Canonical Allele Identifier: CA2610079821
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014682A>G , CM000672.2:g.89014682A>G GRCh38
NC_000010.10:g.90774439A>G , CM000672.1:g.90774439A>G GRCh37
NC_000010.9:g.90764419A>G NCBI36
NG_009089.2:g.29152A>G , LRG_134:g.29152A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1549A>G
ENST00000355740.8:c.*563A>G ENSP00000347979.3:n.*563A>G
ENST00000357339.7:c.*232A>G ENSP00000349896.2:n.*232A>G
ENST00000371857.8:n.2785A>G
ENST00000460510.6:c.*232A>G ENSP00000512812.1:n.*232A>G
ENST00000466081.6:n.2889A>G
ENST00000477270.6:c.*232A>G ENSP00000512813.1:n.*232A>G
ENST00000492756.7:c.*669A>G ENSP00000422453.1:n.*669A>G
ENST00000494799.6:c.*232A>G ENSP00000512834.1:n.*232A>G
ENST00000562983.3:c.*232A>G ENSP00000512845.1:n.*232A>G
ENST00000612663.6:c.*642A>G ENSP00000477997.3:n.*642A>G
ENST00000640140.2:n.1385A>G
ENST00000640250.2:n.739A>G
ENST00000640681.2:n.1344A>G
ENST00000696723.1:n.4873A>G
ENST00000696741.1:n.2878A>G
ENST00000696742.1:n.2605A>G
ENST00000696743.1:n.4008A>G
ENST00000696744.1:n.1279A>G
ENST00000696767.1:n.1574A>G
ENST00000696768.1:c.*563A>G ENSP00000512859.1:n.*563A>G
ENST00000696771.1:c.*232A>G ENSP00000512860.1:n.*232A>G
ENST00000696772.1:n.2843A>G
ENST00000696773.1:n.2582A>G
ENST00000696774.1:n.6350A>G
ENST00000696776.1:c.*232A>G ENSP00000512861.1:n.*232A>G
ENST00000696777.1:n.2648A>G
ENST00000696778.1:n.1676A>G
ENST00000696779.1:c.*232A>G ENSP00000512862.1:n.*232A>G
ENST00000696780.1:c.*232A>G ENSP00000512863.1:n.*232A>G
ENST00000696781.1:c.*232A>G ENSP00000512864.1:n.*232A>G
ENST00000696782.1:c.*642A>G ENSP00000512865.1:n.*642A>G
ENST00000696783.1:n.3108A>G
ENST00000696992.1:n.2357A>G
ENST00000696995.1:n.4769A>G
ENST00000696996.1:n.2682A>G
ENST00000696997.1:c.*870A>G ENSP00000513028.1:n.*870A>G
ENST00000696998.1:n.2494A>G
ENST00000696999.1:c.*232A>G ENSP00000513029.1:n.*232A>G
ENST00000697036.1:c.*656A>G ENSP00000513060.1:n.*656A>G
ENST00000697037.1:n.1275A>G
ENST00000697093.1:n.3476A>G
ENST00000697094.1:n.3823A>G
ENST00000697095.1:c.*2441A>G ENSP00000513104.1:n.*2441A>G
ENST00000697096.1:n.2373A>G
ENST00000697097.1:c.*232A>G ENSP00000513105.1:n.*232A>G
ENST00000562983.2:n.1426A>G
ENST00000690268.1:c.*232A>G ENSP00000509810.1:n.*232A>G
ENST00000355740.7:c.*566A>G ENSP00000347979.3:n.*566A>G
ENST00000640140.1:n.1412A>G
ENST00000640250.1:n.739A>G
ENST00000640681.1:n.1361A>G
ENST00000652046.1:c.*232A>G MANE Select ENSP00000498466.1:n.*232A>G
ENST00000352159.8:c.*557A>G ENSP00000345601.4:n.*557A>G
ENST00000355740.6:c.*232A>G ENSP00000347979.2:n.*232A>G
NM_000043.4:c.*232A>G , LRG_134t1:c.*232A>G NP_000034.1:n.*232A>G
NM_152871.2:c.*232A>G NP_690610.1:n.*232A>G
NM_152872.2:c.*552A>G NP_690611.1:n.*552A>G
NR_028033.2:n.1414A>G
NR_028034.2:n.1276A>G
NR_028035.2:n.1339A>G
NR_028036.2:n.1477A>G
XM_006717819.2:c.*232A>G XP_006717882.1:n.*232A>G
XM_011539764.1:c.*232A>G XP_011538066.1:n.*232A>G
XM_011539765.1:c.*232A>G XP_011538067.1:n.*232A>G
XM_011539766.1:c.*232A>G XP_011538068.1:n.*232A>G
XM_011539767.1:c.*232A>G XP_011538069.1:n.*232A>G
NM_000043.5:c.*232A>G NP_000034.1:n.*232A>G
NM_001320619.1:c.*563A>G NP_001307548.1:n.*563A>G
NM_152871.3:c.*232A>G NP_690610.1:n.*232A>G
NM_152872.3:c.*552A>G NP_690611.1:n.*552A>G
NR_028033.3:n.1386A>G
NR_028034.3:n.1248A>G
NR_028035.3:n.1311A>G
NR_028036.3:n.1449A>G
NR_135313.1:n.1366A>G
NR_135314.1:n.1549A>G
NR_135315.1:n.1302A>G
XM_006717819.3:c.*232A>G XP_006717882.1:n.*232A>G
XM_011539764.2:c.*232A>G XP_011538066.1:n.*232A>G
XM_011539765.2:c.*232A>G XP_011538067.1:n.*232A>G
XM_011539766.2:c.*232A>G XP_011538068.1:n.*232A>G
XM_011539767.3:c.*232A>G XP_011538069.1:n.*232A>G
XR_945732.3:n.1308A>G
XR_945733.2:n.1245A>G
NM_000043.6:c.*232A>G MANE Select NP_000034.1:n.*232A>G
NM_001320619.2:c.*563A>G NP_001307548.1:n.*563A>G
NM_152871.4:c.*232A>G NP_690610.1:n.*232A>G
NM_152872.4:c.*552A>G NP_690611.1:n.*552A>G
NR_028033.4:n.1147A>G
NR_028034.4:n.1009A>G
NR_028035.4:n.1072A>G
NR_028036.4:n.1210A>G
NR_135313.2:n.1127A>G
NR_135314.2:n.1406A>G
NR_135315.2:n.1159A>G