Canonical Allele Identifier: CA5593292
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 301544
ClinVar RCV Id: RCV000287265
dbSNP Id: rs1468063

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89015534C>T , CM000672.2:g.89015534C>T GRCh38
NC_000010.10:g.90775291C>T , CM000672.1:g.90775291C>T GRCh37
NC_000010.9:g.90765271C>T NCBI36
NG_009089.2:g.30004C>T , LRG_134:g.30004C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.2401C>T
ENST00000355740.8:c.*1415C>T ENSP00000347979.3:n.*1415C>T
ENST00000357339.7:c.*1084C>T ENSP00000349896.2:n.*1084C>T
ENST00000460510.6:c.*1084C>T ENSP00000512812.1:n.*1084C>T
ENST00000466081.6:n.3741C>T
ENST00000492756.7:c.*1521C>T ENSP00000422453.1:n.*1521C>T
ENST00000494799.6:c.*1084C>T ENSP00000512834.1:n.*1084C>T
ENST00000562983.3:c.*1084C>T ENSP00000512845.1:n.*1084C>T
ENST00000612663.6:c.*1494C>T ENSP00000477997.3:n.*1494C>T
ENST00000640140.2:n.2237C>T
ENST00000640250.2:n.1591C>T
ENST00000640681.2:n.2196C>T
ENST00000696723.1:n.5725C>T
ENST00000696741.1:n.3730C>T
ENST00000696743.1:n.4860C>T
ENST00000696767.1:n.2426C>T
ENST00000696768.1:c.*1415C>T ENSP00000512859.1:n.*1415C>T
ENST00000696771.1:c.*1084C>T ENSP00000512860.1:n.*1084C>T
ENST00000696773.1:n.3434C>T
ENST00000696774.1:n.7202C>T
ENST00000696778.1:n.2528C>T
ENST00000696779.1:c.*1084C>T ENSP00000512862.1:n.*1084C>T
ENST00000696780.1:c.*1084C>T ENSP00000512863.1:n.*1084C>T
ENST00000696781.1:c.*1084C>T ENSP00000512864.1:n.*1084C>T
ENST00000696782.1:c.*1494C>T ENSP00000512865.1:n.*1494C>T
ENST00000696783.1:n.3960C>T
ENST00000696992.1:n.3209C>T
ENST00000696996.1:n.3534C>T
ENST00000696998.1:n.3346C>T
ENST00000696999.1:c.*1084C>T ENSP00000513029.1:n.*1084C>T
ENST00000697036.1:c.*1508C>T ENSP00000513060.1:n.*1508C>T
ENST00000697037.1:n.2127C>T
ENST00000697094.1:n.4675C>T
ENST00000697097.1:c.*1084C>T ENSP00000513105.1:n.*1084C>T
ENST00000562983.2:n.2278C>T
ENST00000690268.1:c.*1084C>T ENSP00000509810.1:n.*1084C>T
ENST00000355740.7:c.*1418C>T ENSP00000347979.3:n.*1418C>T
ENST00000640250.1:n.1591C>T
ENST00000640681.1:n.2213C>T
ENST00000652046.1:c.*1084C>T MANE Select ENSP00000498466.1:n.*1084C>T
ENST00000355740.6:c.*1084C>T ENSP00000347979.2:n.*1084C>T
NM_000043.4:c.*1084C>T , LRG_134t1:c.*1084C>T NP_000034.1:n.*1084C>T
NM_152871.2:c.*1084C>T NP_690610.1:n.*1084C>T
NM_152872.2:c.*1404C>T NP_690611.1:n.*1404C>T
NR_028033.2:n.2266C>T
NR_028034.2:n.2128C>T
NR_028035.2:n.2191C>T
NR_028036.2:n.2329C>T
XM_006717819.2:c.*1084C>T XP_006717882.1:n.*1084C>T
XM_011539764.1:c.*1084C>T XP_011538066.1:n.*1084C>T
XM_011539765.1:c.*1084C>T XP_011538067.1:n.*1084C>T
XM_011539766.1:c.*1084C>T XP_011538068.1:n.*1084C>T
XM_011539767.1:c.*1084C>T XP_011538069.1:n.*1084C>T
NM_000043.5:c.*1084C>T NP_000034.1:n.*1084C>T
NM_001320619.1:c.*1415C>T NP_001307548.1:n.*1415C>T
NM_152871.3:c.*1084C>T NP_690610.1:n.*1084C>T
NM_152872.3:c.*1404C>T NP_690611.1:n.*1404C>T
NR_028033.3:n.2238C>T
NR_028034.3:n.2100C>T
NR_028035.3:n.2163C>T
NR_028036.3:n.2301C>T
NR_135313.1:n.2218C>T
NR_135314.1:n.2401C>T
NR_135315.1:n.2154C>T
XM_006717819.3:c.*1084C>T XP_006717882.1:n.*1084C>T
XM_011539764.2:c.*1084C>T XP_011538066.1:n.*1084C>T
XM_011539765.2:c.*1084C>T XP_011538067.1:n.*1084C>T
XM_011539766.2:c.*1084C>T XP_011538068.1:n.*1084C>T
XM_011539767.3:c.*1084C>T XP_011538069.1:n.*1084C>T
XR_945732.3:n.2160C>T
XR_945733.2:n.2097C>T
NM_000043.6:c.*1084C>T MANE Select NP_000034.1:n.*1084C>T
NM_001320619.2:c.*1415C>T NP_001307548.1:n.*1415C>T
NM_152871.4:c.*1084C>T NP_690610.1:n.*1084C>T
NM_152872.4:c.*1404C>T NP_690611.1:n.*1404C>T
NR_028033.4:n.1999C>T
NR_028034.4:n.1861C>T
NR_028035.4:n.1924C>T
NR_028036.4:n.2062C>T
NR_135313.2:n.1979C>T
NR_135314.2:n.2258C>T
NR_135315.2:n.2011C>T