Canonical Allele Identifier: CA1926639331
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014188T= , CM000672.2:g.89014188T= GRCh38
NC_000010.10:g.90773945T= , CM000672.1:g.90773945T= GRCh37
NC_000010.9:g.90763925T= NCBI36
NG_009089.2:g.28658T= , LRG_134:g.28658T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1055T=
ENST00000355740.8:c.*69T= ENSP00000347979.3:n.*69T=
ENST00000357339.7:c.683T= ENSP00000349896.2:p.Val228=
ENST00000371857.8:n.2291T=
ENST00000460510.6:c.29T= ENSP00000512812.1:p.Val10=
ENST00000466081.6:n.2395T=
ENST00000477270.6:c.791T= ENSP00000512813.1:p.Val264=
ENST00000479522.6:c.*175T= ENSP00000424113.1:n.*175T=
ENST00000484444.6:c.*187T= ENSP00000420975.1:n.*187T=
ENST00000488877.6:c.637T= ENSP00000425159.1:n.637T=
ENST00000492756.7:c.*175T= ENSP00000422453.1:n.*175T=
ENST00000494799.6:c.29T= ENSP00000512834.1:p.Val10=
ENST00000562983.3:c.29T= ENSP00000512845.1:p.Val10=
ENST00000612663.6:c.*148T= ENSP00000477997.3:n.*148T=
ENST00000640140.2:n.891T=
ENST00000640250.2:n.245T=
ENST00000640681.2:n.850T=
ENST00000696723.1:n.4379T=
ENST00000696741.1:n.2384T=
ENST00000696742.1:n.2111T=
ENST00000696743.1:n.3514T=
ENST00000696744.1:n.785T=
ENST00000696767.1:n.1080T=
ENST00000696768.1:c.*69T= ENSP00000512859.1:n.*69T=
ENST00000696769.1:n.2435T=
ENST00000696771.1:c.29T= ENSP00000512860.1:p.Val10=
ENST00000696772.1:n.2349T=
ENST00000696773.1:n.2088T=
ENST00000696774.1:n.5856T=
ENST00000696776.1:c.839T= ENSP00000512861.1:p.Val280=
ENST00000696777.1:n.2154T=
ENST00000696778.1:n.1182T=
ENST00000696779.1:c.353T= ENSP00000512862.1:p.Val118=
ENST00000696780.1:c.776T= ENSP00000512863.1:p.Val259=
ENST00000696781.1:c.491T= ENSP00000512864.1:p.Val164=
ENST00000696782.1:c.*148T= ENSP00000512865.1:n.*148T=
ENST00000696783.1:n.2614T=
ENST00000696992.1:n.1863T=
ENST00000696995.1:n.4275T=
ENST00000696996.1:n.2188T=
ENST00000696997.1:c.*376T= ENSP00000513028.1:n.*376T=
ENST00000696998.1:n.2000T=
ENST00000696999.1:c.29T= ENSP00000513029.1:p.Val10=
ENST00000697035.1:c.*79T= ENSP00000513059.1:n.*79T=
ENST00000697036.1:c.*162T= ENSP00000513060.1:n.*162T=
ENST00000697037.1:n.781T=
ENST00000697093.1:n.2982T=
ENST00000697094.1:n.3329T=
ENST00000697095.1:c.*1947T= ENSP00000513104.1:n.*1947T=
ENST00000697096.1:n.1879T=
ENST00000697097.1:c.29T= ENSP00000513105.1:p.Val10=
ENST00000562983.2:n.932T=
ENST00000690268.1:c.827T= ENSP00000509810.1:p.Val276=
ENST00000355740.7:c.*72T= ENSP00000347979.3:n.*72T=
ENST00000612663.5:c.*148T= ENSP00000477997.3:n.*148T=
ENST00000640140.1:n.918T=
ENST00000640250.1:n.245T=
ENST00000640681.1:n.867T=
ENST00000652046.1:c.746T= MANE Select ENSP00000498466.1:p.Val249=
ENST00000352159.8:c.*63T= ENSP00000345601.4:n.*63T=
ENST00000355279.2:c.721T= ENSP00000347426.2:n.721T=
ENST00000355740.6:c.746T= ENSP00000347979.2:p.Val249=
ENST00000357339.6:c.683T= ENSP00000349896.2:p.Val228=
ENST00000479522.5:c.*175T= ENSP00000424113.1:n.*175T=
ENST00000484444.5:c.*187T= ENSP00000420975.1:n.*187T=
ENST00000488877.5:c.*187T= ENSP00000425159.1:n.*187T=
ENST00000492756.5:c.574T= ENSP00000422453.1:n.574T=
ENST00000494410.5:c.*104T= ENSP00000423755.1:n.*104T=
ENST00000494799.5:n.653T=
ENST00000612663.4:c.*93T= ENSP00000477997.2:n.*93T=
ENST00000615406.4:c.746T= ENSP00000484575.1:p.Val249=
NM_000043.4:c.746T= , LRG_134t1:c.746T= NP_000034.1:p.Val249=
NM_152871.2:c.683T= NP_690610.1:p.Val228=
NM_152872.2:c.*58T= NP_690611.1:n.*58T=
NR_028033.2:n.920T=
NR_028034.2:n.782T=
NR_028035.2:n.845T=
NR_028036.2:n.983T=
XM_006717819.2:c.827T= XP_006717882.1:p.Val276=
XM_011539764.1:c.908T= XP_011538066.1:p.Val303=
XM_011539765.1:c.845T= XP_011538067.1:p.Val282=
XM_011539766.1:c.827T= XP_011538068.1:p.Val276=
XM_011539767.1:c.791T= XP_011538069.1:p.Val264=
XR_945732.1:n.814T=
XR_945733.1:n.751T=
NM_000043.5:c.746T= NP_000034.1:p.Val249=
NM_001320619.1:c.*69T= NP_001307548.1:n.*69T=
NM_152871.3:c.683T= NP_690610.1:p.Val228=
NM_152872.3:c.*58T= NP_690611.1:n.*58T=
NR_028033.3:n.892T=
NR_028034.3:n.754T=
NR_028035.3:n.817T=
NR_028036.3:n.955T=
NR_135313.1:n.872T=
NR_135314.1:n.1055T=
NR_135315.1:n.808T=
XM_006717819.3:c.827T= XP_006717882.1:p.Val276=
XM_011539764.2:c.908T= XP_011538066.1:p.Val303=
XM_011539765.2:c.845T= XP_011538067.1:p.Val282=
XM_011539766.2:c.827T= XP_011538068.1:p.Val276=
XM_011539767.3:c.791T= XP_011538069.1:p.Val264=
XR_945732.3:n.814T=
XR_945733.2:n.751T=
NM_000043.6:c.746T= MANE Select NP_000034.1:p.Val249=
NM_001320619.2:c.*69T= NP_001307548.1:n.*69T=
NM_152871.4:c.683T= NP_690610.1:p.Val228=
NM_152872.4:c.*58T= NP_690611.1:n.*58T=
NR_028033.4:n.653T=
NR_028034.4:n.515T=
NR_028035.4:n.578T=
NR_028036.4:n.716T=
NR_135313.2:n.633T=
NR_135314.2:n.912T=
NR_135315.2:n.665T=