Canonical Allele Identifier: CA2610079620
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014432_89014433del , CM000672.2:g.89014432_89014433del GRCh38
NC_000010.10:g.90774189_90774190del , CM000672.1:g.90774189_90774190del GRCh37
NC_000010.9:g.90764169_90764170del NCBI36
NG_009089.2:g.28902_28903del , LRG_134:g.28902_28903del

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1299_1300del
ENST00000355740.8:c.*313_*314del ENSP00000347979.3:n.*313_*314del
ENST00000357339.7:c.927_928del ENSP00000349896.2:p.Glu309AspfsTer8
ENST00000371857.8:n.2535_2536del
ENST00000460510.6:c.273_274del ENSP00000512812.1:p.Glu91AspfsTer8
ENST00000466081.6:n.2639_2640del
ENST00000477270.6:c.1035_1036del ENSP00000512813.1:p.Glu345AspfsTer8
ENST00000479522.6:c.*419_*420del ENSP00000424113.1:n.*419_*420del
ENST00000484444.6:c.*431_*432del ENSP00000420975.1:n.*431_*432del
ENST00000488877.6:c.881_882del ENSP00000425159.1:n.881_882del
ENST00000492756.7:c.*419_*420del ENSP00000422453.1:n.*419_*420del
ENST00000494799.6:c.273_274del ENSP00000512834.1:p.Glu91AspfsTer8
ENST00000562983.3:c.273_274del ENSP00000512845.1:p.Glu91AspfsTer8
ENST00000612663.6:c.*392_*393del ENSP00000477997.3:n.*392_*393del
ENST00000640140.2:n.1135_1136del
ENST00000640250.2:n.489_490del
ENST00000640681.2:n.1094_1095del
ENST00000696723.1:n.4623_4624del
ENST00000696741.1:n.2628_2629del
ENST00000696742.1:n.2355_2356del
ENST00000696743.1:n.3758_3759del
ENST00000696744.1:n.1029_1030del
ENST00000696767.1:n.1324_1325del
ENST00000696768.1:c.*313_*314del ENSP00000512859.1:n.*313_*314del
ENST00000696769.1:n.2679_2680del
ENST00000696771.1:c.273_274del ENSP00000512860.1:p.Glu91AspfsTer8
ENST00000696772.1:n.2593_2594del
ENST00000696773.1:n.2332_2333del
ENST00000696774.1:n.6100_6101del
ENST00000696776.1:c.1083_1084del ENSP00000512861.1:p.Glu361AspfsTer8
ENST00000696777.1:n.2398_2399del
ENST00000696778.1:n.1426_1427del
ENST00000696779.1:c.597_598del ENSP00000512862.1:p.Glu199AspfsTer8
ENST00000696780.1:c.1020_1021del ENSP00000512863.1:p.Glu340AspfsTer8
ENST00000696781.1:c.735_736del ENSP00000512864.1:p.Glu245AspfsTer8
ENST00000696782.1:c.*392_*393del ENSP00000512865.1:n.*392_*393del
ENST00000696783.1:n.2858_2859del
ENST00000696992.1:n.2107_2108del
ENST00000696995.1:n.4519_4520del
ENST00000696996.1:n.2432_2433del
ENST00000696997.1:c.*620_*621del ENSP00000513028.1:n.*620_*621del
ENST00000696998.1:n.2244_2245del
ENST00000696999.1:c.273_274del ENSP00000513029.1:p.Glu91AspfsTer8
ENST00000697036.1:c.*406_*407del ENSP00000513060.1:n.*406_*407del
ENST00000697037.1:n.1025_1026del
ENST00000697093.1:n.3226_3227del
ENST00000697094.1:n.3573_3574del
ENST00000697095.1:c.*2191_*2192del ENSP00000513104.1:n.*2191_*2192del
ENST00000697096.1:n.2123_2124del
ENST00000697097.1:c.273_274del ENSP00000513105.1:p.Glu91AspfsTer8
ENST00000562983.2:n.1176_1177del
ENST00000690268.1:c.1071_1072del ENSP00000509810.1:p.Glu357AspfsTer8
ENST00000355740.7:c.*316_*317del ENSP00000347979.3:n.*316_*317del
ENST00000612663.5:c.*392_*393del ENSP00000477997.3:n.*392_*393del
ENST00000640140.1:n.1162_1163del
ENST00000640250.1:n.489_490del
ENST00000640681.1:n.1111_1112del
ENST00000652046.1:c.990_991del MANE Select ENSP00000498466.1:p.Glu330AspfsTer8
ENST00000352159.8:c.*307_*308del ENSP00000345601.4:n.*307_*308del
ENST00000355279.2:c.965_966del ENSP00000347426.2:n.965_966del
ENST00000355740.6:c.990_991del ENSP00000347979.2:p.Glu330AspfsTer8
ENST00000357339.6:c.927_928del ENSP00000349896.2:p.Glu309AspfsTer?
ENST00000479522.5:c.*419_*420del ENSP00000424113.1:n.*419_*420del
ENST00000484444.5:c.*431_*432del ENSP00000420975.1:n.*431_*432del
ENST00000488877.5:c.*431_*432del ENSP00000425159.1:n.*431_*432del
ENST00000492756.5:c.818_819del ENSP00000422453.1:n.818_819del
ENST00000494410.5:c.*348_*349del ENSP00000423755.1:n.*348_*349del
ENST00000612663.4:c.*337_*338del ENSP00000477997.2:n.*337_*338del
NM_000043.4:c.990_991del , LRG_134t1:c.990_991del NP_000034.1:p.Glu330AspfsTer8
NM_152871.2:c.927_928del NP_690610.1:p.Glu309AspfsTer8
NM_152872.2:c.*302_*303del NP_690611.1:n.*302_*303del
NR_028033.2:n.1164_1165del
NR_028034.2:n.1026_1027del
NR_028035.2:n.1089_1090del
NR_028036.2:n.1227_1228del
XM_006717819.2:c.1071_1072del XP_006717882.1:p.Glu357AspfsTer8
XM_011539764.1:c.1152_1153del XP_011538066.1:p.Glu384AspfsTer8
XM_011539765.1:c.1089_1090del XP_011538067.1:p.Glu363AspfsTer8
XM_011539766.1:c.1071_1072del XP_011538068.1:p.Glu357AspfsTer8
XM_011539767.1:c.1035_1036del XP_011538069.1:p.Glu345AspfsTer8
XR_945733.1:n.995_996del
NM_000043.5:c.990_991del NP_000034.1:p.Glu330AspfsTer8
NM_001320619.1:c.*313_*314del NP_001307548.1:n.*313_*314del
NM_152871.3:c.927_928del NP_690610.1:p.Glu309AspfsTer8
NM_152872.3:c.*302_*303del NP_690611.1:n.*302_*303del
NR_028033.3:n.1136_1137del
NR_028034.3:n.998_999del
NR_028035.3:n.1061_1062del
NR_028036.3:n.1199_1200del
NR_135313.1:n.1116_1117del
NR_135314.1:n.1299_1300del
NR_135315.1:n.1052_1053del
XM_006717819.3:c.1071_1072del XP_006717882.1:p.Glu357AspfsTer8
XM_011539764.2:c.1152_1153del XP_011538066.1:p.Glu384AspfsTer8
XM_011539765.2:c.1089_1090del XP_011538067.1:p.Glu363AspfsTer8
XM_011539766.2:c.1071_1072del XP_011538068.1:p.Glu357AspfsTer8
XM_011539767.3:c.1035_1036del XP_011538069.1:p.Glu345AspfsTer8
XR_945732.3:n.1058_1059del
XR_945733.2:n.995_996del
NM_000043.6:c.990_991del MANE Select NP_000034.1:p.Glu330AspfsTer8
NM_001320619.2:c.*313_*314del NP_001307548.1:n.*313_*314del
NM_152871.4:c.927_928del NP_690610.1:p.Glu309AspfsTer8
NM_152872.4:c.*302_*303del NP_690611.1:n.*302_*303del
NR_028033.4:n.897_898del
NR_028034.4:n.759_760del
NR_028035.4:n.822_823del
NR_028036.4:n.960_961del
NR_135313.2:n.877_878del
NR_135314.2:n.1156_1157del
NR_135315.2:n.909_910del