Canonical Allele Identifier: CA1926639514
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014623G= , CM000672.2:g.89014623G= GRCh38
NC_000010.10:g.90774380G= , CM000672.1:g.90774380G= GRCh37
NC_000010.9:g.90764360G= NCBI36
NG_009089.2:g.29093G= , LRG_134:g.29093G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1490G=
ENST00000355740.8:c.*504G= ENSP00000347979.3:n.*504G=
ENST00000357339.7:c.*173G= ENSP00000349896.2:n.*173G=
ENST00000371857.8:n.2726G=
ENST00000460510.6:c.*173G= ENSP00000512812.1:n.*173G=
ENST00000466081.6:n.2830G=
ENST00000477270.6:c.*173G= ENSP00000512813.1:n.*173G=
ENST00000488877.6:c.1072G= ENSP00000425159.1:n.1072G=
ENST00000492756.7:c.*610G= ENSP00000422453.1:n.*610G=
ENST00000494799.6:c.*173G= ENSP00000512834.1:n.*173G=
ENST00000562983.3:c.*173G= ENSP00000512845.1:n.*173G=
ENST00000612663.6:c.*583G= ENSP00000477997.3:n.*583G=
ENST00000640140.2:n.1326G=
ENST00000640250.2:n.680G=
ENST00000640681.2:n.1285G=
ENST00000696723.1:n.4814G=
ENST00000696741.1:n.2819G=
ENST00000696742.1:n.2546G=
ENST00000696743.1:n.3949G=
ENST00000696744.1:n.1220G=
ENST00000696767.1:n.1515G=
ENST00000696768.1:c.*504G= ENSP00000512859.1:n.*504G=
ENST00000696771.1:c.*173G= ENSP00000512860.1:n.*173G=
ENST00000696772.1:n.2784G=
ENST00000696773.1:n.2523G=
ENST00000696774.1:n.6291G=
ENST00000696776.1:c.*173G= ENSP00000512861.1:n.*173G=
ENST00000696777.1:n.2589G=
ENST00000696778.1:n.1617G=
ENST00000696779.1:c.*173G= ENSP00000512862.1:n.*173G=
ENST00000696780.1:c.*173G= ENSP00000512863.1:n.*173G=
ENST00000696781.1:c.*173G= ENSP00000512864.1:n.*173G=
ENST00000696782.1:c.*583G= ENSP00000512865.1:n.*583G=
ENST00000696783.1:n.3049G=
ENST00000696992.1:n.2298G=
ENST00000696995.1:n.4710G=
ENST00000696996.1:n.2623G=
ENST00000696997.1:c.*811G= ENSP00000513028.1:n.*811G=
ENST00000696998.1:n.2435G=
ENST00000696999.1:c.*173G= ENSP00000513029.1:n.*173G=
ENST00000697036.1:c.*597G= ENSP00000513060.1:n.*597G=
ENST00000697037.1:n.1216G=
ENST00000697093.1:n.3417G=
ENST00000697094.1:n.3764G=
ENST00000697095.1:c.*2382G= ENSP00000513104.1:n.*2382G=
ENST00000697096.1:n.2314G=
ENST00000697097.1:c.*173G= ENSP00000513105.1:n.*173G=
ENST00000562983.2:n.1367G=
ENST00000690268.1:c.*173G= ENSP00000509810.1:n.*173G=
ENST00000355740.7:c.*507G= ENSP00000347979.3:n.*507G=
ENST00000640140.1:n.1353G=
ENST00000640250.1:n.680G=
ENST00000640681.1:n.1302G=
ENST00000652046.1:c.*173G= MANE Select ENSP00000498466.1:n.*173G=
ENST00000352159.8:c.*498G= ENSP00000345601.4:n.*498G=
ENST00000355740.6:c.*173G= ENSP00000347979.2:n.*173G=
NM_000043.4:c.*173G= , LRG_134t1:c.*173G= NP_000034.1:n.*173G=
NM_152871.2:c.*173G= NP_690610.1:n.*173G=
NM_152872.2:c.*493G= NP_690611.1:n.*493G=
NR_028033.2:n.1355G=
NR_028034.2:n.1217G=
NR_028035.2:n.1280G=
NR_028036.2:n.1418G=
XM_006717819.2:c.*173G= XP_006717882.1:n.*173G=
XM_011539764.1:c.*173G= XP_011538066.1:n.*173G=
XM_011539765.1:c.*173G= XP_011538067.1:n.*173G=
XM_011539766.1:c.*173G= XP_011538068.1:n.*173G=
XM_011539767.1:c.*173G= XP_011538069.1:n.*173G=
NM_000043.5:c.*173G= NP_000034.1:n.*173G=
NM_001320619.1:c.*504G= NP_001307548.1:n.*504G=
NM_152871.3:c.*173G= NP_690610.1:n.*173G=
NM_152872.3:c.*493G= NP_690611.1:n.*493G=
NR_028033.3:n.1327G=
NR_028034.3:n.1189G=
NR_028035.3:n.1252G=
NR_028036.3:n.1390G=
NR_135313.1:n.1307G=
NR_135314.1:n.1490G=
NR_135315.1:n.1243G=
XM_006717819.3:c.*173G= XP_006717882.1:n.*173G=
XM_011539764.2:c.*173G= XP_011538066.1:n.*173G=
XM_011539765.2:c.*173G= XP_011538067.1:n.*173G=
XM_011539766.2:c.*173G= XP_011538068.1:n.*173G=
XM_011539767.3:c.*173G= XP_011538069.1:n.*173G=
XR_945732.3:n.1249G=
XR_945733.2:n.1186G=
NM_000043.6:c.*173G= MANE Select NP_000034.1:n.*173G=
NM_001320619.2:c.*504G= NP_001307548.1:n.*504G=
NM_152871.4:c.*173G= NP_690610.1:n.*173G=
NM_152872.4:c.*493G= NP_690611.1:n.*493G=
NR_028033.4:n.1088G=
NR_028034.4:n.950G=
NR_028035.4:n.1013G=
NR_028036.4:n.1151G=
NR_135313.2:n.1068G=
NR_135314.2:n.1347G=
NR_135315.2:n.1100G=