Canonical Allele Identifier: CA377510213
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs1848688438

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014407C>T , CM000672.2:g.89014407C>T GRCh38
NC_000010.10:g.90774164C>T , CM000672.1:g.90774164C>T GRCh37
NC_000010.9:g.90764144C>T NCBI36
NG_009089.2:g.28877C>T , LRG_134:g.28877C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1274C>T
ENST00000355740.8:c.*288C>T ENSP00000347979.3:n.*288C>T
ENST00000357339.7:c.902C>T ENSP00000349896.2:p.Ser301Leu
ENST00000371857.8:n.2510C>T
ENST00000460510.6:c.248C>T ENSP00000512812.1:p.Ser83Leu
ENST00000466081.6:n.2614C>T
ENST00000477270.6:c.1010C>T ENSP00000512813.1:p.Ser337Leu
ENST00000479522.6:c.*394C>T ENSP00000424113.1:n.*394C>T
ENST00000484444.6:c.*406C>T ENSP00000420975.1:n.*406C>T
ENST00000488877.6:c.856C>T ENSP00000425159.1:n.856C>T
ENST00000492756.7:c.*394C>T ENSP00000422453.1:n.*394C>T
ENST00000494799.6:c.248C>T ENSP00000512834.1:p.Ser83Leu
ENST00000562983.3:c.248C>T ENSP00000512845.1:p.Ser83Leu
ENST00000612663.6:c.*367C>T ENSP00000477997.3:n.*367C>T
ENST00000640140.2:n.1110C>T
ENST00000640250.2:n.464C>T
ENST00000640681.2:n.1069C>T
ENST00000696723.1:n.4598C>T
ENST00000696741.1:n.2603C>T
ENST00000696742.1:n.2330C>T
ENST00000696743.1:n.3733C>T
ENST00000696744.1:n.1004C>T
ENST00000696767.1:n.1299C>T
ENST00000696768.1:c.*288C>T ENSP00000512859.1:n.*288C>T
ENST00000696769.1:n.2654C>T
ENST00000696771.1:c.248C>T ENSP00000512860.1:p.Ser83Leu
ENST00000696772.1:n.2568C>T
ENST00000696773.1:n.2307C>T
ENST00000696774.1:n.6075C>T
ENST00000696776.1:c.1058C>T ENSP00000512861.1:p.Ser353Leu
ENST00000696777.1:n.2373C>T
ENST00000696778.1:n.1401C>T
ENST00000696779.1:c.572C>T ENSP00000512862.1:p.Ser191Leu
ENST00000696780.1:c.995C>T ENSP00000512863.1:p.Ser332Leu
ENST00000696781.1:c.710C>T ENSP00000512864.1:p.Ser237Leu
ENST00000696782.1:c.*367C>T ENSP00000512865.1:n.*367C>T
ENST00000696783.1:n.2833C>T
ENST00000696992.1:n.2082C>T
ENST00000696995.1:n.4494C>T
ENST00000696996.1:n.2407C>T
ENST00000696997.1:c.*595C>T ENSP00000513028.1:n.*595C>T
ENST00000696998.1:n.2219C>T
ENST00000696999.1:c.248C>T ENSP00000513029.1:p.Ser83Leu
ENST00000697036.1:c.*381C>T ENSP00000513060.1:n.*381C>T
ENST00000697037.1:n.1000C>T
ENST00000697093.1:n.3201C>T
ENST00000697094.1:n.3548C>T
ENST00000697095.1:c.*2166C>T ENSP00000513104.1:n.*2166C>T
ENST00000697096.1:n.2098C>T
ENST00000697097.1:c.248C>T ENSP00000513105.1:p.Ser83Leu
ENST00000562983.2:n.1151C>T
ENST00000690268.1:c.1046C>T ENSP00000509810.1:p.Ser349Leu
ENST00000355740.7:c.*291C>T ENSP00000347979.3:n.*291C>T
ENST00000612663.5:c.*367C>T ENSP00000477997.3:n.*367C>T
ENST00000640140.1:n.1137C>T
ENST00000640250.1:n.464C>T
ENST00000640681.1:n.1086C>T
ENST00000652046.1:c.965C>T MANE Select ENSP00000498466.1:p.Ser322Leu
ENST00000352159.8:c.*282C>T ENSP00000345601.4:n.*282C>T
ENST00000355279.2:c.940C>T ENSP00000347426.2:n.940C>T
ENST00000355740.6:c.965C>T ENSP00000347979.2:p.Ser322Leu
ENST00000357339.6:c.902C>T ENSP00000349896.2:p.Ser301Leu
ENST00000479522.5:c.*394C>T ENSP00000424113.1:n.*394C>T
ENST00000484444.5:c.*406C>T ENSP00000420975.1:n.*406C>T
ENST00000488877.5:c.*406C>T ENSP00000425159.1:n.*406C>T
ENST00000492756.5:c.793C>T ENSP00000422453.1:n.793C>T
ENST00000494410.5:c.*323C>T ENSP00000423755.1:n.*323C>T
ENST00000612663.4:c.*312C>T ENSP00000477997.2:n.*312C>T
NM_000043.4:c.965C>T , LRG_134t1:c.965C>T NP_000034.1:p.Ser322Leu
NM_152871.2:c.902C>T NP_690610.1:p.Ser301Leu
NM_152872.2:c.*277C>T NP_690611.1:n.*277C>T
NR_028033.2:n.1139C>T
NR_028034.2:n.1001C>T
NR_028035.2:n.1064C>T
NR_028036.2:n.1202C>T
XM_006717819.2:c.1046C>T XP_006717882.1:p.Ser349Leu
XM_011539764.1:c.1127C>T XP_011538066.1:p.Ser376Leu
XM_011539765.1:c.1064C>T XP_011538067.1:p.Ser355Leu
XM_011539766.1:c.1046C>T XP_011538068.1:p.Ser349Leu
XM_011539767.1:c.1010C>T XP_011538069.1:p.Ser337Leu
XR_945733.1:n.970C>T
NM_000043.5:c.965C>T NP_000034.1:p.Ser322Leu
NM_001320619.1:c.*288C>T NP_001307548.1:n.*288C>T
NM_152871.3:c.902C>T NP_690610.1:p.Ser301Leu
NM_152872.3:c.*277C>T NP_690611.1:n.*277C>T
NR_028033.3:n.1111C>T
NR_028034.3:n.973C>T
NR_028035.3:n.1036C>T
NR_028036.3:n.1174C>T
NR_135313.1:n.1091C>T
NR_135314.1:n.1274C>T
NR_135315.1:n.1027C>T
XM_006717819.3:c.1046C>T XP_006717882.1:p.Ser349Leu
XM_011539764.2:c.1127C>T XP_011538066.1:p.Ser376Leu
XM_011539765.2:c.1064C>T XP_011538067.1:p.Ser355Leu
XM_011539766.2:c.1046C>T XP_011538068.1:p.Ser349Leu
XM_011539767.3:c.1010C>T XP_011538069.1:p.Ser337Leu
XR_945732.3:n.1033C>T
XR_945733.2:n.970C>T
NM_000043.6:c.965C>T MANE Select NP_000034.1:p.Ser322Leu
NM_001320619.2:c.*288C>T NP_001307548.1:n.*288C>T
NM_152871.4:c.902C>T NP_690610.1:p.Ser301Leu
NM_152872.4:c.*277C>T NP_690611.1:n.*277C>T
NR_028033.4:n.872C>T
NR_028034.4:n.734C>T
NR_028035.4:n.797C>T
NR_028036.4:n.935C>T
NR_135313.2:n.852C>T
NR_135314.2:n.1131C>T
NR_135315.2:n.884C>T