Canonical Allele Identifier: CA1926639541
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014691A= , CM000672.2:g.89014691A= GRCh38
NC_000010.10:g.90774448A= , CM000672.1:g.90774448A= GRCh37
NC_000010.9:g.90764428A= NCBI36
NG_009089.2:g.29161A= , LRG_134:g.29161A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1558A=
ENST00000355740.8:c.*572A= ENSP00000347979.3:n.*572A=
ENST00000357339.7:c.*241A= ENSP00000349896.2:n.*241A=
ENST00000371857.8:n.2794A=
ENST00000460510.6:c.*241A= ENSP00000512812.1:n.*241A=
ENST00000466081.6:n.2898A=
ENST00000477270.6:c.*241A= ENSP00000512813.1:n.*241A=
ENST00000492756.7:c.*678A= ENSP00000422453.1:n.*678A=
ENST00000494799.6:c.*241A= ENSP00000512834.1:n.*241A=
ENST00000562983.3:c.*241A= ENSP00000512845.1:n.*241A=
ENST00000612663.6:c.*651A= ENSP00000477997.3:n.*651A=
ENST00000640140.2:n.1394A=
ENST00000640250.2:n.748A=
ENST00000640681.2:n.1353A=
ENST00000696723.1:n.4882A=
ENST00000696741.1:n.2887A=
ENST00000696742.1:n.2614A=
ENST00000696743.1:n.4017A=
ENST00000696744.1:n.1288A=
ENST00000696767.1:n.1583A=
ENST00000696768.1:c.*572A= ENSP00000512859.1:n.*572A=
ENST00000696771.1:c.*241A= ENSP00000512860.1:n.*241A=
ENST00000696772.1:n.2852A=
ENST00000696773.1:n.2591A=
ENST00000696774.1:n.6359A=
ENST00000696776.1:c.*241A= ENSP00000512861.1:n.*241A=
ENST00000696777.1:n.2657A=
ENST00000696778.1:n.1685A=
ENST00000696779.1:c.*241A= ENSP00000512862.1:n.*241A=
ENST00000696780.1:c.*241A= ENSP00000512863.1:n.*241A=
ENST00000696781.1:c.*241A= ENSP00000512864.1:n.*241A=
ENST00000696782.1:c.*651A= ENSP00000512865.1:n.*651A=
ENST00000696783.1:n.3117A=
ENST00000696992.1:n.2366A=
ENST00000696995.1:n.4778A=
ENST00000696996.1:n.2691A=
ENST00000696997.1:c.*879A= ENSP00000513028.1:n.*879A=
ENST00000696998.1:n.2503A=
ENST00000696999.1:c.*241A= ENSP00000513029.1:n.*241A=
ENST00000697036.1:c.*665A= ENSP00000513060.1:n.*665A=
ENST00000697037.1:n.1284A=
ENST00000697093.1:n.3485A=
ENST00000697094.1:n.3832A=
ENST00000697095.1:c.*2450A= ENSP00000513104.1:n.*2450A=
ENST00000697096.1:n.2382A=
ENST00000697097.1:c.*241A= ENSP00000513105.1:n.*241A=
ENST00000562983.2:n.1435A=
ENST00000690268.1:c.*241A= ENSP00000509810.1:n.*241A=
ENST00000355740.7:c.*575A= ENSP00000347979.3:n.*575A=
ENST00000640140.1:n.1421A=
ENST00000640250.1:n.748A=
ENST00000640681.1:n.1370A=
ENST00000652046.1:c.*241A= MANE Select ENSP00000498466.1:n.*241A=
ENST00000352159.8:c.*566A= ENSP00000345601.4:n.*566A=
ENST00000355740.6:c.*241A= ENSP00000347979.2:n.*241A=
NM_000043.4:c.*241A= , LRG_134t1:c.*241A= NP_000034.1:n.*241A=
NM_152871.2:c.*241A= NP_690610.1:n.*241A=
NM_152872.2:c.*561A= NP_690611.1:n.*561A=
NR_028033.2:n.1423A=
NR_028034.2:n.1285A=
NR_028035.2:n.1348A=
NR_028036.2:n.1486A=
XM_006717819.2:c.*241A= XP_006717882.1:n.*241A=
XM_011539764.1:c.*241A= XP_011538066.1:n.*241A=
XM_011539765.1:c.*241A= XP_011538067.1:n.*241A=
XM_011539766.1:c.*241A= XP_011538068.1:n.*241A=
XM_011539767.1:c.*241A= XP_011538069.1:n.*241A=
NM_000043.5:c.*241A= NP_000034.1:n.*241A=
NM_001320619.1:c.*572A= NP_001307548.1:n.*572A=
NM_152871.3:c.*241A= NP_690610.1:n.*241A=
NM_152872.3:c.*561A= NP_690611.1:n.*561A=
NR_028033.3:n.1395A=
NR_028034.3:n.1257A=
NR_028035.3:n.1320A=
NR_028036.3:n.1458A=
NR_135313.1:n.1375A=
NR_135314.1:n.1558A=
NR_135315.1:n.1311A=
XM_006717819.3:c.*241A= XP_006717882.1:n.*241A=
XM_011539764.2:c.*241A= XP_011538066.1:n.*241A=
XM_011539765.2:c.*241A= XP_011538067.1:n.*241A=
XM_011539766.2:c.*241A= XP_011538068.1:n.*241A=
XM_011539767.3:c.*241A= XP_011538069.1:n.*241A=
XR_945732.3:n.1317A=
XR_945733.2:n.1254A=
NM_000043.6:c.*241A= MANE Select NP_000034.1:n.*241A=
NM_001320619.2:c.*572A= NP_001307548.1:n.*572A=
NM_152871.4:c.*241A= NP_690610.1:n.*241A=
NM_152872.4:c.*561A= NP_690611.1:n.*561A=
NR_028033.4:n.1156A=
NR_028034.4:n.1018A=
NR_028035.4:n.1081A=
NR_028036.4:n.1219A=
NR_135313.2:n.1136A=
NR_135314.2:n.1415A=
NR_135315.2:n.1168A=