Canonical Allele Identifier: CA2722391623
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs2119450989

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014506dup , CM000672.2:g.89014506dup GRCh38
NC_000010.10:g.90774263dup , CM000672.1:g.90774263dup GRCh37
NC_000010.9:g.90764243dup NCBI36
NG_009089.2:g.28976dup , LRG_134:g.28976dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1373dup
ENST00000355740.8:c.*387dup ENSP00000347979.3:n.*387dup
ENST00000357339.7:c.*56dup ENSP00000349896.2:n.*56dup
ENST00000371857.8:n.2609dup
ENST00000460510.6:c.*56dup ENSP00000512812.1:n.*56dup
ENST00000466081.6:n.2713dup
ENST00000477270.6:c.*56dup ENSP00000512813.1:n.*56dup
ENST00000479522.6:c.*493dup ENSP00000424113.1:n.*493dup
ENST00000484444.6:c.*505dup ENSP00000420975.1:n.*505dup
ENST00000488877.6:c.955dup ENSP00000425159.1:n.955dup
ENST00000492756.7:c.*493dup ENSP00000422453.1:n.*493dup
ENST00000494799.6:c.*56dup ENSP00000512834.1:n.*56dup
ENST00000562983.3:c.*56dup ENSP00000512845.1:n.*56dup
ENST00000612663.6:c.*466dup ENSP00000477997.3:n.*466dup
ENST00000640140.2:n.1209dup
ENST00000640250.2:n.563dup
ENST00000640681.2:n.1168dup
ENST00000696723.1:n.4697dup
ENST00000696741.1:n.2702dup
ENST00000696742.1:n.2429dup
ENST00000696743.1:n.3832dup
ENST00000696744.1:n.1103dup
ENST00000696767.1:n.1398dup
ENST00000696768.1:c.*387dup ENSP00000512859.1:n.*387dup
ENST00000696769.1:n.2753dup
ENST00000696771.1:c.*56dup ENSP00000512860.1:n.*56dup
ENST00000696772.1:n.2667dup
ENST00000696773.1:n.2406dup
ENST00000696774.1:n.6174dup
ENST00000696776.1:c.*56dup ENSP00000512861.1:n.*56dup
ENST00000696777.1:n.2472dup
ENST00000696778.1:n.1500dup
ENST00000696779.1:c.*56dup ENSP00000512862.1:n.*56dup
ENST00000696780.1:c.*56dup ENSP00000512863.1:n.*56dup
ENST00000696781.1:c.*56dup ENSP00000512864.1:n.*56dup
ENST00000696782.1:c.*466dup ENSP00000512865.1:n.*466dup
ENST00000696783.1:n.2932dup
ENST00000696992.1:n.2181dup
ENST00000696995.1:n.4593dup
ENST00000696996.1:n.2506dup
ENST00000696997.1:c.*694dup ENSP00000513028.1:n.*694dup
ENST00000696998.1:n.2318dup
ENST00000696999.1:c.*56dup ENSP00000513029.1:n.*56dup
ENST00000697036.1:c.*480dup ENSP00000513060.1:n.*480dup
ENST00000697037.1:n.1099dup
ENST00000697093.1:n.3300dup
ENST00000697094.1:n.3647dup
ENST00000697095.1:c.*2265dup ENSP00000513104.1:n.*2265dup
ENST00000697096.1:n.2197dup
ENST00000697097.1:c.*56dup ENSP00000513105.1:n.*56dup
ENST00000562983.2:n.1250dup
ENST00000690268.1:c.*56dup ENSP00000509810.1:n.*56dup
ENST00000355740.7:c.*390dup ENSP00000347979.3:n.*390dup
ENST00000640140.1:n.1236dup
ENST00000640250.1:n.563dup
ENST00000640681.1:n.1185dup
ENST00000652046.1:c.*56dup MANE Select ENSP00000498466.1:n.*56dup
ENST00000352159.8:c.*381dup ENSP00000345601.4:n.*381dup
ENST00000355740.6:c.*56dup ENSP00000347979.2:n.*56dup
ENST00000479522.5:c.*493dup ENSP00000424113.1:n.*493dup
ENST00000484444.5:c.*505dup ENSP00000420975.1:n.*505dup
ENST00000494410.5:c.*422dup ENSP00000423755.1:n.*422dup
NM_000043.4:c.*56dup , LRG_134t1:c.*56dup NP_000034.1:n.*56dup
NM_152871.2:c.*56dup NP_690610.1:n.*56dup
NM_152872.2:c.*376dup NP_690611.1:n.*376dup
NR_028033.2:n.1238dup
NR_028034.2:n.1100dup
NR_028035.2:n.1163dup
NR_028036.2:n.1301dup
XM_006717819.2:c.*56dup XP_006717882.1:n.*56dup
XM_011539764.1:c.*56dup XP_011538066.1:n.*56dup
XM_011539765.1:c.*56dup XP_011538067.1:n.*56dup
XM_011539766.1:c.*56dup XP_011538068.1:n.*56dup
XM_011539767.1:c.*56dup XP_011538069.1:n.*56dup
NM_000043.5:c.*56dup NP_000034.1:n.*56dup
NM_001320619.1:c.*387dup NP_001307548.1:n.*387dup
NM_152871.3:c.*56dup NP_690610.1:n.*56dup
NM_152872.3:c.*376dup NP_690611.1:n.*376dup
NR_028033.3:n.1210dup
NR_028034.3:n.1072dup
NR_028035.3:n.1135dup
NR_028036.3:n.1273dup
NR_135313.1:n.1190dup
NR_135314.1:n.1373dup
NR_135315.1:n.1126dup
XM_006717819.3:c.*56dup XP_006717882.1:n.*56dup
XM_011539764.2:c.*56dup XP_011538066.1:n.*56dup
XM_011539765.2:c.*56dup XP_011538067.1:n.*56dup
XM_011539766.2:c.*56dup XP_011538068.1:n.*56dup
XM_011539767.3:c.*56dup XP_011538069.1:n.*56dup
XR_945732.3:n.1132dup
XR_945733.2:n.1069dup
NM_000043.6:c.*56dup MANE Select NP_000034.1:n.*56dup
NM_001320619.2:c.*387dup NP_001307548.1:n.*387dup
NM_152871.4:c.*56dup NP_690610.1:n.*56dup
NM_152872.4:c.*376dup NP_690611.1:n.*376dup
NR_028033.4:n.971dup
NR_028034.4:n.833dup
NR_028035.4:n.896dup
NR_028036.4:n.1034dup
NR_135313.2:n.951dup
NR_135314.2:n.1230dup
NR_135315.2:n.983dup