Canonical Allele Identifier: CA2610079802
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014667A>C , CM000672.2:g.89014667A>C GRCh38
NC_000010.10:g.90774424A>C , CM000672.1:g.90774424A>C GRCh37
NC_000010.9:g.90764404A>C NCBI36
NG_009089.2:g.29137A>C , LRG_134:g.29137A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1534A>C
ENST00000355740.8:c.*548A>C ENSP00000347979.3:n.*548A>C
ENST00000357339.7:c.*217A>C ENSP00000349896.2:n.*217A>C
ENST00000371857.8:n.2770A>C
ENST00000460510.6:c.*217A>C ENSP00000512812.1:n.*217A>C
ENST00000466081.6:n.2874A>C
ENST00000477270.6:c.*217A>C ENSP00000512813.1:n.*217A>C
ENST00000492756.7:c.*654A>C ENSP00000422453.1:n.*654A>C
ENST00000494799.6:c.*217A>C ENSP00000512834.1:n.*217A>C
ENST00000562983.3:c.*217A>C ENSP00000512845.1:n.*217A>C
ENST00000612663.6:c.*627A>C ENSP00000477997.3:n.*627A>C
ENST00000640140.2:n.1370A>C
ENST00000640250.2:n.724A>C
ENST00000640681.2:n.1329A>C
ENST00000696723.1:n.4858A>C
ENST00000696741.1:n.2863A>C
ENST00000696742.1:n.2590A>C
ENST00000696743.1:n.3993A>C
ENST00000696744.1:n.1264A>C
ENST00000696767.1:n.1559A>C
ENST00000696768.1:c.*548A>C ENSP00000512859.1:n.*548A>C
ENST00000696771.1:c.*217A>C ENSP00000512860.1:n.*217A>C
ENST00000696772.1:n.2828A>C
ENST00000696773.1:n.2567A>C
ENST00000696774.1:n.6335A>C
ENST00000696776.1:c.*217A>C ENSP00000512861.1:n.*217A>C
ENST00000696777.1:n.2633A>C
ENST00000696778.1:n.1661A>C
ENST00000696779.1:c.*217A>C ENSP00000512862.1:n.*217A>C
ENST00000696780.1:c.*217A>C ENSP00000512863.1:n.*217A>C
ENST00000696781.1:c.*217A>C ENSP00000512864.1:n.*217A>C
ENST00000696782.1:c.*627A>C ENSP00000512865.1:n.*627A>C
ENST00000696783.1:n.3093A>C
ENST00000696992.1:n.2342A>C
ENST00000696995.1:n.4754A>C
ENST00000696996.1:n.2667A>C
ENST00000696997.1:c.*855A>C ENSP00000513028.1:n.*855A>C
ENST00000696998.1:n.2479A>C
ENST00000696999.1:c.*217A>C ENSP00000513029.1:n.*217A>C
ENST00000697036.1:c.*641A>C ENSP00000513060.1:n.*641A>C
ENST00000697037.1:n.1260A>C
ENST00000697093.1:n.3461A>C
ENST00000697094.1:n.3808A>C
ENST00000697095.1:c.*2426A>C ENSP00000513104.1:n.*2426A>C
ENST00000697096.1:n.2358A>C
ENST00000697097.1:c.*217A>C ENSP00000513105.1:n.*217A>C
ENST00000562983.2:n.1411A>C
ENST00000690268.1:c.*217A>C ENSP00000509810.1:n.*217A>C
ENST00000355740.7:c.*551A>C ENSP00000347979.3:n.*551A>C
ENST00000640140.1:n.1397A>C
ENST00000640250.1:n.724A>C
ENST00000640681.1:n.1346A>C
ENST00000652046.1:c.*217A>C MANE Select ENSP00000498466.1:n.*217A>C
ENST00000352159.8:c.*542A>C ENSP00000345601.4:n.*542A>C
ENST00000355740.6:c.*217A>C ENSP00000347979.2:n.*217A>C
NM_000043.4:c.*217A>C , LRG_134t1:c.*217A>C NP_000034.1:n.*217A>C
NM_152871.2:c.*217A>C NP_690610.1:n.*217A>C
NM_152872.2:c.*537A>C NP_690611.1:n.*537A>C
NR_028033.2:n.1399A>C
NR_028034.2:n.1261A>C
NR_028035.2:n.1324A>C
NR_028036.2:n.1462A>C
XM_006717819.2:c.*217A>C XP_006717882.1:n.*217A>C
XM_011539764.1:c.*217A>C XP_011538066.1:n.*217A>C
XM_011539765.1:c.*217A>C XP_011538067.1:n.*217A>C
XM_011539766.1:c.*217A>C XP_011538068.1:n.*217A>C
XM_011539767.1:c.*217A>C XP_011538069.1:n.*217A>C
NM_000043.5:c.*217A>C NP_000034.1:n.*217A>C
NM_001320619.1:c.*548A>C NP_001307548.1:n.*548A>C
NM_152871.3:c.*217A>C NP_690610.1:n.*217A>C
NM_152872.3:c.*537A>C NP_690611.1:n.*537A>C
NR_028033.3:n.1371A>C
NR_028034.3:n.1233A>C
NR_028035.3:n.1296A>C
NR_028036.3:n.1434A>C
NR_135313.1:n.1351A>C
NR_135314.1:n.1534A>C
NR_135315.1:n.1287A>C
XM_006717819.3:c.*217A>C XP_006717882.1:n.*217A>C
XM_011539764.2:c.*217A>C XP_011538066.1:n.*217A>C
XM_011539765.2:c.*217A>C XP_011538067.1:n.*217A>C
XM_011539766.2:c.*217A>C XP_011538068.1:n.*217A>C
XM_011539767.3:c.*217A>C XP_011538069.1:n.*217A>C
XR_945732.3:n.1293A>C
XR_945733.2:n.1230A>C
NM_000043.6:c.*217A>C MANE Select NP_000034.1:n.*217A>C
NM_001320619.2:c.*548A>C NP_001307548.1:n.*548A>C
NM_152871.4:c.*217A>C NP_690610.1:n.*217A>C
NM_152872.4:c.*537A>C NP_690611.1:n.*537A>C
NR_028033.4:n.1132A>C
NR_028034.4:n.994A>C
NR_028035.4:n.1057A>C
NR_028036.4:n.1195A>C
NR_135313.2:n.1112A>C
NR_135314.2:n.1391A>C
NR_135315.2:n.1144A>C