Canonical Allele Identifier: CA1926639312
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014144_89014147delinsCACT , CM000672.2:g.89014144_89014147delinsCACT GRCh38
NC_000010.10:g.90773901_90773904delinsCACT , CM000672.1:g.90773901_90773904delinsCACT GRCh37
NC_000010.9:g.90763881_90763884delinsCACT NCBI36
NG_009089.2:g.28614_28617delinsCACT , LRG_134:g.28614_28617delinsCACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1011_1014delinsCACT
ENST00000355740.8:c.*25_*28delinsCACT ENSP00000347979.3:n.*25_*28delinsCACT
ENST00000357339.7:c.639_642delinsCACT ENSP00000349896.2:p.Thr213=
ENST00000371857.8:n.2247_2250delinsCACT
ENST00000460510.6:c.-16_-13delinsCACT ENSP00000512812.1:n.-16_-13delinsCACT
ENST00000466081.6:n.2351_2354delinsCACT
ENST00000477270.6:c.747_750delinsCACT ENSP00000512813.1:p.Thr249=
ENST00000479522.6:c.*131_*134delinsCACT ENSP00000424113.1:n.*131_*134delinsCACT
ENST00000484444.6:c.*143_*146delinsCACT ENSP00000420975.1:n.*143_*146delinsCACT
ENST00000488877.6:c.593_596delinsCACT ENSP00000425159.1:n.593_596delinsCACT
ENST00000492756.7:c.*131_*134delinsCACT ENSP00000422453.1:n.*131_*134delinsCACT
ENST00000494799.6:c.-16_-13delinsCACT ENSP00000512834.1:n.-16_-13delinsCACT
ENST00000562983.3:c.-16_-13delinsCACT ENSP00000512845.1:n.-16_-13delinsCACT
ENST00000612663.6:c.*104_*107delinsCACT ENSP00000477997.3:n.*104_*107delinsCACT
ENST00000640140.2:n.847_850delinsCACT
ENST00000640250.2:n.201_204delinsCACT
ENST00000640681.2:n.806_809delinsCACT
ENST00000696723.1:n.4335_4338delinsCACT
ENST00000696741.1:n.2340_2343delinsCACT
ENST00000696742.1:n.2067_2070delinsCACT
ENST00000696743.1:n.3470_3473delinsCACT
ENST00000696744.1:n.741_744delinsCACT
ENST00000696767.1:n.1036_1039delinsCACT
ENST00000696768.1:c.*25_*28delinsCACT ENSP00000512859.1:n.*25_*28delinsCACT
ENST00000696769.1:n.2391_2394delinsCACT
ENST00000696771.1:c.-16_-13delinsCACT ENSP00000512860.1:n.-16_-13delinsCACT
ENST00000696772.1:n.2305_2308delinsCACT
ENST00000696773.1:n.2044_2047delinsCACT
ENST00000696774.1:n.5812_5815delinsCACT
ENST00000696776.1:c.795_798delinsCACT ENSP00000512861.1:p.Thr265=
ENST00000696777.1:n.2110_2113delinsCACT
ENST00000696778.1:n.1138_1141delinsCACT
ENST00000696779.1:c.309_312delinsCACT ENSP00000512862.1:p.Thr103=
ENST00000696780.1:c.732_735delinsCACT ENSP00000512863.1:p.Thr244=
ENST00000696781.1:c.447_450delinsCACT ENSP00000512864.1:p.Thr149=
ENST00000696782.1:c.*104_*107delinsCACT ENSP00000512865.1:n.*104_*107delinsCACT
ENST00000696783.1:n.2570_2573delinsCACT
ENST00000696992.1:n.1819_1822delinsCACT
ENST00000696995.1:n.4231_4234delinsCACT
ENST00000696996.1:n.2144_2147delinsCACT
ENST00000696997.1:c.*332_*335delinsCACT ENSP00000513028.1:n.*332_*335delinsCACT
ENST00000696998.1:n.1956_1959delinsCACT
ENST00000696999.1:c.-16_-13delinsCACT ENSP00000513029.1:n.-16_-13delinsCACT
ENST00000697035.1:c.*35_*38delinsCACT ENSP00000513059.1:n.*35_*38delinsCACT
ENST00000697036.1:c.*118_*121delinsCACT ENSP00000513060.1:n.*118_*121delinsCACT
ENST00000697037.1:n.737_740delinsCACT
ENST00000697093.1:n.2938_2941delinsCACT
ENST00000697094.1:n.3285_3288delinsCACT
ENST00000697095.1:c.*1903_*1906delinsCACT ENSP00000513104.1:n.*1903_*1906delinsCACT
ENST00000697096.1:n.1835_1838delinsCACT
ENST00000697097.1:c.-16_-13delinsCACT ENSP00000513105.1:n.-16_-13delinsCACT
ENST00000562983.2:n.888_891delinsCACT
ENST00000690268.1:c.783_786delinsCACT ENSP00000509810.1:p.Thr261=
ENST00000355740.7:c.*28_*31delinsCACT ENSP00000347979.3:n.*28_*31delinsCACT
ENST00000612663.5:c.*104_*107delinsCACT ENSP00000477997.3:n.*104_*107delinsCACT
ENST00000640140.1:n.874_877delinsCACT
ENST00000640250.1:n.201_204delinsCACT
ENST00000640681.1:n.823_826delinsCACT
ENST00000652046.1:c.702_705delinsCACT MANE Select ENSP00000498466.1:p.Thr234=
ENST00000313771.9:n.1011_1014delinsCACT
ENST00000352159.8:c.*19_*22delinsCACT ENSP00000345601.4:n.*19_*22delinsCACT
ENST00000355279.2:c.677_680delinsCACT ENSP00000347426.2:n.677_680delinsCACT
ENST00000355740.6:c.702_705delinsCACT ENSP00000347979.2:p.Thr234=
ENST00000357339.6:c.639_642delinsCACT ENSP00000349896.2:p.Thr213=
ENST00000479522.5:c.*131_*134delinsCACT ENSP00000424113.1:n.*131_*134delinsCACT
ENST00000484444.5:c.*143_*146delinsCACT ENSP00000420975.1:n.*143_*146delinsCACT
ENST00000488877.5:c.*143_*146delinsCACT ENSP00000425159.1:n.*143_*146delinsCACT
ENST00000492756.5:c.530_533delinsCACT ENSP00000422453.1:n.530_533delinsCACT
ENST00000494410.5:c.*60_*63delinsCACT ENSP00000423755.1:n.*60_*63delinsCACT
ENST00000494799.5:n.609_612delinsCACT
ENST00000612663.4:c.*49_*52delinsCACT ENSP00000477997.2:n.*49_*52delinsCACT
ENST00000615406.4:c.702_705delinsCACT ENSP00000484575.1:p.Thr234=
ENST00000626542.2:c.700_703delinsCACT ENSP00000485876.1:p.His234=
NM_000043.4:c.702_705delinsCACT , LRG_134t1:c.702_705delinsCACT NP_000034.1:p.Thr234=
NM_152871.2:c.639_642delinsCACT NP_690610.1:p.Thr213=
NM_152872.2:c.*14_*17delinsCACT NP_690611.1:n.*14_*17delinsCACT
NR_028033.2:n.876_879delinsCACT
NR_028034.2:n.738_741delinsCACT
NR_028035.2:n.801_804delinsCACT
NR_028036.2:n.939_942delinsCACT
XM_006717819.2:c.783_786delinsCACT XP_006717882.1:p.Thr261=
XM_011539764.1:c.864_867delinsCACT XP_011538066.1:p.Thr288=
XM_011539765.1:c.801_804delinsCACT XP_011538067.1:p.Thr267=
XM_011539766.1:c.783_786delinsCACT XP_011538068.1:p.Thr261=
XM_011539767.1:c.747_750delinsCACT XP_011538069.1:p.Thr249=
XR_945732.1:n.770_773delinsCACT
XR_945733.1:n.707_710delinsCACT
NM_000043.5:c.702_705delinsCACT NP_000034.1:p.Thr234=
NM_001320619.1:c.*25_*28delinsCACT NP_001307548.1:n.*25_*28delinsCACT
NM_152871.3:c.639_642delinsCACT NP_690610.1:p.Thr213=
NM_152872.3:c.*14_*17delinsCACT NP_690611.1:n.*14_*17delinsCACT
NR_028033.3:n.848_851delinsCACT
NR_028034.3:n.710_713delinsCACT
NR_028035.3:n.773_776delinsCACT
NR_028036.3:n.911_914delinsCACT
NR_135313.1:n.828_831delinsCACT
NR_135314.1:n.1011_1014delinsCACT
NR_135315.1:n.764_767delinsCACT
XM_006717819.3:c.783_786delinsCACT XP_006717882.1:p.Thr261=
XM_011539764.2:c.864_867delinsCACT XP_011538066.1:p.Thr288=
XM_011539765.2:c.801_804delinsCACT XP_011538067.1:p.Thr267=
XM_011539766.2:c.783_786delinsCACT XP_011538068.1:p.Thr261=
XM_011539767.3:c.747_750delinsCACT XP_011538069.1:p.Thr249=
XR_945732.3:n.770_773delinsCACT
XR_945733.2:n.707_710delinsCACT
NM_000043.6:c.702_705delinsCACT MANE Select NP_000034.1:p.Thr234=
NM_001320619.2:c.*25_*28delinsCACT NP_001307548.1:n.*25_*28delinsCACT
NM_152871.4:c.639_642delinsCACT NP_690610.1:p.Thr213=
NM_152872.4:c.*14_*17delinsCACT NP_690611.1:n.*14_*17delinsCACT
NR_028033.4:n.609_612delinsCACT
NR_028034.4:n.471_474delinsCACT
NR_028035.4:n.534_537delinsCACT
NR_028036.4:n.672_675delinsCACT
NR_135313.2:n.589_592delinsCACT
NR_135314.2:n.868_871delinsCACT
NR_135315.2:n.621_624delinsCACT