Canonical Allele Identifier: CA2610079822
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014684G>T , CM000672.2:g.89014684G>T GRCh38
NC_000010.10:g.90774441G>T , CM000672.1:g.90774441G>T GRCh37
NC_000010.9:g.90764421G>T NCBI36
NG_009089.2:g.29154G>T , LRG_134:g.29154G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1551G>T
ENST00000355740.8:c.*565G>T ENSP00000347979.3:n.*565G>T
ENST00000357339.7:c.*234G>T ENSP00000349896.2:n.*234G>T
ENST00000371857.8:n.2787G>T
ENST00000460510.6:c.*234G>T ENSP00000512812.1:n.*234G>T
ENST00000466081.6:n.2891G>T
ENST00000477270.6:c.*234G>T ENSP00000512813.1:n.*234G>T
ENST00000492756.7:c.*671G>T ENSP00000422453.1:n.*671G>T
ENST00000494799.6:c.*234G>T ENSP00000512834.1:n.*234G>T
ENST00000562983.3:c.*234G>T ENSP00000512845.1:n.*234G>T
ENST00000612663.6:c.*644G>T ENSP00000477997.3:n.*644G>T
ENST00000640140.2:n.1387G>T
ENST00000640250.2:n.741G>T
ENST00000640681.2:n.1346G>T
ENST00000696723.1:n.4875G>T
ENST00000696741.1:n.2880G>T
ENST00000696742.1:n.2607G>T
ENST00000696743.1:n.4010G>T
ENST00000696744.1:n.1281G>T
ENST00000696767.1:n.1576G>T
ENST00000696768.1:c.*565G>T ENSP00000512859.1:n.*565G>T
ENST00000696771.1:c.*234G>T ENSP00000512860.1:n.*234G>T
ENST00000696772.1:n.2845G>T
ENST00000696773.1:n.2584G>T
ENST00000696774.1:n.6352G>T
ENST00000696776.1:c.*234G>T ENSP00000512861.1:n.*234G>T
ENST00000696777.1:n.2650G>T
ENST00000696778.1:n.1678G>T
ENST00000696779.1:c.*234G>T ENSP00000512862.1:n.*234G>T
ENST00000696780.1:c.*234G>T ENSP00000512863.1:n.*234G>T
ENST00000696781.1:c.*234G>T ENSP00000512864.1:n.*234G>T
ENST00000696782.1:c.*644G>T ENSP00000512865.1:n.*644G>T
ENST00000696783.1:n.3110G>T
ENST00000696992.1:n.2359G>T
ENST00000696995.1:n.4771G>T
ENST00000696996.1:n.2684G>T
ENST00000696997.1:c.*872G>T ENSP00000513028.1:n.*872G>T
ENST00000696998.1:n.2496G>T
ENST00000696999.1:c.*234G>T ENSP00000513029.1:n.*234G>T
ENST00000697036.1:c.*658G>T ENSP00000513060.1:n.*658G>T
ENST00000697037.1:n.1277G>T
ENST00000697093.1:n.3478G>T
ENST00000697094.1:n.3825G>T
ENST00000697095.1:c.*2443G>T ENSP00000513104.1:n.*2443G>T
ENST00000697096.1:n.2375G>T
ENST00000697097.1:c.*234G>T ENSP00000513105.1:n.*234G>T
ENST00000562983.2:n.1428G>T
ENST00000690268.1:c.*234G>T ENSP00000509810.1:n.*234G>T
ENST00000355740.7:c.*568G>T ENSP00000347979.3:n.*568G>T
ENST00000640140.1:n.1414G>T
ENST00000640250.1:n.741G>T
ENST00000640681.1:n.1363G>T
ENST00000652046.1:c.*234G>T MANE Select ENSP00000498466.1:n.*234G>T
ENST00000352159.8:c.*559G>T ENSP00000345601.4:n.*559G>T
ENST00000355740.6:c.*234G>T ENSP00000347979.2:n.*234G>T
NM_000043.4:c.*234G>T , LRG_134t1:c.*234G>T NP_000034.1:n.*234G>T
NM_152871.2:c.*234G>T NP_690610.1:n.*234G>T
NM_152872.2:c.*554G>T NP_690611.1:n.*554G>T
NR_028033.2:n.1416G>T
NR_028034.2:n.1278G>T
NR_028035.2:n.1341G>T
NR_028036.2:n.1479G>T
XM_006717819.2:c.*234G>T XP_006717882.1:n.*234G>T
XM_011539764.1:c.*234G>T XP_011538066.1:n.*234G>T
XM_011539765.1:c.*234G>T XP_011538067.1:n.*234G>T
XM_011539766.1:c.*234G>T XP_011538068.1:n.*234G>T
XM_011539767.1:c.*234G>T XP_011538069.1:n.*234G>T
NM_000043.5:c.*234G>T NP_000034.1:n.*234G>T
NM_001320619.1:c.*565G>T NP_001307548.1:n.*565G>T
NM_152871.3:c.*234G>T NP_690610.1:n.*234G>T
NM_152872.3:c.*554G>T NP_690611.1:n.*554G>T
NR_028033.3:n.1388G>T
NR_028034.3:n.1250G>T
NR_028035.3:n.1313G>T
NR_028036.3:n.1451G>T
NR_135313.1:n.1368G>T
NR_135314.1:n.1551G>T
NR_135315.1:n.1304G>T
XM_006717819.3:c.*234G>T XP_006717882.1:n.*234G>T
XM_011539764.2:c.*234G>T XP_011538066.1:n.*234G>T
XM_011539765.2:c.*234G>T XP_011538067.1:n.*234G>T
XM_011539766.2:c.*234G>T XP_011538068.1:n.*234G>T
XM_011539767.3:c.*234G>T XP_011538069.1:n.*234G>T
XR_945732.3:n.1310G>T
XR_945733.2:n.1247G>T
NM_000043.6:c.*234G>T MANE Select NP_000034.1:n.*234G>T
NM_001320619.2:c.*565G>T NP_001307548.1:n.*565G>T
NM_152871.4:c.*234G>T NP_690610.1:n.*234G>T
NM_152872.4:c.*554G>T NP_690611.1:n.*554G>T
NR_028033.4:n.1149G>T
NR_028034.4:n.1011G>T
NR_028035.4:n.1074G>T
NR_028036.4:n.1212G>T
NR_135313.2:n.1129G>T
NR_135314.2:n.1408G>T
NR_135315.2:n.1161G>T