_1614-402insGCT
NR_045667.2:n.740-403_740-402insGCT
NR_104293.1:n.2048-403_2048-402insGCT
XR_933239.1:n.2055-403_2055-402insGCT
XR_933240.1:n.2052-403_2052-402insGCT
XR_933241.1:n.1809-403_1809-402insGCT
NR_147928.1:n.2092-403_2092-402insGCT
NR_147929.1:n.1846-403_1846-402insGCT
XM_017023020.2:c.-3491-403_-3491-402insGCT	XP_016878509.1:n.-3491-403_-3491-402insGCT
XM_024450187.1:c.819-403_819-402insGCT	XP_024305955.1:n.819-403_819-402insGCT
XR_001751864.2:n.1861-403_1861-402insGCT
XR_933240.3:n.2051-403_2051-402insGCT
NM_001127214.4:c.1614-403_1614-402insGCT	NP_001120686.1:n.1614-403_1614-402insGCT
NM_001243279.3:c.1614-403_1614-402insGCT MANE Select	NP_001230208.1:n.1614-403_1614-402insGCT
NM_001284316.2:c.819-403_819-402insGCT	NP_001271245.1:n.819-403_819-402insGCT
NM_174917.5:c.1614-403_1614-402insGCT	NP_777577.2:n.1614-403_1614-402insGCT
NR_104293.2:n.2005-403_2005-402insGCT
NR_147928.2:n.2049-403_2049-402insGCT
NR_147929.2:n.1803-403_1803-402insGCT