Canonical Allele Identifier: CA377509822
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1505824
ClinVar RCV Id: RCV001999610
dbSNP Id: rs2119446116

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014234T>G , CM000672.2:g.89014234T>G GRCh38
NC_000010.10:g.90773991T>G , CM000672.1:g.90773991T>G GRCh37
NC_000010.9:g.90763971T>G NCBI36
NG_009089.2:g.28704T>G , LRG_134:g.28704T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1101T>G
ENST00000355740.8:c.*115T>G ENSP00000347979.3:n.*115T>G
ENST00000357339.7:c.729T>G ENSP00000349896.2:p.Asn243Lys
ENST00000371857.8:n.2337T>G
ENST00000460510.6:c.75T>G ENSP00000512812.1:p.Asn25Lys
ENST00000466081.6:n.2441T>G
ENST00000477270.6:c.837T>G ENSP00000512813.1:p.Asn279Lys
ENST00000479522.6:c.*221T>G ENSP00000424113.1:n.*221T>G
ENST00000484444.6:c.*233T>G ENSP00000420975.1:n.*233T>G
ENST00000488877.6:c.683T>G ENSP00000425159.1:n.683T>G
ENST00000492756.7:c.*221T>G ENSP00000422453.1:n.*221T>G
ENST00000494799.6:c.75T>G ENSP00000512834.1:p.Asn25Lys
ENST00000562983.3:c.75T>G ENSP00000512845.1:p.Asn25Lys
ENST00000612663.6:c.*194T>G ENSP00000477997.3:n.*194T>G
ENST00000640140.2:n.937T>G
ENST00000640250.2:n.291T>G
ENST00000640681.2:n.896T>G
ENST00000696723.1:n.4425T>G
ENST00000696741.1:n.2430T>G
ENST00000696742.1:n.2157T>G
ENST00000696743.1:n.3560T>G
ENST00000696744.1:n.831T>G
ENST00000696767.1:n.1126T>G
ENST00000696768.1:c.*115T>G ENSP00000512859.1:n.*115T>G
ENST00000696769.1:n.2481T>G
ENST00000696771.1:c.75T>G ENSP00000512860.1:p.Asn25Lys
ENST00000696772.1:n.2395T>G
ENST00000696773.1:n.2134T>G
ENST00000696774.1:n.5902T>G
ENST00000696776.1:c.885T>G ENSP00000512861.1:p.Asn295Lys
ENST00000696777.1:n.2200T>G
ENST00000696778.1:n.1228T>G
ENST00000696779.1:c.399T>G ENSP00000512862.1:p.Asn133Lys
ENST00000696780.1:c.822T>G ENSP00000512863.1:p.Asn274Lys
ENST00000696781.1:c.537T>G ENSP00000512864.1:p.Asn179Lys
ENST00000696782.1:c.*194T>G ENSP00000512865.1:n.*194T>G
ENST00000696783.1:n.2660T>G
ENST00000696992.1:n.1909T>G
ENST00000696995.1:n.4321T>G
ENST00000696996.1:n.2234T>G
ENST00000696997.1:c.*422T>G ENSP00000513028.1:n.*422T>G
ENST00000696998.1:n.2046T>G
ENST00000696999.1:c.75T>G ENSP00000513029.1:p.Asn25Lys
ENST00000697035.1:c.*125T>G ENSP00000513059.1:n.*125T>G
ENST00000697036.1:c.*208T>G ENSP00000513060.1:n.*208T>G
ENST00000697037.1:n.827T>G
ENST00000697093.1:n.3028T>G
ENST00000697094.1:n.3375T>G
ENST00000697095.1:c.*1993T>G ENSP00000513104.1:n.*1993T>G
ENST00000697096.1:n.1925T>G
ENST00000697097.1:c.75T>G ENSP00000513105.1:p.Asn25Lys
ENST00000562983.2:n.978T>G
ENST00000690268.1:c.873T>G ENSP00000509810.1:p.Asn291Lys
ENST00000355740.7:c.*118T>G ENSP00000347979.3:n.*118T>G
ENST00000612663.5:c.*194T>G ENSP00000477997.3:n.*194T>G
ENST00000640140.1:n.964T>G
ENST00000640250.1:n.291T>G
ENST00000640681.1:n.913T>G
ENST00000652046.1:c.792T>G MANE Select ENSP00000498466.1:p.Asn264Lys
ENST00000352159.8:c.*109T>G ENSP00000345601.4:n.*109T>G
ENST00000355279.2:c.767T>G ENSP00000347426.2:n.767T>G
ENST00000355740.6:c.792T>G ENSP00000347979.2:p.Asn264Lys
ENST00000357339.6:c.729T>G ENSP00000349896.2:p.Asn243Lys
ENST00000479522.5:c.*221T>G ENSP00000424113.1:n.*221T>G
ENST00000484444.5:c.*233T>G ENSP00000420975.1:n.*233T>G
ENST00000488877.5:c.*233T>G ENSP00000425159.1:n.*233T>G
ENST00000492756.5:c.620T>G ENSP00000422453.1:n.620T>G
ENST00000494410.5:c.*150T>G ENSP00000423755.1:n.*150T>G
ENST00000612663.4:c.*139T>G ENSP00000477997.2:n.*139T>G
NM_000043.4:c.792T>G , LRG_134t1:c.792T>G NP_000034.1:p.Asn264Lys
NM_152871.2:c.729T>G NP_690610.1:p.Asn243Lys
NM_152872.2:c.*104T>G NP_690611.1:n.*104T>G
NR_028033.2:n.966T>G
NR_028034.2:n.828T>G
NR_028035.2:n.891T>G
NR_028036.2:n.1029T>G
XM_006717819.2:c.873T>G XP_006717882.1:p.Asn291Lys
XM_011539764.1:c.954T>G XP_011538066.1:p.Asn318Lys
XM_011539765.1:c.891T>G XP_011538067.1:p.Asn297Lys
XM_011539766.1:c.873T>G XP_011538068.1:p.Asn291Lys
XM_011539767.1:c.837T>G XP_011538069.1:p.Asn279Lys
XR_945732.1:n.860T>G
XR_945733.1:n.797T>G
NM_000043.5:c.792T>G NP_000034.1:p.Asn264Lys
NM_001320619.1:c.*115T>G NP_001307548.1:n.*115T>G
NM_152871.3:c.729T>G NP_690610.1:p.Asn243Lys
NM_152872.3:c.*104T>G NP_690611.1:n.*104T>G
NR_028033.3:n.938T>G
NR_028034.3:n.800T>G
NR_028035.3:n.863T>G
NR_028036.3:n.1001T>G
NR_135313.1:n.918T>G
NR_135314.1:n.1101T>G
NR_135315.1:n.854T>G
XM_006717819.3:c.873T>G XP_006717882.1:p.Asn291Lys
XM_011539764.2:c.954T>G XP_011538066.1:p.Asn318Lys
XM_011539765.2:c.891T>G XP_011538067.1:p.Asn297Lys
XM_011539766.2:c.873T>G XP_011538068.1:p.Asn291Lys
XM_011539767.3:c.837T>G XP_011538069.1:p.Asn279Lys
XR_945732.3:n.860T>G
XR_945733.2:n.797T>G
NM_000043.6:c.792T>G MANE Select NP_000034.1:p.Asn264Lys
NM_001320619.2:c.*115T>G NP_001307548.1:n.*115T>G
NM_152871.4:c.729T>G NP_690610.1:p.Asn243Lys
NM_152872.4:c.*104T>G NP_690611.1:n.*104T>G
NR_028033.4:n.699T>G
NR_028034.4:n.561T>G
NR_028035.4:n.624T>G
NR_028036.4:n.762T>G
NR_135313.2:n.679T>G
NR_135314.2:n.958T>G
NR_135315.2:n.711T>G