Canonical Allele Identifier: CA645542421

Gene: FAS

Linked Data

• COSMIC: COSM5946575

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014180del , CM000672.2:g.89014180del	GRCh38
NC_000010.10:g.90773937del , CM000672.1:g.90773937del	GRCh37
NC_000010.9:g.90763917del	NCBI36
NG_009089.2:g.28650del , LRG_134:g.28650del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1047del
ENST00000355740.8:c.*61del	ENSP00000347979.3:n.*61del
ENST00000357339.7:c.675del	ENSP00000349896.2:p.Gly226AlafsTer13
ENST00000371857.8:n.2283del
ENST00000460510.6:c.21del	ENSP00000512812.1:p.Gly8AlafsTer13
ENST00000466081.6:n.2387del
ENST00000477270.6:c.783del	ENSP00000512813.1:p.Gly262AlafsTer13
ENST00000479522.6:c.*167del	ENSP00000424113.1:n.*167del
ENST00000484444.6:c.*179del	ENSP00000420975.1:n.*179del
ENST00000488877.6:c.629del	ENSP00000425159.1:n.629del
ENST00000492756.7:c.*167del	ENSP00000422453.1:n.*167del
ENST00000494799.6:c.21del	ENSP00000512834.1:p.Gly8AlafsTer13
ENST00000562983.3:c.21del	ENSP00000512845.1:p.Gly8AlafsTer13
ENST00000612663.6:c.*140del	ENSP00000477997.3:n.*140del
ENST00000640140.2:n.883del
ENST00000640250.2:n.237del
ENST00000640681.2:n.842del
ENST00000696723.1:n.4371del
ENST00000696741.1:n.2376del
ENST00000696742.1:n.2103del
ENST00000696743.1:n.3506del
ENST00000696744.1:n.777del
ENST00000696767.1:n.1072del
ENST00000696768.1:c.*61del	ENSP00000512859.1:n.*61del
ENST00000696769.1:n.2427del
ENST00000696771.1:c.21del	ENSP00000512860.1:p.Gly8AlafsTer13
ENST00000696772.1:n.2341del
ENST00000696773.1:n.2080del
ENST00000696774.1:n.5848del
ENST00000696776.1:c.831del	ENSP00000512861.1:p.Gly278AlafsTer13
ENST00000696777.1:n.2146del
ENST00000696778.1:n.1174del
ENST00000696779.1:c.345del	ENSP00000512862.1:p.Gly116AlafsTer13
ENST00000696780.1:c.768del	ENSP00000512863.1:p.Gly257AlafsTer13
ENST00000696781.1:c.483del	ENSP00000512864.1:p.Gly162AlafsTer13
ENST00000696782.1:c.*140del	ENSP00000512865.1:n.*140del
ENST00000696783.1:n.2606del
ENST00000696992.1:n.1855del
ENST00000696995.1:n.4267del
ENST00000696996.1:n.2180del
ENST00000696997.1:c.*368del	ENSP00000513028.1:n.*368del
ENST00000696998.1:n.1992del
ENST00000696999.1:c.21del	ENSP00000513029.1:p.Gly8AlafsTer13
ENST00000697035.1:c.*71del	ENSP00000513059.1:n.*71del
ENST00000697036.1:c.*154del	ENSP00000513060.1:n.*154del
ENST00000697037.1:n.773del
ENST00000697093.1:n.2974del
ENST00000697094.1:n.3321del
ENST00000697095.1:c.*1939del	ENSP00000513104.1:n.*1939del
ENST00000697096.1:n.1871del
ENST00000697097.1:c.21del	ENSP00000513105.1:p.Gly8AlafsTer13
ENST00000562983.2:n.924del
ENST00000690268.1:c.819del	ENSP00000509810.1:p.Gly274AlafsTer13
ENST00000355740.7:c.*64del	ENSP00000347979.3:n.*64del
ENST00000612663.5:c.*140del	ENSP00000477997.3:n.*140del
ENST00000640140.1:n.910del
ENST00000640250.1:n.237del
ENST00000640681.1:n.859del
ENST00000652046.1:c.738del MANE Select	ENSP00000498466.1:p.Gly247AlafsTer13
ENST00000352159.8:c.*55del	ENSP00000345601.4:n.*55del
ENST00000355279.2:c.713del	ENSP00000347426.2:n.713del
ENST00000355740.6:c.738del	ENSP00000347979.2:p.Gly247AlafsTer13
ENST00000357339.6:c.675del	ENSP00000349896.2:p.Gly226AlafsTer13
ENST00000479522.5:c.*167del	ENSP00000424113.1:n.*167del
ENST00000484444.5:c.*179del	ENSP00000420975.1:n.*179del
ENST00000488877.5:c.*179del	ENSP00000425159.1:n.*179del
ENST00000492756.5:c.566del	ENSP00000422453.1:n.566del
ENST00000494410.5:c.*96del	ENSP00000423755.1:n.*96del
ENST00000494799.5:n.645del
ENST00000612663.4:c.*85del	ENSP00000477997.2:n.*85del
ENST00000615406.4:c.738del	ENSP00000484575.1:p.Gly247AlafsTer?
NM_000043.4:c.738del , LRG_134t1:c.738del	NP_000034.1:p.Gly247AlafsTer13
NM_152871.2:c.675del	NP_690610.1:p.Gly226AlafsTer13
NM_152872.2:c.*50del	NP_690611.1:n.*50del
NR_028033.2:n.912del
NR_028034.2:n.774del
NR_028035.2:n.837del
NR_028036.2:n.975del
XM_006717819.2:c.819del	XP_006717882.1:p.Gly274AlafsTer13
XM_011539764.1:c.900del	XP_011538066.1:p.Gly301AlafsTer13
XM_011539765.1:c.837del	XP_011538067.1:p.Gly280AlafsTer13
XM_011539766.1:c.819del	XP_011538068.1:p.Gly274AlafsTer13
XM_011539767.1:c.783del	XP_011538069.1:p.Gly262AlafsTer13
XR_945732.1:n.806del
XR_945733.1:n.743del
NM_000043.5:c.738del	NP_000034.1:p.Gly247AlafsTer13
NM_001320619.1:c.*61del	NP_001307548.1:n.*61del
NM_152871.3:c.675del	NP_690610.1:p.Gly226AlafsTer13
NM_152872.3:c.*50del	NP_690611.1:n.*50del
NR_028033.3:n.884del
NR_028034.3:n.746del
NR_028035.3:n.809del
NR_028036.3:n.947del
NR_135313.1:n.864del
NR_135314.1:n.1047del
NR_135315.1:n.800del
XM_006717819.3:c.819del	XP_006717882.1:p.Gly274AlafsTer13
XM_011539764.2:c.900del	XP_011538066.1:p.Gly301AlafsTer13
XM_011539765.2:c.837del	XP_011538067.1:p.Gly280AlafsTer13
XM_011539766.2:c.819del	XP_011538068.1:p.Gly274AlafsTer13
XM_011539767.3:c.783del	XP_011538069.1:p.Gly262AlafsTer13
XR_945732.3:n.806del
XR_945733.2:n.743del
NM_000043.6:c.738del MANE Select	NP_000034.1:p.Gly247AlafsTer13
NM_001320619.2:c.*61del	NP_001307548.1:n.*61del
NM_152871.4:c.675del	NP_690610.1:p.Gly226AlafsTer13
NM_152872.4:c.*50del	NP_690611.1:n.*50del
NR_028033.4:n.645del
NR_028034.4:n.507del
NR_028035.4:n.570del
NR_028036.4:n.708del
NR_135313.2:n.625del
NR_135314.2:n.904del
NR_135315.2:n.657del