Canonical Allele Identifier: CA2634920775
Gene: ACSF3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89146048dup , CM000678.2:g.89146048dup GRCh38
NC_000016.9:g.89212456dup , CM000678.1:g.89212456dup GRCh37
NC_000016.8:g.87739957dup NCBI36
NG_031961.1:g.57240dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000317447.9:c.1612dup ENSP00000320646.4:p.Arg538LysfsTer28
ENST00000614302.5:c.1612dup MANE Select ENSP00000479130.1:p.Arg538LysfsTer28
ENST00000649953.1:c.1822dup ENSP00000497456.1:p.Arg608LysfsTer28
ENST00000317447.8:c.1612dup ENSP00000320646.4:p.Arg538LysfsTer28
ENST00000378345.8:c.817dup ENSP00000367596.4:p.Arg273LysfsTer28
ENST00000406948.7:c.1612dup ENSP00000384627.3:p.Arg538LysfsTer28
ENST00000535176.1:c.99dup
ENST00000537116.5:n.738dup
ENST00000537155.1:n.352dup
ENST00000542688.5:c.*356dup ENSP00000446281.1:n.*356dup
ENST00000614302.4:c.1612dup ENSP00000479130.1:p.Arg538LysfsTer28
NM_001127214.3:c.1612dup NP_001120686.1:p.Arg538LysfsTer28
NM_001243279.2:c.1612dup NP_001230208.1:p.Arg538LysfsTer28
NM_001284316.1:c.817dup NP_001271245.1:p.Arg273LysfsTer28
NM_174917.4:c.1612dup NP_777577.2:p.Arg538LysfsTer28
NR_045667.2:n.738dup
NR_104293.1:n.2046dup
XM_005256293.1:c.1612dup XP_005256350.1:p.Arg538LysfsTer?
XM_011522942.1:c.1612dup XP_011521244.1:p.Arg538LysfsTer?
XM_011522943.1:c.1612dup XP_011521245.1:p.Arg538LysfsTer?
XR_933239.1:n.2053dup
XR_933240.1:n.2050dup
XR_933241.1:n.1807dup
NR_147928.1:n.2090dup
NR_147929.1:n.1844dup
XM_005256293.2:c.1612dup XP_005256350.1:p.Arg538LysfsTer?
XM_017023018.1:c.1612dup XP_016878507.1:p.Arg538LysfsTer?
XM_017023019.1:c.1612dup XP_016878508.1:p.Arg538LysfsTer16
XM_017023020.2:c.-3493dup XP_016878509.1:n.-3493dup
XM_017023022.1:c.745dup XP_016878511.1:p.Arg249LysfsTer?
XM_024450186.1:c.817dup XP_024305954.1:p.Arg273LysfsTer?
XM_024450187.1:c.817dup XP_024305955.1:p.Arg273LysfsTer28
XR_001751864.2:n.1859dup
XR_001751865.1:n.1806dup
XR_933240.3:n.2049dup
NM_001127214.4:c.1612dup NP_001120686.1:p.Arg538LysfsTer28
NM_001243279.3:c.1612dup MANE Select NP_001230208.1:p.Arg538LysfsTer28
NM_001284316.2:c.817dup NP_001271245.1:p.Arg273LysfsTer28
NM_174917.5:c.1612dup NP_777577.2:p.Arg538LysfsTer28
NR_104293.2:n.2003dup
NR_147928.2:n.2047dup
NR_147929.2:n.1801dup