Canonical Allele Identifier: CA377509809
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014229A>T , CM000672.2:g.89014229A>T GRCh38
NC_000010.10:g.90773986A>T , CM000672.1:g.90773986A>T GRCh37
NC_000010.9:g.90763966A>T NCBI36
NG_009089.2:g.28699A>T , LRG_134:g.28699A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1096A>T
ENST00000355740.8:c.*110A>T ENSP00000347979.3:n.*110A>T
ENST00000357339.7:c.724A>T ENSP00000349896.2:p.Lys242Ter
ENST00000371857.8:n.2332A>T
ENST00000460510.6:c.70A>T ENSP00000512812.1:p.Lys24Ter
ENST00000466081.6:n.2436A>T
ENST00000477270.6:c.832A>T ENSP00000512813.1:p.Lys278Ter
ENST00000479522.6:c.*216A>T ENSP00000424113.1:n.*216A>T
ENST00000484444.6:c.*228A>T ENSP00000420975.1:n.*228A>T
ENST00000488877.6:c.678A>T ENSP00000425159.1:n.678A>T
ENST00000492756.7:c.*216A>T ENSP00000422453.1:n.*216A>T
ENST00000494799.6:c.70A>T ENSP00000512834.1:p.Lys24Ter
ENST00000562983.3:c.70A>T ENSP00000512845.1:p.Lys24Ter
ENST00000612663.6:c.*189A>T ENSP00000477997.3:n.*189A>T
ENST00000640140.2:n.932A>T
ENST00000640250.2:n.286A>T
ENST00000640681.2:n.891A>T
ENST00000696723.1:n.4420A>T
ENST00000696741.1:n.2425A>T
ENST00000696742.1:n.2152A>T
ENST00000696743.1:n.3555A>T
ENST00000696744.1:n.826A>T
ENST00000696767.1:n.1121A>T
ENST00000696768.1:c.*110A>T ENSP00000512859.1:n.*110A>T
ENST00000696769.1:n.2476A>T
ENST00000696771.1:c.70A>T ENSP00000512860.1:p.Lys24Ter
ENST00000696772.1:n.2390A>T
ENST00000696773.1:n.2129A>T
ENST00000696774.1:n.5897A>T
ENST00000696776.1:c.880A>T ENSP00000512861.1:p.Lys294Ter
ENST00000696777.1:n.2195A>T
ENST00000696778.1:n.1223A>T
ENST00000696779.1:c.394A>T ENSP00000512862.1:p.Lys132Ter
ENST00000696780.1:c.817A>T ENSP00000512863.1:p.Lys273Ter
ENST00000696781.1:c.532A>T ENSP00000512864.1:p.Lys178Ter
ENST00000696782.1:c.*189A>T ENSP00000512865.1:n.*189A>T
ENST00000696783.1:n.2655A>T
ENST00000696992.1:n.1904A>T
ENST00000696995.1:n.4316A>T
ENST00000696996.1:n.2229A>T
ENST00000696997.1:c.*417A>T ENSP00000513028.1:n.*417A>T
ENST00000696998.1:n.2041A>T
ENST00000696999.1:c.70A>T ENSP00000513029.1:p.Lys24Ter
ENST00000697035.1:c.*120A>T ENSP00000513059.1:n.*120A>T
ENST00000697036.1:c.*203A>T ENSP00000513060.1:n.*203A>T
ENST00000697037.1:n.822A>T
ENST00000697093.1:n.3023A>T
ENST00000697094.1:n.3370A>T
ENST00000697095.1:c.*1988A>T ENSP00000513104.1:n.*1988A>T
ENST00000697096.1:n.1920A>T
ENST00000697097.1:c.70A>T ENSP00000513105.1:p.Lys24Ter
ENST00000562983.2:n.973A>T
ENST00000690268.1:c.868A>T ENSP00000509810.1:p.Lys290Ter
ENST00000355740.7:c.*113A>T ENSP00000347979.3:n.*113A>T
ENST00000612663.5:c.*189A>T ENSP00000477997.3:n.*189A>T
ENST00000640140.1:n.959A>T
ENST00000640250.1:n.286A>T
ENST00000640681.1:n.908A>T
ENST00000652046.1:c.787A>T MANE Select ENSP00000498466.1:p.Lys263Ter
ENST00000352159.8:c.*104A>T ENSP00000345601.4:n.*104A>T
ENST00000355279.2:c.762A>T ENSP00000347426.2:n.762A>T
ENST00000355740.6:c.787A>T ENSP00000347979.2:p.Lys263Ter
ENST00000357339.6:c.724A>T ENSP00000349896.2:p.Lys242Ter
ENST00000479522.5:c.*216A>T ENSP00000424113.1:n.*216A>T
ENST00000484444.5:c.*228A>T ENSP00000420975.1:n.*228A>T
ENST00000488877.5:c.*228A>T ENSP00000425159.1:n.*228A>T
ENST00000492756.5:c.615A>T ENSP00000422453.1:n.615A>T
ENST00000494410.5:c.*145A>T ENSP00000423755.1:n.*145A>T
ENST00000612663.4:c.*134A>T ENSP00000477997.2:n.*134A>T
NM_000043.4:c.787A>T , LRG_134t1:c.787A>T NP_000034.1:p.Lys263Ter
NM_152871.2:c.724A>T NP_690610.1:p.Lys242Ter
NM_152872.2:c.*99A>T NP_690611.1:n.*99A>T
NR_028033.2:n.961A>T
NR_028034.2:n.823A>T
NR_028035.2:n.886A>T
NR_028036.2:n.1024A>T
XM_006717819.2:c.868A>T XP_006717882.1:p.Lys290Ter
XM_011539764.1:c.949A>T XP_011538066.1:p.Lys317Ter
XM_011539765.1:c.886A>T XP_011538067.1:p.Lys296Ter
XM_011539766.1:c.868A>T XP_011538068.1:p.Lys290Ter
XM_011539767.1:c.832A>T XP_011538069.1:p.Lys278Ter
XR_945732.1:n.855A>T
XR_945733.1:n.792A>T
NM_000043.5:c.787A>T NP_000034.1:p.Lys263Ter
NM_001320619.1:c.*110A>T NP_001307548.1:n.*110A>T
NM_152871.3:c.724A>T NP_690610.1:p.Lys242Ter
NM_152872.3:c.*99A>T NP_690611.1:n.*99A>T
NR_028033.3:n.933A>T
NR_028034.3:n.795A>T
NR_028035.3:n.858A>T
NR_028036.3:n.996A>T
NR_135313.1:n.913A>T
NR_135314.1:n.1096A>T
NR_135315.1:n.849A>T
XM_006717819.3:c.868A>T XP_006717882.1:p.Lys290Ter
XM_011539764.2:c.949A>T XP_011538066.1:p.Lys317Ter
XM_011539765.2:c.886A>T XP_011538067.1:p.Lys296Ter
XM_011539766.2:c.868A>T XP_011538068.1:p.Lys290Ter
XM_011539767.3:c.832A>T XP_011538069.1:p.Lys278Ter
XR_945732.3:n.855A>T
XR_945733.2:n.792A>T
NM_000043.6:c.787A>T MANE Select NP_000034.1:p.Lys263Ter
NM_001320619.2:c.*110A>T NP_001307548.1:n.*110A>T
NM_152871.4:c.724A>T NP_690610.1:p.Lys242Ter
NM_152872.4:c.*99A>T NP_690611.1:n.*99A>T
NR_028033.4:n.694A>T
NR_028034.4:n.556A>T
NR_028035.4:n.619A>T
NR_028036.4:n.757A>T
NR_135313.2:n.674A>T
NR_135314.2:n.953A>T
NR_135315.2:n.706A>T