Canonical Allele Identifier: CA1926639497
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014590A= , CM000672.2:g.89014590A= GRCh38
NC_000010.10:g.90774347A= , CM000672.1:g.90774347A= GRCh37
NC_000010.9:g.90764327A= NCBI36
NG_009089.2:g.29060A= , LRG_134:g.29060A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1457A=
ENST00000355740.8:c.*471A= ENSP00000347979.3:n.*471A=
ENST00000357339.7:c.*140A= ENSP00000349896.2:n.*140A=
ENST00000371857.8:n.2693A=
ENST00000460510.6:c.*140A= ENSP00000512812.1:n.*140A=
ENST00000466081.6:n.2797A=
ENST00000477270.6:c.*140A= ENSP00000512813.1:n.*140A=
ENST00000488877.6:c.1039A= ENSP00000425159.1:n.1039A=
ENST00000492756.7:c.*577A= ENSP00000422453.1:n.*577A=
ENST00000494799.6:c.*140A= ENSP00000512834.1:n.*140A=
ENST00000562983.3:c.*140A= ENSP00000512845.1:n.*140A=
ENST00000612663.6:c.*550A= ENSP00000477997.3:n.*550A=
ENST00000640140.2:n.1293A=
ENST00000640250.2:n.647A=
ENST00000640681.2:n.1252A=
ENST00000696723.1:n.4781A=
ENST00000696741.1:n.2786A=
ENST00000696742.1:n.2513A=
ENST00000696743.1:n.3916A=
ENST00000696744.1:n.1187A=
ENST00000696767.1:n.1482A=
ENST00000696768.1:c.*471A= ENSP00000512859.1:n.*471A=
ENST00000696771.1:c.*140A= ENSP00000512860.1:n.*140A=
ENST00000696772.1:n.2751A=
ENST00000696773.1:n.2490A=
ENST00000696774.1:n.6258A=
ENST00000696776.1:c.*140A= ENSP00000512861.1:n.*140A=
ENST00000696777.1:n.2556A=
ENST00000696778.1:n.1584A=
ENST00000696779.1:c.*140A= ENSP00000512862.1:n.*140A=
ENST00000696780.1:c.*140A= ENSP00000512863.1:n.*140A=
ENST00000696781.1:c.*140A= ENSP00000512864.1:n.*140A=
ENST00000696782.1:c.*550A= ENSP00000512865.1:n.*550A=
ENST00000696783.1:n.3016A=
ENST00000696992.1:n.2265A=
ENST00000696995.1:n.4677A=
ENST00000696996.1:n.2590A=
ENST00000696997.1:c.*778A= ENSP00000513028.1:n.*778A=
ENST00000696998.1:n.2402A=
ENST00000696999.1:c.*140A= ENSP00000513029.1:n.*140A=
ENST00000697036.1:c.*564A= ENSP00000513060.1:n.*564A=
ENST00000697037.1:n.1183A=
ENST00000697093.1:n.3384A=
ENST00000697094.1:n.3731A=
ENST00000697095.1:c.*2349A= ENSP00000513104.1:n.*2349A=
ENST00000697096.1:n.2281A=
ENST00000697097.1:c.*140A= ENSP00000513105.1:n.*140A=
ENST00000562983.2:n.1334A=
ENST00000690268.1:c.*140A= ENSP00000509810.1:n.*140A=
ENST00000355740.7:c.*474A= ENSP00000347979.3:n.*474A=
ENST00000640140.1:n.1320A=
ENST00000640250.1:n.647A=
ENST00000640681.1:n.1269A=
ENST00000652046.1:c.*140A= MANE Select ENSP00000498466.1:n.*140A=
ENST00000352159.8:c.*465A= ENSP00000345601.4:n.*465A=
ENST00000355740.6:c.*140A= ENSP00000347979.2:n.*140A=
ENST00000484444.5:c.*589A= ENSP00000420975.1:n.*589A=
NM_000043.4:c.*140A= , LRG_134t1:c.*140A= NP_000034.1:n.*140A=
NM_152871.2:c.*140A= NP_690610.1:n.*140A=
NM_152872.2:c.*460A= NP_690611.1:n.*460A=
NR_028033.2:n.1322A=
NR_028034.2:n.1184A=
NR_028035.2:n.1247A=
NR_028036.2:n.1385A=
XM_006717819.2:c.*140A= XP_006717882.1:n.*140A=
XM_011539764.1:c.*140A= XP_011538066.1:n.*140A=
XM_011539765.1:c.*140A= XP_011538067.1:n.*140A=
XM_011539766.1:c.*140A= XP_011538068.1:n.*140A=
XM_011539767.1:c.*140A= XP_011538069.1:n.*140A=
NM_000043.5:c.*140A= NP_000034.1:n.*140A=
NM_001320619.1:c.*471A= NP_001307548.1:n.*471A=
NM_152871.3:c.*140A= NP_690610.1:n.*140A=
NM_152872.3:c.*460A= NP_690611.1:n.*460A=
NR_028033.3:n.1294A=
NR_028034.3:n.1156A=
NR_028035.3:n.1219A=
NR_028036.3:n.1357A=
NR_135313.1:n.1274A=
NR_135314.1:n.1457A=
NR_135315.1:n.1210A=
XM_006717819.3:c.*140A= XP_006717882.1:n.*140A=
XM_011539764.2:c.*140A= XP_011538066.1:n.*140A=
XM_011539765.2:c.*140A= XP_011538067.1:n.*140A=
XM_011539766.2:c.*140A= XP_011538068.1:n.*140A=
XM_011539767.3:c.*140A= XP_011538069.1:n.*140A=
XR_945732.3:n.1216A=
XR_945733.2:n.1153A=
NM_000043.6:c.*140A= MANE Select NP_000034.1:n.*140A=
NM_001320619.2:c.*471A= NP_001307548.1:n.*471A=
NM_152871.4:c.*140A= NP_690610.1:n.*140A=
NM_152872.4:c.*460A= NP_690611.1:n.*460A=
NR_028033.4:n.1055A=
NR_028034.4:n.917A=
NR_028035.4:n.980A=
NR_028036.4:n.1118A=
NR_135313.2:n.1035A=
NR_135314.2:n.1314A=
NR_135315.2:n.1067A=