Canonical Allele Identifier: CA645542425

Gene: FAS

Linked Data

• dbSNP Id: rs1848680833
• COSMIC: COSM5703788

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014314_89014315del , CM000672.2:g.89014314_89014315del	GRCh38
NC_000010.10:g.90774071_90774072del , CM000672.1:g.90774071_90774072del	GRCh37
NC_000010.9:g.90764051_90764052del	NCBI36
NG_009089.2:g.28784_28785del , LRG_134:g.28784_28785del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1181_1182del
ENST00000355740.8:c.*195_*196del	ENSP00000347979.3:n.*195_*196del
ENST00000357339.7:c.809_810del	ENSP00000349896.2:p.Tyr270Ter
ENST00000371857.8:n.2417_2418del
ENST00000460510.6:c.155_156del	ENSP00000512812.1:p.Tyr52Ter
ENST00000466081.6:n.2521_2522del
ENST00000477270.6:c.917_918del	ENSP00000512813.1:p.Tyr306Ter
ENST00000479522.6:c.*301_*302del	ENSP00000424113.1:n.*301_*302del
ENST00000484444.6:c.*313_*314del	ENSP00000420975.1:n.*313_*314del
ENST00000488877.6:c.763_764del	ENSP00000425159.1:n.763_764del
ENST00000492756.7:c.*301_*302del	ENSP00000422453.1:n.*301_*302del
ENST00000494799.6:c.155_156del	ENSP00000512834.1:p.Tyr52Ter
ENST00000562983.3:c.155_156del	ENSP00000512845.1:p.Tyr52Ter
ENST00000612663.6:c.*274_*275del	ENSP00000477997.3:n.*274_*275del
ENST00000640140.2:n.1017_1018del
ENST00000640250.2:n.371_372del
ENST00000640681.2:n.976_977del
ENST00000696723.1:n.4505_4506del
ENST00000696741.1:n.2510_2511del
ENST00000696742.1:n.2237_2238del
ENST00000696743.1:n.3640_3641del
ENST00000696744.1:n.911_912del
ENST00000696767.1:n.1206_1207del
ENST00000696768.1:c.*195_*196del	ENSP00000512859.1:n.*195_*196del
ENST00000696769.1:n.2561_2562del
ENST00000696771.1:c.155_156del	ENSP00000512860.1:p.Tyr52Ter
ENST00000696772.1:n.2475_2476del
ENST00000696773.1:n.2214_2215del
ENST00000696774.1:n.5982_5983del
ENST00000696776.1:c.965_966del	ENSP00000512861.1:p.Tyr322Ter
ENST00000696777.1:n.2280_2281del
ENST00000696778.1:n.1308_1309del
ENST00000696779.1:c.479_480del	ENSP00000512862.1:p.Tyr160Ter
ENST00000696780.1:c.902_903del	ENSP00000512863.1:p.Tyr301Ter
ENST00000696781.1:c.617_618del	ENSP00000512864.1:p.Tyr206Ter
ENST00000696782.1:c.*274_*275del	ENSP00000512865.1:n.*274_*275del
ENST00000696783.1:n.2740_2741del
ENST00000696992.1:n.1989_1990del
ENST00000696995.1:n.4401_4402del
ENST00000696996.1:n.2314_2315del
ENST00000696997.1:c.*502_*503del	ENSP00000513028.1:n.*502_*503del
ENST00000696998.1:n.2126_2127del
ENST00000696999.1:c.155_156del	ENSP00000513029.1:p.Tyr52Ter
ENST00000697036.1:c.*288_*289del	ENSP00000513060.1:n.*288_*289del
ENST00000697037.1:n.907_908del
ENST00000697093.1:n.3108_3109del
ENST00000697094.1:n.3455_3456del
ENST00000697095.1:c.*2073_*2074del	ENSP00000513104.1:n.*2073_*2074del
ENST00000697096.1:n.2005_2006del
ENST00000697097.1:c.155_156del	ENSP00000513105.1:p.Tyr52Ter
ENST00000562983.2:n.1058_1059del
ENST00000690268.1:c.953_954del	ENSP00000509810.1:p.Tyr318Ter
ENST00000355740.7:c.*198_*199del	ENSP00000347979.3:n.*198_*199del
ENST00000612663.5:c.*274_*275del	ENSP00000477997.3:n.*274_*275del
ENST00000640140.1:n.1044_1045del
ENST00000640250.1:n.371_372del
ENST00000640681.1:n.993_994del
ENST00000652046.1:c.872_873del MANE Select	ENSP00000498466.1:p.Tyr291Ter
ENST00000352159.8:c.*189_*190del	ENSP00000345601.4:n.*189_*190del
ENST00000355279.2:c.847_848del	ENSP00000347426.2:n.847_848del
ENST00000355740.6:c.872_873del	ENSP00000347979.2:p.Tyr291Ter
ENST00000357339.6:c.809_810del	ENSP00000349896.2:p.Tyr270Ter
ENST00000479522.5:c.*301_*302del	ENSP00000424113.1:n.*301_*302del
ENST00000484444.5:c.*313_*314del	ENSP00000420975.1:n.*313_*314del
ENST00000488877.5:c.*313_*314del	ENSP00000425159.1:n.*313_*314del
ENST00000492756.5:c.700_701del	ENSP00000422453.1:n.700_701del
ENST00000494410.5:c.*230_*231del	ENSP00000423755.1:n.*230_*231del
ENST00000612663.4:c.*219_*220del	ENSP00000477997.2:n.*219_*220del
NM_000043.4:c.872_873del , LRG_134t1:c.872_873del	NP_000034.1:p.Tyr291Ter
NM_152871.2:c.809_810del	NP_690610.1:p.Tyr270Ter
NM_152872.2:c.*184_*185del	NP_690611.1:n.*184_*185del
NR_028033.2:n.1046_1047del
NR_028034.2:n.908_909del
NR_028035.2:n.971_972del
NR_028036.2:n.1109_1110del
XM_006717819.2:c.953_954del	XP_006717882.1:p.Tyr318Ter
XM_011539764.1:c.1034_1035del	XP_011538066.1:p.Tyr345Ter
XM_011539765.1:c.971_972del	XP_011538067.1:p.Tyr324Ter
XM_011539766.1:c.953_954del	XP_011538068.1:p.Tyr318Ter
XM_011539767.1:c.917_918del	XP_011538069.1:p.Tyr306Ter
XR_945732.1:n.940_941del
XR_945733.1:n.877_878del
NM_000043.5:c.872_873del	NP_000034.1:p.Tyr291Ter
NM_001320619.1:c.*195_*196del	NP_001307548.1:n.*195_*196del
NM_152871.3:c.809_810del	NP_690610.1:p.Tyr270Ter
NM_152872.3:c.*184_*185del	NP_690611.1:n.*184_*185del
NR_028033.3:n.1018_1019del
NR_028034.3:n.880_881del
NR_028035.3:n.943_944del
NR_028036.3:n.1081_1082del
NR_135313.1:n.998_999del
NR_135314.1:n.1181_1182del
NR_135315.1:n.934_935del
XM_006717819.3:c.953_954del	XP_006717882.1:p.Tyr318Ter
XM_011539764.2:c.1034_1035del	XP_011538066.1:p.Tyr345Ter
XM_011539765.2:c.971_972del	XP_011538067.1:p.Tyr324Ter
XM_011539766.2:c.953_954del	XP_011538068.1:p.Tyr318Ter
XM_011539767.3:c.917_918del	XP_011538069.1:p.Tyr306Ter
XR_945732.3:n.940_941del
XR_945733.2:n.877_878del
NM_000043.6:c.872_873del MANE Select	NP_000034.1:p.Tyr291Ter
NM_001320619.2:c.*195_*196del	NP_001307548.1:n.*195_*196del
NM_152871.4:c.809_810del	NP_690610.1:p.Tyr270Ter
NM_152872.4:c.*184_*185del	NP_690611.1:n.*184_*185del
NR_028033.4:n.779_780del
NR_028034.4:n.641_642del
NR_028035.4:n.704_705del
NR_028036.4:n.842_843del
NR_135313.2:n.759_760del
NR_135314.2:n.1038_1039del
NR_135315.2:n.791_792del