Canonical Allele Identifier: CA2634928230
Gene: ACSF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89153713_89153724del , CM000678.2:g.89153713_89153724del GRCh38
NC_000016.9:g.89220121_89220132del , CM000678.1:g.89220121_89220132del GRCh37
NC_000016.8:g.87747622_87747633del NCBI36
NG_031961.1:g.64905_64916del

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1614-377_1614-366del ENSP00000320646.4:n.1614-377_1614-366del
ENST00000614302.5:c.1614-377_1614-366del MANE Select ENSP00000479130.1:n.1614-377_1614-366del
ENST00000649953.1:c.1824-377_1824-366del ENSP00000497456.1:n.1824-377_1824-366del
ENST00000317447.8:c.1614-377_1614-366del ENSP00000320646.4:n.1614-377_1614-366del
ENST00000378345.8:c.819-377_819-366del ENSP00000367596.4:n.819-377_819-366del
ENST00000393145.5:n.6147_6158del
ENST00000406948.7:c.1614-377_1614-366del ENSP00000384627.3:n.1614-377_1614-366del
ENST00000537116.5:n.740-377_740-366del
ENST00000537155.1:n.354-377_354-366del
ENST00000542688.5:c.*358-377_*358-366del ENSP00000446281.1:n.*358-377_*358-366del
ENST00000614302.4:c.1614-377_1614-366del ENSP00000479130.1:n.1614-377_1614-366del
NM_001127214.3:c.1614-377_1614-366del NP_001120686.1:n.1614-377_1614-366del
NM_001243279.2:c.1614-377_1614-366del NP_001230208.1:n.1614-377_1614-366del
NM_001284316.1:c.819-377_819-366del NP_001271245.1:n.819-377_819-366del
NM_174917.4:c.1614-377_1614-366del NP_777577.2:n.1614-377_1614-366del
NR_045667.2:n.740-377_740-366del
NR_104293.1:n.2048-377_2048-366del
XR_933239.1:n.2055-377_2055-366del
XR_933240.1:n.2052-377_2052-366del
XR_933241.1:n.1809-377_1809-366del
NR_147928.1:n.2092-377_2092-366del
NR_147929.1:n.1846-377_1846-366del
XM_017023020.2:c.-3491-377_-3491-366del XP_016878509.1:n.-3491-377_-3491-366del
XM_024450187.1:c.819-377_819-366del XP_024305955.1:n.819-377_819-366del
XR_001751864.2:n.1861-377_1861-366del
XR_933240.3:n.2051-377_2051-366del
NM_001127214.4:c.1614-377_1614-366del NP_001120686.1:n.1614-377_1614-366del
NM_001243279.3:c.1614-377_1614-366del MANE Select NP_001230208.1:n.1614-377_1614-366del
NM_001284316.2:c.819-377_819-366del NP_001271245.1:n.819-377_819-366del
NM_174917.5:c.1614-377_1614-366del NP_777577.2:n.1614-377_1614-366del
NR_104293.2:n.2005-377_2005-366del
NR_147928.2:n.2049-377_2049-366del
NR_147929.2:n.1803-377_1803-366del