Canonical Allele Identifier: CA2610079787
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014656A>C , CM000672.2:g.89014656A>C GRCh38
NC_000010.10:g.90774413A>C , CM000672.1:g.90774413A>C GRCh37
NC_000010.9:g.90764393A>C NCBI36
NG_009089.2:g.29126A>C , LRG_134:g.29126A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1523A>C
ENST00000355740.8:c.*537A>C ENSP00000347979.3:n.*537A>C
ENST00000357339.7:c.*206A>C ENSP00000349896.2:n.*206A>C
ENST00000371857.8:n.2759A>C
ENST00000460510.6:c.*206A>C ENSP00000512812.1:n.*206A>C
ENST00000466081.6:n.2863A>C
ENST00000477270.6:c.*206A>C ENSP00000512813.1:n.*206A>C
ENST00000492756.7:c.*643A>C ENSP00000422453.1:n.*643A>C
ENST00000494799.6:c.*206A>C ENSP00000512834.1:n.*206A>C
ENST00000562983.3:c.*206A>C ENSP00000512845.1:n.*206A>C
ENST00000612663.6:c.*616A>C ENSP00000477997.3:n.*616A>C
ENST00000640140.2:n.1359A>C
ENST00000640250.2:n.713A>C
ENST00000640681.2:n.1318A>C
ENST00000696723.1:n.4847A>C
ENST00000696741.1:n.2852A>C
ENST00000696742.1:n.2579A>C
ENST00000696743.1:n.3982A>C
ENST00000696744.1:n.1253A>C
ENST00000696767.1:n.1548A>C
ENST00000696768.1:c.*537A>C ENSP00000512859.1:n.*537A>C
ENST00000696771.1:c.*206A>C ENSP00000512860.1:n.*206A>C
ENST00000696772.1:n.2817A>C
ENST00000696773.1:n.2556A>C
ENST00000696774.1:n.6324A>C
ENST00000696776.1:c.*206A>C ENSP00000512861.1:n.*206A>C
ENST00000696777.1:n.2622A>C
ENST00000696778.1:n.1650A>C
ENST00000696779.1:c.*206A>C ENSP00000512862.1:n.*206A>C
ENST00000696780.1:c.*206A>C ENSP00000512863.1:n.*206A>C
ENST00000696781.1:c.*206A>C ENSP00000512864.1:n.*206A>C
ENST00000696782.1:c.*616A>C ENSP00000512865.1:n.*616A>C
ENST00000696783.1:n.3082A>C
ENST00000696992.1:n.2331A>C
ENST00000696995.1:n.4743A>C
ENST00000696996.1:n.2656A>C
ENST00000696997.1:c.*844A>C ENSP00000513028.1:n.*844A>C
ENST00000696998.1:n.2468A>C
ENST00000696999.1:c.*206A>C ENSP00000513029.1:n.*206A>C
ENST00000697036.1:c.*630A>C ENSP00000513060.1:n.*630A>C
ENST00000697037.1:n.1249A>C
ENST00000697093.1:n.3450A>C
ENST00000697094.1:n.3797A>C
ENST00000697095.1:c.*2415A>C ENSP00000513104.1:n.*2415A>C
ENST00000697096.1:n.2347A>C
ENST00000697097.1:c.*206A>C ENSP00000513105.1:n.*206A>C
ENST00000562983.2:n.1400A>C
ENST00000690268.1:c.*206A>C ENSP00000509810.1:n.*206A>C
ENST00000355740.7:c.*540A>C ENSP00000347979.3:n.*540A>C
ENST00000640140.1:n.1386A>C
ENST00000640250.1:n.713A>C
ENST00000640681.1:n.1335A>C
ENST00000652046.1:c.*206A>C MANE Select ENSP00000498466.1:n.*206A>C
ENST00000352159.8:c.*531A>C ENSP00000345601.4:n.*531A>C
ENST00000355740.6:c.*206A>C ENSP00000347979.2:n.*206A>C
NM_000043.4:c.*206A>C , LRG_134t1:c.*206A>C NP_000034.1:n.*206A>C
NM_152871.2:c.*206A>C NP_690610.1:n.*206A>C
NM_152872.2:c.*526A>C NP_690611.1:n.*526A>C
NR_028033.2:n.1388A>C
NR_028034.2:n.1250A>C
NR_028035.2:n.1313A>C
NR_028036.2:n.1451A>C
XM_006717819.2:c.*206A>C XP_006717882.1:n.*206A>C
XM_011539764.1:c.*206A>C XP_011538066.1:n.*206A>C
XM_011539765.1:c.*206A>C XP_011538067.1:n.*206A>C
XM_011539766.1:c.*206A>C XP_011538068.1:n.*206A>C
XM_011539767.1:c.*206A>C XP_011538069.1:n.*206A>C
NM_000043.5:c.*206A>C NP_000034.1:n.*206A>C
NM_001320619.1:c.*537A>C NP_001307548.1:n.*537A>C
NM_152871.3:c.*206A>C NP_690610.1:n.*206A>C
NM_152872.3:c.*526A>C NP_690611.1:n.*526A>C
NR_028033.3:n.1360A>C
NR_028034.3:n.1222A>C
NR_028035.3:n.1285A>C
NR_028036.3:n.1423A>C
NR_135313.1:n.1340A>C
NR_135314.1:n.1523A>C
NR_135315.1:n.1276A>C
XM_006717819.3:c.*206A>C XP_006717882.1:n.*206A>C
XM_011539764.2:c.*206A>C XP_011538066.1:n.*206A>C
XM_011539765.2:c.*206A>C XP_011538067.1:n.*206A>C
XM_011539766.2:c.*206A>C XP_011538068.1:n.*206A>C
XM_011539767.3:c.*206A>C XP_011538069.1:n.*206A>C
XR_945732.3:n.1282A>C
XR_945733.2:n.1219A>C
NM_000043.6:c.*206A>C MANE Select NP_000034.1:n.*206A>C
NM_001320619.2:c.*537A>C NP_001307548.1:n.*537A>C
NM_152871.4:c.*206A>C NP_690610.1:n.*206A>C
NM_152872.4:c.*526A>C NP_690611.1:n.*526A>C
NR_028033.4:n.1121A>C
NR_028034.4:n.983A>C
NR_028035.4:n.1046A>C
NR_028036.4:n.1184A>C
NR_135313.2:n.1101A>C
NR_135314.2:n.1380A>C
NR_135315.2:n.1133A>C