Canonical Allele Identifier: CA3001247810
Gene: ACSF3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89114444dup , CM000678.2:g.89114444dup GRCh38
NC_000016.9:g.89180852dup , CM000678.1:g.89180852dup GRCh37
NC_000016.8:g.87708353dup NCBI36
NG_031961.1:g.25636dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1083dup ENSP00000320646.4:p.Met362HisfsTer?
ENST00000614302.5:c.1083dup MANE Select ENSP00000479130.1:p.Met362HisfsTer?
ENST00000649953.1:c.1083dup ENSP00000497456.1:p.Met362HisfsTer?
ENST00000317447.8:c.1083dup ENSP00000320646.4:p.Met362HisfsTer?
ENST00000378345.8:c.288dup ENSP00000367596.4:p.Met97HisfsTer?
ENST00000406948.7:c.1083dup ENSP00000384627.3:p.Met362HisfsTer?
ENST00000537895.5:c.288dup ENSP00000439201.1:p.Met97HisfsTer?
ENST00000538340.5:c.302+2198dup ENSP00000445870.1:n.302+2198dup
ENST00000540697.5:c.288dup ENSP00000445397.1:p.Met97HisfsTer?
ENST00000542688.5:c.977+2198dup ENSP00000446281.1:n.977+2198dup
ENST00000543676.1:c.325dup
ENST00000544543.5:c.288dup ENSP00000442781.1:p.Met97HisfsTer?
ENST00000562204.1:n.46+2198dup
ENST00000614302.4:c.1083dup ENSP00000479130.1:p.Met362HisfsTer?
NM_001127214.3:c.1083dup NP_001120686.1:p.Met362HisfsTer?
NM_001243279.2:c.1083dup NP_001230208.1:p.Met362HisfsTer?
NM_001284316.1:c.288dup NP_001271245.1:p.Met97HisfsTer?
NM_174917.4:c.1083dup NP_777577.2:p.Met362HisfsTer?
NR_104293.1:n.1464dup
XM_005256293.1:c.1083dup XP_005256350.1:p.Met362HisfsTer?
XM_011522942.1:c.1083dup XP_011521244.1:p.Met362HisfsTer?
XM_011522943.1:c.1083dup XP_011521245.1:p.Met362HisfsTer?
XM_011522944.1:c.1083dup XP_011521246.1:p.Met362HisfsTer?
XR_933238.1:n.1427dup
XR_933239.1:n.1427dup
XR_933240.1:n.1427dup
XR_933241.1:n.1321+2198dup
NR_147928.1:n.1464dup
NR_147929.1:n.1358+2198dup
XM_005256293.2:c.1083dup XP_005256350.1:p.Met362HisfsTer?
XM_017023018.1:c.1083dup XP_016878507.1:p.Met362HisfsTer?
XM_017023019.1:c.1083dup XP_016878508.1:p.Met362HisfsTer?
XM_017023020.2:c.-4032+2198dup XP_016878509.1:n.-4032+2198dup
XM_017023021.1:c.1083dup XP_016878510.1:p.Met362HisfsTer?
XM_024450186.1:c.288dup XP_024305954.1:p.Met97HisfsTer?
XM_024450187.1:c.288dup XP_024305955.1:p.Met97HisfsTer?
XR_001751864.2:n.1320+2198dup
XR_001751865.1:n.1320+2198dup
XR_933238.2:n.1426dup
XR_933240.3:n.1426dup
NM_001127214.4:c.1083dup NP_001120686.1:p.Met362HisfsTer?
NM_001243279.3:c.1083dup MANE Select NP_001230208.1:p.Met362HisfsTer?
NM_001284316.2:c.288dup NP_001271245.1:p.Met97HisfsTer?
NM_174917.5:c.1083dup NP_777577.2:p.Met362HisfsTer?
NR_104293.2:n.1421dup
NR_147928.2:n.1421dup
NR_147929.2:n.1315+2198dup