Canonical Allele Identifier: CA377510185
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs1848687177

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014395T>A , CM000672.2:g.89014395T>A GRCh38
NC_000010.10:g.90774152T>A , CM000672.1:g.90774152T>A GRCh37
NC_000010.9:g.90764132T>A NCBI36
NG_009089.2:g.28865T>A , LRG_134:g.28865T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1262T>A
ENST00000355740.8:c.*276T>A ENSP00000347979.3:n.*276T>A
ENST00000357339.7:c.890T>A ENSP00000349896.2:p.Ile297Asn
ENST00000371857.8:n.2498T>A
ENST00000460510.6:c.236T>A ENSP00000512812.1:p.Ile79Asn
ENST00000466081.6:n.2602T>A
ENST00000477270.6:c.998T>A ENSP00000512813.1:p.Ile333Asn
ENST00000479522.6:c.*382T>A ENSP00000424113.1:n.*382T>A
ENST00000484444.6:c.*394T>A ENSP00000420975.1:n.*394T>A
ENST00000488877.6:c.844T>A ENSP00000425159.1:n.844T>A
ENST00000492756.7:c.*382T>A ENSP00000422453.1:n.*382T>A
ENST00000494799.6:c.236T>A ENSP00000512834.1:p.Ile79Asn
ENST00000562983.3:c.236T>A ENSP00000512845.1:p.Ile79Asn
ENST00000612663.6:c.*355T>A ENSP00000477997.3:n.*355T>A
ENST00000640140.2:n.1098T>A
ENST00000640250.2:n.452T>A
ENST00000640681.2:n.1057T>A
ENST00000696723.1:n.4586T>A
ENST00000696741.1:n.2591T>A
ENST00000696742.1:n.2318T>A
ENST00000696743.1:n.3721T>A
ENST00000696744.1:n.992T>A
ENST00000696767.1:n.1287T>A
ENST00000696768.1:c.*276T>A ENSP00000512859.1:n.*276T>A
ENST00000696769.1:n.2642T>A
ENST00000696771.1:c.236T>A ENSP00000512860.1:p.Ile79Asn
ENST00000696772.1:n.2556T>A
ENST00000696773.1:n.2295T>A
ENST00000696774.1:n.6063T>A
ENST00000696776.1:c.1046T>A ENSP00000512861.1:p.Ile349Asn
ENST00000696777.1:n.2361T>A
ENST00000696778.1:n.1389T>A
ENST00000696779.1:c.560T>A ENSP00000512862.1:p.Ile187Asn
ENST00000696780.1:c.983T>A ENSP00000512863.1:p.Ile328Asn
ENST00000696781.1:c.698T>A ENSP00000512864.1:p.Ile233Asn
ENST00000696782.1:c.*355T>A ENSP00000512865.1:n.*355T>A
ENST00000696783.1:n.2821T>A
ENST00000696992.1:n.2070T>A
ENST00000696995.1:n.4482T>A
ENST00000696996.1:n.2395T>A
ENST00000696997.1:c.*583T>A ENSP00000513028.1:n.*583T>A
ENST00000696998.1:n.2207T>A
ENST00000696999.1:c.236T>A ENSP00000513029.1:p.Ile79Asn
ENST00000697036.1:c.*369T>A ENSP00000513060.1:n.*369T>A
ENST00000697037.1:n.988T>A
ENST00000697093.1:n.3189T>A
ENST00000697094.1:n.3536T>A
ENST00000697095.1:c.*2154T>A ENSP00000513104.1:n.*2154T>A
ENST00000697096.1:n.2086T>A
ENST00000697097.1:c.236T>A ENSP00000513105.1:p.Ile79Asn
ENST00000562983.2:n.1139T>A
ENST00000690268.1:c.1034T>A ENSP00000509810.1:p.Ile345Asn
ENST00000355740.7:c.*279T>A ENSP00000347979.3:n.*279T>A
ENST00000612663.5:c.*355T>A ENSP00000477997.3:n.*355T>A
ENST00000640140.1:n.1125T>A
ENST00000640250.1:n.452T>A
ENST00000640681.1:n.1074T>A
ENST00000652046.1:c.953T>A MANE Select ENSP00000498466.1:p.Ile318Asn
ENST00000352159.8:c.*270T>A ENSP00000345601.4:n.*270T>A
ENST00000355279.2:c.928T>A ENSP00000347426.2:n.928T>A
ENST00000355740.6:c.953T>A ENSP00000347979.2:p.Ile318Asn
ENST00000357339.6:c.890T>A ENSP00000349896.2:p.Ile297Asn
ENST00000479522.5:c.*382T>A ENSP00000424113.1:n.*382T>A
ENST00000484444.5:c.*394T>A ENSP00000420975.1:n.*394T>A
ENST00000488877.5:c.*394T>A ENSP00000425159.1:n.*394T>A
ENST00000492756.5:c.781T>A ENSP00000422453.1:n.781T>A
ENST00000494410.5:c.*311T>A ENSP00000423755.1:n.*311T>A
ENST00000612663.4:c.*300T>A ENSP00000477997.2:n.*300T>A
NM_000043.4:c.953T>A , LRG_134t1:c.953T>A NP_000034.1:p.Ile318Asn
NM_152871.2:c.890T>A NP_690610.1:p.Ile297Asn
NM_152872.2:c.*265T>A NP_690611.1:n.*265T>A
NR_028033.2:n.1127T>A
NR_028034.2:n.989T>A
NR_028035.2:n.1052T>A
NR_028036.2:n.1190T>A
XM_006717819.2:c.1034T>A XP_006717882.1:p.Ile345Asn
XM_011539764.1:c.1115T>A XP_011538066.1:p.Ile372Asn
XM_011539765.1:c.1052T>A XP_011538067.1:p.Ile351Asn
XM_011539766.1:c.1034T>A XP_011538068.1:p.Ile345Asn
XM_011539767.1:c.998T>A XP_011538069.1:p.Ile333Asn
XR_945733.1:n.958T>A
NM_000043.5:c.953T>A NP_000034.1:p.Ile318Asn
NM_001320619.1:c.*276T>A NP_001307548.1:n.*276T>A
NM_152871.3:c.890T>A NP_690610.1:p.Ile297Asn
NM_152872.3:c.*265T>A NP_690611.1:n.*265T>A
NR_028033.3:n.1099T>A
NR_028034.3:n.961T>A
NR_028035.3:n.1024T>A
NR_028036.3:n.1162T>A
NR_135313.1:n.1079T>A
NR_135314.1:n.1262T>A
NR_135315.1:n.1015T>A
XM_006717819.3:c.1034T>A XP_006717882.1:p.Ile345Asn
XM_011539764.2:c.1115T>A XP_011538066.1:p.Ile372Asn
XM_011539765.2:c.1052T>A XP_011538067.1:p.Ile351Asn
XM_011539766.2:c.1034T>A XP_011538068.1:p.Ile345Asn
XM_011539767.3:c.998T>A XP_011538069.1:p.Ile333Asn
XR_945732.3:n.1021T>A
XR_945733.2:n.958T>A
NM_000043.6:c.953T>A MANE Select NP_000034.1:p.Ile318Asn
NM_001320619.2:c.*276T>A NP_001307548.1:n.*276T>A
NM_152871.4:c.890T>A NP_690610.1:p.Ile297Asn
NM_152872.4:c.*265T>A NP_690611.1:n.*265T>A
NR_028033.4:n.860T>A
NR_028034.4:n.722T>A
NR_028035.4:n.785T>A
NR_028036.4:n.923T>A
NR_135313.2:n.840T>A
NR_135314.2:n.1119T>A
NR_135315.2:n.872T>A