Canonical Allele Identifier: CA377509806
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs2119446066

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014228C>G , CM000672.2:g.89014228C>G GRCh38
NC_000010.10:g.90773985C>G , CM000672.1:g.90773985C>G GRCh37
NC_000010.9:g.90763965C>G NCBI36
NG_009089.2:g.28698C>G , LRG_134:g.28698C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1095C>G
ENST00000355740.8:c.*109C>G ENSP00000347979.3:n.*109C>G
ENST00000357339.7:c.723C>G ENSP00000349896.2:p.Ile241Met
ENST00000371857.8:n.2331C>G
ENST00000460510.6:c.69C>G ENSP00000512812.1:p.Ile23Met
ENST00000466081.6:n.2435C>G
ENST00000477270.6:c.831C>G ENSP00000512813.1:p.Ile277Met
ENST00000479522.6:c.*215C>G ENSP00000424113.1:n.*215C>G
ENST00000484444.6:c.*227C>G ENSP00000420975.1:n.*227C>G
ENST00000488877.6:c.677C>G ENSP00000425159.1:n.677C>G
ENST00000492756.7:c.*215C>G ENSP00000422453.1:n.*215C>G
ENST00000494799.6:c.69C>G ENSP00000512834.1:p.Ile23Met
ENST00000562983.3:c.69C>G ENSP00000512845.1:p.Ile23Met
ENST00000612663.6:c.*188C>G ENSP00000477997.3:n.*188C>G
ENST00000640140.2:n.931C>G
ENST00000640250.2:n.285C>G
ENST00000640681.2:n.890C>G
ENST00000696723.1:n.4419C>G
ENST00000696741.1:n.2424C>G
ENST00000696742.1:n.2151C>G
ENST00000696743.1:n.3554C>G
ENST00000696744.1:n.825C>G
ENST00000696767.1:n.1120C>G
ENST00000696768.1:c.*109C>G ENSP00000512859.1:n.*109C>G
ENST00000696769.1:n.2475C>G
ENST00000696771.1:c.69C>G ENSP00000512860.1:p.Ile23Met
ENST00000696772.1:n.2389C>G
ENST00000696773.1:n.2128C>G
ENST00000696774.1:n.5896C>G
ENST00000696776.1:c.879C>G ENSP00000512861.1:p.Ile293Met
ENST00000696777.1:n.2194C>G
ENST00000696778.1:n.1222C>G
ENST00000696779.1:c.393C>G ENSP00000512862.1:p.Ile131Met
ENST00000696780.1:c.816C>G ENSP00000512863.1:p.Ile272Met
ENST00000696781.1:c.531C>G ENSP00000512864.1:p.Ile177Met
ENST00000696782.1:c.*188C>G ENSP00000512865.1:n.*188C>G
ENST00000696783.1:n.2654C>G
ENST00000696992.1:n.1903C>G
ENST00000696995.1:n.4315C>G
ENST00000696996.1:n.2228C>G
ENST00000696997.1:c.*416C>G ENSP00000513028.1:n.*416C>G
ENST00000696998.1:n.2040C>G
ENST00000696999.1:c.69C>G ENSP00000513029.1:p.Ile23Met
ENST00000697035.1:c.*119C>G ENSP00000513059.1:n.*119C>G
ENST00000697036.1:c.*202C>G ENSP00000513060.1:n.*202C>G
ENST00000697037.1:n.821C>G
ENST00000697093.1:n.3022C>G
ENST00000697094.1:n.3369C>G
ENST00000697095.1:c.*1987C>G ENSP00000513104.1:n.*1987C>G
ENST00000697096.1:n.1919C>G
ENST00000697097.1:c.69C>G ENSP00000513105.1:p.Ile23Met
ENST00000562983.2:n.972C>G
ENST00000690268.1:c.867C>G ENSP00000509810.1:p.Ile289Met
ENST00000355740.7:c.*112C>G ENSP00000347979.3:n.*112C>G
ENST00000612663.5:c.*188C>G ENSP00000477997.3:n.*188C>G
ENST00000640140.1:n.958C>G
ENST00000640250.1:n.285C>G
ENST00000640681.1:n.907C>G
ENST00000652046.1:c.786C>G MANE Select ENSP00000498466.1:p.Ile262Met
ENST00000352159.8:c.*103C>G ENSP00000345601.4:n.*103C>G
ENST00000355279.2:c.761C>G ENSP00000347426.2:n.761C>G
ENST00000355740.6:c.786C>G ENSP00000347979.2:p.Ile262Met
ENST00000357339.6:c.723C>G ENSP00000349896.2:p.Ile241Met
ENST00000479522.5:c.*215C>G ENSP00000424113.1:n.*215C>G
ENST00000484444.5:c.*227C>G ENSP00000420975.1:n.*227C>G
ENST00000488877.5:c.*227C>G ENSP00000425159.1:n.*227C>G
ENST00000492756.5:c.614C>G ENSP00000422453.1:n.614C>G
ENST00000494410.5:c.*144C>G ENSP00000423755.1:n.*144C>G
ENST00000612663.4:c.*133C>G ENSP00000477997.2:n.*133C>G
NM_000043.4:c.786C>G , LRG_134t1:c.786C>G NP_000034.1:p.Ile262Met
NM_152871.2:c.723C>G NP_690610.1:p.Ile241Met
NM_152872.2:c.*98C>G NP_690611.1:n.*98C>G
NR_028033.2:n.960C>G
NR_028034.2:n.822C>G
NR_028035.2:n.885C>G
NR_028036.2:n.1023C>G
XM_006717819.2:c.867C>G XP_006717882.1:p.Ile289Met
XM_011539764.1:c.948C>G XP_011538066.1:p.Ile316Met
XM_011539765.1:c.885C>G XP_011538067.1:p.Ile295Met
XM_011539766.1:c.867C>G XP_011538068.1:p.Ile289Met
XM_011539767.1:c.831C>G XP_011538069.1:p.Ile277Met
XR_945732.1:n.854C>G
XR_945733.1:n.791C>G
NM_000043.5:c.786C>G NP_000034.1:p.Ile262Met
NM_001320619.1:c.*109C>G NP_001307548.1:n.*109C>G
NM_152871.3:c.723C>G NP_690610.1:p.Ile241Met
NM_152872.3:c.*98C>G NP_690611.1:n.*98C>G
NR_028033.3:n.932C>G
NR_028034.3:n.794C>G
NR_028035.3:n.857C>G
NR_028036.3:n.995C>G
NR_135313.1:n.912C>G
NR_135314.1:n.1095C>G
NR_135315.1:n.848C>G
XM_006717819.3:c.867C>G XP_006717882.1:p.Ile289Met
XM_011539764.2:c.948C>G XP_011538066.1:p.Ile316Met
XM_011539765.2:c.885C>G XP_011538067.1:p.Ile295Met
XM_011539766.2:c.867C>G XP_011538068.1:p.Ile289Met
XM_011539767.3:c.831C>G XP_011538069.1:p.Ile277Met
XR_945732.3:n.854C>G
XR_945733.2:n.791C>G
NM_000043.6:c.786C>G MANE Select NP_000034.1:p.Ile262Met
NM_001320619.2:c.*109C>G NP_001307548.1:n.*109C>G
NM_152871.4:c.723C>G NP_690610.1:p.Ile241Met
NM_152872.4:c.*98C>G NP_690611.1:n.*98C>G
NR_028033.4:n.693C>G
NR_028034.4:n.555C>G
NR_028035.4:n.618C>G
NR_028036.4:n.756C>G
NR_135313.2:n.673C>G
NR_135314.2:n.952C>G
NR_135315.2:n.705C>G