Canonical Allele Identifier: CA1926639534
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014676C= , CM000672.2:g.89014676C= GRCh38
NC_000010.10:g.90774433C= , CM000672.1:g.90774433C= GRCh37
NC_000010.9:g.90764413C= NCBI36
NG_009089.2:g.29146C= , LRG_134:g.29146C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1543C=
ENST00000355740.8:c.*557C= ENSP00000347979.3:n.*557C=
ENST00000357339.7:c.*226C= ENSP00000349896.2:n.*226C=
ENST00000371857.8:n.2779C=
ENST00000460510.6:c.*226C= ENSP00000512812.1:n.*226C=
ENST00000466081.6:n.2883C=
ENST00000477270.6:c.*226C= ENSP00000512813.1:n.*226C=
ENST00000492756.7:c.*663C= ENSP00000422453.1:n.*663C=
ENST00000494799.6:c.*226C= ENSP00000512834.1:n.*226C=
ENST00000562983.3:c.*226C= ENSP00000512845.1:n.*226C=
ENST00000612663.6:c.*636C= ENSP00000477997.3:n.*636C=
ENST00000640140.2:n.1379C=
ENST00000640250.2:n.733C=
ENST00000640681.2:n.1338C=
ENST00000696723.1:n.4867C=
ENST00000696741.1:n.2872C=
ENST00000696742.1:n.2599C=
ENST00000696743.1:n.4002C=
ENST00000696744.1:n.1273C=
ENST00000696767.1:n.1568C=
ENST00000696768.1:c.*557C= ENSP00000512859.1:n.*557C=
ENST00000696771.1:c.*226C= ENSP00000512860.1:n.*226C=
ENST00000696772.1:n.2837C=
ENST00000696773.1:n.2576C=
ENST00000696774.1:n.6344C=
ENST00000696776.1:c.*226C= ENSP00000512861.1:n.*226C=
ENST00000696777.1:n.2642C=
ENST00000696778.1:n.1670C=
ENST00000696779.1:c.*226C= ENSP00000512862.1:n.*226C=
ENST00000696780.1:c.*226C= ENSP00000512863.1:n.*226C=
ENST00000696781.1:c.*226C= ENSP00000512864.1:n.*226C=
ENST00000696782.1:c.*636C= ENSP00000512865.1:n.*636C=
ENST00000696783.1:n.3102C=
ENST00000696992.1:n.2351C=
ENST00000696995.1:n.4763C=
ENST00000696996.1:n.2676C=
ENST00000696997.1:c.*864C= ENSP00000513028.1:n.*864C=
ENST00000696998.1:n.2488C=
ENST00000696999.1:c.*226C= ENSP00000513029.1:n.*226C=
ENST00000697036.1:c.*650C= ENSP00000513060.1:n.*650C=
ENST00000697037.1:n.1269C=
ENST00000697093.1:n.3470C=
ENST00000697094.1:n.3817C=
ENST00000697095.1:c.*2435C= ENSP00000513104.1:n.*2435C=
ENST00000697096.1:n.2367C=
ENST00000697097.1:c.*226C= ENSP00000513105.1:n.*226C=
ENST00000562983.2:n.1420C=
ENST00000690268.1:c.*226C= ENSP00000509810.1:n.*226C=
ENST00000355740.7:c.*560C= ENSP00000347979.3:n.*560C=
ENST00000640140.1:n.1406C=
ENST00000640250.1:n.733C=
ENST00000640681.1:n.1355C=
ENST00000652046.1:c.*226C= MANE Select ENSP00000498466.1:n.*226C=
ENST00000352159.8:c.*551C= ENSP00000345601.4:n.*551C=
ENST00000355740.6:c.*226C= ENSP00000347979.2:n.*226C=
NM_000043.4:c.*226C= , LRG_134t1:c.*226C= NP_000034.1:n.*226C=
NM_152871.2:c.*226C= NP_690610.1:n.*226C=
NM_152872.2:c.*546C= NP_690611.1:n.*546C=
NR_028033.2:n.1408C=
NR_028034.2:n.1270C=
NR_028035.2:n.1333C=
NR_028036.2:n.1471C=
XM_006717819.2:c.*226C= XP_006717882.1:n.*226C=
XM_011539764.1:c.*226C= XP_011538066.1:n.*226C=
XM_011539765.1:c.*226C= XP_011538067.1:n.*226C=
XM_011539766.1:c.*226C= XP_011538068.1:n.*226C=
XM_011539767.1:c.*226C= XP_011538069.1:n.*226C=
NM_000043.5:c.*226C= NP_000034.1:n.*226C=
NM_001320619.1:c.*557C= NP_001307548.1:n.*557C=
NM_152871.3:c.*226C= NP_690610.1:n.*226C=
NM_152872.3:c.*546C= NP_690611.1:n.*546C=
NR_028033.3:n.1380C=
NR_028034.3:n.1242C=
NR_028035.3:n.1305C=
NR_028036.3:n.1443C=
NR_135313.1:n.1360C=
NR_135314.1:n.1543C=
NR_135315.1:n.1296C=
XM_006717819.3:c.*226C= XP_006717882.1:n.*226C=
XM_011539764.2:c.*226C= XP_011538066.1:n.*226C=
XM_011539765.2:c.*226C= XP_011538067.1:n.*226C=
XM_011539766.2:c.*226C= XP_011538068.1:n.*226C=
XM_011539767.3:c.*226C= XP_011538069.1:n.*226C=
XR_945732.3:n.1302C=
XR_945733.2:n.1239C=
NM_000043.6:c.*226C= MANE Select NP_000034.1:n.*226C=
NM_001320619.2:c.*557C= NP_001307548.1:n.*557C=
NM_152871.4:c.*226C= NP_690610.1:n.*226C=
NM_152872.4:c.*546C= NP_690611.1:n.*546C=
NR_028033.4:n.1141C=
NR_028034.4:n.1003C=
NR_028035.4:n.1066C=
NR_028036.4:n.1204C=
NR_135313.2:n.1121C=
NR_135314.2:n.1400C=
NR_135315.2:n.1153C=