Canonical Allele Identifier: CA211335091
Gene: FAS HGNC NCBI

Linked Data

dbSNP Id: rs112369298

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014264A>G , CM000672.2:g.89014264A>G GRCh38
NC_000010.10:g.90774021A>G , CM000672.1:g.90774021A>G GRCh37
NC_000010.9:g.90764001A>G NCBI36
NG_009089.2:g.28734A>G , LRG_134:g.28734A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1131A>G
ENST00000355740.8:c.*145A>G ENSP00000347979.3:n.*145A>G
ENST00000357339.7:c.759A>G ENSP00000349896.2:p.Lys253=
ENST00000371857.8:n.2367A>G
ENST00000460510.6:c.105A>G ENSP00000512812.1:p.Lys35=
ENST00000466081.6:n.2471A>G
ENST00000477270.6:c.867A>G ENSP00000512813.1:p.Lys289=
ENST00000479522.6:c.*251A>G ENSP00000424113.1:n.*251A>G
ENST00000484444.6:c.*263A>G ENSP00000420975.1:n.*263A>G
ENST00000488877.6:c.713A>G ENSP00000425159.1:n.713A>G
ENST00000492756.7:c.*251A>G ENSP00000422453.1:n.*251A>G
ENST00000494799.6:c.105A>G ENSP00000512834.1:p.Lys35=
ENST00000562983.3:c.105A>G ENSP00000512845.1:p.Lys35=
ENST00000612663.6:c.*224A>G ENSP00000477997.3:n.*224A>G
ENST00000640140.2:n.967A>G
ENST00000640250.2:n.321A>G
ENST00000640681.2:n.926A>G
ENST00000696723.1:n.4455A>G
ENST00000696741.1:n.2460A>G
ENST00000696742.1:n.2187A>G
ENST00000696743.1:n.3590A>G
ENST00000696744.1:n.861A>G
ENST00000696767.1:n.1156A>G
ENST00000696768.1:c.*145A>G ENSP00000512859.1:n.*145A>G
ENST00000696769.1:n.2511A>G
ENST00000696771.1:c.105A>G ENSP00000512860.1:p.Lys35=
ENST00000696772.1:n.2425A>G
ENST00000696773.1:n.2164A>G
ENST00000696774.1:n.5932A>G
ENST00000696776.1:c.915A>G ENSP00000512861.1:p.Lys305=
ENST00000696777.1:n.2230A>G
ENST00000696778.1:n.1258A>G
ENST00000696779.1:c.429A>G ENSP00000512862.1:p.Lys143=
ENST00000696780.1:c.852A>G ENSP00000512863.1:p.Lys284=
ENST00000696781.1:c.567A>G ENSP00000512864.1:p.Lys189=
ENST00000696782.1:c.*224A>G ENSP00000512865.1:n.*224A>G
ENST00000696783.1:n.2690A>G
ENST00000696992.1:n.1939A>G
ENST00000696995.1:n.4351A>G
ENST00000696996.1:n.2264A>G
ENST00000696997.1:c.*452A>G ENSP00000513028.1:n.*452A>G
ENST00000696998.1:n.2076A>G
ENST00000696999.1:c.105A>G ENSP00000513029.1:p.Lys35=
ENST00000697035.1:c.*155A>G ENSP00000513059.1:n.*155A>G
ENST00000697036.1:c.*238A>G ENSP00000513060.1:n.*238A>G
ENST00000697037.1:n.857A>G
ENST00000697093.1:n.3058A>G
ENST00000697094.1:n.3405A>G
ENST00000697095.1:c.*2023A>G ENSP00000513104.1:n.*2023A>G
ENST00000697096.1:n.1955A>G
ENST00000697097.1:c.105A>G ENSP00000513105.1:p.Lys35=
ENST00000562983.2:n.1008A>G
ENST00000690268.1:c.903A>G ENSP00000509810.1:p.Lys301=
ENST00000355740.7:c.*148A>G ENSP00000347979.3:n.*148A>G
ENST00000612663.5:c.*224A>G ENSP00000477997.3:n.*224A>G
ENST00000640140.1:n.994A>G
ENST00000640250.1:n.321A>G
ENST00000640681.1:n.943A>G
ENST00000652046.1:c.822A>G MANE Select ENSP00000498466.1:p.Lys274=
ENST00000352159.8:c.*139A>G ENSP00000345601.4:n.*139A>G
ENST00000355279.2:c.797A>G ENSP00000347426.2:n.797A>G
ENST00000355740.6:c.822A>G ENSP00000347979.2:p.Lys274=
ENST00000357339.6:c.759A>G ENSP00000349896.2:p.Lys253=
ENST00000479522.5:c.*251A>G ENSP00000424113.1:n.*251A>G
ENST00000484444.5:c.*263A>G ENSP00000420975.1:n.*263A>G
ENST00000488877.5:c.*263A>G ENSP00000425159.1:n.*263A>G
ENST00000492756.5:c.650A>G ENSP00000422453.1:n.650A>G
ENST00000494410.5:c.*180A>G ENSP00000423755.1:n.*180A>G
ENST00000612663.4:c.*169A>G ENSP00000477997.2:n.*169A>G
NM_000043.4:c.822A>G , LRG_134t1:c.822A>G NP_000034.1:p.Lys274=
NM_152871.2:c.759A>G NP_690610.1:p.Lys253=
NM_152872.2:c.*134A>G NP_690611.1:n.*134A>G
NR_028033.2:n.996A>G
NR_028034.2:n.858A>G
NR_028035.2:n.921A>G
NR_028036.2:n.1059A>G
XM_006717819.2:c.903A>G XP_006717882.1:p.Lys301=
XM_011539764.1:c.984A>G XP_011538066.1:p.Lys328=
XM_011539765.1:c.921A>G XP_011538067.1:p.Lys307=
XM_011539766.1:c.903A>G XP_011538068.1:p.Lys301=
XM_011539767.1:c.867A>G XP_011538069.1:p.Lys289=
XR_945732.1:n.890A>G
XR_945733.1:n.827A>G
NM_000043.5:c.822A>G NP_000034.1:p.Lys274=
NM_001320619.1:c.*145A>G NP_001307548.1:n.*145A>G
NM_152871.3:c.759A>G NP_690610.1:p.Lys253=
NM_152872.3:c.*134A>G NP_690611.1:n.*134A>G
NR_028033.3:n.968A>G
NR_028034.3:n.830A>G
NR_028035.3:n.893A>G
NR_028036.3:n.1031A>G
NR_135313.1:n.948A>G
NR_135314.1:n.1131A>G
NR_135315.1:n.884A>G
XM_006717819.3:c.903A>G XP_006717882.1:p.Lys301=
XM_011539764.2:c.984A>G XP_011538066.1:p.Lys328=
XM_011539765.2:c.921A>G XP_011538067.1:p.Lys307=
XM_011539766.2:c.903A>G XP_011538068.1:p.Lys301=
XM_011539767.3:c.867A>G XP_011538069.1:p.Lys289=
XR_945732.3:n.890A>G
XR_945733.2:n.827A>G
NM_000043.6:c.822A>G MANE Select NP_000034.1:p.Lys274=
NM_001320619.2:c.*145A>G NP_001307548.1:n.*145A>G
NM_152871.4:c.759A>G NP_690610.1:p.Lys253=
NM_152872.4:c.*134A>G NP_690611.1:n.*134A>G
NR_028033.4:n.729A>G
NR_028034.4:n.591A>G
NR_028035.4:n.654A>G
NR_028036.4:n.792A>G
NR_135313.2:n.709A>G
NR_135314.2:n.988A>G
NR_135315.2:n.741A>G