Canonical Allele Identifier: CA2610079799
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014664T>A , CM000672.2:g.89014664T>A GRCh38
NC_000010.10:g.90774421T>A , CM000672.1:g.90774421T>A GRCh37
NC_000010.9:g.90764401T>A NCBI36
NG_009089.2:g.29134T>A , LRG_134:g.29134T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1531T>A
ENST00000355740.8:c.*545T>A ENSP00000347979.3:n.*545T>A
ENST00000357339.7:c.*214T>A ENSP00000349896.2:n.*214T>A
ENST00000371857.8:n.2767T>A
ENST00000460510.6:c.*214T>A ENSP00000512812.1:n.*214T>A
ENST00000466081.6:n.2871T>A
ENST00000477270.6:c.*214T>A ENSP00000512813.1:n.*214T>A
ENST00000492756.7:c.*651T>A ENSP00000422453.1:n.*651T>A
ENST00000494799.6:c.*214T>A ENSP00000512834.1:n.*214T>A
ENST00000562983.3:c.*214T>A ENSP00000512845.1:n.*214T>A
ENST00000612663.6:c.*624T>A ENSP00000477997.3:n.*624T>A
ENST00000640140.2:n.1367T>A
ENST00000640250.2:n.721T>A
ENST00000640681.2:n.1326T>A
ENST00000696723.1:n.4855T>A
ENST00000696741.1:n.2860T>A
ENST00000696742.1:n.2587T>A
ENST00000696743.1:n.3990T>A
ENST00000696744.1:n.1261T>A
ENST00000696767.1:n.1556T>A
ENST00000696768.1:c.*545T>A ENSP00000512859.1:n.*545T>A
ENST00000696771.1:c.*214T>A ENSP00000512860.1:n.*214T>A
ENST00000696772.1:n.2825T>A
ENST00000696773.1:n.2564T>A
ENST00000696774.1:n.6332T>A
ENST00000696776.1:c.*214T>A ENSP00000512861.1:n.*214T>A
ENST00000696777.1:n.2630T>A
ENST00000696778.1:n.1658T>A
ENST00000696779.1:c.*214T>A ENSP00000512862.1:n.*214T>A
ENST00000696780.1:c.*214T>A ENSP00000512863.1:n.*214T>A
ENST00000696781.1:c.*214T>A ENSP00000512864.1:n.*214T>A
ENST00000696782.1:c.*624T>A ENSP00000512865.1:n.*624T>A
ENST00000696783.1:n.3090T>A
ENST00000696992.1:n.2339T>A
ENST00000696995.1:n.4751T>A
ENST00000696996.1:n.2664T>A
ENST00000696997.1:c.*852T>A ENSP00000513028.1:n.*852T>A
ENST00000696998.1:n.2476T>A
ENST00000696999.1:c.*214T>A ENSP00000513029.1:n.*214T>A
ENST00000697036.1:c.*638T>A ENSP00000513060.1:n.*638T>A
ENST00000697037.1:n.1257T>A
ENST00000697093.1:n.3458T>A
ENST00000697094.1:n.3805T>A
ENST00000697095.1:c.*2423T>A ENSP00000513104.1:n.*2423T>A
ENST00000697096.1:n.2355T>A
ENST00000697097.1:c.*214T>A ENSP00000513105.1:n.*214T>A
ENST00000562983.2:n.1408T>A
ENST00000690268.1:c.*214T>A ENSP00000509810.1:n.*214T>A
ENST00000355740.7:c.*548T>A ENSP00000347979.3:n.*548T>A
ENST00000640140.1:n.1394T>A
ENST00000640250.1:n.721T>A
ENST00000640681.1:n.1343T>A
ENST00000652046.1:c.*214T>A MANE Select ENSP00000498466.1:n.*214T>A
ENST00000352159.8:c.*539T>A ENSP00000345601.4:n.*539T>A
ENST00000355740.6:c.*214T>A ENSP00000347979.2:n.*214T>A
NM_000043.4:c.*214T>A , LRG_134t1:c.*214T>A NP_000034.1:n.*214T>A
NM_152871.2:c.*214T>A NP_690610.1:n.*214T>A
NM_152872.2:c.*534T>A NP_690611.1:n.*534T>A
NR_028033.2:n.1396T>A
NR_028034.2:n.1258T>A
NR_028035.2:n.1321T>A
NR_028036.2:n.1459T>A
XM_006717819.2:c.*214T>A XP_006717882.1:n.*214T>A
XM_011539764.1:c.*214T>A XP_011538066.1:n.*214T>A
XM_011539765.1:c.*214T>A XP_011538067.1:n.*214T>A
XM_011539766.1:c.*214T>A XP_011538068.1:n.*214T>A
XM_011539767.1:c.*214T>A XP_011538069.1:n.*214T>A
NM_000043.5:c.*214T>A NP_000034.1:n.*214T>A
NM_001320619.1:c.*545T>A NP_001307548.1:n.*545T>A
NM_152871.3:c.*214T>A NP_690610.1:n.*214T>A
NM_152872.3:c.*534T>A NP_690611.1:n.*534T>A
NR_028033.3:n.1368T>A
NR_028034.3:n.1230T>A
NR_028035.3:n.1293T>A
NR_028036.3:n.1431T>A
NR_135313.1:n.1348T>A
NR_135314.1:n.1531T>A
NR_135315.1:n.1284T>A
XM_006717819.3:c.*214T>A XP_006717882.1:n.*214T>A
XM_011539764.2:c.*214T>A XP_011538066.1:n.*214T>A
XM_011539765.2:c.*214T>A XP_011538067.1:n.*214T>A
XM_011539766.2:c.*214T>A XP_011538068.1:n.*214T>A
XM_011539767.3:c.*214T>A XP_011538069.1:n.*214T>A
XR_945732.3:n.1290T>A
XR_945733.2:n.1227T>A
NM_000043.6:c.*214T>A MANE Select NP_000034.1:n.*214T>A
NM_001320619.2:c.*545T>A NP_001307548.1:n.*545T>A
NM_152871.4:c.*214T>A NP_690610.1:n.*214T>A
NM_152872.4:c.*534T>A NP_690611.1:n.*534T>A
NR_028033.4:n.1129T>A
NR_028034.4:n.991T>A
NR_028035.4:n.1054T>A
NR_028036.4:n.1192T>A
NR_135313.2:n.1109T>A
NR_135314.2:n.1388T>A
NR_135315.2:n.1141T>A