Canonical Allele Identifier: CA2695212382
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014147del , CM000672.2:g.89014147del GRCh38
NC_000010.10:g.90773904del , CM000672.1:g.90773904del GRCh37
NC_000010.9:g.90763884del NCBI36
NG_009089.2:g.28617del , LRG_134:g.28617del

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1014del
ENST00000355740.8:c.*28del ENSP00000347979.3:n.*28del
ENST00000357339.7:c.642del ENSP00000349896.2:p.Ile215LeufsTer5
ENST00000371857.8:n.2250del
ENST00000460510.6:c.-13del ENSP00000512812.1:n.-13del
ENST00000466081.6:n.2354del
ENST00000477270.6:c.750del ENSP00000512813.1:p.Ile251LeufsTer5
ENST00000479522.6:c.*134del ENSP00000424113.1:n.*134del
ENST00000484444.6:c.*146del ENSP00000420975.1:n.*146del
ENST00000488877.6:c.596del ENSP00000425159.1:n.596del
ENST00000492756.7:c.*134del ENSP00000422453.1:n.*134del
ENST00000494799.6:c.-13del ENSP00000512834.1:n.-13del
ENST00000562983.3:c.-13del ENSP00000512845.1:n.-13del
ENST00000612663.6:c.*107del ENSP00000477997.3:n.*107del
ENST00000640140.2:n.850del
ENST00000640250.2:n.204del
ENST00000640681.2:n.809del
ENST00000696723.1:n.4338del
ENST00000696741.1:n.2343del
ENST00000696742.1:n.2070del
ENST00000696743.1:n.3473del
ENST00000696744.1:n.744del
ENST00000696767.1:n.1039del
ENST00000696768.1:c.*28del ENSP00000512859.1:n.*28del
ENST00000696769.1:n.2394del
ENST00000696771.1:c.-13del ENSP00000512860.1:n.-13del
ENST00000696772.1:n.2308del
ENST00000696773.1:n.2047del
ENST00000696774.1:n.5815del
ENST00000696776.1:c.798del ENSP00000512861.1:p.Ile267LeufsTer5
ENST00000696777.1:n.2113del
ENST00000696778.1:n.1141del
ENST00000696779.1:c.312del ENSP00000512862.1:p.Ile105LeufsTer5
ENST00000696780.1:c.735del ENSP00000512863.1:p.Ile246LeufsTer5
ENST00000696781.1:c.450del ENSP00000512864.1:p.Ile151LeufsTer5
ENST00000696782.1:c.*107del ENSP00000512865.1:n.*107del
ENST00000696783.1:n.2573del
ENST00000696992.1:n.1822del
ENST00000696995.1:n.4234del
ENST00000696996.1:n.2147del
ENST00000696997.1:c.*335del ENSP00000513028.1:n.*335del
ENST00000696998.1:n.1959del
ENST00000696999.1:c.-13del ENSP00000513029.1:n.-13del
ENST00000697035.1:c.*38del ENSP00000513059.1:n.*38del
ENST00000697036.1:c.*121del ENSP00000513060.1:n.*121del
ENST00000697037.1:n.740del
ENST00000697093.1:n.2941del
ENST00000697094.1:n.3288del
ENST00000697095.1:c.*1906del ENSP00000513104.1:n.*1906del
ENST00000697096.1:n.1838del
ENST00000697097.1:c.-13del ENSP00000513105.1:n.-13del
ENST00000562983.2:n.891del
ENST00000690268.1:c.786del ENSP00000509810.1:p.Ile263LeufsTer5
ENST00000355740.7:c.*31del ENSP00000347979.3:n.*31del
ENST00000612663.5:c.*107del ENSP00000477997.3:n.*107del
ENST00000640140.1:n.877del
ENST00000640250.1:n.204del
ENST00000640681.1:n.826del
ENST00000652046.1:c.705del MANE Select ENSP00000498466.1:p.Ile236LeufsTer5
ENST00000313771.9:n.1014del
ENST00000352159.8:c.*22del ENSP00000345601.4:n.*22del
ENST00000355279.2:c.680del ENSP00000347426.2:n.680del
ENST00000355740.6:c.705del ENSP00000347979.2:p.Ile236LeufsTer5
ENST00000357339.6:c.642del ENSP00000349896.2:p.Ile215LeufsTer5
ENST00000479522.5:c.*134del ENSP00000424113.1:n.*134del
ENST00000484444.5:c.*146del ENSP00000420975.1:n.*146del
ENST00000488877.5:c.*146del ENSP00000425159.1:n.*146del
ENST00000492756.5:c.533del ENSP00000422453.1:n.533del
ENST00000494410.5:c.*63del ENSP00000423755.1:n.*63del
ENST00000494799.5:n.612del
ENST00000612663.4:c.*52del ENSP00000477997.2:n.*52del
ENST00000615406.4:c.705del ENSP00000484575.1:p.Ile236LeufsTer5
ENST00000626542.2:c.703del ENSP00000485876.1:p.Tyr235IlefsTer?
NM_000043.4:c.705del , LRG_134t1:c.705del NP_000034.1:p.Ile236LeufsTer5
NM_152871.2:c.642del NP_690610.1:p.Ile215LeufsTer5
NM_152872.2:c.*17del NP_690611.1:n.*17del
NR_028033.2:n.879del
NR_028034.2:n.741del
NR_028035.2:n.804del
NR_028036.2:n.942del
XM_006717819.2:c.786del XP_006717882.1:p.Ile263LeufsTer5
XM_011539764.1:c.867del XP_011538066.1:p.Ile290LeufsTer5
XM_011539765.1:c.804del XP_011538067.1:p.Ile269LeufsTer5
XM_011539766.1:c.786del XP_011538068.1:p.Ile263LeufsTer5
XM_011539767.1:c.750del XP_011538069.1:p.Ile251LeufsTer5
XR_945732.1:n.773del
XR_945733.1:n.710del
NM_000043.5:c.705del NP_000034.1:p.Ile236LeufsTer5
NM_001320619.1:c.*28del NP_001307548.1:n.*28del
NM_152871.3:c.642del NP_690610.1:p.Ile215LeufsTer5
NM_152872.3:c.*17del NP_690611.1:n.*17del
NR_028033.3:n.851del
NR_028034.3:n.713del
NR_028035.3:n.776del
NR_028036.3:n.914del
NR_135313.1:n.831del
NR_135314.1:n.1014del
NR_135315.1:n.767del
XM_006717819.3:c.786del XP_006717882.1:p.Ile263LeufsTer5
XM_011539764.2:c.867del XP_011538066.1:p.Ile290LeufsTer5
XM_011539765.2:c.804del XP_011538067.1:p.Ile269LeufsTer5
XM_011539766.2:c.786del XP_011538068.1:p.Ile263LeufsTer5
XM_011539767.3:c.750del XP_011538069.1:p.Ile251LeufsTer5
XR_945732.3:n.773del
XR_945733.2:n.710del
NM_000043.6:c.705del MANE Select NP_000034.1:p.Ile236LeufsTer5
NM_001320619.2:c.*28del NP_001307548.1:n.*28del
NM_152871.4:c.642del NP_690610.1:p.Ile215LeufsTer5
NM_152872.4:c.*17del NP_690611.1:n.*17del
NR_028033.4:n.612del
NR_028034.4:n.474del
NR_028035.4:n.537del
NR_028036.4:n.675del
NR_135313.2:n.592del
NR_135314.2:n.871del
NR_135315.2:n.624del