Canonical Allele Identifier: CA1926639317

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014156A= , CM000672.2:g.89014156A=	GRCh38
NC_000010.10:g.90773913A= , CM000672.1:g.90773913A=	GRCh37
NC_000010.9:g.90763893A=	NCBI36
NG_009089.2:g.28626A= , LRG_134:g.28626A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1023A=
ENST00000355740.8:c.*37A=	ENSP00000347979.3:n.*37A=
ENST00000357339.7:c.651A=	ENSP00000349896.2:p.Gly217=
ENST00000371857.8:n.2259A=
ENST00000460510.6:c.-4A=	ENSP00000512812.1:n.-4A=
ENST00000466081.6:n.2363A=
ENST00000477270.6:c.759A=	ENSP00000512813.1:p.Gly253=
ENST00000479522.6:c.*143A=	ENSP00000424113.1:n.*143A=
ENST00000484444.6:c.*155A=	ENSP00000420975.1:n.*155A=
ENST00000488877.6:c.605A=	ENSP00000425159.1:n.605A=
ENST00000492756.7:c.*143A=	ENSP00000422453.1:n.*143A=
ENST00000494799.6:c.-4A=	ENSP00000512834.1:n.-4A=
ENST00000562983.3:c.-4A=	ENSP00000512845.1:n.-4A=
ENST00000612663.6:c.*116A=	ENSP00000477997.3:n.*116A=
ENST00000640140.2:n.859A=
ENST00000640250.2:n.213A=
ENST00000640681.2:n.818A=
ENST00000696723.1:n.4347A=
ENST00000696741.1:n.2352A=
ENST00000696742.1:n.2079A=
ENST00000696743.1:n.3482A=
ENST00000696744.1:n.753A=
ENST00000696767.1:n.1048A=
ENST00000696768.1:c.*37A=	ENSP00000512859.1:n.*37A=
ENST00000696769.1:n.2403A=
ENST00000696771.1:c.-4A=	ENSP00000512860.1:n.-4A=
ENST00000696772.1:n.2317A=
ENST00000696773.1:n.2056A=
ENST00000696774.1:n.5824A=
ENST00000696776.1:c.807A=	ENSP00000512861.1:p.Gly269=
ENST00000696777.1:n.2122A=
ENST00000696778.1:n.1150A=
ENST00000696779.1:c.321A=	ENSP00000512862.1:p.Gly107=
ENST00000696780.1:c.744A=	ENSP00000512863.1:p.Gly248=
ENST00000696781.1:c.459A=	ENSP00000512864.1:p.Gly153=
ENST00000696782.1:c.*116A=	ENSP00000512865.1:n.*116A=
ENST00000696783.1:n.2582A=
ENST00000696992.1:n.1831A=
ENST00000696995.1:n.4243A=
ENST00000696996.1:n.2156A=
ENST00000696997.1:c.*344A=	ENSP00000513028.1:n.*344A=
ENST00000696998.1:n.1968A=
ENST00000696999.1:c.-4A=	ENSP00000513029.1:n.-4A=
ENST00000697035.1:c.*47A=	ENSP00000513059.1:n.*47A=
ENST00000697036.1:c.*130A=	ENSP00000513060.1:n.*130A=
ENST00000697037.1:n.749A=
ENST00000697093.1:n.2950A=
ENST00000697094.1:n.3297A=
ENST00000697095.1:c.*1915A=	ENSP00000513104.1:n.*1915A=
ENST00000697096.1:n.1847A=
ENST00000697097.1:c.-4A=	ENSP00000513105.1:n.-4A=
ENST00000562983.2:n.900A=
ENST00000690268.1:c.795A=	ENSP00000509810.1:p.Gly265=
ENST00000355740.7:c.*40A=	ENSP00000347979.3:n.*40A=
ENST00000612663.5:c.*116A=	ENSP00000477997.3:n.*116A=
ENST00000640140.1:n.886A=
ENST00000640250.1:n.213A=
ENST00000640681.1:n.835A=
ENST00000652046.1:c.714A= MANE Select	ENSP00000498466.1:p.Gly238=
ENST00000313771.9:n.1023A=
ENST00000352159.8:c.*31A=	ENSP00000345601.4:n.*31A=
ENST00000355279.2:c.689A=	ENSP00000347426.2:n.689A=
ENST00000355740.6:c.714A=	ENSP00000347979.2:p.Gly238=
ENST00000357339.6:c.651A=	ENSP00000349896.2:p.Gly217=
ENST00000479522.5:c.*143A=	ENSP00000424113.1:n.*143A=
ENST00000484444.5:c.*155A=	ENSP00000420975.1:n.*155A=
ENST00000488877.5:c.*155A=	ENSP00000425159.1:n.*155A=
ENST00000492756.5:c.542A=	ENSP00000422453.1:n.542A=
ENST00000494410.5:c.*72A=	ENSP00000423755.1:n.*72A=
ENST00000494799.5:n.621A=
ENST00000612663.4:c.*61A=	ENSP00000477997.2:n.*61A=
ENST00000615406.4:c.714A=	ENSP00000484575.1:p.Gly238=
ENST00000626542.2:c.712A=	ENSP00000485876.1:p.Ser238=
NM_000043.4:c.714A= , LRG_134t1:c.714A=	NP_000034.1:p.Gly238=
NM_152871.2:c.651A=	NP_690610.1:p.Gly217=
NM_152872.2:c.*26A=	NP_690611.1:n.*26A=
NR_028033.2:n.888A=
NR_028034.2:n.750A=
NR_028035.2:n.813A=
NR_028036.2:n.951A=
XM_006717819.2:c.795A=	XP_006717882.1:p.Gly265=
XM_011539764.1:c.876A=	XP_011538066.1:p.Gly292=
XM_011539765.1:c.813A=	XP_011538067.1:p.Gly271=
XM_011539766.1:c.795A=	XP_011538068.1:p.Gly265=
XM_011539767.1:c.759A=	XP_011538069.1:p.Gly253=
XR_945732.1:n.782A=
XR_945733.1:n.719A=
NM_000043.5:c.714A=	NP_000034.1:p.Gly238=
NM_001320619.1:c.*37A=	NP_001307548.1:n.*37A=
NM_152871.3:c.651A=	NP_690610.1:p.Gly217=
NM_152872.3:c.*26A=	NP_690611.1:n.*26A=
NR_028033.3:n.860A=
NR_028034.3:n.722A=
NR_028035.3:n.785A=
NR_028036.3:n.923A=
NR_135313.1:n.840A=
NR_135314.1:n.1023A=
NR_135315.1:n.776A=
XM_006717819.3:c.795A=	XP_006717882.1:p.Gly265=
XM_011539764.2:c.876A=	XP_011538066.1:p.Gly292=
XM_011539765.2:c.813A=	XP_011538067.1:p.Gly271=
XM_011539766.2:c.795A=	XP_011538068.1:p.Gly265=
XM_011539767.3:c.759A=	XP_011538069.1:p.Gly253=
XR_945732.3:n.782A=
XR_945733.2:n.719A=
NM_000043.6:c.714A= MANE Select	NP_000034.1:p.Gly238=
NM_001320619.2:c.*37A=	NP_001307548.1:n.*37A=
NM_152871.4:c.651A=	NP_690610.1:p.Gly217=
NM_152872.4:c.*26A=	NP_690611.1:n.*26A=
NR_028033.4:n.621A=
NR_028034.4:n.483A=
NR_028035.4:n.546A=
NR_028036.4:n.684A=
NR_135313.2:n.601A=
NR_135314.2:n.880A=
NR_135315.2:n.633A=