Canonical Allele Identifier: CA377510063
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs1330397439

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014340A>C , CM000672.2:g.89014340A>C GRCh38
NC_000010.10:g.90774097A>C , CM000672.1:g.90774097A>C GRCh37
NC_000010.9:g.90764077A>C NCBI36
NG_009089.2:g.28810A>C , LRG_134:g.28810A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1207A>C
ENST00000355740.8:c.*221A>C ENSP00000347979.3:n.*221A>C
ENST00000357339.7:c.835A>C ENSP00000349896.2:p.Lys279Gln
ENST00000371857.8:n.2443A>C
ENST00000460510.6:c.181A>C ENSP00000512812.1:p.Lys61Gln
ENST00000466081.6:n.2547A>C
ENST00000477270.6:c.943A>C ENSP00000512813.1:p.Lys315Gln
ENST00000479522.6:c.*327A>C ENSP00000424113.1:n.*327A>C
ENST00000484444.6:c.*339A>C ENSP00000420975.1:n.*339A>C
ENST00000488877.6:c.789A>C ENSP00000425159.1:n.789A>C
ENST00000492756.7:c.*327A>C ENSP00000422453.1:n.*327A>C
ENST00000494799.6:c.181A>C ENSP00000512834.1:p.Lys61Gln
ENST00000562983.3:c.181A>C ENSP00000512845.1:p.Lys61Gln
ENST00000612663.6:c.*300A>C ENSP00000477997.3:n.*300A>C
ENST00000640140.2:n.1043A>C
ENST00000640250.2:n.397A>C
ENST00000640681.2:n.1002A>C
ENST00000696723.1:n.4531A>C
ENST00000696741.1:n.2536A>C
ENST00000696742.1:n.2263A>C
ENST00000696743.1:n.3666A>C
ENST00000696744.1:n.937A>C
ENST00000696767.1:n.1232A>C
ENST00000696768.1:c.*221A>C ENSP00000512859.1:n.*221A>C
ENST00000696769.1:n.2587A>C
ENST00000696771.1:c.181A>C ENSP00000512860.1:p.Lys61Gln
ENST00000696772.1:n.2501A>C
ENST00000696773.1:n.2240A>C
ENST00000696774.1:n.6008A>C
ENST00000696776.1:c.991A>C ENSP00000512861.1:p.Lys331Gln
ENST00000696777.1:n.2306A>C
ENST00000696778.1:n.1334A>C
ENST00000696779.1:c.505A>C ENSP00000512862.1:p.Lys169Gln
ENST00000696780.1:c.928A>C ENSP00000512863.1:p.Lys310Gln
ENST00000696781.1:c.643A>C ENSP00000512864.1:p.Lys215Gln
ENST00000696782.1:c.*300A>C ENSP00000512865.1:n.*300A>C
ENST00000696783.1:n.2766A>C
ENST00000696992.1:n.2015A>C
ENST00000696995.1:n.4427A>C
ENST00000696996.1:n.2340A>C
ENST00000696997.1:c.*528A>C ENSP00000513028.1:n.*528A>C
ENST00000696998.1:n.2152A>C
ENST00000696999.1:c.181A>C ENSP00000513029.1:p.Lys61Gln
ENST00000697036.1:c.*314A>C ENSP00000513060.1:n.*314A>C
ENST00000697037.1:n.933A>C
ENST00000697093.1:n.3134A>C
ENST00000697094.1:n.3481A>C
ENST00000697095.1:c.*2099A>C ENSP00000513104.1:n.*2099A>C
ENST00000697096.1:n.2031A>C
ENST00000697097.1:c.181A>C ENSP00000513105.1:p.Lys61Gln
ENST00000562983.2:n.1084A>C
ENST00000690268.1:c.979A>C ENSP00000509810.1:p.Lys327Gln
ENST00000355740.7:c.*224A>C ENSP00000347979.3:n.*224A>C
ENST00000612663.5:c.*300A>C ENSP00000477997.3:n.*300A>C
ENST00000640140.1:n.1070A>C
ENST00000640250.1:n.397A>C
ENST00000640681.1:n.1019A>C
ENST00000652046.1:c.898A>C MANE Select ENSP00000498466.1:p.Lys300Gln
ENST00000352159.8:c.*215A>C ENSP00000345601.4:n.*215A>C
ENST00000355279.2:c.873A>C ENSP00000347426.2:n.873A>C
ENST00000355740.6:c.898A>C ENSP00000347979.2:p.Lys300Gln
ENST00000357339.6:c.835A>C ENSP00000349896.2:p.Lys279Gln
ENST00000479522.5:c.*327A>C ENSP00000424113.1:n.*327A>C
ENST00000484444.5:c.*339A>C ENSP00000420975.1:n.*339A>C
ENST00000488877.5:c.*339A>C ENSP00000425159.1:n.*339A>C
ENST00000492756.5:c.726A>C ENSP00000422453.1:n.726A>C
ENST00000494410.5:c.*256A>C ENSP00000423755.1:n.*256A>C
ENST00000612663.4:c.*245A>C ENSP00000477997.2:n.*245A>C
NM_000043.4:c.898A>C , LRG_134t1:c.898A>C NP_000034.1:p.Lys300Gln
NM_152871.2:c.835A>C NP_690610.1:p.Lys279Gln
NM_152872.2:c.*210A>C NP_690611.1:n.*210A>C
NR_028033.2:n.1072A>C
NR_028034.2:n.934A>C
NR_028035.2:n.997A>C
NR_028036.2:n.1135A>C
XM_006717819.2:c.979A>C XP_006717882.1:p.Lys327Gln
XM_011539764.1:c.1060A>C XP_011538066.1:p.Lys354Gln
XM_011539765.1:c.997A>C XP_011538067.1:p.Lys333Gln
XM_011539766.1:c.979A>C XP_011538068.1:p.Lys327Gln
XM_011539767.1:c.943A>C XP_011538069.1:p.Lys315Gln
XR_945732.1:n.966A>C
XR_945733.1:n.903A>C
NM_000043.5:c.898A>C NP_000034.1:p.Lys300Gln
NM_001320619.1:c.*221A>C NP_001307548.1:n.*221A>C
NM_152871.3:c.835A>C NP_690610.1:p.Lys279Gln
NM_152872.3:c.*210A>C NP_690611.1:n.*210A>C
NR_028033.3:n.1044A>C
NR_028034.3:n.906A>C
NR_028035.3:n.969A>C
NR_028036.3:n.1107A>C
NR_135313.1:n.1024A>C
NR_135314.1:n.1207A>C
NR_135315.1:n.960A>C
XM_006717819.3:c.979A>C XP_006717882.1:p.Lys327Gln
XM_011539764.2:c.1060A>C XP_011538066.1:p.Lys354Gln
XM_011539765.2:c.997A>C XP_011538067.1:p.Lys333Gln
XM_011539766.2:c.979A>C XP_011538068.1:p.Lys327Gln
XM_011539767.3:c.943A>C XP_011538069.1:p.Lys315Gln
XR_945732.3:n.966A>C
XR_945733.2:n.903A>C
NM_000043.6:c.898A>C MANE Select NP_000034.1:p.Lys300Gln
NM_001320619.2:c.*221A>C NP_001307548.1:n.*221A>C
NM_152871.4:c.835A>C NP_690610.1:p.Lys279Gln
NM_152872.4:c.*210A>C NP_690611.1:n.*210A>C
NR_028033.4:n.805A>C
NR_028034.4:n.667A>C
NR_028035.4:n.730A>C
NR_028036.4:n.868A>C
NR_135313.2:n.785A>C
NR_135314.2:n.1064A>C
NR_135315.2:n.817A>C