Canonical Allele Identifier: CA377510160
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014384C>G , CM000672.2:g.89014384C>G GRCh38
NC_000010.10:g.90774141C>G , CM000672.1:g.90774141C>G GRCh37
NC_000010.9:g.90764121C>G NCBI36
NG_009089.2:g.28854C>G , LRG_134:g.28854C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1251C>G
ENST00000355740.8:c.*265C>G ENSP00000347979.3:n.*265C>G
ENST00000357339.7:c.879C>G ENSP00000349896.2:p.Ile293Met
ENST00000371857.8:n.2487C>G
ENST00000460510.6:c.225C>G ENSP00000512812.1:p.Ile75Met
ENST00000466081.6:n.2591C>G
ENST00000477270.6:c.987C>G ENSP00000512813.1:p.Ile329Met
ENST00000479522.6:c.*371C>G ENSP00000424113.1:n.*371C>G
ENST00000484444.6:c.*383C>G ENSP00000420975.1:n.*383C>G
ENST00000488877.6:c.833C>G ENSP00000425159.1:n.833C>G
ENST00000492756.7:c.*371C>G ENSP00000422453.1:n.*371C>G
ENST00000494799.6:c.225C>G ENSP00000512834.1:p.Ile75Met
ENST00000562983.3:c.225C>G ENSP00000512845.1:p.Ile75Met
ENST00000612663.6:c.*344C>G ENSP00000477997.3:n.*344C>G
ENST00000640140.2:n.1087C>G
ENST00000640250.2:n.441C>G
ENST00000640681.2:n.1046C>G
ENST00000696723.1:n.4575C>G
ENST00000696741.1:n.2580C>G
ENST00000696742.1:n.2307C>G
ENST00000696743.1:n.3710C>G
ENST00000696744.1:n.981C>G
ENST00000696767.1:n.1276C>G
ENST00000696768.1:c.*265C>G ENSP00000512859.1:n.*265C>G
ENST00000696769.1:n.2631C>G
ENST00000696771.1:c.225C>G ENSP00000512860.1:p.Ile75Met
ENST00000696772.1:n.2545C>G
ENST00000696773.1:n.2284C>G
ENST00000696774.1:n.6052C>G
ENST00000696776.1:c.1035C>G ENSP00000512861.1:p.Ile345Met
ENST00000696777.1:n.2350C>G
ENST00000696778.1:n.1378C>G
ENST00000696779.1:c.549C>G ENSP00000512862.1:p.Ile183Met
ENST00000696780.1:c.972C>G ENSP00000512863.1:p.Ile324Met
ENST00000696781.1:c.687C>G ENSP00000512864.1:p.Ile229Met
ENST00000696782.1:c.*344C>G ENSP00000512865.1:n.*344C>G
ENST00000696783.1:n.2810C>G
ENST00000696992.1:n.2059C>G
ENST00000696995.1:n.4471C>G
ENST00000696996.1:n.2384C>G
ENST00000696997.1:c.*572C>G ENSP00000513028.1:n.*572C>G
ENST00000696998.1:n.2196C>G
ENST00000696999.1:c.225C>G ENSP00000513029.1:p.Ile75Met
ENST00000697036.1:c.*358C>G ENSP00000513060.1:n.*358C>G
ENST00000697037.1:n.977C>G
ENST00000697093.1:n.3178C>G
ENST00000697094.1:n.3525C>G
ENST00000697095.1:c.*2143C>G ENSP00000513104.1:n.*2143C>G
ENST00000697096.1:n.2075C>G
ENST00000697097.1:c.225C>G ENSP00000513105.1:p.Ile75Met
ENST00000562983.2:n.1128C>G
ENST00000690268.1:c.1023C>G ENSP00000509810.1:p.Ile341Met
ENST00000355740.7:c.*268C>G ENSP00000347979.3:n.*268C>G
ENST00000612663.5:c.*344C>G ENSP00000477997.3:n.*344C>G
ENST00000640140.1:n.1114C>G
ENST00000640250.1:n.441C>G
ENST00000640681.1:n.1063C>G
ENST00000652046.1:c.942C>G MANE Select ENSP00000498466.1:p.Ile314Met
ENST00000352159.8:c.*259C>G ENSP00000345601.4:n.*259C>G
ENST00000355279.2:c.917C>G ENSP00000347426.2:n.917C>G
ENST00000355740.6:c.942C>G ENSP00000347979.2:p.Ile314Met
ENST00000357339.6:c.879C>G ENSP00000349896.2:p.Ile293Met
ENST00000479522.5:c.*371C>G ENSP00000424113.1:n.*371C>G
ENST00000484444.5:c.*383C>G ENSP00000420975.1:n.*383C>G
ENST00000488877.5:c.*383C>G ENSP00000425159.1:n.*383C>G
ENST00000492756.5:c.770C>G ENSP00000422453.1:n.770C>G
ENST00000494410.5:c.*300C>G ENSP00000423755.1:n.*300C>G
ENST00000612663.4:c.*289C>G ENSP00000477997.2:n.*289C>G
NM_000043.4:c.942C>G , LRG_134t1:c.942C>G NP_000034.1:p.Ile314Met
NM_152871.2:c.879C>G NP_690610.1:p.Ile293Met
NM_152872.2:c.*254C>G NP_690611.1:n.*254C>G
NR_028033.2:n.1116C>G
NR_028034.2:n.978C>G
NR_028035.2:n.1041C>G
NR_028036.2:n.1179C>G
XM_006717819.2:c.1023C>G XP_006717882.1:p.Ile341Met
XM_011539764.1:c.1104C>G XP_011538066.1:p.Ile368Met
XM_011539765.1:c.1041C>G XP_011538067.1:p.Ile347Met
XM_011539766.1:c.1023C>G XP_011538068.1:p.Ile341Met
XM_011539767.1:c.987C>G XP_011538069.1:p.Ile329Met
XR_945733.1:n.947C>G
NM_000043.5:c.942C>G NP_000034.1:p.Ile314Met
NM_001320619.1:c.*265C>G NP_001307548.1:n.*265C>G
NM_152871.3:c.879C>G NP_690610.1:p.Ile293Met
NM_152872.3:c.*254C>G NP_690611.1:n.*254C>G
NR_028033.3:n.1088C>G
NR_028034.3:n.950C>G
NR_028035.3:n.1013C>G
NR_028036.3:n.1151C>G
NR_135313.1:n.1068C>G
NR_135314.1:n.1251C>G
NR_135315.1:n.1004C>G
XM_006717819.3:c.1023C>G XP_006717882.1:p.Ile341Met
XM_011539764.2:c.1104C>G XP_011538066.1:p.Ile368Met
XM_011539765.2:c.1041C>G XP_011538067.1:p.Ile347Met
XM_011539766.2:c.1023C>G XP_011538068.1:p.Ile341Met
XM_011539767.3:c.987C>G XP_011538069.1:p.Ile329Met
XR_945732.3:n.1010C>G
XR_945733.2:n.947C>G
NM_000043.6:c.942C>G MANE Select NP_000034.1:p.Ile314Met
NM_001320619.2:c.*265C>G NP_001307548.1:n.*265C>G
NM_152871.4:c.879C>G NP_690610.1:p.Ile293Met
NM_152872.4:c.*254C>G NP_690611.1:n.*254C>G
NR_028033.4:n.849C>G
NR_028034.4:n.711C>G
NR_028035.4:n.774C>G
NR_028036.4:n.912C>G
NR_135313.2:n.829C>G
NR_135314.2:n.1108C>G
NR_135315.2:n.861C>G