Canonical Allele Identifier: CA2722370163
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs1817191692

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014342del , CM000672.2:g.89014342del GRCh38
NC_000010.10:g.90774099del , CM000672.1:g.90774099del GRCh37
NC_000010.9:g.90764079del NCBI36
NG_009089.2:g.28812del , LRG_134:g.28812del

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1209del
ENST00000355740.8:c.*223del ENSP00000347979.3:n.*223del
ENST00000357339.7:c.837del ENSP00000349896.2:p.Ala280ProfsTer?
ENST00000371857.8:n.2445del
ENST00000460510.6:c.183del ENSP00000512812.1:p.Ala62ProfsTer?
ENST00000466081.6:n.2549del
ENST00000477270.6:c.945del ENSP00000512813.1:p.Ala316ProfsTer?
ENST00000479522.6:c.*329del ENSP00000424113.1:n.*329del
ENST00000484444.6:c.*341del ENSP00000420975.1:n.*341del
ENST00000488877.6:c.791del ENSP00000425159.1:n.791del
ENST00000492756.7:c.*329del ENSP00000422453.1:n.*329del
ENST00000494799.6:c.183del ENSP00000512834.1:p.Ala62ProfsTer?
ENST00000562983.3:c.183del ENSP00000512845.1:p.Ala62ProfsTer?
ENST00000612663.6:c.*302del ENSP00000477997.3:n.*302del
ENST00000640140.2:n.1045del
ENST00000640250.2:n.399del
ENST00000640681.2:n.1004del
ENST00000696723.1:n.4533del
ENST00000696741.1:n.2538del
ENST00000696742.1:n.2265del
ENST00000696743.1:n.3668del
ENST00000696744.1:n.939del
ENST00000696767.1:n.1234del
ENST00000696768.1:c.*223del ENSP00000512859.1:n.*223del
ENST00000696769.1:n.2589del
ENST00000696771.1:c.183del ENSP00000512860.1:p.Ala62ProfsTer?
ENST00000696772.1:n.2503del
ENST00000696773.1:n.2242del
ENST00000696774.1:n.6010del
ENST00000696776.1:c.993del ENSP00000512861.1:p.Ala332ProfsTer?
ENST00000696777.1:n.2308del
ENST00000696778.1:n.1336del
ENST00000696779.1:c.507del ENSP00000512862.1:p.Ala170ProfsTer?
ENST00000696780.1:c.930del ENSP00000512863.1:p.Ala311ProfsTer?
ENST00000696781.1:c.645del ENSP00000512864.1:p.Ala216ProfsTer?
ENST00000696782.1:c.*302del ENSP00000512865.1:n.*302del
ENST00000696783.1:n.2768del
ENST00000696992.1:n.2017del
ENST00000696995.1:n.4429del
ENST00000696996.1:n.2342del
ENST00000696997.1:c.*530del ENSP00000513028.1:n.*530del
ENST00000696998.1:n.2154del
ENST00000696999.1:c.183del ENSP00000513029.1:p.Ala62ProfsTer?
ENST00000697036.1:c.*316del ENSP00000513060.1:n.*316del
ENST00000697037.1:n.935del
ENST00000697093.1:n.3136del
ENST00000697094.1:n.3483del
ENST00000697095.1:c.*2101del ENSP00000513104.1:n.*2101del
ENST00000697096.1:n.2033del
ENST00000697097.1:c.183del ENSP00000513105.1:p.Ala62ProfsTer?
ENST00000562983.2:n.1086del
ENST00000690268.1:c.981del ENSP00000509810.1:p.Ala328ProfsTer?
ENST00000355740.7:c.*226del ENSP00000347979.3:n.*226del
ENST00000612663.5:c.*302del ENSP00000477997.3:n.*302del
ENST00000640140.1:n.1072del
ENST00000640250.1:n.399del
ENST00000640681.1:n.1021del
ENST00000652046.1:c.900del MANE Select ENSP00000498466.1:p.Ala301ProfsTer?
ENST00000352159.8:c.*217del ENSP00000345601.4:n.*217del
ENST00000355279.2:c.875del ENSP00000347426.2:n.875del
ENST00000355740.6:c.900del ENSP00000347979.2:p.Ala301ProfsTer?
ENST00000357339.6:c.837del ENSP00000349896.2:p.Ala280ProfsTer?
ENST00000479522.5:c.*329del ENSP00000424113.1:n.*329del
ENST00000484444.5:c.*341del ENSP00000420975.1:n.*341del
ENST00000488877.5:c.*341del ENSP00000425159.1:n.*341del
ENST00000492756.5:c.728del ENSP00000422453.1:n.728del
ENST00000494410.5:c.*258del ENSP00000423755.1:n.*258del
ENST00000612663.4:c.*247del ENSP00000477997.2:n.*247del
NM_000043.4:c.900del , LRG_134t1:c.900del NP_000034.1:p.Ala301ProfsTer?
NM_152871.2:c.837del NP_690610.1:p.Ala280ProfsTer?
NM_152872.2:c.*212del NP_690611.1:n.*212del
NR_028033.2:n.1074del
NR_028034.2:n.936del
NR_028035.2:n.999del
NR_028036.2:n.1137del
XM_006717819.2:c.981del XP_006717882.1:p.Ala328ProfsTer?
XM_011539764.1:c.1062del XP_011538066.1:p.Ala355ProfsTer?
XM_011539765.1:c.999del XP_011538067.1:p.Ala334ProfsTer?
XM_011539766.1:c.981del XP_011538068.1:p.Ala328ProfsTer?
XM_011539767.1:c.945del XP_011538069.1:p.Ala316ProfsTer?
XR_945732.1:n.968del
XR_945733.1:n.905del
NM_000043.5:c.900del NP_000034.1:p.Ala301ProfsTer?
NM_001320619.1:c.*223del NP_001307548.1:n.*223del
NM_152871.3:c.837del NP_690610.1:p.Ala280ProfsTer?
NM_152872.3:c.*212del NP_690611.1:n.*212del
NR_028033.3:n.1046del
NR_028034.3:n.908del
NR_028035.3:n.971del
NR_028036.3:n.1109del
NR_135313.1:n.1026del
NR_135314.1:n.1209del
NR_135315.1:n.962del
XM_006717819.3:c.981del XP_006717882.1:p.Ala328ProfsTer?
XM_011539764.2:c.1062del XP_011538066.1:p.Ala355ProfsTer?
XM_011539765.2:c.999del XP_011538067.1:p.Ala334ProfsTer?
XM_011539766.2:c.981del XP_011538068.1:p.Ala328ProfsTer?
XM_011539767.3:c.945del XP_011538069.1:p.Ala316ProfsTer?
XR_945732.3:n.968del
XR_945733.2:n.905del
NM_000043.6:c.900del MANE Select NP_000034.1:p.Ala301ProfsTer?
NM_001320619.2:c.*223del NP_001307548.1:n.*223del
NM_152871.4:c.837del NP_690610.1:p.Ala280ProfsTer?
NM_152872.4:c.*212del NP_690611.1:n.*212del
NR_028033.4:n.807del
NR_028034.4:n.669del
NR_028035.4:n.732del
NR_028036.4:n.870del
NR_135313.2:n.787del
NR_135314.2:n.1066del
NR_135315.2:n.819del