Canonical Allele Identifier: CA1926639330

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014186T= , CM000672.2:g.89014186T=	GRCh38
NC_000010.10:g.90773943T= , CM000672.1:g.90773943T=	GRCh37
NC_000010.9:g.90763923T=	NCBI36
NG_009089.2:g.28656T= , LRG_134:g.28656T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1053T=
ENST00000355740.8:c.*67T=	ENSP00000347979.3:n.*67T=
ENST00000357339.7:c.681T=	ENSP00000349896.2:p.Phe227=
ENST00000371857.8:n.2289T=
ENST00000460510.6:c.27T=	ENSP00000512812.1:p.Phe9=
ENST00000466081.6:n.2393T=
ENST00000477270.6:c.789T=	ENSP00000512813.1:p.Phe263=
ENST00000479522.6:c.*173T=	ENSP00000424113.1:n.*173T=
ENST00000484444.6:c.*185T=	ENSP00000420975.1:n.*185T=
ENST00000488877.6:c.635T=	ENSP00000425159.1:n.635T=
ENST00000492756.7:c.*173T=	ENSP00000422453.1:n.*173T=
ENST00000494799.6:c.27T=	ENSP00000512834.1:p.Phe9=
ENST00000562983.3:c.27T=	ENSP00000512845.1:p.Phe9=
ENST00000612663.6:c.*146T=	ENSP00000477997.3:n.*146T=
ENST00000640140.2:n.889T=
ENST00000640250.2:n.243T=
ENST00000640681.2:n.848T=
ENST00000696723.1:n.4377T=
ENST00000696741.1:n.2382T=
ENST00000696742.1:n.2109T=
ENST00000696743.1:n.3512T=
ENST00000696744.1:n.783T=
ENST00000696767.1:n.1078T=
ENST00000696768.1:c.*67T=	ENSP00000512859.1:n.*67T=
ENST00000696769.1:n.2433T=
ENST00000696771.1:c.27T=	ENSP00000512860.1:p.Phe9=
ENST00000696772.1:n.2347T=
ENST00000696773.1:n.2086T=
ENST00000696774.1:n.5854T=
ENST00000696776.1:c.837T=	ENSP00000512861.1:p.Phe279=
ENST00000696777.1:n.2152T=
ENST00000696778.1:n.1180T=
ENST00000696779.1:c.351T=	ENSP00000512862.1:p.Phe117=
ENST00000696780.1:c.774T=	ENSP00000512863.1:p.Phe258=
ENST00000696781.1:c.489T=	ENSP00000512864.1:p.Phe163=
ENST00000696782.1:c.*146T=	ENSP00000512865.1:n.*146T=
ENST00000696783.1:n.2612T=
ENST00000696992.1:n.1861T=
ENST00000696995.1:n.4273T=
ENST00000696996.1:n.2186T=
ENST00000696997.1:c.*374T=	ENSP00000513028.1:n.*374T=
ENST00000696998.1:n.1998T=
ENST00000696999.1:c.27T=	ENSP00000513029.1:p.Phe9=
ENST00000697035.1:c.*77T=	ENSP00000513059.1:n.*77T=
ENST00000697036.1:c.*160T=	ENSP00000513060.1:n.*160T=
ENST00000697037.1:n.779T=
ENST00000697093.1:n.2980T=
ENST00000697094.1:n.3327T=
ENST00000697095.1:c.*1945T=	ENSP00000513104.1:n.*1945T=
ENST00000697096.1:n.1877T=
ENST00000697097.1:c.27T=	ENSP00000513105.1:p.Phe9=
ENST00000562983.2:n.930T=
ENST00000690268.1:c.825T=	ENSP00000509810.1:p.Phe275=
ENST00000355740.7:c.*70T=	ENSP00000347979.3:n.*70T=
ENST00000612663.5:c.*146T=	ENSP00000477997.3:n.*146T=
ENST00000640140.1:n.916T=
ENST00000640250.1:n.243T=
ENST00000640681.1:n.865T=
ENST00000652046.1:c.744T= MANE Select	ENSP00000498466.1:p.Phe248=
ENST00000352159.8:c.*61T=	ENSP00000345601.4:n.*61T=
ENST00000355279.2:c.719T=	ENSP00000347426.2:n.719T=
ENST00000355740.6:c.744T=	ENSP00000347979.2:p.Phe248=
ENST00000357339.6:c.681T=	ENSP00000349896.2:p.Phe227=
ENST00000479522.5:c.*173T=	ENSP00000424113.1:n.*173T=
ENST00000484444.5:c.*185T=	ENSP00000420975.1:n.*185T=
ENST00000488877.5:c.*185T=	ENSP00000425159.1:n.*185T=
ENST00000492756.5:c.572T=	ENSP00000422453.1:n.572T=
ENST00000494410.5:c.*102T=	ENSP00000423755.1:n.*102T=
ENST00000494799.5:n.651T=
ENST00000612663.4:c.*91T=	ENSP00000477997.2:n.*91T=
ENST00000615406.4:c.744T=	ENSP00000484575.1:p.Phe248=
NM_000043.4:c.744T= , LRG_134t1:c.744T=	NP_000034.1:p.Phe248=
NM_152871.2:c.681T=	NP_690610.1:p.Phe227=
NM_152872.2:c.*56T=	NP_690611.1:n.*56T=
NR_028033.2:n.918T=
NR_028034.2:n.780T=
NR_028035.2:n.843T=
NR_028036.2:n.981T=
XM_006717819.2:c.825T=	XP_006717882.1:p.Phe275=
XM_011539764.1:c.906T=	XP_011538066.1:p.Phe302=
XM_011539765.1:c.843T=	XP_011538067.1:p.Phe281=
XM_011539766.1:c.825T=	XP_011538068.1:p.Phe275=
XM_011539767.1:c.789T=	XP_011538069.1:p.Phe263=
XR_945732.1:n.812T=
XR_945733.1:n.749T=
NM_000043.5:c.744T=	NP_000034.1:p.Phe248=
NM_001320619.1:c.*67T=	NP_001307548.1:n.*67T=
NM_152871.3:c.681T=	NP_690610.1:p.Phe227=
NM_152872.3:c.*56T=	NP_690611.1:n.*56T=
NR_028033.3:n.890T=
NR_028034.3:n.752T=
NR_028035.3:n.815T=
NR_028036.3:n.953T=
NR_135313.1:n.870T=
NR_135314.1:n.1053T=
NR_135315.1:n.806T=
XM_006717819.3:c.825T=	XP_006717882.1:p.Phe275=
XM_011539764.2:c.906T=	XP_011538066.1:p.Phe302=
XM_011539765.2:c.843T=	XP_011538067.1:p.Phe281=
XM_011539766.2:c.825T=	XP_011538068.1:p.Phe275=
XM_011539767.3:c.789T=	XP_011538069.1:p.Phe263=
XR_945732.3:n.812T=
XR_945733.2:n.749T=
NM_000043.6:c.744T= MANE Select	NP_000034.1:p.Phe248=
NM_001320619.2:c.*67T=	NP_001307548.1:n.*67T=
NM_152871.4:c.681T=	NP_690610.1:p.Phe227=
NM_152872.4:c.*56T=	NP_690611.1:n.*56T=
NR_028033.4:n.651T=
NR_028034.4:n.513T=
NR_028035.4:n.576T=
NR_028036.4:n.714T=
NR_135313.2:n.631T=
NR_135314.2:n.910T=
NR_135315.2:n.663T=