Canonical Allele Identifier: CA377509927
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs762629344

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014282T>A , CM000672.2:g.89014282T>A GRCh38
NC_000010.10:g.90774039T>A , CM000672.1:g.90774039T>A GRCh37
NC_000010.9:g.90764019T>A NCBI36
NG_009089.2:g.28752T>A , LRG_134:g.28752T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1149T>A
ENST00000355740.8:c.*163T>A ENSP00000347979.3:n.*163T>A
ENST00000357339.7:c.777T>A ENSP00000349896.2:p.Asn259Lys
ENST00000371857.8:n.2385T>A
ENST00000460510.6:c.123T>A ENSP00000512812.1:p.Asn41Lys
ENST00000466081.6:n.2489T>A
ENST00000477270.6:c.885T>A ENSP00000512813.1:p.Asn295Lys
ENST00000479522.6:c.*269T>A ENSP00000424113.1:n.*269T>A
ENST00000484444.6:c.*281T>A ENSP00000420975.1:n.*281T>A
ENST00000488877.6:c.731T>A ENSP00000425159.1:n.731T>A
ENST00000492756.7:c.*269T>A ENSP00000422453.1:n.*269T>A
ENST00000494799.6:c.123T>A ENSP00000512834.1:p.Asn41Lys
ENST00000562983.3:c.123T>A ENSP00000512845.1:p.Asn41Lys
ENST00000612663.6:c.*242T>A ENSP00000477997.3:n.*242T>A
ENST00000640140.2:n.985T>A
ENST00000640250.2:n.339T>A
ENST00000640681.2:n.944T>A
ENST00000696723.1:n.4473T>A
ENST00000696741.1:n.2478T>A
ENST00000696742.1:n.2205T>A
ENST00000696743.1:n.3608T>A
ENST00000696744.1:n.879T>A
ENST00000696767.1:n.1174T>A
ENST00000696768.1:c.*163T>A ENSP00000512859.1:n.*163T>A
ENST00000696769.1:n.2529T>A
ENST00000696771.1:c.123T>A ENSP00000512860.1:p.Asn41Lys
ENST00000696772.1:n.2443T>A
ENST00000696773.1:n.2182T>A
ENST00000696774.1:n.5950T>A
ENST00000696776.1:c.933T>A ENSP00000512861.1:p.Asn311Lys
ENST00000696777.1:n.2248T>A
ENST00000696778.1:n.1276T>A
ENST00000696779.1:c.447T>A ENSP00000512862.1:p.Asn149Lys
ENST00000696780.1:c.870T>A ENSP00000512863.1:p.Asn290Lys
ENST00000696781.1:c.585T>A ENSP00000512864.1:p.Asn195Lys
ENST00000696782.1:c.*242T>A ENSP00000512865.1:n.*242T>A
ENST00000696783.1:n.2708T>A
ENST00000696992.1:n.1957T>A
ENST00000696995.1:n.4369T>A
ENST00000696996.1:n.2282T>A
ENST00000696997.1:c.*470T>A ENSP00000513028.1:n.*470T>A
ENST00000696998.1:n.2094T>A
ENST00000696999.1:c.123T>A ENSP00000513029.1:p.Asn41Lys
ENST00000697035.1:c.*173T>A ENSP00000513059.1:n.*173T>A
ENST00000697036.1:c.*256T>A ENSP00000513060.1:n.*256T>A
ENST00000697037.1:n.875T>A
ENST00000697093.1:n.3076T>A
ENST00000697094.1:n.3423T>A
ENST00000697095.1:c.*2041T>A ENSP00000513104.1:n.*2041T>A
ENST00000697096.1:n.1973T>A
ENST00000697097.1:c.123T>A ENSP00000513105.1:p.Asn41Lys
ENST00000562983.2:n.1026T>A
ENST00000690268.1:c.921T>A ENSP00000509810.1:p.Asn307Lys
ENST00000355740.7:c.*166T>A ENSP00000347979.3:n.*166T>A
ENST00000612663.5:c.*242T>A ENSP00000477997.3:n.*242T>A
ENST00000640140.1:n.1012T>A
ENST00000640250.1:n.339T>A
ENST00000640681.1:n.961T>A
ENST00000652046.1:c.840T>A MANE Select ENSP00000498466.1:p.Asn280Lys
ENST00000352159.8:c.*157T>A ENSP00000345601.4:n.*157T>A
ENST00000355279.2:c.815T>A ENSP00000347426.2:n.815T>A
ENST00000355740.6:c.840T>A ENSP00000347979.2:p.Asn280Lys
ENST00000357339.6:c.777T>A ENSP00000349896.2:p.Asn259Lys
ENST00000479522.5:c.*269T>A ENSP00000424113.1:n.*269T>A
ENST00000484444.5:c.*281T>A ENSP00000420975.1:n.*281T>A
ENST00000488877.5:c.*281T>A ENSP00000425159.1:n.*281T>A
ENST00000492756.5:c.668T>A ENSP00000422453.1:n.668T>A
ENST00000494410.5:c.*198T>A ENSP00000423755.1:n.*198T>A
ENST00000612663.4:c.*187T>A ENSP00000477997.2:n.*187T>A
NM_000043.4:c.840T>A , LRG_134t1:c.840T>A NP_000034.1:p.Asn280Lys
NM_152871.2:c.777T>A NP_690610.1:p.Asn259Lys
NM_152872.2:c.*152T>A NP_690611.1:n.*152T>A
NR_028033.2:n.1014T>A
NR_028034.2:n.876T>A
NR_028035.2:n.939T>A
NR_028036.2:n.1077T>A
XM_006717819.2:c.921T>A XP_006717882.1:p.Asn307Lys
XM_011539764.1:c.1002T>A XP_011538066.1:p.Asn334Lys
XM_011539765.1:c.939T>A XP_011538067.1:p.Asn313Lys
XM_011539766.1:c.921T>A XP_011538068.1:p.Asn307Lys
XM_011539767.1:c.885T>A XP_011538069.1:p.Asn295Lys
XR_945732.1:n.908T>A
XR_945733.1:n.845T>A
NM_000043.5:c.840T>A NP_000034.1:p.Asn280Lys
NM_001320619.1:c.*163T>A NP_001307548.1:n.*163T>A
NM_152871.3:c.777T>A NP_690610.1:p.Asn259Lys
NM_152872.3:c.*152T>A NP_690611.1:n.*152T>A
NR_028033.3:n.986T>A
NR_028034.3:n.848T>A
NR_028035.3:n.911T>A
NR_028036.3:n.1049T>A
NR_135313.1:n.966T>A
NR_135314.1:n.1149T>A
NR_135315.1:n.902T>A
XM_006717819.3:c.921T>A XP_006717882.1:p.Asn307Lys
XM_011539764.2:c.1002T>A XP_011538066.1:p.Asn334Lys
XM_011539765.2:c.939T>A XP_011538067.1:p.Asn313Lys
XM_011539766.2:c.921T>A XP_011538068.1:p.Asn307Lys
XM_011539767.3:c.885T>A XP_011538069.1:p.Asn295Lys
XR_945732.3:n.908T>A
XR_945733.2:n.845T>A
NM_000043.6:c.840T>A MANE Select NP_000034.1:p.Asn280Lys
NM_001320619.2:c.*163T>A NP_001307548.1:n.*163T>A
NM_152871.4:c.777T>A NP_690610.1:p.Asn259Lys
NM_152872.4:c.*152T>A NP_690611.1:n.*152T>A
NR_028033.4:n.747T>A
NR_028034.4:n.609T>A
NR_028035.4:n.672T>A
NR_028036.4:n.810T>A
NR_135313.2:n.727T>A
NR_135314.2:n.1006T>A
NR_135315.2:n.759T>A