Canonical Allele Identifier: CA2610079843
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014708A>C , CM000672.2:g.89014708A>C GRCh38
NC_000010.10:g.90774465A>C , CM000672.1:g.90774465A>C GRCh37
NC_000010.9:g.90764445A>C NCBI36
NG_009089.2:g.29178A>C , LRG_134:g.29178A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1575A>C
ENST00000355740.8:c.*589A>C ENSP00000347979.3:n.*589A>C
ENST00000357339.7:c.*258A>C ENSP00000349896.2:n.*258A>C
ENST00000371857.8:n.2811A>C
ENST00000460510.6:c.*258A>C ENSP00000512812.1:n.*258A>C
ENST00000466081.6:n.2915A>C
ENST00000477270.6:c.*258A>C ENSP00000512813.1:n.*258A>C
ENST00000492756.7:c.*695A>C ENSP00000422453.1:n.*695A>C
ENST00000494799.6:c.*258A>C ENSP00000512834.1:n.*258A>C
ENST00000562983.3:c.*258A>C ENSP00000512845.1:n.*258A>C
ENST00000612663.6:c.*668A>C ENSP00000477997.3:n.*668A>C
ENST00000640140.2:n.1411A>C
ENST00000640250.2:n.765A>C
ENST00000640681.2:n.1370A>C
ENST00000696723.1:n.4899A>C
ENST00000696741.1:n.2904A>C
ENST00000696742.1:n.2631A>C
ENST00000696743.1:n.4034A>C
ENST00000696744.1:n.1305A>C
ENST00000696767.1:n.1600A>C
ENST00000696768.1:c.*589A>C ENSP00000512859.1:n.*589A>C
ENST00000696771.1:c.*258A>C ENSP00000512860.1:n.*258A>C
ENST00000696772.1:n.2869A>C
ENST00000696773.1:n.2608A>C
ENST00000696774.1:n.6376A>C
ENST00000696776.1:c.*258A>C ENSP00000512861.1:n.*258A>C
ENST00000696777.1:n.2674A>C
ENST00000696778.1:n.1702A>C
ENST00000696779.1:c.*258A>C ENSP00000512862.1:n.*258A>C
ENST00000696780.1:c.*258A>C ENSP00000512863.1:n.*258A>C
ENST00000696781.1:c.*258A>C ENSP00000512864.1:n.*258A>C
ENST00000696782.1:c.*668A>C ENSP00000512865.1:n.*668A>C
ENST00000696783.1:n.3134A>C
ENST00000696992.1:n.2383A>C
ENST00000696995.1:n.4795A>C
ENST00000696996.1:n.2708A>C
ENST00000696997.1:c.*896A>C ENSP00000513028.1:n.*896A>C
ENST00000696998.1:n.2520A>C
ENST00000696999.1:c.*258A>C ENSP00000513029.1:n.*258A>C
ENST00000697036.1:c.*682A>C ENSP00000513060.1:n.*682A>C
ENST00000697037.1:n.1301A>C
ENST00000697093.1:n.3502A>C
ENST00000697094.1:n.3849A>C
ENST00000697095.1:c.*2467A>C ENSP00000513104.1:n.*2467A>C
ENST00000697096.1:n.2399A>C
ENST00000697097.1:c.*258A>C ENSP00000513105.1:n.*258A>C
ENST00000562983.2:n.1452A>C
ENST00000690268.1:c.*258A>C ENSP00000509810.1:n.*258A>C
ENST00000355740.7:c.*592A>C ENSP00000347979.3:n.*592A>C
ENST00000640140.1:n.1438A>C
ENST00000640250.1:n.765A>C
ENST00000640681.1:n.1387A>C
ENST00000652046.1:c.*258A>C MANE Select ENSP00000498466.1:n.*258A>C
ENST00000352159.8:c.*583A>C ENSP00000345601.4:n.*583A>C
ENST00000355740.6:c.*258A>C ENSP00000347979.2:n.*258A>C
NM_000043.4:c.*258A>C , LRG_134t1:c.*258A>C NP_000034.1:n.*258A>C
NM_152871.2:c.*258A>C NP_690610.1:n.*258A>C
NM_152872.2:c.*578A>C NP_690611.1:n.*578A>C
NR_028033.2:n.1440A>C
NR_028034.2:n.1302A>C
NR_028035.2:n.1365A>C
NR_028036.2:n.1503A>C
XM_006717819.2:c.*258A>C XP_006717882.1:n.*258A>C
XM_011539764.1:c.*258A>C XP_011538066.1:n.*258A>C
XM_011539765.1:c.*258A>C XP_011538067.1:n.*258A>C
XM_011539766.1:c.*258A>C XP_011538068.1:n.*258A>C
XM_011539767.1:c.*258A>C XP_011538069.1:n.*258A>C
NM_000043.5:c.*258A>C NP_000034.1:n.*258A>C
NM_001320619.1:c.*589A>C NP_001307548.1:n.*589A>C
NM_152871.3:c.*258A>C NP_690610.1:n.*258A>C
NM_152872.3:c.*578A>C NP_690611.1:n.*578A>C
NR_028033.3:n.1412A>C
NR_028034.3:n.1274A>C
NR_028035.3:n.1337A>C
NR_028036.3:n.1475A>C
NR_135313.1:n.1392A>C
NR_135314.1:n.1575A>C
NR_135315.1:n.1328A>C
XM_006717819.3:c.*258A>C XP_006717882.1:n.*258A>C
XM_011539764.2:c.*258A>C XP_011538066.1:n.*258A>C
XM_011539765.2:c.*258A>C XP_011538067.1:n.*258A>C
XM_011539766.2:c.*258A>C XP_011538068.1:n.*258A>C
XM_011539767.3:c.*258A>C XP_011538069.1:n.*258A>C
XR_945732.3:n.1334A>C
XR_945733.2:n.1271A>C
NM_000043.6:c.*258A>C MANE Select NP_000034.1:n.*258A>C
NM_001320619.2:c.*589A>C NP_001307548.1:n.*589A>C
NM_152871.4:c.*258A>C NP_690610.1:n.*258A>C
NM_152872.4:c.*578A>C NP_690611.1:n.*578A>C
NR_028033.4:n.1173A>C
NR_028034.4:n.1035A>C
NR_028035.4:n.1098A>C
NR_028036.4:n.1236A>C
NR_135313.2:n.1153A>C
NR_135314.2:n.1432A>C
NR_135315.2:n.1185A>C