Canonical Allele Identifier: CA2610079784
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014652C>A , CM000672.2:g.89014652C>A GRCh38
NC_000010.10:g.90774409C>A , CM000672.1:g.90774409C>A GRCh37
NC_000010.9:g.90764389C>A NCBI36
NG_009089.2:g.29122C>A , LRG_134:g.29122C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1519C>A
ENST00000355740.8:c.*533C>A ENSP00000347979.3:n.*533C>A
ENST00000357339.7:c.*202C>A ENSP00000349896.2:n.*202C>A
ENST00000371857.8:n.2755C>A
ENST00000460510.6:c.*202C>A ENSP00000512812.1:n.*202C>A
ENST00000466081.6:n.2859C>A
ENST00000477270.6:c.*202C>A ENSP00000512813.1:n.*202C>A
ENST00000492756.7:c.*639C>A ENSP00000422453.1:n.*639C>A
ENST00000494799.6:c.*202C>A ENSP00000512834.1:n.*202C>A
ENST00000562983.3:c.*202C>A ENSP00000512845.1:n.*202C>A
ENST00000612663.6:c.*612C>A ENSP00000477997.3:n.*612C>A
ENST00000640140.2:n.1355C>A
ENST00000640250.2:n.709C>A
ENST00000640681.2:n.1314C>A
ENST00000696723.1:n.4843C>A
ENST00000696741.1:n.2848C>A
ENST00000696742.1:n.2575C>A
ENST00000696743.1:n.3978C>A
ENST00000696744.1:n.1249C>A
ENST00000696767.1:n.1544C>A
ENST00000696768.1:c.*533C>A ENSP00000512859.1:n.*533C>A
ENST00000696771.1:c.*202C>A ENSP00000512860.1:n.*202C>A
ENST00000696772.1:n.2813C>A
ENST00000696773.1:n.2552C>A
ENST00000696774.1:n.6320C>A
ENST00000696776.1:c.*202C>A ENSP00000512861.1:n.*202C>A
ENST00000696777.1:n.2618C>A
ENST00000696778.1:n.1646C>A
ENST00000696779.1:c.*202C>A ENSP00000512862.1:n.*202C>A
ENST00000696780.1:c.*202C>A ENSP00000512863.1:n.*202C>A
ENST00000696781.1:c.*202C>A ENSP00000512864.1:n.*202C>A
ENST00000696782.1:c.*612C>A ENSP00000512865.1:n.*612C>A
ENST00000696783.1:n.3078C>A
ENST00000696992.1:n.2327C>A
ENST00000696995.1:n.4739C>A
ENST00000696996.1:n.2652C>A
ENST00000696997.1:c.*840C>A ENSP00000513028.1:n.*840C>A
ENST00000696998.1:n.2464C>A
ENST00000696999.1:c.*202C>A ENSP00000513029.1:n.*202C>A
ENST00000697036.1:c.*626C>A ENSP00000513060.1:n.*626C>A
ENST00000697037.1:n.1245C>A
ENST00000697093.1:n.3446C>A
ENST00000697094.1:n.3793C>A
ENST00000697095.1:c.*2411C>A ENSP00000513104.1:n.*2411C>A
ENST00000697096.1:n.2343C>A
ENST00000697097.1:c.*202C>A ENSP00000513105.1:n.*202C>A
ENST00000562983.2:n.1396C>A
ENST00000690268.1:c.*202C>A ENSP00000509810.1:n.*202C>A
ENST00000355740.7:c.*536C>A ENSP00000347979.3:n.*536C>A
ENST00000640140.1:n.1382C>A
ENST00000640250.1:n.709C>A
ENST00000640681.1:n.1331C>A
ENST00000652046.1:c.*202C>A MANE Select ENSP00000498466.1:n.*202C>A
ENST00000352159.8:c.*527C>A ENSP00000345601.4:n.*527C>A
ENST00000355740.6:c.*202C>A ENSP00000347979.2:n.*202C>A
NM_000043.4:c.*202C>A , LRG_134t1:c.*202C>A NP_000034.1:n.*202C>A
NM_152871.2:c.*202C>A NP_690610.1:n.*202C>A
NM_152872.2:c.*522C>A NP_690611.1:n.*522C>A
NR_028033.2:n.1384C>A
NR_028034.2:n.1246C>A
NR_028035.2:n.1309C>A
NR_028036.2:n.1447C>A
XM_006717819.2:c.*202C>A XP_006717882.1:n.*202C>A
XM_011539764.1:c.*202C>A XP_011538066.1:n.*202C>A
XM_011539765.1:c.*202C>A XP_011538067.1:n.*202C>A
XM_011539766.1:c.*202C>A XP_011538068.1:n.*202C>A
XM_011539767.1:c.*202C>A XP_011538069.1:n.*202C>A
NM_000043.5:c.*202C>A NP_000034.1:n.*202C>A
NM_001320619.1:c.*533C>A NP_001307548.1:n.*533C>A
NM_152871.3:c.*202C>A NP_690610.1:n.*202C>A
NM_152872.3:c.*522C>A NP_690611.1:n.*522C>A
NR_028033.3:n.1356C>A
NR_028034.3:n.1218C>A
NR_028035.3:n.1281C>A
NR_028036.3:n.1419C>A
NR_135313.1:n.1336C>A
NR_135314.1:n.1519C>A
NR_135315.1:n.1272C>A
XM_006717819.3:c.*202C>A XP_006717882.1:n.*202C>A
XM_011539764.2:c.*202C>A XP_011538066.1:n.*202C>A
XM_011539765.2:c.*202C>A XP_011538067.1:n.*202C>A
XM_011539766.2:c.*202C>A XP_011538068.1:n.*202C>A
XM_011539767.3:c.*202C>A XP_011538069.1:n.*202C>A
XR_945732.3:n.1278C>A
XR_945733.2:n.1215C>A
NM_000043.6:c.*202C>A MANE Select NP_000034.1:n.*202C>A
NM_001320619.2:c.*533C>A NP_001307548.1:n.*533C>A
NM_152871.4:c.*202C>A NP_690610.1:n.*202C>A
NM_152872.4:c.*522C>A NP_690611.1:n.*522C>A
NR_028033.4:n.1117C>A
NR_028034.4:n.979C>A
NR_028035.4:n.1042C>A
NR_028036.4:n.1180C>A
NR_135313.2:n.1097C>A
NR_135314.2:n.1376C>A
NR_135315.2:n.1129C>A