Canonical Allele Identifier: CA1926639527
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014660A= , CM000672.2:g.89014660A= GRCh38
NC_000010.10:g.90774417A= , CM000672.1:g.90774417A= GRCh37
NC_000010.9:g.90764397A= NCBI36
NG_009089.2:g.29130A= , LRG_134:g.29130A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1527A=
ENST00000355740.8:c.*541A= ENSP00000347979.3:n.*541A=
ENST00000357339.7:c.*210A= ENSP00000349896.2:n.*210A=
ENST00000371857.8:n.2763A=
ENST00000460510.6:c.*210A= ENSP00000512812.1:n.*210A=
ENST00000466081.6:n.2867A=
ENST00000477270.6:c.*210A= ENSP00000512813.1:n.*210A=
ENST00000492756.7:c.*647A= ENSP00000422453.1:n.*647A=
ENST00000494799.6:c.*210A= ENSP00000512834.1:n.*210A=
ENST00000562983.3:c.*210A= ENSP00000512845.1:n.*210A=
ENST00000612663.6:c.*620A= ENSP00000477997.3:n.*620A=
ENST00000640140.2:n.1363A=
ENST00000640250.2:n.717A=
ENST00000640681.2:n.1322A=
ENST00000696723.1:n.4851A=
ENST00000696741.1:n.2856A=
ENST00000696742.1:n.2583A=
ENST00000696743.1:n.3986A=
ENST00000696744.1:n.1257A=
ENST00000696767.1:n.1552A=
ENST00000696768.1:c.*541A= ENSP00000512859.1:n.*541A=
ENST00000696771.1:c.*210A= ENSP00000512860.1:n.*210A=
ENST00000696772.1:n.2821A=
ENST00000696773.1:n.2560A=
ENST00000696774.1:n.6328A=
ENST00000696776.1:c.*210A= ENSP00000512861.1:n.*210A=
ENST00000696777.1:n.2626A=
ENST00000696778.1:n.1654A=
ENST00000696779.1:c.*210A= ENSP00000512862.1:n.*210A=
ENST00000696780.1:c.*210A= ENSP00000512863.1:n.*210A=
ENST00000696781.1:c.*210A= ENSP00000512864.1:n.*210A=
ENST00000696782.1:c.*620A= ENSP00000512865.1:n.*620A=
ENST00000696783.1:n.3086A=
ENST00000696992.1:n.2335A=
ENST00000696995.1:n.4747A=
ENST00000696996.1:n.2660A=
ENST00000696997.1:c.*848A= ENSP00000513028.1:n.*848A=
ENST00000696998.1:n.2472A=
ENST00000696999.1:c.*210A= ENSP00000513029.1:n.*210A=
ENST00000697036.1:c.*634A= ENSP00000513060.1:n.*634A=
ENST00000697037.1:n.1253A=
ENST00000697093.1:n.3454A=
ENST00000697094.1:n.3801A=
ENST00000697095.1:c.*2419A= ENSP00000513104.1:n.*2419A=
ENST00000697096.1:n.2351A=
ENST00000697097.1:c.*210A= ENSP00000513105.1:n.*210A=
ENST00000562983.2:n.1404A=
ENST00000690268.1:c.*210A= ENSP00000509810.1:n.*210A=
ENST00000355740.7:c.*544A= ENSP00000347979.3:n.*544A=
ENST00000640140.1:n.1390A=
ENST00000640250.1:n.717A=
ENST00000640681.1:n.1339A=
ENST00000652046.1:c.*210A= MANE Select ENSP00000498466.1:n.*210A=
ENST00000352159.8:c.*535A= ENSP00000345601.4:n.*535A=
ENST00000355740.6:c.*210A= ENSP00000347979.2:n.*210A=
NM_000043.4:c.*210A= , LRG_134t1:c.*210A= NP_000034.1:n.*210A=
NM_152871.2:c.*210A= NP_690610.1:n.*210A=
NM_152872.2:c.*530A= NP_690611.1:n.*530A=
NR_028033.2:n.1392A=
NR_028034.2:n.1254A=
NR_028035.2:n.1317A=
NR_028036.2:n.1455A=
XM_006717819.2:c.*210A= XP_006717882.1:n.*210A=
XM_011539764.1:c.*210A= XP_011538066.1:n.*210A=
XM_011539765.1:c.*210A= XP_011538067.1:n.*210A=
XM_011539766.1:c.*210A= XP_011538068.1:n.*210A=
XM_011539767.1:c.*210A= XP_011538069.1:n.*210A=
NM_000043.5:c.*210A= NP_000034.1:n.*210A=
NM_001320619.1:c.*541A= NP_001307548.1:n.*541A=
NM_152871.3:c.*210A= NP_690610.1:n.*210A=
NM_152872.3:c.*530A= NP_690611.1:n.*530A=
NR_028033.3:n.1364A=
NR_028034.3:n.1226A=
NR_028035.3:n.1289A=
NR_028036.3:n.1427A=
NR_135313.1:n.1344A=
NR_135314.1:n.1527A=
NR_135315.1:n.1280A=
XM_006717819.3:c.*210A= XP_006717882.1:n.*210A=
XM_011539764.2:c.*210A= XP_011538066.1:n.*210A=
XM_011539765.2:c.*210A= XP_011538067.1:n.*210A=
XM_011539766.2:c.*210A= XP_011538068.1:n.*210A=
XM_011539767.3:c.*210A= XP_011538069.1:n.*210A=
XR_945732.3:n.1286A=
XR_945733.2:n.1223A=
NM_000043.6:c.*210A= MANE Select NP_000034.1:n.*210A=
NM_001320619.2:c.*541A= NP_001307548.1:n.*541A=
NM_152871.4:c.*210A= NP_690610.1:n.*210A=
NM_152872.4:c.*530A= NP_690611.1:n.*530A=
NR_028033.4:n.1125A=
NR_028034.4:n.987A=
NR_028035.4:n.1050A=
NR_028036.4:n.1188A=
NR_135313.2:n.1105A=
NR_135314.2:n.1384A=
NR_135315.2:n.1137A=