Canonical Allele Identifier: CA1926639329

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014182G= , CM000672.2:g.89014182G=	GRCh38
NC_000010.10:g.90773939G= , CM000672.1:g.90773939G=	GRCh37
NC_000010.9:g.90763919G=	NCBI36
NG_009089.2:g.28652G= , LRG_134:g.28652G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1049G=
ENST00000355740.8:c.*63G=	ENSP00000347979.3:n.*63G=
ENST00000357339.7:c.677G=	ENSP00000349896.2:p.Gly226=
ENST00000371857.8:n.2285G=
ENST00000460510.6:c.23G=	ENSP00000512812.1:p.Gly8=
ENST00000466081.6:n.2389G=
ENST00000477270.6:c.785G=	ENSP00000512813.1:p.Gly262=
ENST00000479522.6:c.*169G=	ENSP00000424113.1:n.*169G=
ENST00000484444.6:c.*181G=	ENSP00000420975.1:n.*181G=
ENST00000488877.6:c.631G=	ENSP00000425159.1:n.631G=
ENST00000492756.7:c.*169G=	ENSP00000422453.1:n.*169G=
ENST00000494799.6:c.23G=	ENSP00000512834.1:p.Gly8=
ENST00000562983.3:c.23G=	ENSP00000512845.1:p.Gly8=
ENST00000612663.6:c.*142G=	ENSP00000477997.3:n.*142G=
ENST00000640140.2:n.885G=
ENST00000640250.2:n.239G=
ENST00000640681.2:n.844G=
ENST00000696723.1:n.4373G=
ENST00000696741.1:n.2378G=
ENST00000696742.1:n.2105G=
ENST00000696743.1:n.3508G=
ENST00000696744.1:n.779G=
ENST00000696767.1:n.1074G=
ENST00000696768.1:c.*63G=	ENSP00000512859.1:n.*63G=
ENST00000696769.1:n.2429G=
ENST00000696771.1:c.23G=	ENSP00000512860.1:p.Gly8=
ENST00000696772.1:n.2343G=
ENST00000696773.1:n.2082G=
ENST00000696774.1:n.5850G=
ENST00000696776.1:c.833G=	ENSP00000512861.1:p.Gly278=
ENST00000696777.1:n.2148G=
ENST00000696778.1:n.1176G=
ENST00000696779.1:c.347G=	ENSP00000512862.1:p.Gly116=
ENST00000696780.1:c.770G=	ENSP00000512863.1:p.Gly257=
ENST00000696781.1:c.485G=	ENSP00000512864.1:p.Gly162=
ENST00000696782.1:c.*142G=	ENSP00000512865.1:n.*142G=
ENST00000696783.1:n.2608G=
ENST00000696992.1:n.1857G=
ENST00000696995.1:n.4269G=
ENST00000696996.1:n.2182G=
ENST00000696997.1:c.*370G=	ENSP00000513028.1:n.*370G=
ENST00000696998.1:n.1994G=
ENST00000696999.1:c.23G=	ENSP00000513029.1:p.Gly8=
ENST00000697035.1:c.*73G=	ENSP00000513059.1:n.*73G=
ENST00000697036.1:c.*156G=	ENSP00000513060.1:n.*156G=
ENST00000697037.1:n.775G=
ENST00000697093.1:n.2976G=
ENST00000697094.1:n.3323G=
ENST00000697095.1:c.*1941G=	ENSP00000513104.1:n.*1941G=
ENST00000697096.1:n.1873G=
ENST00000697097.1:c.23G=	ENSP00000513105.1:p.Gly8=
ENST00000562983.2:n.926G=
ENST00000690268.1:c.821G=	ENSP00000509810.1:p.Gly274=
ENST00000355740.7:c.*66G=	ENSP00000347979.3:n.*66G=
ENST00000612663.5:c.*142G=	ENSP00000477997.3:n.*142G=
ENST00000640140.1:n.912G=
ENST00000640250.1:n.239G=
ENST00000640681.1:n.861G=
ENST00000652046.1:c.740G= MANE Select	ENSP00000498466.1:p.Gly247=
ENST00000352159.8:c.*57G=	ENSP00000345601.4:n.*57G=
ENST00000355279.2:c.715G=	ENSP00000347426.2:n.715G=
ENST00000355740.6:c.740G=	ENSP00000347979.2:p.Gly247=
ENST00000357339.6:c.677G=	ENSP00000349896.2:p.Gly226=
ENST00000479522.5:c.*169G=	ENSP00000424113.1:n.*169G=
ENST00000484444.5:c.*181G=	ENSP00000420975.1:n.*181G=
ENST00000488877.5:c.*181G=	ENSP00000425159.1:n.*181G=
ENST00000492756.5:c.568G=	ENSP00000422453.1:n.568G=
ENST00000494410.5:c.*98G=	ENSP00000423755.1:n.*98G=
ENST00000494799.5:n.647G=
ENST00000612663.4:c.*87G=	ENSP00000477997.2:n.*87G=
ENST00000615406.4:c.740G=	ENSP00000484575.1:p.Gly247=
NM_000043.4:c.740G= , LRG_134t1:c.740G=	NP_000034.1:p.Gly247=
NM_152871.2:c.677G=	NP_690610.1:p.Gly226=
NM_152872.2:c.*52G=	NP_690611.1:n.*52G=
NR_028033.2:n.914G=
NR_028034.2:n.776G=
NR_028035.2:n.839G=
NR_028036.2:n.977G=
XM_006717819.2:c.821G=	XP_006717882.1:p.Gly274=
XM_011539764.1:c.902G=	XP_011538066.1:p.Gly301=
XM_011539765.1:c.839G=	XP_011538067.1:p.Gly280=
XM_011539766.1:c.821G=	XP_011538068.1:p.Gly274=
XM_011539767.1:c.785G=	XP_011538069.1:p.Gly262=
XR_945732.1:n.808G=
XR_945733.1:n.745G=
NM_000043.5:c.740G=	NP_000034.1:p.Gly247=
NM_001320619.1:c.*63G=	NP_001307548.1:n.*63G=
NM_152871.3:c.677G=	NP_690610.1:p.Gly226=
NM_152872.3:c.*52G=	NP_690611.1:n.*52G=
NR_028033.3:n.886G=
NR_028034.3:n.748G=
NR_028035.3:n.811G=
NR_028036.3:n.949G=
NR_135313.1:n.866G=
NR_135314.1:n.1049G=
NR_135315.1:n.802G=
XM_006717819.3:c.821G=	XP_006717882.1:p.Gly274=
XM_011539764.2:c.902G=	XP_011538066.1:p.Gly301=
XM_011539765.2:c.839G=	XP_011538067.1:p.Gly280=
XM_011539766.2:c.821G=	XP_011538068.1:p.Gly274=
XM_011539767.3:c.785G=	XP_011538069.1:p.Gly262=
XR_945732.3:n.808G=
XR_945733.2:n.745G=
NM_000043.6:c.740G= MANE Select	NP_000034.1:p.Gly247=
NM_001320619.2:c.*63G=	NP_001307548.1:n.*63G=
NM_152871.4:c.677G=	NP_690610.1:p.Gly226=
NM_152872.4:c.*52G=	NP_690611.1:n.*52G=
NR_028033.4:n.647G=
NR_028034.4:n.509G=
NR_028035.4:n.572G=
NR_028036.4:n.710G=
NR_135313.2:n.627G=
NR_135314.2:n.906G=
NR_135315.2:n.659G=