Canonical Allele Identifier: CA126581
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 16504
ClinVar RCV Id: RCV000017968 RCV002513090
dbSNP Id: rs28929498
MyVariant Identifiers: chr10:g.90773978A>T (hg19) chr10:g.89014221A>T (hg38)
PubMed: PMID:9821419
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014221A>T , CM000672.2:g.89014221A>T GRCh38
NC_000010.10:g.90773978A>T , CM000672.1:g.90773978A>T GRCh37
NC_000010.9:g.90763958A>T NCBI36
NG_009089.2:g.28691A>T , LRG_134:g.28691A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.1088A>T
ENST00000355740.8:c.*102A>T ENSP00000347979.3:n.*102A>T
ENST00000357339.7:c.716A>T ENSP00000349896.2:p.Asp239Val
ENST00000371857.8:n.2324A>T
ENST00000460510.6:c.62A>T ENSP00000512812.1:p.Asp21Val
ENST00000466081.6:n.2428A>T
ENST00000477270.6:c.824A>T ENSP00000512813.1:p.Asp275Val
ENST00000479522.6:c.*208A>T ENSP00000424113.1:n.*208A>T
ENST00000484444.6:c.*220A>T ENSP00000420975.1:n.*220A>T
ENST00000488877.6:c.670A>T ENSP00000425159.1:n.670A>T
ENST00000492756.7:c.*208A>T ENSP00000422453.1:n.*208A>T
ENST00000494799.6:c.62A>T ENSP00000512834.1:p.Asp21Val
ENST00000562983.3:c.62A>T ENSP00000512845.1:p.Asp21Val
ENST00000612663.6:c.*181A>T ENSP00000477997.3:n.*181A>T
ENST00000640140.2:n.924A>T
ENST00000640250.2:n.278A>T
ENST00000640681.2:n.883A>T
ENST00000696723.1:n.4412A>T
ENST00000696741.1:n.2417A>T
ENST00000696742.1:n.2144A>T
ENST00000696743.1:n.3547A>T
ENST00000696744.1:n.818A>T
ENST00000696767.1:n.1113A>T
ENST00000696768.1:c.*102A>T ENSP00000512859.1:n.*102A>T
ENST00000696769.1:n.2468A>T
ENST00000696771.1:c.62A>T ENSP00000512860.1:p.Asp21Val
ENST00000696772.1:n.2382A>T
ENST00000696773.1:n.2121A>T
ENST00000696774.1:n.5889A>T
ENST00000696776.1:c.872A>T ENSP00000512861.1:p.Asp291Val
ENST00000696777.1:n.2187A>T
ENST00000696778.1:n.1215A>T
ENST00000696779.1:c.386A>T ENSP00000512862.1:p.Asp129Val
ENST00000696780.1:c.809A>T ENSP00000512863.1:p.Asp270Val
ENST00000696781.1:c.524A>T ENSP00000512864.1:p.Asp175Val
ENST00000696782.1:c.*181A>T ENSP00000512865.1:n.*181A>T
ENST00000696783.1:n.2647A>T
ENST00000696992.1:n.1896A>T
ENST00000696995.1:n.4308A>T
ENST00000696996.1:n.2221A>T
ENST00000696997.1:c.*409A>T ENSP00000513028.1:n.*409A>T
ENST00000696998.1:n.2033A>T
ENST00000696999.1:c.62A>T ENSP00000513029.1:p.Asp21Val
ENST00000697035.1:c.*112A>T ENSP00000513059.1:n.*112A>T
ENST00000697036.1:c.*195A>T ENSP00000513060.1:n.*195A>T
ENST00000697037.1:n.814A>T
ENST00000697093.1:n.3015A>T
ENST00000697094.1:n.3362A>T
ENST00000697095.1:c.*1980A>T ENSP00000513104.1:n.*1980A>T
ENST00000697096.1:n.1912A>T
ENST00000697097.1:c.62A>T ENSP00000513105.1:p.Asp21Val
ENST00000562983.2:n.965A>T
ENST00000690268.1:c.860A>T ENSP00000509810.1:p.Asp287Val
ENST00000355740.7:c.*105A>T ENSP00000347979.3:n.*105A>T
ENST00000612663.5:c.*181A>T ENSP00000477997.3:n.*181A>T
ENST00000640140.1:n.951A>T
ENST00000640250.1:n.278A>T
ENST00000640681.1:n.900A>T
ENST00000652046.1:c.779A>T MANE Select ENSP00000498466.1:p.Asp260Val
ENST00000352159.8:c.*96A>T ENSP00000345601.4:n.*96A>T
ENST00000355279.2:c.754A>T ENSP00000347426.2:n.754A>T
ENST00000355740.6:c.779A>T ENSP00000347979.2:p.Asp260Val
ENST00000357339.6:c.716A>T ENSP00000349896.2:p.Asp239Val
ENST00000479522.5:c.*208A>T ENSP00000424113.1:n.*208A>T
ENST00000484444.5:c.*220A>T ENSP00000420975.1:n.*220A>T
ENST00000488877.5:c.*220A>T ENSP00000425159.1:n.*220A>T
ENST00000492756.5:c.607A>T ENSP00000422453.1:n.607A>T
ENST00000494410.5:c.*137A>T ENSP00000423755.1:n.*137A>T
ENST00000612663.4:c.*126A>T ENSP00000477997.2:n.*126A>T
NM_000043.4:c.779A>T , LRG_134t1:c.779A>T NP_000034.1:p.Asp260Val
NM_152871.2:c.716A>T NP_690610.1:p.Asp239Val
NM_152872.2:c.*91A>T NP_690611.1:n.*91A>T
NR_028033.2:n.953A>T
NR_028034.2:n.815A>T
NR_028035.2:n.878A>T
NR_028036.2:n.1016A>T
XM_006717819.2:c.860A>T XP_006717882.1:p.Asp287Val
XM_011539764.1:c.941A>T XP_011538066.1:p.Asp314Val
XM_011539765.1:c.878A>T XP_011538067.1:p.Asp293Val
XM_011539766.1:c.860A>T XP_011538068.1:p.Asp287Val
XM_011539767.1:c.824A>T XP_011538069.1:p.Asp275Val
XR_945732.1:n.847A>T
XR_945733.1:n.784A>T
NM_000043.5:c.779A>T NP_000034.1:p.Asp260Val
NM_001320619.1:c.*102A>T NP_001307548.1:n.*102A>T
NM_152871.3:c.716A>T NP_690610.1:p.Asp239Val
NM_152872.3:c.*91A>T NP_690611.1:n.*91A>T
NR_028033.3:n.925A>T
NR_028034.3:n.787A>T
NR_028035.3:n.850A>T
NR_028036.3:n.988A>T
NR_135313.1:n.905A>T
NR_135314.1:n.1088A>T
NR_135315.1:n.841A>T
XM_006717819.3:c.860A>T XP_006717882.1:p.Asp287Val
XM_011539764.2:c.941A>T XP_011538066.1:p.Asp314Val
XM_011539765.2:c.878A>T XP_011538067.1:p.Asp293Val
XM_011539766.2:c.860A>T XP_011538068.1:p.Asp287Val
XM_011539767.3:c.824A>T XP_011538069.1:p.Asp275Val
XR_945732.3:n.847A>T
XR_945733.2:n.784A>T
NM_000043.6:c.779A>T MANE Select NP_000034.1:p.Asp260Val
NM_001320619.2:c.*102A>T NP_001307548.1:n.*102A>T
NM_152871.4:c.716A>T NP_690610.1:p.Asp239Val
NM_152872.4:c.*91A>T NP_690611.1:n.*91A>T
NR_028033.4:n.686A>T
NR_028034.4:n.548A>T
NR_028035.4:n.611A>T
NR_028036.4:n.749A>T
NR_135313.2:n.666A>T
NR_135314.2:n.945A>T
NR_135315.2:n.698A>T
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