Canonical Allele Identifier: CA1926639542
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014692A= , CM000672.2:g.89014692A= GRCh38
NC_000010.10:g.90774449A= , CM000672.1:g.90774449A= GRCh37
NC_000010.9:g.90764429A= NCBI36
NG_009089.2:g.29162A= , LRG_134:g.29162A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1559A=
ENST00000355740.8:c.*573A= ENSP00000347979.3:n.*573A=
ENST00000357339.7:c.*242A= ENSP00000349896.2:n.*242A=
ENST00000371857.8:n.2795A=
ENST00000460510.6:c.*242A= ENSP00000512812.1:n.*242A=
ENST00000466081.6:n.2899A=
ENST00000477270.6:c.*242A= ENSP00000512813.1:n.*242A=
ENST00000492756.7:c.*679A= ENSP00000422453.1:n.*679A=
ENST00000494799.6:c.*242A= ENSP00000512834.1:n.*242A=
ENST00000562983.3:c.*242A= ENSP00000512845.1:n.*242A=
ENST00000612663.6:c.*652A= ENSP00000477997.3:n.*652A=
ENST00000640140.2:n.1395A=
ENST00000640250.2:n.749A=
ENST00000640681.2:n.1354A=
ENST00000696723.1:n.4883A=
ENST00000696741.1:n.2888A=
ENST00000696742.1:n.2615A=
ENST00000696743.1:n.4018A=
ENST00000696744.1:n.1289A=
ENST00000696767.1:n.1584A=
ENST00000696768.1:c.*573A= ENSP00000512859.1:n.*573A=
ENST00000696771.1:c.*242A= ENSP00000512860.1:n.*242A=
ENST00000696772.1:n.2853A=
ENST00000696773.1:n.2592A=
ENST00000696774.1:n.6360A=
ENST00000696776.1:c.*242A= ENSP00000512861.1:n.*242A=
ENST00000696777.1:n.2658A=
ENST00000696778.1:n.1686A=
ENST00000696779.1:c.*242A= ENSP00000512862.1:n.*242A=
ENST00000696780.1:c.*242A= ENSP00000512863.1:n.*242A=
ENST00000696781.1:c.*242A= ENSP00000512864.1:n.*242A=
ENST00000696782.1:c.*652A= ENSP00000512865.1:n.*652A=
ENST00000696783.1:n.3118A=
ENST00000696992.1:n.2367A=
ENST00000696995.1:n.4779A=
ENST00000696996.1:n.2692A=
ENST00000696997.1:c.*880A= ENSP00000513028.1:n.*880A=
ENST00000696998.1:n.2504A=
ENST00000696999.1:c.*242A= ENSP00000513029.1:n.*242A=
ENST00000697036.1:c.*666A= ENSP00000513060.1:n.*666A=
ENST00000697037.1:n.1285A=
ENST00000697093.1:n.3486A=
ENST00000697094.1:n.3833A=
ENST00000697095.1:c.*2451A= ENSP00000513104.1:n.*2451A=
ENST00000697096.1:n.2383A=
ENST00000697097.1:c.*242A= ENSP00000513105.1:n.*242A=
ENST00000562983.2:n.1436A=
ENST00000690268.1:c.*242A= ENSP00000509810.1:n.*242A=
ENST00000355740.7:c.*576A= ENSP00000347979.3:n.*576A=
ENST00000640140.1:n.1422A=
ENST00000640250.1:n.749A=
ENST00000640681.1:n.1371A=
ENST00000652046.1:c.*242A= MANE Select ENSP00000498466.1:n.*242A=
ENST00000352159.8:c.*567A= ENSP00000345601.4:n.*567A=
ENST00000355740.6:c.*242A= ENSP00000347979.2:n.*242A=
NM_000043.4:c.*242A= , LRG_134t1:c.*242A= NP_000034.1:n.*242A=
NM_152871.2:c.*242A= NP_690610.1:n.*242A=
NM_152872.2:c.*562A= NP_690611.1:n.*562A=
NR_028033.2:n.1424A=
NR_028034.2:n.1286A=
NR_028035.2:n.1349A=
NR_028036.2:n.1487A=
XM_006717819.2:c.*242A= XP_006717882.1:n.*242A=
XM_011539764.1:c.*242A= XP_011538066.1:n.*242A=
XM_011539765.1:c.*242A= XP_011538067.1:n.*242A=
XM_011539766.1:c.*242A= XP_011538068.1:n.*242A=
XM_011539767.1:c.*242A= XP_011538069.1:n.*242A=
NM_000043.5:c.*242A= NP_000034.1:n.*242A=
NM_001320619.1:c.*573A= NP_001307548.1:n.*573A=
NM_152871.3:c.*242A= NP_690610.1:n.*242A=
NM_152872.3:c.*562A= NP_690611.1:n.*562A=
NR_028033.3:n.1396A=
NR_028034.3:n.1258A=
NR_028035.3:n.1321A=
NR_028036.3:n.1459A=
NR_135313.1:n.1376A=
NR_135314.1:n.1559A=
NR_135315.1:n.1312A=
XM_006717819.3:c.*242A= XP_006717882.1:n.*242A=
XM_011539764.2:c.*242A= XP_011538066.1:n.*242A=
XM_011539765.2:c.*242A= XP_011538067.1:n.*242A=
XM_011539766.2:c.*242A= XP_011538068.1:n.*242A=
XM_011539767.3:c.*242A= XP_011538069.1:n.*242A=
XR_945732.3:n.1318A=
XR_945733.2:n.1255A=
NM_000043.6:c.*242A= MANE Select NP_000034.1:n.*242A=
NM_001320619.2:c.*573A= NP_001307548.1:n.*573A=
NM_152871.4:c.*242A= NP_690610.1:n.*242A=
NM_152872.4:c.*562A= NP_690611.1:n.*562A=
NR_028033.4:n.1157A=
NR_028034.4:n.1019A=
NR_028035.4:n.1082A=
NR_028036.4:n.1220A=
NR_135313.2:n.1137A=
NR_135314.2:n.1416A=
NR_135315.2:n.1169A=