Canonical Allele Identifier: CA377510087
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014349C>T , CM000672.2:g.89014349C>T GRCh38
NC_000010.10:g.90774106C>T , CM000672.1:g.90774106C>T GRCh37
NC_000010.9:g.90764086C>T NCBI36
NG_009089.2:g.28819C>T , LRG_134:g.28819C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1216C>T
ENST00000355740.8:c.*230C>T ENSP00000347979.3:n.*230C>T
ENST00000357339.7:c.844C>T ENSP00000349896.2:p.Leu282Phe
ENST00000371857.8:n.2452C>T
ENST00000460510.6:c.190C>T ENSP00000512812.1:p.Leu64Phe
ENST00000466081.6:n.2556C>T
ENST00000477270.6:c.952C>T ENSP00000512813.1:p.Leu318Phe
ENST00000479522.6:c.*336C>T ENSP00000424113.1:n.*336C>T
ENST00000484444.6:c.*348C>T ENSP00000420975.1:n.*348C>T
ENST00000488877.6:c.798C>T ENSP00000425159.1:n.798C>T
ENST00000492756.7:c.*336C>T ENSP00000422453.1:n.*336C>T
ENST00000494799.6:c.190C>T ENSP00000512834.1:p.Leu64Phe
ENST00000562983.3:c.190C>T ENSP00000512845.1:p.Leu64Phe
ENST00000612663.6:c.*309C>T ENSP00000477997.3:n.*309C>T
ENST00000640140.2:n.1052C>T
ENST00000640250.2:n.406C>T
ENST00000640681.2:n.1011C>T
ENST00000696723.1:n.4540C>T
ENST00000696741.1:n.2545C>T
ENST00000696742.1:n.2272C>T
ENST00000696743.1:n.3675C>T
ENST00000696744.1:n.946C>T
ENST00000696767.1:n.1241C>T
ENST00000696768.1:c.*230C>T ENSP00000512859.1:n.*230C>T
ENST00000696769.1:n.2596C>T
ENST00000696771.1:c.190C>T ENSP00000512860.1:p.Leu64Phe
ENST00000696772.1:n.2510C>T
ENST00000696773.1:n.2249C>T
ENST00000696774.1:n.6017C>T
ENST00000696776.1:c.1000C>T ENSP00000512861.1:p.Leu334Phe
ENST00000696777.1:n.2315C>T
ENST00000696778.1:n.1343C>T
ENST00000696779.1:c.514C>T ENSP00000512862.1:p.Leu172Phe
ENST00000696780.1:c.937C>T ENSP00000512863.1:p.Leu313Phe
ENST00000696781.1:c.652C>T ENSP00000512864.1:p.Leu218Phe
ENST00000696782.1:c.*309C>T ENSP00000512865.1:n.*309C>T
ENST00000696783.1:n.2775C>T
ENST00000696992.1:n.2024C>T
ENST00000696995.1:n.4436C>T
ENST00000696996.1:n.2349C>T
ENST00000696997.1:c.*537C>T ENSP00000513028.1:n.*537C>T
ENST00000696998.1:n.2161C>T
ENST00000696999.1:c.190C>T ENSP00000513029.1:p.Leu64Phe
ENST00000697036.1:c.*323C>T ENSP00000513060.1:n.*323C>T
ENST00000697037.1:n.942C>T
ENST00000697093.1:n.3143C>T
ENST00000697094.1:n.3490C>T
ENST00000697095.1:c.*2108C>T ENSP00000513104.1:n.*2108C>T
ENST00000697096.1:n.2040C>T
ENST00000697097.1:c.190C>T ENSP00000513105.1:p.Leu64Phe
ENST00000562983.2:n.1093C>T
ENST00000690268.1:c.988C>T ENSP00000509810.1:p.Leu330Phe
ENST00000355740.7:c.*233C>T ENSP00000347979.3:n.*233C>T
ENST00000612663.5:c.*309C>T ENSP00000477997.3:n.*309C>T
ENST00000640140.1:n.1079C>T
ENST00000640250.1:n.406C>T
ENST00000640681.1:n.1028C>T
ENST00000652046.1:c.907C>T MANE Select ENSP00000498466.1:p.Leu303Phe
ENST00000352159.8:c.*224C>T ENSP00000345601.4:n.*224C>T
ENST00000355279.2:c.882C>T ENSP00000347426.2:n.882C>T
ENST00000355740.6:c.907C>T ENSP00000347979.2:p.Leu303Phe
ENST00000357339.6:c.844C>T ENSP00000349896.2:p.Leu282Phe
ENST00000479522.5:c.*336C>T ENSP00000424113.1:n.*336C>T
ENST00000484444.5:c.*348C>T ENSP00000420975.1:n.*348C>T
ENST00000488877.5:c.*348C>T ENSP00000425159.1:n.*348C>T
ENST00000492756.5:c.735C>T ENSP00000422453.1:n.735C>T
ENST00000494410.5:c.*265C>T ENSP00000423755.1:n.*265C>T
ENST00000612663.4:c.*254C>T ENSP00000477997.2:n.*254C>T
NM_000043.4:c.907C>T , LRG_134t1:c.907C>T NP_000034.1:p.Leu303Phe
NM_152871.2:c.844C>T NP_690610.1:p.Leu282Phe
NM_152872.2:c.*219C>T NP_690611.1:n.*219C>T
NR_028033.2:n.1081C>T
NR_028034.2:n.943C>T
NR_028035.2:n.1006C>T
NR_028036.2:n.1144C>T
XM_006717819.2:c.988C>T XP_006717882.1:p.Leu330Phe
XM_011539764.1:c.1069C>T XP_011538066.1:p.Leu357Phe
XM_011539765.1:c.1006C>T XP_011538067.1:p.Leu336Phe
XM_011539766.1:c.988C>T XP_011538068.1:p.Leu330Phe
XM_011539767.1:c.952C>T XP_011538069.1:p.Leu318Phe
XR_945732.1:n.975C>T
XR_945733.1:n.912C>T
NM_000043.5:c.907C>T NP_000034.1:p.Leu303Phe
NM_001320619.1:c.*230C>T NP_001307548.1:n.*230C>T
NM_152871.3:c.844C>T NP_690610.1:p.Leu282Phe
NM_152872.3:c.*219C>T NP_690611.1:n.*219C>T
NR_028033.3:n.1053C>T
NR_028034.3:n.915C>T
NR_028035.3:n.978C>T
NR_028036.3:n.1116C>T
NR_135313.1:n.1033C>T
NR_135314.1:n.1216C>T
NR_135315.1:n.969C>T
XM_006717819.3:c.988C>T XP_006717882.1:p.Leu330Phe
XM_011539764.2:c.1069C>T XP_011538066.1:p.Leu357Phe
XM_011539765.2:c.1006C>T XP_011538067.1:p.Leu336Phe
XM_011539766.2:c.988C>T XP_011538068.1:p.Leu330Phe
XM_011539767.3:c.952C>T XP_011538069.1:p.Leu318Phe
XR_945732.3:n.975C>T
XR_945733.2:n.912C>T
NM_000043.6:c.907C>T MANE Select NP_000034.1:p.Leu303Phe
NM_001320619.2:c.*230C>T NP_001307548.1:n.*230C>T
NM_152871.4:c.844C>T NP_690610.1:p.Leu282Phe
NM_152872.4:c.*219C>T NP_690611.1:n.*219C>T
NR_028033.4:n.814C>T
NR_028034.4:n.676C>T
NR_028035.4:n.739C>T
NR_028036.4:n.877C>T
NR_135313.2:n.794C>T
NR_135314.2:n.1073C>T
NR_135315.2:n.826C>T