Canonical Allele Identifier: CA2241520241

Gene: ACSF3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89153689_89153692delinsGCCT , CM000678.2:g.89153689_89153692delinsGCCT	GRCh38
NC_000016.9:g.89220097_89220100delinsGCCT , CM000678.1:g.89220097_89220100delinsGCCT	GRCh37
NC_000016.8:g.87747598_87747601delinsGCCT	NCBI36
NG_031961.1:g.64881_64884delinsGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000317447.9:c.1614-401_1614-398delinsGCCT	ENSP00000320646.4:n.1614-401_1614-398delinsGCCT
ENST00000614302.5:c.1614-401_1614-398delinsGCCT MANE Select	ENSP00000479130.1:n.1614-401_1614-398delinsGCCT
ENST00000649953.1:c.1824-401_1824-398delinsGCCT	ENSP00000497456.1:n.1824-401_1824-398delinsGCCT
ENST00000317447.8:c.1614-401_1614-398delinsGCCT	ENSP00000320646.4:n.1614-401_1614-398delinsGCCT
ENST00000378345.8:c.819-401_819-398delinsGCCT	ENSP00000367596.4:n.819-401_819-398delinsGCCT
ENST00000393145.5:n.6123_6126delinsGCCT
ENST00000406948.7:c.1614-401_1614-398delinsGCCT	ENSP00000384627.3:n.1614-401_1614-398delinsGCCT
ENST00000537116.5:n.740-401_740-398delinsGCCT
ENST00000537155.1:n.354-401_354-398delinsGCCT
ENST00000542688.5:c.*358-401_*358-398delinsGCCT	ENSP00000446281.1:n.*358-401_*358-398delinsGCCT
ENST00000614302.4:c.1614-401_1614-398delinsGCCT	ENSP00000479130.1:n.1614-401_1614-398delinsGCCT
NM_001127214.3:c.1614-401_1614-398delinsGCCT	NP_001120686.1:n.1614-401_1614-398delinsGCCT
NM_001243279.2:c.1614-401_1614-398delinsGCCT	NP_001230208.1:n.1614-401_1614-398delinsGCCT
NM_001284316.1:c.819-401_819-398delinsGCCT	NP_001271245.1:n.819-401_819-398delinsGCCT
NM_174917.4:c.1614-401_1614-398delinsGCCT	NP_777577.2:n.1614-401_1614-398delinsGCCT
NR_045667.2:n.740-401_740-398delinsGCCT
NR_104293.1:n.2048-401_2048-398delinsGCCT
XR_933239.1:n.2055-401_2055-398delinsGCCT
XR_933240.1:n.2052-401_2052-398delinsGCCT
XR_933241.1:n.1809-401_1809-398delinsGCCT
NR_147928.1:n.2092-401_2092-398delinsGCCT
NR_147929.1:n.1846-401_1846-398delinsGCCT
XM_017023020.2:c.-3491-401_-3491-398delinsGCCT	XP_016878509.1:n.-3491-401_-3491-398delinsGCCT
XM_024450187.1:c.819-401_819-398delinsGCCT	XP_024305955.1:n.819-401_819-398delinsGCCT
XR_001751864.2:n.1861-401_1861-398delinsGCCT
XR_933240.3:n.2051-401_2051-398delinsGCCT
NM_001127214.4:c.1614-401_1614-398delinsGCCT	NP_001120686.1:n.1614-401_1614-398delinsGCCT
NM_001243279.3:c.1614-401_1614-398delinsGCCT MANE Select	NP_001230208.1:n.1614-401_1614-398delinsGCCT
NM_001284316.2:c.819-401_819-398delinsGCCT	NP_001271245.1:n.819-401_819-398delinsGCCT
NM_174917.5:c.1614-401_1614-398delinsGCCT	NP_777577.2:n.1614-401_1614-398delinsGCCT
NR_104293.2:n.2005-401_2005-398delinsGCCT
NR_147928.2:n.2049-401_2049-398delinsGCCT
NR_147929.2:n.1803-401_1803-398delinsGCCT