Canonical Allele Identifier: CA1926639508
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014605C= , CM000672.2:g.89014605C= GRCh38
NC_000010.10:g.90774362C= , CM000672.1:g.90774362C= GRCh37
NC_000010.9:g.90764342C= NCBI36
NG_009089.2:g.29075C= , LRG_134:g.29075C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1472C=
ENST00000355740.8:c.*486C= ENSP00000347979.3:n.*486C=
ENST00000357339.7:c.*155C= ENSP00000349896.2:n.*155C=
ENST00000371857.8:n.2708C=
ENST00000460510.6:c.*155C= ENSP00000512812.1:n.*155C=
ENST00000466081.6:n.2812C=
ENST00000477270.6:c.*155C= ENSP00000512813.1:n.*155C=
ENST00000488877.6:c.1054C= ENSP00000425159.1:n.1054C=
ENST00000492756.7:c.*592C= ENSP00000422453.1:n.*592C=
ENST00000494799.6:c.*155C= ENSP00000512834.1:n.*155C=
ENST00000562983.3:c.*155C= ENSP00000512845.1:n.*155C=
ENST00000612663.6:c.*565C= ENSP00000477997.3:n.*565C=
ENST00000640140.2:n.1308C=
ENST00000640250.2:n.662C=
ENST00000640681.2:n.1267C=
ENST00000696723.1:n.4796C=
ENST00000696741.1:n.2801C=
ENST00000696742.1:n.2528C=
ENST00000696743.1:n.3931C=
ENST00000696744.1:n.1202C=
ENST00000696767.1:n.1497C=
ENST00000696768.1:c.*486C= ENSP00000512859.1:n.*486C=
ENST00000696771.1:c.*155C= ENSP00000512860.1:n.*155C=
ENST00000696772.1:n.2766C=
ENST00000696773.1:n.2505C=
ENST00000696774.1:n.6273C=
ENST00000696776.1:c.*155C= ENSP00000512861.1:n.*155C=
ENST00000696777.1:n.2571C=
ENST00000696778.1:n.1599C=
ENST00000696779.1:c.*155C= ENSP00000512862.1:n.*155C=
ENST00000696780.1:c.*155C= ENSP00000512863.1:n.*155C=
ENST00000696781.1:c.*155C= ENSP00000512864.1:n.*155C=
ENST00000696782.1:c.*565C= ENSP00000512865.1:n.*565C=
ENST00000696783.1:n.3031C=
ENST00000696992.1:n.2280C=
ENST00000696995.1:n.4692C=
ENST00000696996.1:n.2605C=
ENST00000696997.1:c.*793C= ENSP00000513028.1:n.*793C=
ENST00000696998.1:n.2417C=
ENST00000696999.1:c.*155C= ENSP00000513029.1:n.*155C=
ENST00000697036.1:c.*579C= ENSP00000513060.1:n.*579C=
ENST00000697037.1:n.1198C=
ENST00000697093.1:n.3399C=
ENST00000697094.1:n.3746C=
ENST00000697095.1:c.*2364C= ENSP00000513104.1:n.*2364C=
ENST00000697096.1:n.2296C=
ENST00000697097.1:c.*155C= ENSP00000513105.1:n.*155C=
ENST00000562983.2:n.1349C=
ENST00000690268.1:c.*155C= ENSP00000509810.1:n.*155C=
ENST00000355740.7:c.*489C= ENSP00000347979.3:n.*489C=
ENST00000640140.1:n.1335C=
ENST00000640250.1:n.662C=
ENST00000640681.1:n.1284C=
ENST00000652046.1:c.*155C= MANE Select ENSP00000498466.1:n.*155C=
ENST00000352159.8:c.*480C= ENSP00000345601.4:n.*480C=
ENST00000355740.6:c.*155C= ENSP00000347979.2:n.*155C=
ENST00000484444.5:c.*604C= ENSP00000420975.1:n.*604C=
NM_000043.4:c.*155C= , LRG_134t1:c.*155C= NP_000034.1:n.*155C=
NM_152871.2:c.*155C= NP_690610.1:n.*155C=
NM_152872.2:c.*475C= NP_690611.1:n.*475C=
NR_028033.2:n.1337C=
NR_028034.2:n.1199C=
NR_028035.2:n.1262C=
NR_028036.2:n.1400C=
XM_006717819.2:c.*155C= XP_006717882.1:n.*155C=
XM_011539764.1:c.*155C= XP_011538066.1:n.*155C=
XM_011539765.1:c.*155C= XP_011538067.1:n.*155C=
XM_011539766.1:c.*155C= XP_011538068.1:n.*155C=
XM_011539767.1:c.*155C= XP_011538069.1:n.*155C=
NM_000043.5:c.*155C= NP_000034.1:n.*155C=
NM_001320619.1:c.*486C= NP_001307548.1:n.*486C=
NM_152871.3:c.*155C= NP_690610.1:n.*155C=
NM_152872.3:c.*475C= NP_690611.1:n.*475C=
NR_028033.3:n.1309C=
NR_028034.3:n.1171C=
NR_028035.3:n.1234C=
NR_028036.3:n.1372C=
NR_135313.1:n.1289C=
NR_135314.1:n.1472C=
NR_135315.1:n.1225C=
XM_006717819.3:c.*155C= XP_006717882.1:n.*155C=
XM_011539764.2:c.*155C= XP_011538066.1:n.*155C=
XM_011539765.2:c.*155C= XP_011538067.1:n.*155C=
XM_011539766.2:c.*155C= XP_011538068.1:n.*155C=
XM_011539767.3:c.*155C= XP_011538069.1:n.*155C=
XR_945732.3:n.1231C=
XR_945733.2:n.1168C=
NM_000043.6:c.*155C= MANE Select NP_000034.1:n.*155C=
NM_001320619.2:c.*486C= NP_001307548.1:n.*486C=
NM_152871.4:c.*155C= NP_690610.1:n.*155C=
NM_152872.4:c.*475C= NP_690611.1:n.*475C=
NR_028033.4:n.1070C=
NR_028034.4:n.932C=
NR_028035.4:n.995C=
NR_028036.4:n.1133C=
NR_135313.2:n.1050C=
NR_135314.2:n.1329C=
NR_135315.2:n.1082C=