Canonical Allele Identifier: CA377509947
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs2119446799

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014289C>G , CM000672.2:g.89014289C>G GRCh38
NC_000010.10:g.90774046C>G , CM000672.1:g.90774046C>G GRCh37
NC_000010.9:g.90764026C>G NCBI36
NG_009089.2:g.28759C>G , LRG_134:g.28759C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1156C>G
ENST00000355740.8:c.*170C>G ENSP00000347979.3:n.*170C>G
ENST00000357339.7:c.784C>G ENSP00000349896.2:p.Gln262Glu
ENST00000371857.8:n.2392C>G
ENST00000460510.6:c.130C>G ENSP00000512812.1:p.Gln44Glu
ENST00000466081.6:n.2496C>G
ENST00000477270.6:c.892C>G ENSP00000512813.1:p.Gln298Glu
ENST00000479522.6:c.*276C>G ENSP00000424113.1:n.*276C>G
ENST00000484444.6:c.*288C>G ENSP00000420975.1:n.*288C>G
ENST00000488877.6:c.738C>G ENSP00000425159.1:n.738C>G
ENST00000492756.7:c.*276C>G ENSP00000422453.1:n.*276C>G
ENST00000494799.6:c.130C>G ENSP00000512834.1:p.Gln44Glu
ENST00000562983.3:c.130C>G ENSP00000512845.1:p.Gln44Glu
ENST00000612663.6:c.*249C>G ENSP00000477997.3:n.*249C>G
ENST00000640140.2:n.992C>G
ENST00000640250.2:n.346C>G
ENST00000640681.2:n.951C>G
ENST00000696723.1:n.4480C>G
ENST00000696741.1:n.2485C>G
ENST00000696742.1:n.2212C>G
ENST00000696743.1:n.3615C>G
ENST00000696744.1:n.886C>G
ENST00000696767.1:n.1181C>G
ENST00000696768.1:c.*170C>G ENSP00000512859.1:n.*170C>G
ENST00000696769.1:n.2536C>G
ENST00000696771.1:c.130C>G ENSP00000512860.1:p.Gln44Glu
ENST00000696772.1:n.2450C>G
ENST00000696773.1:n.2189C>G
ENST00000696774.1:n.5957C>G
ENST00000696776.1:c.940C>G ENSP00000512861.1:p.Gln314Glu
ENST00000696777.1:n.2255C>G
ENST00000696778.1:n.1283C>G
ENST00000696779.1:c.454C>G ENSP00000512862.1:p.Gln152Glu
ENST00000696780.1:c.877C>G ENSP00000512863.1:p.Gln293Glu
ENST00000696781.1:c.592C>G ENSP00000512864.1:p.Gln198Glu
ENST00000696782.1:c.*249C>G ENSP00000512865.1:n.*249C>G
ENST00000696783.1:n.2715C>G
ENST00000696992.1:n.1964C>G
ENST00000696995.1:n.4376C>G
ENST00000696996.1:n.2289C>G
ENST00000696997.1:c.*477C>G ENSP00000513028.1:n.*477C>G
ENST00000696998.1:n.2101C>G
ENST00000696999.1:c.130C>G ENSP00000513029.1:p.Gln44Glu
ENST00000697035.1:c.*180C>G ENSP00000513059.1:n.*180C>G
ENST00000697036.1:c.*263C>G ENSP00000513060.1:n.*263C>G
ENST00000697037.1:n.882C>G
ENST00000697093.1:n.3083C>G
ENST00000697094.1:n.3430C>G
ENST00000697095.1:c.*2048C>G ENSP00000513104.1:n.*2048C>G
ENST00000697096.1:n.1980C>G
ENST00000697097.1:c.130C>G ENSP00000513105.1:p.Gln44Glu
ENST00000562983.2:n.1033C>G
ENST00000690268.1:c.928C>G ENSP00000509810.1:p.Gln310Glu
ENST00000355740.7:c.*173C>G ENSP00000347979.3:n.*173C>G
ENST00000612663.5:c.*249C>G ENSP00000477997.3:n.*249C>G
ENST00000640140.1:n.1019C>G
ENST00000640250.1:n.346C>G
ENST00000640681.1:n.968C>G
ENST00000652046.1:c.847C>G MANE Select ENSP00000498466.1:p.Gln283Glu
ENST00000352159.8:c.*164C>G ENSP00000345601.4:n.*164C>G
ENST00000355279.2:c.822C>G ENSP00000347426.2:n.822C>G
ENST00000355740.6:c.847C>G ENSP00000347979.2:p.Gln283Glu
ENST00000357339.6:c.784C>G ENSP00000349896.2:p.Gln262Glu
ENST00000479522.5:c.*276C>G ENSP00000424113.1:n.*276C>G
ENST00000484444.5:c.*288C>G ENSP00000420975.1:n.*288C>G
ENST00000488877.5:c.*288C>G ENSP00000425159.1:n.*288C>G
ENST00000492756.5:c.675C>G ENSP00000422453.1:n.675C>G
ENST00000494410.5:c.*205C>G ENSP00000423755.1:n.*205C>G
ENST00000612663.4:c.*194C>G ENSP00000477997.2:n.*194C>G
NM_000043.4:c.847C>G , LRG_134t1:c.847C>G NP_000034.1:p.Gln283Glu
NM_152871.2:c.784C>G NP_690610.1:p.Gln262Glu
NM_152872.2:c.*159C>G NP_690611.1:n.*159C>G
NR_028033.2:n.1021C>G
NR_028034.2:n.883C>G
NR_028035.2:n.946C>G
NR_028036.2:n.1084C>G
XM_006717819.2:c.928C>G XP_006717882.1:p.Gln310Glu
XM_011539764.1:c.1009C>G XP_011538066.1:p.Gln337Glu
XM_011539765.1:c.946C>G XP_011538067.1:p.Gln316Glu
XM_011539766.1:c.928C>G XP_011538068.1:p.Gln310Glu
XM_011539767.1:c.892C>G XP_011538069.1:p.Gln298Glu
XR_945732.1:n.915C>G
XR_945733.1:n.852C>G
NM_000043.5:c.847C>G NP_000034.1:p.Gln283Glu
NM_001320619.1:c.*170C>G NP_001307548.1:n.*170C>G
NM_152871.3:c.784C>G NP_690610.1:p.Gln262Glu
NM_152872.3:c.*159C>G NP_690611.1:n.*159C>G
NR_028033.3:n.993C>G
NR_028034.3:n.855C>G
NR_028035.3:n.918C>G
NR_028036.3:n.1056C>G
NR_135313.1:n.973C>G
NR_135314.1:n.1156C>G
NR_135315.1:n.909C>G
XM_006717819.3:c.928C>G XP_006717882.1:p.Gln310Glu
XM_011539764.2:c.1009C>G XP_011538066.1:p.Gln337Glu
XM_011539765.2:c.946C>G XP_011538067.1:p.Gln316Glu
XM_011539766.2:c.928C>G XP_011538068.1:p.Gln310Glu
XM_011539767.3:c.892C>G XP_011538069.1:p.Gln298Glu
XR_945732.3:n.915C>G
XR_945733.2:n.852C>G
NM_000043.6:c.847C>G MANE Select NP_000034.1:p.Gln283Glu
NM_001320619.2:c.*170C>G NP_001307548.1:n.*170C>G
NM_152871.4:c.784C>G NP_690610.1:p.Gln262Glu
NM_152872.4:c.*159C>G NP_690611.1:n.*159C>G
NR_028033.4:n.754C>G
NR_028034.4:n.616C>G
NR_028035.4:n.679C>G
NR_028036.4:n.817C>G
NR_135313.2:n.734C>G
NR_135314.2:n.1013C>G
NR_135315.2:n.766C>G