Canonical Allele Identifier: CA1926639303
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014126C= , CM000672.2:g.89014126C= GRCh38
NC_000010.10:g.90773883C= , CM000672.1:g.90773883C= GRCh37
NC_000010.9:g.90763863C= NCBI36
NG_009089.2:g.28596C= , LRG_134:g.28596C=

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.993C=
ENST00000355740.8:c.*7C= ENSP00000347979.3:n.*7C=
ENST00000357339.7:c.621C= ENSP00000349896.2:p.Asp207=
ENST00000371857.8:n.2229C=
ENST00000460510.6:c.-34C= ENSP00000512812.1:n.-34C=
ENST00000466081.6:n.2333C=
ENST00000477270.6:c.729C= ENSP00000512813.1:p.Asp243=
ENST00000479522.6:c.*113C= ENSP00000424113.1:n.*113C=
ENST00000484444.6:c.*125C= ENSP00000420975.1:n.*125C=
ENST00000488877.6:c.575C= ENSP00000425159.1:n.575C=
ENST00000492756.7:c.*113C= ENSP00000422453.1:n.*113C=
ENST00000494799.6:c.-34C= ENSP00000512834.1:n.-34C=
ENST00000562983.3:c.-34C= ENSP00000512845.1:n.-34C=
ENST00000612663.6:c.*86C= ENSP00000477997.3:n.*86C=
ENST00000640140.2:n.829C=
ENST00000640250.2:n.183C=
ENST00000640681.2:n.788C=
ENST00000696723.1:n.4317C=
ENST00000696741.1:n.2322C=
ENST00000696742.1:n.2049C=
ENST00000696743.1:n.3452C=
ENST00000696744.1:n.723C=
ENST00000696767.1:n.1018C=
ENST00000696768.1:c.*7C= ENSP00000512859.1:n.*7C=
ENST00000696769.1:n.2373C=
ENST00000696771.1:c.-34C= ENSP00000512860.1:n.-34C=
ENST00000696772.1:n.2287C=
ENST00000696773.1:n.2026C=
ENST00000696774.1:n.5794C=
ENST00000696776.1:c.777C= ENSP00000512861.1:p.Asp259=
ENST00000696777.1:n.2092C=
ENST00000696778.1:n.1120C=
ENST00000696779.1:c.291C= ENSP00000512862.1:p.Asp97=
ENST00000696780.1:c.714C= ENSP00000512863.1:p.Asp238=
ENST00000696781.1:c.429C= ENSP00000512864.1:p.Asp143=
ENST00000696782.1:c.*86C= ENSP00000512865.1:n.*86C=
ENST00000696783.1:n.2552C=
ENST00000696992.1:n.1801C=
ENST00000696995.1:n.4213C=
ENST00000696996.1:n.2126C=
ENST00000696997.1:c.*314C= ENSP00000513028.1:n.*314C=
ENST00000696998.1:n.1938C=
ENST00000696999.1:c.-34C= ENSP00000513029.1:n.-34C=
ENST00000697035.1:c.*17C= ENSP00000513059.1:n.*17C=
ENST00000697036.1:c.*100C= ENSP00000513060.1:n.*100C=
ENST00000697037.1:n.719C=
ENST00000697093.1:n.2920C=
ENST00000697094.1:n.3267C=
ENST00000697095.1:c.*1885C= ENSP00000513104.1:n.*1885C=
ENST00000697096.1:n.1817C=
ENST00000697097.1:c.-34C= ENSP00000513105.1:n.-34C=
ENST00000562983.2:n.870C=
ENST00000690268.1:c.765C= ENSP00000509810.1:p.Asp255=
ENST00000355740.7:c.*10C= ENSP00000347979.3:n.*10C=
ENST00000612663.5:c.*86C= ENSP00000477997.3:n.*86C=
ENST00000640140.1:n.856C=
ENST00000640250.1:n.183C=
ENST00000640681.1:n.805C=
ENST00000652046.1:c.684C= MANE Select ENSP00000498466.1:p.Asp228=
ENST00000313771.9:n.993C=
ENST00000352159.8:c.*1C= ENSP00000345601.4:n.*1C=
ENST00000355279.2:c.659C= ENSP00000347426.2:p.Thr220=
ENST00000355740.6:c.684C= ENSP00000347979.2:p.Asp228=
ENST00000357339.6:c.621C= ENSP00000349896.2:p.Asp207=
ENST00000479522.5:c.*113C= ENSP00000424113.1:n.*113C=
ENST00000484444.5:c.*125C= ENSP00000420975.1:n.*125C=
ENST00000488877.5:c.*125C= ENSP00000425159.1:n.*125C=
ENST00000492756.5:c.512C= ENSP00000422453.1:n.512C=
ENST00000494410.5:c.*42C= ENSP00000423755.1:n.*42C=
ENST00000494799.5:n.591C=
ENST00000612663.4:c.*31C= ENSP00000477997.2:n.*31C=
ENST00000615406.4:c.684C= ENSP00000484575.1:p.Asp228=
ENST00000626542.2:c.684C= ENSP00000485876.1:p.Asp228=
NM_000043.4:c.684C= , LRG_134t1:c.684C= NP_000034.1:p.Asp228=
NM_152871.2:c.621C= NP_690610.1:p.Asp207=
NM_152872.2:c.659C= NP_690611.1:p.Thr220=
NR_028033.2:n.858C=
NR_028034.2:n.720C=
NR_028035.2:n.783C=
NR_028036.2:n.921C=
XM_006717819.2:c.765C= XP_006717882.1:p.Asp255=
XM_011539764.1:c.846C= XP_011538066.1:p.Asp282=
XM_011539765.1:c.783C= XP_011538067.1:p.Asp261=
XM_011539766.1:c.765C= XP_011538068.1:p.Asp255=
XM_011539767.1:c.729C= XP_011538069.1:p.Asp243=
XR_945732.1:n.752C=
XR_945733.1:n.689C=
NM_000043.5:c.684C= NP_000034.1:p.Asp228=
NM_001320619.1:c.*7C= NP_001307548.1:n.*7C=
NM_152871.3:c.621C= NP_690610.1:p.Asp207=
NM_152872.3:c.659C= NP_690611.1:p.Thr220=
NR_028033.3:n.830C=
NR_028034.3:n.692C=
NR_028035.3:n.755C=
NR_028036.3:n.893C=
NR_135313.1:n.810C=
NR_135314.1:n.993C=
NR_135315.1:n.746C=
XM_006717819.3:c.765C= XP_006717882.1:p.Asp255=
XM_011539764.2:c.846C= XP_011538066.1:p.Asp282=
XM_011539765.2:c.783C= XP_011538067.1:p.Asp261=
XM_011539766.2:c.765C= XP_011538068.1:p.Asp255=
XM_011539767.3:c.729C= XP_011538069.1:p.Asp243=
XR_945732.3:n.752C=
XR_945733.2:n.689C=
NM_000043.6:c.684C= MANE Select NP_000034.1:p.Asp228=
NM_001320619.2:c.*7C= NP_001307548.1:n.*7C=
NM_152871.4:c.621C= NP_690610.1:p.Asp207=
NM_152872.4:c.659C= NP_690611.1:p.Thr220=
NR_028033.4:n.591C=
NR_028034.4:n.453C=
NR_028035.4:n.516C=
NR_028036.4:n.654C=
NR_135313.2:n.571C=
NR_135314.2:n.850C=
NR_135315.2:n.603C=