Canonical Allele Identifier: CA377510306
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014448T>A , CM000672.2:g.89014448T>A GRCh38
NC_000010.10:g.90774205T>A , CM000672.1:g.90774205T>A GRCh37
NC_000010.9:g.90764185T>A NCBI36
NG_009089.2:g.28918T>A , LRG_134:g.28918T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1315T>A
ENST00000355740.8:c.*329T>A ENSP00000347979.3:n.*329T>A
ENST00000357339.7:c.943T>A ENSP00000349896.2:p.Ter315Lys
ENST00000371857.8:n.2551T>A
ENST00000460510.6:c.289T>A ENSP00000512812.1:p.Ter97Lys
ENST00000466081.6:n.2655T>A
ENST00000477270.6:c.1051T>A ENSP00000512813.1:p.Ter351Lys
ENST00000479522.6:c.*435T>A ENSP00000424113.1:n.*435T>A
ENST00000484444.6:c.*447T>A ENSP00000420975.1:n.*447T>A
ENST00000488877.6:c.897T>A ENSP00000425159.1:n.897T>A
ENST00000492756.7:c.*435T>A ENSP00000422453.1:n.*435T>A
ENST00000494799.6:c.289T>A ENSP00000512834.1:p.Ter97Lys
ENST00000562983.3:c.289T>A ENSP00000512845.1:p.Ter97Lys
ENST00000612663.6:c.*408T>A ENSP00000477997.3:n.*408T>A
ENST00000640140.2:n.1151T>A
ENST00000640250.2:n.505T>A
ENST00000640681.2:n.1110T>A
ENST00000696723.1:n.4639T>A
ENST00000696741.1:n.2644T>A
ENST00000696742.1:n.2371T>A
ENST00000696743.1:n.3774T>A
ENST00000696744.1:n.1045T>A
ENST00000696767.1:n.1340T>A
ENST00000696768.1:c.*329T>A ENSP00000512859.1:n.*329T>A
ENST00000696769.1:n.2695T>A
ENST00000696771.1:c.289T>A ENSP00000512860.1:p.Ter97Lys
ENST00000696772.1:n.2609T>A
ENST00000696773.1:n.2348T>A
ENST00000696774.1:n.6116T>A
ENST00000696776.1:c.1099T>A ENSP00000512861.1:p.Ter367Lys
ENST00000696777.1:n.2414T>A
ENST00000696778.1:n.1442T>A
ENST00000696779.1:c.613T>A ENSP00000512862.1:p.Ter205Lys
ENST00000696780.1:c.1036T>A ENSP00000512863.1:p.Ter346Lys
ENST00000696781.1:c.751T>A ENSP00000512864.1:p.Ter251Lys
ENST00000696782.1:c.*408T>A ENSP00000512865.1:n.*408T>A
ENST00000696783.1:n.2874T>A
ENST00000696992.1:n.2123T>A
ENST00000696995.1:n.4535T>A
ENST00000696996.1:n.2448T>A
ENST00000696997.1:c.*636T>A ENSP00000513028.1:n.*636T>A
ENST00000696998.1:n.2260T>A
ENST00000696999.1:c.289T>A ENSP00000513029.1:p.Ter97Lys
ENST00000697036.1:c.*422T>A ENSP00000513060.1:n.*422T>A
ENST00000697037.1:n.1041T>A
ENST00000697093.1:n.3242T>A
ENST00000697094.1:n.3589T>A
ENST00000697095.1:c.*2207T>A ENSP00000513104.1:n.*2207T>A
ENST00000697096.1:n.2139T>A
ENST00000697097.1:c.289T>A ENSP00000513105.1:p.Ter97Lys
ENST00000562983.2:n.1192T>A
ENST00000690268.1:c.1087T>A ENSP00000509810.1:p.Ter363Lys
ENST00000355740.7:c.*332T>A ENSP00000347979.3:n.*332T>A
ENST00000612663.5:c.*408T>A ENSP00000477997.3:n.*408T>A
ENST00000640140.1:n.1178T>A
ENST00000640250.1:n.505T>A
ENST00000640681.1:n.1127T>A
ENST00000652046.1:c.1006T>A MANE Select ENSP00000498466.1:p.Ter336Lys
ENST00000352159.8:c.*323T>A ENSP00000345601.4:n.*323T>A
ENST00000355279.2:c.981T>A ENSP00000347426.2:n.981T>A
ENST00000355740.6:c.1006T>A ENSP00000347979.2:p.Ter336Lys
ENST00000357339.6:c.943T>A ENSP00000349896.2:p.Ter315Lys
ENST00000479522.5:c.*435T>A ENSP00000424113.1:n.*435T>A
ENST00000484444.5:c.*447T>A ENSP00000420975.1:n.*447T>A
ENST00000488877.5:c.*447T>A ENSP00000425159.1:n.*447T>A
ENST00000492756.5:c.834T>A ENSP00000422453.1:n.834T>A
ENST00000494410.5:c.*364T>A ENSP00000423755.1:n.*364T>A
ENST00000612663.4:c.*353T>A ENSP00000477997.2:n.*353T>A
NM_000043.4:c.1006T>A , LRG_134t1:c.1006T>A NP_000034.1:p.Ter336Lys
NM_152871.2:c.943T>A NP_690610.1:p.Ter315Lys
NM_152872.2:c.*318T>A NP_690611.1:n.*318T>A
NR_028033.2:n.1180T>A
NR_028034.2:n.1042T>A
NR_028035.2:n.1105T>A
NR_028036.2:n.1243T>A
XM_006717819.2:c.1087T>A XP_006717882.1:p.Ter363Lys
XM_011539764.1:c.1168T>A XP_011538066.1:p.Ter390Lys
XM_011539765.1:c.1105T>A XP_011538067.1:p.Ter369Lys
XM_011539766.1:c.1087T>A XP_011538068.1:p.Ter363Lys
XM_011539767.1:c.1051T>A XP_011538069.1:p.Ter351Lys
XR_945733.1:n.1011T>A
NM_000043.5:c.1006T>A NP_000034.1:p.Ter336Lys
NM_001320619.1:c.*329T>A NP_001307548.1:n.*329T>A
NM_152871.3:c.943T>A NP_690610.1:p.Ter315Lys
NM_152872.3:c.*318T>A NP_690611.1:n.*318T>A
NR_028033.3:n.1152T>A
NR_028034.3:n.1014T>A
NR_028035.3:n.1077T>A
NR_028036.3:n.1215T>A
NR_135313.1:n.1132T>A
NR_135314.1:n.1315T>A
NR_135315.1:n.1068T>A
XM_006717819.3:c.1087T>A XP_006717882.1:p.Ter363Lys
XM_011539764.2:c.1168T>A XP_011538066.1:p.Ter390Lys
XM_011539765.2:c.1105T>A XP_011538067.1:p.Ter369Lys
XM_011539766.2:c.1087T>A XP_011538068.1:p.Ter363Lys
XM_011539767.3:c.1051T>A XP_011538069.1:p.Ter351Lys
XR_945732.3:n.1074T>A
XR_945733.2:n.1011T>A
NM_000043.6:c.1006T>A MANE Select NP_000034.1:p.Ter336Lys
NM_001320619.2:c.*329T>A NP_001307548.1:n.*329T>A
NM_152871.4:c.943T>A NP_690610.1:p.Ter315Lys
NM_152872.4:c.*318T>A NP_690611.1:n.*318T>A
NR_028033.4:n.913T>A
NR_028034.4:n.775T>A
NR_028035.4:n.838T>A
NR_028036.4:n.976T>A
NR_135313.2:n.893T>A
NR_135314.2:n.1172T>A
NR_135315.2:n.925T>A