Canonical Allele Identifier: CA1926639522
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014645A= , CM000672.2:g.89014645A= GRCh38
NC_000010.10:g.90774402A= , CM000672.1:g.90774402A= GRCh37
NC_000010.9:g.90764382A= NCBI36
NG_009089.2:g.29115A= , LRG_134:g.29115A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1512A=
ENST00000355740.8:c.*526A= ENSP00000347979.3:n.*526A=
ENST00000357339.7:c.*195A= ENSP00000349896.2:n.*195A=
ENST00000371857.8:n.2748A=
ENST00000460510.6:c.*195A= ENSP00000512812.1:n.*195A=
ENST00000466081.6:n.2852A=
ENST00000477270.6:c.*195A= ENSP00000512813.1:n.*195A=
ENST00000488877.6:c.1094A= ENSP00000425159.1:n.1094A=
ENST00000492756.7:c.*632A= ENSP00000422453.1:n.*632A=
ENST00000494799.6:c.*195A= ENSP00000512834.1:n.*195A=
ENST00000562983.3:c.*195A= ENSP00000512845.1:n.*195A=
ENST00000612663.6:c.*605A= ENSP00000477997.3:n.*605A=
ENST00000640140.2:n.1348A=
ENST00000640250.2:n.702A=
ENST00000640681.2:n.1307A=
ENST00000696723.1:n.4836A=
ENST00000696741.1:n.2841A=
ENST00000696742.1:n.2568A=
ENST00000696743.1:n.3971A=
ENST00000696744.1:n.1242A=
ENST00000696767.1:n.1537A=
ENST00000696768.1:c.*526A= ENSP00000512859.1:n.*526A=
ENST00000696771.1:c.*195A= ENSP00000512860.1:n.*195A=
ENST00000696772.1:n.2806A=
ENST00000696773.1:n.2545A=
ENST00000696774.1:n.6313A=
ENST00000696776.1:c.*195A= ENSP00000512861.1:n.*195A=
ENST00000696777.1:n.2611A=
ENST00000696778.1:n.1639A=
ENST00000696779.1:c.*195A= ENSP00000512862.1:n.*195A=
ENST00000696780.1:c.*195A= ENSP00000512863.1:n.*195A=
ENST00000696781.1:c.*195A= ENSP00000512864.1:n.*195A=
ENST00000696782.1:c.*605A= ENSP00000512865.1:n.*605A=
ENST00000696783.1:n.3071A=
ENST00000696992.1:n.2320A=
ENST00000696995.1:n.4732A=
ENST00000696996.1:n.2645A=
ENST00000696997.1:c.*833A= ENSP00000513028.1:n.*833A=
ENST00000696998.1:n.2457A=
ENST00000696999.1:c.*195A= ENSP00000513029.1:n.*195A=
ENST00000697036.1:c.*619A= ENSP00000513060.1:n.*619A=
ENST00000697037.1:n.1238A=
ENST00000697093.1:n.3439A=
ENST00000697094.1:n.3786A=
ENST00000697095.1:c.*2404A= ENSP00000513104.1:n.*2404A=
ENST00000697096.1:n.2336A=
ENST00000697097.1:c.*195A= ENSP00000513105.1:n.*195A=
ENST00000562983.2:n.1389A=
ENST00000690268.1:c.*195A= ENSP00000509810.1:n.*195A=
ENST00000355740.7:c.*529A= ENSP00000347979.3:n.*529A=
ENST00000640140.1:n.1375A=
ENST00000640250.1:n.702A=
ENST00000640681.1:n.1324A=
ENST00000652046.1:c.*195A= MANE Select ENSP00000498466.1:n.*195A=
ENST00000352159.8:c.*520A= ENSP00000345601.4:n.*520A=
ENST00000355740.6:c.*195A= ENSP00000347979.2:n.*195A=
NM_000043.4:c.*195A= , LRG_134t1:c.*195A= NP_000034.1:n.*195A=
NM_152871.2:c.*195A= NP_690610.1:n.*195A=
NM_152872.2:c.*515A= NP_690611.1:n.*515A=
NR_028033.2:n.1377A=
NR_028034.2:n.1239A=
NR_028035.2:n.1302A=
NR_028036.2:n.1440A=
XM_006717819.2:c.*195A= XP_006717882.1:n.*195A=
XM_011539764.1:c.*195A= XP_011538066.1:n.*195A=
XM_011539765.1:c.*195A= XP_011538067.1:n.*195A=
XM_011539766.1:c.*195A= XP_011538068.1:n.*195A=
XM_011539767.1:c.*195A= XP_011538069.1:n.*195A=
NM_000043.5:c.*195A= NP_000034.1:n.*195A=
NM_001320619.1:c.*526A= NP_001307548.1:n.*526A=
NM_152871.3:c.*195A= NP_690610.1:n.*195A=
NM_152872.3:c.*515A= NP_690611.1:n.*515A=
NR_028033.3:n.1349A=
NR_028034.3:n.1211A=
NR_028035.3:n.1274A=
NR_028036.3:n.1412A=
NR_135313.1:n.1329A=
NR_135314.1:n.1512A=
NR_135315.1:n.1265A=
XM_006717819.3:c.*195A= XP_006717882.1:n.*195A=
XM_011539764.2:c.*195A= XP_011538066.1:n.*195A=
XM_011539765.2:c.*195A= XP_011538067.1:n.*195A=
XM_011539766.2:c.*195A= XP_011538068.1:n.*195A=
XM_011539767.3:c.*195A= XP_011538069.1:n.*195A=
XR_945732.3:n.1271A=
XR_945733.2:n.1208A=
NM_000043.6:c.*195A= MANE Select NP_000034.1:n.*195A=
NM_001320619.2:c.*526A= NP_001307548.1:n.*526A=
NM_152871.4:c.*195A= NP_690610.1:n.*195A=
NM_152872.4:c.*515A= NP_690611.1:n.*515A=
NR_028033.4:n.1110A=
NR_028034.4:n.972A=
NR_028035.4:n.1035A=
NR_028036.4:n.1173A=
NR_135313.2:n.1090A=
NR_135314.2:n.1369A=
NR_135315.2:n.1122A=