Canonical Allele Identifier: CA377509950

Gene: FAS

Linked Data

• COSMIC: COSM4610602
• MyVariant Identifiers: chr10:g.90774047A>G (hg19) ; chr10:g.89014290A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014290A>G , CM000672.2:g.89014290A>G	GRCh38
NC_000010.10:g.90774047A>G , CM000672.1:g.90774047A>G	GRCh37
NC_000010.9:g.90764027A>G	NCBI36
NG_009089.2:g.28760A>G , LRG_134:g.28760A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1157A>G
ENST00000355740.8:c.*171A>G	ENSP00000347979.3:n.*171A>G
ENST00000357339.7:c.785A>G	ENSP00000349896.2:p.Gln262Arg
ENST00000371857.8:n.2393A>G
ENST00000460510.6:c.131A>G	ENSP00000512812.1:p.Gln44Arg
ENST00000466081.6:n.2497A>G
ENST00000477270.6:c.893A>G	ENSP00000512813.1:p.Gln298Arg
ENST00000479522.6:c.*277A>G	ENSP00000424113.1:n.*277A>G
ENST00000484444.6:c.*289A>G	ENSP00000420975.1:n.*289A>G
ENST00000488877.6:c.739A>G	ENSP00000425159.1:n.739A>G
ENST00000492756.7:c.*277A>G	ENSP00000422453.1:n.*277A>G
ENST00000494799.6:c.131A>G	ENSP00000512834.1:p.Gln44Arg
ENST00000562983.3:c.131A>G	ENSP00000512845.1:p.Gln44Arg
ENST00000612663.6:c.*250A>G	ENSP00000477997.3:n.*250A>G
ENST00000640140.2:n.993A>G
ENST00000640250.2:n.347A>G
ENST00000640681.2:n.952A>G
ENST00000696723.1:n.4481A>G
ENST00000696741.1:n.2486A>G
ENST00000696742.1:n.2213A>G
ENST00000696743.1:n.3616A>G
ENST00000696744.1:n.887A>G
ENST00000696767.1:n.1182A>G
ENST00000696768.1:c.*171A>G	ENSP00000512859.1:n.*171A>G
ENST00000696769.1:n.2537A>G
ENST00000696771.1:c.131A>G	ENSP00000512860.1:p.Gln44Arg
ENST00000696772.1:n.2451A>G
ENST00000696773.1:n.2190A>G
ENST00000696774.1:n.5958A>G
ENST00000696776.1:c.941A>G	ENSP00000512861.1:p.Gln314Arg
ENST00000696777.1:n.2256A>G
ENST00000696778.1:n.1284A>G
ENST00000696779.1:c.455A>G	ENSP00000512862.1:p.Gln152Arg
ENST00000696780.1:c.878A>G	ENSP00000512863.1:p.Gln293Arg
ENST00000696781.1:c.593A>G	ENSP00000512864.1:p.Gln198Arg
ENST00000696782.1:c.*250A>G	ENSP00000512865.1:n.*250A>G
ENST00000696783.1:n.2716A>G
ENST00000696992.1:n.1965A>G
ENST00000696995.1:n.4377A>G
ENST00000696996.1:n.2290A>G
ENST00000696997.1:c.*478A>G	ENSP00000513028.1:n.*478A>G
ENST00000696998.1:n.2102A>G
ENST00000696999.1:c.131A>G	ENSP00000513029.1:p.Gln44Arg
ENST00000697035.1:c.*181A>G	ENSP00000513059.1:n.*181A>G
ENST00000697036.1:c.*264A>G	ENSP00000513060.1:n.*264A>G
ENST00000697037.1:n.883A>G
ENST00000697093.1:n.3084A>G
ENST00000697094.1:n.3431A>G
ENST00000697095.1:c.*2049A>G	ENSP00000513104.1:n.*2049A>G
ENST00000697096.1:n.1981A>G
ENST00000697097.1:c.131A>G	ENSP00000513105.1:p.Gln44Arg
ENST00000562983.2:n.1034A>G
ENST00000690268.1:c.929A>G	ENSP00000509810.1:p.Gln310Arg
ENST00000355740.7:c.*174A>G	ENSP00000347979.3:n.*174A>G
ENST00000612663.5:c.*250A>G	ENSP00000477997.3:n.*250A>G
ENST00000640140.1:n.1020A>G
ENST00000640250.1:n.347A>G
ENST00000640681.1:n.969A>G
ENST00000652046.1:c.848A>G MANE Select	ENSP00000498466.1:p.Gln283Arg
ENST00000352159.8:c.*165A>G	ENSP00000345601.4:n.*165A>G
ENST00000355279.2:c.823A>G	ENSP00000347426.2:n.823A>G
ENST00000355740.6:c.848A>G	ENSP00000347979.2:p.Gln283Arg
ENST00000357339.6:c.785A>G	ENSP00000349896.2:p.Gln262Arg
ENST00000479522.5:c.*277A>G	ENSP00000424113.1:n.*277A>G
ENST00000484444.5:c.*289A>G	ENSP00000420975.1:n.*289A>G
ENST00000488877.5:c.*289A>G	ENSP00000425159.1:n.*289A>G
ENST00000492756.5:c.676A>G	ENSP00000422453.1:n.676A>G
ENST00000494410.5:c.*206A>G	ENSP00000423755.1:n.*206A>G
ENST00000612663.4:c.*195A>G	ENSP00000477997.2:n.*195A>G
NM_000043.4:c.848A>G , LRG_134t1:c.848A>G	NP_000034.1:p.Gln283Arg
NM_152871.2:c.785A>G	NP_690610.1:p.Gln262Arg
NM_152872.2:c.*160A>G	NP_690611.1:n.*160A>G
NR_028033.2:n.1022A>G
NR_028034.2:n.884A>G
NR_028035.2:n.947A>G
NR_028036.2:n.1085A>G
XM_006717819.2:c.929A>G	XP_006717882.1:p.Gln310Arg
XM_011539764.1:c.1010A>G	XP_011538066.1:p.Gln337Arg
XM_011539765.1:c.947A>G	XP_011538067.1:p.Gln316Arg
XM_011539766.1:c.929A>G	XP_011538068.1:p.Gln310Arg
XM_011539767.1:c.893A>G	XP_011538069.1:p.Gln298Arg
XR_945732.1:n.916A>G
XR_945733.1:n.853A>G
NM_000043.5:c.848A>G	NP_000034.1:p.Gln283Arg
NM_001320619.1:c.*171A>G	NP_001307548.1:n.*171A>G
NM_152871.3:c.785A>G	NP_690610.1:p.Gln262Arg
NM_152872.3:c.*160A>G	NP_690611.1:n.*160A>G
NR_028033.3:n.994A>G
NR_028034.3:n.856A>G
NR_028035.3:n.919A>G
NR_028036.3:n.1057A>G
NR_135313.1:n.974A>G
NR_135314.1:n.1157A>G
NR_135315.1:n.910A>G
XM_006717819.3:c.929A>G	XP_006717882.1:p.Gln310Arg
XM_011539764.2:c.1010A>G	XP_011538066.1:p.Gln337Arg
XM_011539765.2:c.947A>G	XP_011538067.1:p.Gln316Arg
XM_011539766.2:c.929A>G	XP_011538068.1:p.Gln310Arg
XM_011539767.3:c.893A>G	XP_011538069.1:p.Gln298Arg
XR_945732.3:n.916A>G
XR_945733.2:n.853A>G
NM_000043.6:c.848A>G MANE Select	NP_000034.1:p.Gln283Arg
NM_001320619.2:c.*171A>G	NP_001307548.1:n.*171A>G
NM_152871.4:c.785A>G	NP_690610.1:p.Gln262Arg
NM_152872.4:c.*160A>G	NP_690611.1:n.*160A>G
NR_028033.4:n.755A>G
NR_028034.4:n.617A>G
NR_028035.4:n.680A>G
NR_028036.4:n.818A>G
NR_135313.2:n.735A>G
NR_135314.2:n.1014A>G
NR_135315.2:n.767A>G