Canonical Allele Identifier: CA2610079841
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014705C>T , CM000672.2:g.89014705C>T GRCh38
NC_000010.10:g.90774462C>T , CM000672.1:g.90774462C>T GRCh37
NC_000010.9:g.90764442C>T NCBI36
NG_009089.2:g.29175C>T , LRG_134:g.29175C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1572C>T
ENST00000355740.8:c.*586C>T ENSP00000347979.3:n.*586C>T
ENST00000357339.7:c.*255C>T ENSP00000349896.2:n.*255C>T
ENST00000371857.8:n.2808C>T
ENST00000460510.6:c.*255C>T ENSP00000512812.1:n.*255C>T
ENST00000466081.6:n.2912C>T
ENST00000477270.6:c.*255C>T ENSP00000512813.1:n.*255C>T
ENST00000492756.7:c.*692C>T ENSP00000422453.1:n.*692C>T
ENST00000494799.6:c.*255C>T ENSP00000512834.1:n.*255C>T
ENST00000562983.3:c.*255C>T ENSP00000512845.1:n.*255C>T
ENST00000612663.6:c.*665C>T ENSP00000477997.3:n.*665C>T
ENST00000640140.2:n.1408C>T
ENST00000640250.2:n.762C>T
ENST00000640681.2:n.1367C>T
ENST00000696723.1:n.4896C>T
ENST00000696741.1:n.2901C>T
ENST00000696742.1:n.2628C>T
ENST00000696743.1:n.4031C>T
ENST00000696744.1:n.1302C>T
ENST00000696767.1:n.1597C>T
ENST00000696768.1:c.*586C>T ENSP00000512859.1:n.*586C>T
ENST00000696771.1:c.*255C>T ENSP00000512860.1:n.*255C>T
ENST00000696772.1:n.2866C>T
ENST00000696773.1:n.2605C>T
ENST00000696774.1:n.6373C>T
ENST00000696776.1:c.*255C>T ENSP00000512861.1:n.*255C>T
ENST00000696777.1:n.2671C>T
ENST00000696778.1:n.1699C>T
ENST00000696779.1:c.*255C>T ENSP00000512862.1:n.*255C>T
ENST00000696780.1:c.*255C>T ENSP00000512863.1:n.*255C>T
ENST00000696781.1:c.*255C>T ENSP00000512864.1:n.*255C>T
ENST00000696782.1:c.*665C>T ENSP00000512865.1:n.*665C>T
ENST00000696783.1:n.3131C>T
ENST00000696992.1:n.2380C>T
ENST00000696995.1:n.4792C>T
ENST00000696996.1:n.2705C>T
ENST00000696997.1:c.*893C>T ENSP00000513028.1:n.*893C>T
ENST00000696998.1:n.2517C>T
ENST00000696999.1:c.*255C>T ENSP00000513029.1:n.*255C>T
ENST00000697036.1:c.*679C>T ENSP00000513060.1:n.*679C>T
ENST00000697037.1:n.1298C>T
ENST00000697093.1:n.3499C>T
ENST00000697094.1:n.3846C>T
ENST00000697095.1:c.*2464C>T ENSP00000513104.1:n.*2464C>T
ENST00000697096.1:n.2396C>T
ENST00000697097.1:c.*255C>T ENSP00000513105.1:n.*255C>T
ENST00000562983.2:n.1449C>T
ENST00000690268.1:c.*255C>T ENSP00000509810.1:n.*255C>T
ENST00000355740.7:c.*589C>T ENSP00000347979.3:n.*589C>T
ENST00000640140.1:n.1435C>T
ENST00000640250.1:n.762C>T
ENST00000640681.1:n.1384C>T
ENST00000652046.1:c.*255C>T MANE Select ENSP00000498466.1:n.*255C>T
ENST00000352159.8:c.*580C>T ENSP00000345601.4:n.*580C>T
ENST00000355740.6:c.*255C>T ENSP00000347979.2:n.*255C>T
NM_000043.4:c.*255C>T , LRG_134t1:c.*255C>T NP_000034.1:n.*255C>T
NM_152871.2:c.*255C>T NP_690610.1:n.*255C>T
NM_152872.2:c.*575C>T NP_690611.1:n.*575C>T
NR_028033.2:n.1437C>T
NR_028034.2:n.1299C>T
NR_028035.2:n.1362C>T
NR_028036.2:n.1500C>T
XM_006717819.2:c.*255C>T XP_006717882.1:n.*255C>T
XM_011539764.1:c.*255C>T XP_011538066.1:n.*255C>T
XM_011539765.1:c.*255C>T XP_011538067.1:n.*255C>T
XM_011539766.1:c.*255C>T XP_011538068.1:n.*255C>T
XM_011539767.1:c.*255C>T XP_011538069.1:n.*255C>T
NM_000043.5:c.*255C>T NP_000034.1:n.*255C>T
NM_001320619.1:c.*586C>T NP_001307548.1:n.*586C>T
NM_152871.3:c.*255C>T NP_690610.1:n.*255C>T
NM_152872.3:c.*575C>T NP_690611.1:n.*575C>T
NR_028033.3:n.1409C>T
NR_028034.3:n.1271C>T
NR_028035.3:n.1334C>T
NR_028036.3:n.1472C>T
NR_135313.1:n.1389C>T
NR_135314.1:n.1572C>T
NR_135315.1:n.1325C>T
XM_006717819.3:c.*255C>T XP_006717882.1:n.*255C>T
XM_011539764.2:c.*255C>T XP_011538066.1:n.*255C>T
XM_011539765.2:c.*255C>T XP_011538067.1:n.*255C>T
XM_011539766.2:c.*255C>T XP_011538068.1:n.*255C>T
XM_011539767.3:c.*255C>T XP_011538069.1:n.*255C>T
XR_945732.3:n.1331C>T
XR_945733.2:n.1268C>T
NM_000043.6:c.*255C>T MANE Select NP_000034.1:n.*255C>T
NM_001320619.2:c.*586C>T NP_001307548.1:n.*586C>T
NM_152871.4:c.*255C>T NP_690610.1:n.*255C>T
NM_152872.4:c.*575C>T NP_690611.1:n.*575C>T
NR_028033.4:n.1170C>T
NR_028034.4:n.1032C>T
NR_028035.4:n.1095C>T
NR_028036.4:n.1233C>T
NR_135313.2:n.1150C>T
NR_135314.2:n.1429C>T
NR_135315.2:n.1182C>T