Canonical Allele Identifier: CA1926639397

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014353G= , CM000672.2:g.89014353G=	GRCh38
NC_000010.10:g.90774110G= , CM000672.1:g.90774110G=	GRCh37
NC_000010.9:g.90764090G=	NCBI36
NG_009089.2:g.28823G= , LRG_134:g.28823G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1220G=
ENST00000355740.8:c.*234G=	ENSP00000347979.3:n.*234G=
ENST00000357339.7:c.848G=	ENSP00000349896.2:p.Cys283=
ENST00000371857.8:n.2456G=
ENST00000460510.6:c.194G=	ENSP00000512812.1:p.Cys65=
ENST00000466081.6:n.2560G=
ENST00000477270.6:c.956G=	ENSP00000512813.1:p.Cys319=
ENST00000479522.6:c.*340G=	ENSP00000424113.1:n.*340G=
ENST00000484444.6:c.*352G=	ENSP00000420975.1:n.*352G=
ENST00000488877.6:c.802G=	ENSP00000425159.1:n.802G=
ENST00000492756.7:c.*340G=	ENSP00000422453.1:n.*340G=
ENST00000494799.6:c.194G=	ENSP00000512834.1:p.Cys65=
ENST00000562983.3:c.194G=	ENSP00000512845.1:p.Cys65=
ENST00000612663.6:c.*313G=	ENSP00000477997.3:n.*313G=
ENST00000640140.2:n.1056G=
ENST00000640250.2:n.410G=
ENST00000640681.2:n.1015G=
ENST00000696723.1:n.4544G=
ENST00000696741.1:n.2549G=
ENST00000696742.1:n.2276G=
ENST00000696743.1:n.3679G=
ENST00000696744.1:n.950G=
ENST00000696767.1:n.1245G=
ENST00000696768.1:c.*234G=	ENSP00000512859.1:n.*234G=
ENST00000696769.1:n.2600G=
ENST00000696771.1:c.194G=	ENSP00000512860.1:p.Cys65=
ENST00000696772.1:n.2514G=
ENST00000696773.1:n.2253G=
ENST00000696774.1:n.6021G=
ENST00000696776.1:c.1004G=	ENSP00000512861.1:p.Cys335=
ENST00000696777.1:n.2319G=
ENST00000696778.1:n.1347G=
ENST00000696779.1:c.518G=	ENSP00000512862.1:p.Cys173=
ENST00000696780.1:c.941G=	ENSP00000512863.1:p.Cys314=
ENST00000696781.1:c.656G=	ENSP00000512864.1:p.Cys219=
ENST00000696782.1:c.*313G=	ENSP00000512865.1:n.*313G=
ENST00000696783.1:n.2779G=
ENST00000696992.1:n.2028G=
ENST00000696995.1:n.4440G=
ENST00000696996.1:n.2353G=
ENST00000696997.1:c.*541G=	ENSP00000513028.1:n.*541G=
ENST00000696998.1:n.2165G=
ENST00000696999.1:c.194G=	ENSP00000513029.1:p.Cys65=
ENST00000697036.1:c.*327G=	ENSP00000513060.1:n.*327G=
ENST00000697037.1:n.946G=
ENST00000697093.1:n.3147G=
ENST00000697094.1:n.3494G=
ENST00000697095.1:c.*2112G=	ENSP00000513104.1:n.*2112G=
ENST00000697096.1:n.2044G=
ENST00000697097.1:c.194G=	ENSP00000513105.1:p.Cys65=
ENST00000562983.2:n.1097G=
ENST00000690268.1:c.992G=	ENSP00000509810.1:p.Cys331=
ENST00000355740.7:c.*237G=	ENSP00000347979.3:n.*237G=
ENST00000612663.5:c.*313G=	ENSP00000477997.3:n.*313G=
ENST00000640140.1:n.1083G=
ENST00000640250.1:n.410G=
ENST00000640681.1:n.1032G=
ENST00000652046.1:c.911G= MANE Select	ENSP00000498466.1:p.Cys304=
ENST00000352159.8:c.*228G=	ENSP00000345601.4:n.*228G=
ENST00000355279.2:c.886G=	ENSP00000347426.2:n.886G=
ENST00000355740.6:c.911G=	ENSP00000347979.2:p.Cys304=
ENST00000357339.6:c.848G=	ENSP00000349896.2:p.Cys283=
ENST00000479522.5:c.*340G=	ENSP00000424113.1:n.*340G=
ENST00000484444.5:c.*352G=	ENSP00000420975.1:n.*352G=
ENST00000488877.5:c.*352G=	ENSP00000425159.1:n.*352G=
ENST00000492756.5:c.739G=	ENSP00000422453.1:n.739G=
ENST00000494410.5:c.*269G=	ENSP00000423755.1:n.*269G=
ENST00000612663.4:c.*258G=	ENSP00000477997.2:n.*258G=
NM_000043.4:c.911G= , LRG_134t1:c.911G=	NP_000034.1:p.Cys304=
NM_152871.2:c.848G=	NP_690610.1:p.Cys283=
NM_152872.2:c.*223G=	NP_690611.1:n.*223G=
NR_028033.2:n.1085G=
NR_028034.2:n.947G=
NR_028035.2:n.1010G=
NR_028036.2:n.1148G=
XM_006717819.2:c.992G=	XP_006717882.1:p.Cys331=
XM_011539764.1:c.1073G=	XP_011538066.1:p.Cys358=
XM_011539765.1:c.1010G=	XP_011538067.1:p.Cys337=
XM_011539766.1:c.992G=	XP_011538068.1:p.Cys331=
XM_011539767.1:c.956G=	XP_011538069.1:p.Cys319=
XR_945732.1:n.979G=
XR_945733.1:n.916G=
NM_000043.5:c.911G=	NP_000034.1:p.Cys304=
NM_001320619.1:c.*234G=	NP_001307548.1:n.*234G=
NM_152871.3:c.848G=	NP_690610.1:p.Cys283=
NM_152872.3:c.*223G=	NP_690611.1:n.*223G=
NR_028033.3:n.1057G=
NR_028034.3:n.919G=
NR_028035.3:n.982G=
NR_028036.3:n.1120G=
NR_135313.1:n.1037G=
NR_135314.1:n.1220G=
NR_135315.1:n.973G=
XM_006717819.3:c.992G=	XP_006717882.1:p.Cys331=
XM_011539764.2:c.1073G=	XP_011538066.1:p.Cys358=
XM_011539765.2:c.1010G=	XP_011538067.1:p.Cys337=
XM_011539766.2:c.992G=	XP_011538068.1:p.Cys331=
XM_011539767.3:c.956G=	XP_011538069.1:p.Cys319=
XR_945732.3:n.979G=
XR_945733.2:n.916G=
NM_000043.6:c.911G= MANE Select	NP_000034.1:p.Cys304=
NM_001320619.2:c.*234G=	NP_001307548.1:n.*234G=
NM_152871.4:c.848G=	NP_690610.1:p.Cys283=
NM_152872.4:c.*223G=	NP_690611.1:n.*223G=
NR_028033.4:n.818G=
NR_028034.4:n.680G=
NR_028035.4:n.743G=
NR_028036.4:n.881G=
NR_135313.2:n.798G=
NR_135314.2:n.1077G=
NR_135315.2:n.830G=