Canonical Allele Identifier: CA13271822
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1291170
dbSNP Id: rs2296600

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89010682C>G , CM000672.2:g.89010682C>G GRCh38
NC_000010.10:g.90770439C>G , CM000672.1:g.90770439C>G GRCh37
NC_000010.9:g.90760419C>G NCBI36
NG_009089.2:g.25152C>G , LRG_134:g.25152C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.815-71C>G
ENST00000355740.8:c.506-71C>G ENSP00000347979.3:n.506-71C>G
ENST00000357339.7:c.505+82C>G ENSP00000349896.2:n.505+82C>G
ENST00000371857.8:n.797C>G
ENST00000460510.6:c.-212-71C>G ENSP00000512812.1:n.-212-71C>G
ENST00000466081.6:n.647C>G
ENST00000477270.6:c.551-71C>G ENSP00000512813.1:n.551-71C>G
ENST00000479522.6:c.258+82C>G ENSP00000424113.1:n.258+82C>G
ENST00000484444.6:c.259-71C>G ENSP00000420975.1:n.259-71C>G
ENST00000488877.6:c.397-71C>G ENSP00000425159.1:n.397-71C>G
ENST00000492756.7:c.396+82C>G ENSP00000422453.1:n.396+82C>G
ENST00000494799.6:c.-212-71C>G ENSP00000512834.1:n.-212-71C>G
ENST00000562983.3:c.-212-71C>G ENSP00000512845.1:n.-212-71C>G
ENST00000612663.6:c.506-71C>G ENSP00000477997.3:n.506-71C>G
ENST00000640140.2:n.651-71C>G
ENST00000640681.2:n.610-71C>G
ENST00000696723.1:n.4139-71C>G
ENST00000696741.1:n.890C>G
ENST00000696742.1:n.688-71C>G
ENST00000696743.1:n.759C>G
ENST00000696744.1:n.545-71C>G
ENST00000696767.1:n.769C>G
ENST00000696768.1:c.505+82C>G ENSP00000512859.1:n.505+82C>G
ENST00000696769.1:n.941C>G
ENST00000696770.1:n.3362C>G
ENST00000696771.1:c.-150+82C>G ENSP00000512860.1:n.-150+82C>G
ENST00000696772.1:n.672-71C>G
ENST00000696773.1:n.665-71C>G
ENST00000696774.1:n.2350C>G
ENST00000696776.1:c.599-71C>G ENSP00000512861.1:n.599-71C>G
ENST00000696777.1:n.660C>G
ENST00000696778.1:n.688-71C>G
ENST00000696779.1:c.258+82C>G ENSP00000512862.1:n.258+82C>G
ENST00000696780.1:c.598+82C>G ENSP00000512863.1:n.598+82C>G
ENST00000696781.1:c.396+82C>G ENSP00000512864.1:n.396+82C>G
ENST00000696782.1:c.505+82C>G ENSP00000512865.1:n.505+82C>G
ENST00000696783.1:n.1120C>G
ENST00000696992.1:n.1623-71C>G
ENST00000696995.1:n.769C>G
ENST00000696996.1:n.687-71C>G
ENST00000696997.1:c.*136-71C>G ENSP00000513028.1:n.*136-71C>G
ENST00000696998.1:n.506C>G
ENST00000696999.1:c.-150+82C>G ENSP00000513029.1:n.-150+82C>G
ENST00000697035.1:c.506-71C>G ENSP00000513059.1:n.506-71C>G
ENST00000697036.1:c.397-71C>G ENSP00000513060.1:n.397-71C>G
ENST00000697037.1:n.541-71C>G
ENST00000697093.1:n.730-71C>G
ENST00000697094.1:n.645-71C>G
ENST00000697095.1:c.*1707-71C>G ENSP00000513104.1:n.*1707-71C>G
ENST00000697096.1:n.643C>G
ENST00000697097.1:c.-212-71C>G ENSP00000513105.1:n.-212-71C>G
ENST00000562983.2:n.692-71C>G
ENST00000690268.1:c.587-71C>G ENSP00000509810.1:n.587-71C>G
ENST00000355740.7:c.506-71C>G ENSP00000347979.3:n.506-71C>G
ENST00000612663.5:c.506-71C>G ENSP00000477997.3:n.506-71C>G
ENST00000640140.1:n.678-71C>G
ENST00000640681.1:n.627-71C>G
ENST00000652046.1:c.506-71C>G MANE Select ENSP00000498466.1:n.506-71C>G
ENST00000313771.9:n.815-71C>G
ENST00000352159.8:c.506-71C>G ENSP00000345601.4:n.506-71C>G
ENST00000355279.2:c.506-71C>G ENSP00000347426.2:n.506-71C>G
ENST00000355740.6:c.506-71C>G ENSP00000347979.2:n.506-71C>G
ENST00000357339.6:c.505+82C>G ENSP00000349896.2:n.505+82C>G
ENST00000371857.7:n.753C>G
ENST00000477270.5:n.669-71C>G
ENST00000479522.5:c.258+82C>G ENSP00000424113.1:n.258+82C>G
ENST00000484444.5:c.259-71C>G ENSP00000420975.1:n.259-71C>G
ENST00000487314.1:n.655-71C>G
ENST00000488877.5:c.397-71C>G ENSP00000425159.1:n.397-71C>G
ENST00000492756.5:c.396+82C>G ENSP00000422453.1:n.396+82C>G
ENST00000494410.5:c.397-71C>G ENSP00000423755.1:n.397-71C>G
ENST00000494799.5:n.413-71C>G
ENST00000612663.4:c.506-71C>G ENSP00000477997.2:n.506-71C>G
ENST00000615406.4:c.506-71C>G ENSP00000484575.1:n.506-71C>G
ENST00000626542.2:c.506-71C>G ENSP00000485876.1:n.506-71C>G
NM_000043.4:c.506-71C>G , LRG_134t1:c.506-71C>G NP_000034.1:n.506-71C>G
NM_152871.2:c.505+82C>G NP_690610.1:n.505+82C>G
NM_152872.2:c.506-71C>G NP_690611.1:n.506-71C>G
NR_028033.2:n.742+82C>G
NR_028034.2:n.604+82C>G
NR_028035.2:n.605-71C>G
NR_028036.2:n.743-71C>G
XM_006717819.2:c.587-71C>G XP_006717882.1:n.587-71C>G
XM_011539764.1:c.668-71C>G XP_011538066.1:n.668-71C>G
XM_011539765.1:c.667+82C>G XP_011538067.1:n.667+82C>G
XM_011539766.1:c.587-71C>G XP_011538068.1:n.587-71C>G
XM_011539767.1:c.551-71C>G XP_011538069.1:n.551-71C>G
XR_945732.1:n.574-71C>G
XR_945733.1:n.573+82C>G
NM_000043.5:c.506-71C>G NP_000034.1:n.506-71C>G
NM_001320619.1:c.506-71C>G NP_001307548.1:n.506-71C>G
NM_152871.3:c.505+82C>G NP_690610.1:n.505+82C>G
NM_152872.3:c.506-71C>G NP_690611.1:n.506-71C>G
NR_028033.3:n.714+82C>G
NR_028034.3:n.576+82C>G
NR_028035.3:n.577-71C>G
NR_028036.3:n.715-71C>G
NR_135313.1:n.715-71C>G
NR_135314.1:n.815-71C>G
NR_135315.1:n.568-71C>G
XM_006717819.3:c.587-71C>G XP_006717882.1:n.587-71C>G
XM_011539764.2:c.668-71C>G XP_011538066.1:n.668-71C>G
XM_011539765.2:c.667+82C>G XP_011538067.1:n.667+82C>G
XM_011539766.2:c.587-71C>G XP_011538068.1:n.587-71C>G
XM_011539767.3:c.551-71C>G XP_011538069.1:n.551-71C>G
XR_945732.3:n.574-71C>G
XR_945733.2:n.573+82C>G
NM_000043.6:c.506-71C>G MANE Select NP_000034.1:n.506-71C>G
NM_001320619.2:c.506-71C>G NP_001307548.1:n.506-71C>G
NM_152871.4:c.505+82C>G NP_690610.1:n.505+82C>G
NM_152872.4:c.506-71C>G NP_690611.1:n.506-71C>G
NR_028033.4:n.475+82C>G
NR_028034.4:n.337+82C>G
NR_028035.4:n.338-71C>G
NR_028036.4:n.476-71C>G
NR_135313.2:n.476-71C>G
NR_135314.2:n.672-71C>G
NR_135315.2:n.425-71C>G