Canonical Allele Identifier: CA2610079785
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014654T>A , CM000672.2:g.89014654T>A GRCh38
NC_000010.10:g.90774411T>A , CM000672.1:g.90774411T>A GRCh37
NC_000010.9:g.90764391T>A NCBI36
NG_009089.2:g.29124T>A , LRG_134:g.29124T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1521T>A
ENST00000355740.8:c.*535T>A ENSP00000347979.3:n.*535T>A
ENST00000357339.7:c.*204T>A ENSP00000349896.2:n.*204T>A
ENST00000371857.8:n.2757T>A
ENST00000460510.6:c.*204T>A ENSP00000512812.1:n.*204T>A
ENST00000466081.6:n.2861T>A
ENST00000477270.6:c.*204T>A ENSP00000512813.1:n.*204T>A
ENST00000492756.7:c.*641T>A ENSP00000422453.1:n.*641T>A
ENST00000494799.6:c.*204T>A ENSP00000512834.1:n.*204T>A
ENST00000562983.3:c.*204T>A ENSP00000512845.1:n.*204T>A
ENST00000612663.6:c.*614T>A ENSP00000477997.3:n.*614T>A
ENST00000640140.2:n.1357T>A
ENST00000640250.2:n.711T>A
ENST00000640681.2:n.1316T>A
ENST00000696723.1:n.4845T>A
ENST00000696741.1:n.2850T>A
ENST00000696742.1:n.2577T>A
ENST00000696743.1:n.3980T>A
ENST00000696744.1:n.1251T>A
ENST00000696767.1:n.1546T>A
ENST00000696768.1:c.*535T>A ENSP00000512859.1:n.*535T>A
ENST00000696771.1:c.*204T>A ENSP00000512860.1:n.*204T>A
ENST00000696772.1:n.2815T>A
ENST00000696773.1:n.2554T>A
ENST00000696774.1:n.6322T>A
ENST00000696776.1:c.*204T>A ENSP00000512861.1:n.*204T>A
ENST00000696777.1:n.2620T>A
ENST00000696778.1:n.1648T>A
ENST00000696779.1:c.*204T>A ENSP00000512862.1:n.*204T>A
ENST00000696780.1:c.*204T>A ENSP00000512863.1:n.*204T>A
ENST00000696781.1:c.*204T>A ENSP00000512864.1:n.*204T>A
ENST00000696782.1:c.*614T>A ENSP00000512865.1:n.*614T>A
ENST00000696783.1:n.3080T>A
ENST00000696992.1:n.2329T>A
ENST00000696995.1:n.4741T>A
ENST00000696996.1:n.2654T>A
ENST00000696997.1:c.*842T>A ENSP00000513028.1:n.*842T>A
ENST00000696998.1:n.2466T>A
ENST00000696999.1:c.*204T>A ENSP00000513029.1:n.*204T>A
ENST00000697036.1:c.*628T>A ENSP00000513060.1:n.*628T>A
ENST00000697037.1:n.1247T>A
ENST00000697093.1:n.3448T>A
ENST00000697094.1:n.3795T>A
ENST00000697095.1:c.*2413T>A ENSP00000513104.1:n.*2413T>A
ENST00000697096.1:n.2345T>A
ENST00000697097.1:c.*204T>A ENSP00000513105.1:n.*204T>A
ENST00000562983.2:n.1398T>A
ENST00000690268.1:c.*204T>A ENSP00000509810.1:n.*204T>A
ENST00000355740.7:c.*538T>A ENSP00000347979.3:n.*538T>A
ENST00000640140.1:n.1384T>A
ENST00000640250.1:n.711T>A
ENST00000640681.1:n.1333T>A
ENST00000652046.1:c.*204T>A MANE Select ENSP00000498466.1:n.*204T>A
ENST00000352159.8:c.*529T>A ENSP00000345601.4:n.*529T>A
ENST00000355740.6:c.*204T>A ENSP00000347979.2:n.*204T>A
NM_000043.4:c.*204T>A , LRG_134t1:c.*204T>A NP_000034.1:n.*204T>A
NM_152871.2:c.*204T>A NP_690610.1:n.*204T>A
NM_152872.2:c.*524T>A NP_690611.1:n.*524T>A
NR_028033.2:n.1386T>A
NR_028034.2:n.1248T>A
NR_028035.2:n.1311T>A
NR_028036.2:n.1449T>A
XM_006717819.2:c.*204T>A XP_006717882.1:n.*204T>A
XM_011539764.1:c.*204T>A XP_011538066.1:n.*204T>A
XM_011539765.1:c.*204T>A XP_011538067.1:n.*204T>A
XM_011539766.1:c.*204T>A XP_011538068.1:n.*204T>A
XM_011539767.1:c.*204T>A XP_011538069.1:n.*204T>A
NM_000043.5:c.*204T>A NP_000034.1:n.*204T>A
NM_001320619.1:c.*535T>A NP_001307548.1:n.*535T>A
NM_152871.3:c.*204T>A NP_690610.1:n.*204T>A
NM_152872.3:c.*524T>A NP_690611.1:n.*524T>A
NR_028033.3:n.1358T>A
NR_028034.3:n.1220T>A
NR_028035.3:n.1283T>A
NR_028036.3:n.1421T>A
NR_135313.1:n.1338T>A
NR_135314.1:n.1521T>A
NR_135315.1:n.1274T>A
XM_006717819.3:c.*204T>A XP_006717882.1:n.*204T>A
XM_011539764.2:c.*204T>A XP_011538066.1:n.*204T>A
XM_011539765.2:c.*204T>A XP_011538067.1:n.*204T>A
XM_011539766.2:c.*204T>A XP_011538068.1:n.*204T>A
XM_011539767.3:c.*204T>A XP_011538069.1:n.*204T>A
XR_945732.3:n.1280T>A
XR_945733.2:n.1217T>A
NM_000043.6:c.*204T>A MANE Select NP_000034.1:n.*204T>A
NM_001320619.2:c.*535T>A NP_001307548.1:n.*535T>A
NM_152871.4:c.*204T>A NP_690610.1:n.*204T>A
NM_152872.4:c.*524T>A NP_690611.1:n.*524T>A
NR_028033.4:n.1119T>A
NR_028034.4:n.981T>A
NR_028035.4:n.1044T>A
NR_028036.4:n.1182T>A
NR_135313.2:n.1099T>A
NR_135314.2:n.1378T>A
NR_135315.2:n.1131T>A