Canonical Allele Identifier: CA2610079813
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014674G>T , CM000672.2:g.89014674G>T GRCh38
NC_000010.10:g.90774431G>T , CM000672.1:g.90774431G>T GRCh37
NC_000010.9:g.90764411G>T NCBI36
NG_009089.2:g.29144G>T , LRG_134:g.29144G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1541G>T
ENST00000355740.8:c.*555G>T ENSP00000347979.3:n.*555G>T
ENST00000357339.7:c.*224G>T ENSP00000349896.2:n.*224G>T
ENST00000371857.8:n.2777G>T
ENST00000460510.6:c.*224G>T ENSP00000512812.1:n.*224G>T
ENST00000466081.6:n.2881G>T
ENST00000477270.6:c.*224G>T ENSP00000512813.1:n.*224G>T
ENST00000492756.7:c.*661G>T ENSP00000422453.1:n.*661G>T
ENST00000494799.6:c.*224G>T ENSP00000512834.1:n.*224G>T
ENST00000562983.3:c.*224G>T ENSP00000512845.1:n.*224G>T
ENST00000612663.6:c.*634G>T ENSP00000477997.3:n.*634G>T
ENST00000640140.2:n.1377G>T
ENST00000640250.2:n.731G>T
ENST00000640681.2:n.1336G>T
ENST00000696723.1:n.4865G>T
ENST00000696741.1:n.2870G>T
ENST00000696742.1:n.2597G>T
ENST00000696743.1:n.4000G>T
ENST00000696744.1:n.1271G>T
ENST00000696767.1:n.1566G>T
ENST00000696768.1:c.*555G>T ENSP00000512859.1:n.*555G>T
ENST00000696771.1:c.*224G>T ENSP00000512860.1:n.*224G>T
ENST00000696772.1:n.2835G>T
ENST00000696773.1:n.2574G>T
ENST00000696774.1:n.6342G>T
ENST00000696776.1:c.*224G>T ENSP00000512861.1:n.*224G>T
ENST00000696777.1:n.2640G>T
ENST00000696778.1:n.1668G>T
ENST00000696779.1:c.*224G>T ENSP00000512862.1:n.*224G>T
ENST00000696780.1:c.*224G>T ENSP00000512863.1:n.*224G>T
ENST00000696781.1:c.*224G>T ENSP00000512864.1:n.*224G>T
ENST00000696782.1:c.*634G>T ENSP00000512865.1:n.*634G>T
ENST00000696783.1:n.3100G>T
ENST00000696992.1:n.2349G>T
ENST00000696995.1:n.4761G>T
ENST00000696996.1:n.2674G>T
ENST00000696997.1:c.*862G>T ENSP00000513028.1:n.*862G>T
ENST00000696998.1:n.2486G>T
ENST00000696999.1:c.*224G>T ENSP00000513029.1:n.*224G>T
ENST00000697036.1:c.*648G>T ENSP00000513060.1:n.*648G>T
ENST00000697037.1:n.1267G>T
ENST00000697093.1:n.3468G>T
ENST00000697094.1:n.3815G>T
ENST00000697095.1:c.*2433G>T ENSP00000513104.1:n.*2433G>T
ENST00000697096.1:n.2365G>T
ENST00000697097.1:c.*224G>T ENSP00000513105.1:n.*224G>T
ENST00000562983.2:n.1418G>T
ENST00000690268.1:c.*224G>T ENSP00000509810.1:n.*224G>T
ENST00000355740.7:c.*558G>T ENSP00000347979.3:n.*558G>T
ENST00000640140.1:n.1404G>T
ENST00000640250.1:n.731G>T
ENST00000640681.1:n.1353G>T
ENST00000652046.1:c.*224G>T MANE Select ENSP00000498466.1:n.*224G>T
ENST00000352159.8:c.*549G>T ENSP00000345601.4:n.*549G>T
ENST00000355740.6:c.*224G>T ENSP00000347979.2:n.*224G>T
NM_000043.4:c.*224G>T , LRG_134t1:c.*224G>T NP_000034.1:n.*224G>T
NM_152871.2:c.*224G>T NP_690610.1:n.*224G>T
NM_152872.2:c.*544G>T NP_690611.1:n.*544G>T
NR_028033.2:n.1406G>T
NR_028034.2:n.1268G>T
NR_028035.2:n.1331G>T
NR_028036.2:n.1469G>T
XM_006717819.2:c.*224G>T XP_006717882.1:n.*224G>T
XM_011539764.1:c.*224G>T XP_011538066.1:n.*224G>T
XM_011539765.1:c.*224G>T XP_011538067.1:n.*224G>T
XM_011539766.1:c.*224G>T XP_011538068.1:n.*224G>T
XM_011539767.1:c.*224G>T XP_011538069.1:n.*224G>T
NM_000043.5:c.*224G>T NP_000034.1:n.*224G>T
NM_001320619.1:c.*555G>T NP_001307548.1:n.*555G>T
NM_152871.3:c.*224G>T NP_690610.1:n.*224G>T
NM_152872.3:c.*544G>T NP_690611.1:n.*544G>T
NR_028033.3:n.1378G>T
NR_028034.3:n.1240G>T
NR_028035.3:n.1303G>T
NR_028036.3:n.1441G>T
NR_135313.1:n.1358G>T
NR_135314.1:n.1541G>T
NR_135315.1:n.1294G>T
XM_006717819.3:c.*224G>T XP_006717882.1:n.*224G>T
XM_011539764.2:c.*224G>T XP_011538066.1:n.*224G>T
XM_011539765.2:c.*224G>T XP_011538067.1:n.*224G>T
XM_011539766.2:c.*224G>T XP_011538068.1:n.*224G>T
XM_011539767.3:c.*224G>T XP_011538069.1:n.*224G>T
XR_945732.3:n.1300G>T
XR_945733.2:n.1237G>T
NM_000043.6:c.*224G>T MANE Select NP_000034.1:n.*224G>T
NM_001320619.2:c.*555G>T NP_001307548.1:n.*555G>T
NM_152871.4:c.*224G>T NP_690610.1:n.*224G>T
NM_152872.4:c.*544G>T NP_690611.1:n.*544G>T
NR_028033.4:n.1139G>T
NR_028034.4:n.1001G>T
NR_028035.4:n.1064G>T
NR_028036.4:n.1202G>T
NR_135313.2:n.1119G>T
NR_135314.2:n.1398G>T
NR_135315.2:n.1151G>T