Canonical Allele Identifier: CA377509805
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014227T>G , CM000672.2:g.89014227T>G GRCh38
NC_000010.10:g.90773984T>G , CM000672.1:g.90773984T>G GRCh37
NC_000010.9:g.90763964T>G NCBI36
NG_009089.2:g.28697T>G , LRG_134:g.28697T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1094T>G
ENST00000355740.8:c.*108T>G ENSP00000347979.3:n.*108T>G
ENST00000357339.7:c.722T>G ENSP00000349896.2:p.Ile241Ser
ENST00000371857.8:n.2330T>G
ENST00000460510.6:c.68T>G ENSP00000512812.1:p.Ile23Ser
ENST00000466081.6:n.2434T>G
ENST00000477270.6:c.830T>G ENSP00000512813.1:p.Ile277Ser
ENST00000479522.6:c.*214T>G ENSP00000424113.1:n.*214T>G
ENST00000484444.6:c.*226T>G ENSP00000420975.1:n.*226T>G
ENST00000488877.6:c.676T>G ENSP00000425159.1:n.676T>G
ENST00000492756.7:c.*214T>G ENSP00000422453.1:n.*214T>G
ENST00000494799.6:c.68T>G ENSP00000512834.1:p.Ile23Ser
ENST00000562983.3:c.68T>G ENSP00000512845.1:p.Ile23Ser
ENST00000612663.6:c.*187T>G ENSP00000477997.3:n.*187T>G
ENST00000640140.2:n.930T>G
ENST00000640250.2:n.284T>G
ENST00000640681.2:n.889T>G
ENST00000696723.1:n.4418T>G
ENST00000696741.1:n.2423T>G
ENST00000696742.1:n.2150T>G
ENST00000696743.1:n.3553T>G
ENST00000696744.1:n.824T>G
ENST00000696767.1:n.1119T>G
ENST00000696768.1:c.*108T>G ENSP00000512859.1:n.*108T>G
ENST00000696769.1:n.2474T>G
ENST00000696771.1:c.68T>G ENSP00000512860.1:p.Ile23Ser
ENST00000696772.1:n.2388T>G
ENST00000696773.1:n.2127T>G
ENST00000696774.1:n.5895T>G
ENST00000696776.1:c.878T>G ENSP00000512861.1:p.Ile293Ser
ENST00000696777.1:n.2193T>G
ENST00000696778.1:n.1221T>G
ENST00000696779.1:c.392T>G ENSP00000512862.1:p.Ile131Ser
ENST00000696780.1:c.815T>G ENSP00000512863.1:p.Ile272Ser
ENST00000696781.1:c.530T>G ENSP00000512864.1:p.Ile177Ser
ENST00000696782.1:c.*187T>G ENSP00000512865.1:n.*187T>G
ENST00000696783.1:n.2653T>G
ENST00000696992.1:n.1902T>G
ENST00000696995.1:n.4314T>G
ENST00000696996.1:n.2227T>G
ENST00000696997.1:c.*415T>G ENSP00000513028.1:n.*415T>G
ENST00000696998.1:n.2039T>G
ENST00000696999.1:c.68T>G ENSP00000513029.1:p.Ile23Ser
ENST00000697035.1:c.*118T>G ENSP00000513059.1:n.*118T>G
ENST00000697036.1:c.*201T>G ENSP00000513060.1:n.*201T>G
ENST00000697037.1:n.820T>G
ENST00000697093.1:n.3021T>G
ENST00000697094.1:n.3368T>G
ENST00000697095.1:c.*1986T>G ENSP00000513104.1:n.*1986T>G
ENST00000697096.1:n.1918T>G
ENST00000697097.1:c.68T>G ENSP00000513105.1:p.Ile23Ser
ENST00000562983.2:n.971T>G
ENST00000690268.1:c.866T>G ENSP00000509810.1:p.Ile289Ser
ENST00000355740.7:c.*111T>G ENSP00000347979.3:n.*111T>G
ENST00000612663.5:c.*187T>G ENSP00000477997.3:n.*187T>G
ENST00000640140.1:n.957T>G
ENST00000640250.1:n.284T>G
ENST00000640681.1:n.906T>G
ENST00000652046.1:c.785T>G MANE Select ENSP00000498466.1:p.Ile262Ser
ENST00000352159.8:c.*102T>G ENSP00000345601.4:n.*102T>G
ENST00000355279.2:c.760T>G ENSP00000347426.2:n.760T>G
ENST00000355740.6:c.785T>G ENSP00000347979.2:p.Ile262Ser
ENST00000357339.6:c.722T>G ENSP00000349896.2:p.Ile241Ser
ENST00000479522.5:c.*214T>G ENSP00000424113.1:n.*214T>G
ENST00000484444.5:c.*226T>G ENSP00000420975.1:n.*226T>G
ENST00000488877.5:c.*226T>G ENSP00000425159.1:n.*226T>G
ENST00000492756.5:c.613T>G ENSP00000422453.1:n.613T>G
ENST00000494410.5:c.*143T>G ENSP00000423755.1:n.*143T>G
ENST00000612663.4:c.*132T>G ENSP00000477997.2:n.*132T>G
NM_000043.4:c.785T>G , LRG_134t1:c.785T>G NP_000034.1:p.Ile262Ser
NM_152871.2:c.722T>G NP_690610.1:p.Ile241Ser
NM_152872.2:c.*97T>G NP_690611.1:n.*97T>G
NR_028033.2:n.959T>G
NR_028034.2:n.821T>G
NR_028035.2:n.884T>G
NR_028036.2:n.1022T>G
XM_006717819.2:c.866T>G XP_006717882.1:p.Ile289Ser
XM_011539764.1:c.947T>G XP_011538066.1:p.Ile316Ser
XM_011539765.1:c.884T>G XP_011538067.1:p.Ile295Ser
XM_011539766.1:c.866T>G XP_011538068.1:p.Ile289Ser
XM_011539767.1:c.830T>G XP_011538069.1:p.Ile277Ser
XR_945732.1:n.853T>G
XR_945733.1:n.790T>G
NM_000043.5:c.785T>G NP_000034.1:p.Ile262Ser
NM_001320619.1:c.*108T>G NP_001307548.1:n.*108T>G
NM_152871.3:c.722T>G NP_690610.1:p.Ile241Ser
NM_152872.3:c.*97T>G NP_690611.1:n.*97T>G
NR_028033.3:n.931T>G
NR_028034.3:n.793T>G
NR_028035.3:n.856T>G
NR_028036.3:n.994T>G
NR_135313.1:n.911T>G
NR_135314.1:n.1094T>G
NR_135315.1:n.847T>G
XM_006717819.3:c.866T>G XP_006717882.1:p.Ile289Ser
XM_011539764.2:c.947T>G XP_011538066.1:p.Ile316Ser
XM_011539765.2:c.884T>G XP_011538067.1:p.Ile295Ser
XM_011539766.2:c.866T>G XP_011538068.1:p.Ile289Ser
XM_011539767.3:c.830T>G XP_011538069.1:p.Ile277Ser
XR_945732.3:n.853T>G
XR_945733.2:n.790T>G
NM_000043.6:c.785T>G MANE Select NP_000034.1:p.Ile262Ser
NM_001320619.2:c.*108T>G NP_001307548.1:n.*108T>G
NM_152871.4:c.722T>G NP_690610.1:p.Ile241Ser
NM_152872.4:c.*97T>G NP_690611.1:n.*97T>G
NR_028033.4:n.692T>G
NR_028034.4:n.554T>G
NR_028035.4:n.617T>G
NR_028036.4:n.755T>G
NR_135313.2:n.672T>G
NR_135314.2:n.951T>G
NR_135315.2:n.704T>G