Canonical Allele Identifier: CA1926639382

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014324G= , CM000672.2:g.89014324G=	GRCh38
NC_000010.10:g.90774081G= , CM000672.1:g.90774081G=	GRCh37
NC_000010.9:g.90764061G=	NCBI36
NG_009089.2:g.28794G= , LRG_134:g.28794G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1191G=
ENST00000355740.8:c.*205G=	ENSP00000347979.3:n.*205G=
ENST00000357339.7:c.819G=	ENSP00000349896.2:p.Leu273=
ENST00000371857.8:n.2427G=
ENST00000460510.6:c.165G=	ENSP00000512812.1:p.Leu55=
ENST00000466081.6:n.2531G=
ENST00000477270.6:c.927G=	ENSP00000512813.1:p.Leu309=
ENST00000479522.6:c.*311G=	ENSP00000424113.1:n.*311G=
ENST00000484444.6:c.*323G=	ENSP00000420975.1:n.*323G=
ENST00000488877.6:c.773G=	ENSP00000425159.1:n.773G=
ENST00000492756.7:c.*311G=	ENSP00000422453.1:n.*311G=
ENST00000494799.6:c.165G=	ENSP00000512834.1:p.Leu55=
ENST00000562983.3:c.165G=	ENSP00000512845.1:p.Leu55=
ENST00000612663.6:c.*284G=	ENSP00000477997.3:n.*284G=
ENST00000640140.2:n.1027G=
ENST00000640250.2:n.381G=
ENST00000640681.2:n.986G=
ENST00000696723.1:n.4515G=
ENST00000696741.1:n.2520G=
ENST00000696742.1:n.2247G=
ENST00000696743.1:n.3650G=
ENST00000696744.1:n.921G=
ENST00000696767.1:n.1216G=
ENST00000696768.1:c.*205G=	ENSP00000512859.1:n.*205G=
ENST00000696769.1:n.2571G=
ENST00000696771.1:c.165G=	ENSP00000512860.1:p.Leu55=
ENST00000696772.1:n.2485G=
ENST00000696773.1:n.2224G=
ENST00000696774.1:n.5992G=
ENST00000696776.1:c.975G=	ENSP00000512861.1:p.Leu325=
ENST00000696777.1:n.2290G=
ENST00000696778.1:n.1318G=
ENST00000696779.1:c.489G=	ENSP00000512862.1:p.Leu163=
ENST00000696780.1:c.912G=	ENSP00000512863.1:p.Leu304=
ENST00000696781.1:c.627G=	ENSP00000512864.1:p.Leu209=
ENST00000696782.1:c.*284G=	ENSP00000512865.1:n.*284G=
ENST00000696783.1:n.2750G=
ENST00000696992.1:n.1999G=
ENST00000696995.1:n.4411G=
ENST00000696996.1:n.2324G=
ENST00000696997.1:c.*512G=	ENSP00000513028.1:n.*512G=
ENST00000696998.1:n.2136G=
ENST00000696999.1:c.165G=	ENSP00000513029.1:p.Leu55=
ENST00000697036.1:c.*298G=	ENSP00000513060.1:n.*298G=
ENST00000697037.1:n.917G=
ENST00000697093.1:n.3118G=
ENST00000697094.1:n.3465G=
ENST00000697095.1:c.*2083G=	ENSP00000513104.1:n.*2083G=
ENST00000697096.1:n.2015G=
ENST00000697097.1:c.165G=	ENSP00000513105.1:p.Leu55=
ENST00000562983.2:n.1068G=
ENST00000690268.1:c.963G=	ENSP00000509810.1:p.Leu321=
ENST00000355740.7:c.*208G=	ENSP00000347979.3:n.*208G=
ENST00000612663.5:c.*284G=	ENSP00000477997.3:n.*284G=
ENST00000640140.1:n.1054G=
ENST00000640250.1:n.381G=
ENST00000640681.1:n.1003G=
ENST00000652046.1:c.882G= MANE Select	ENSP00000498466.1:p.Leu294=
ENST00000352159.8:c.*199G=	ENSP00000345601.4:n.*199G=
ENST00000355279.2:c.857G=	ENSP00000347426.2:n.857G=
ENST00000355740.6:c.882G=	ENSP00000347979.2:p.Leu294=
ENST00000357339.6:c.819G=	ENSP00000349896.2:p.Leu273=
ENST00000479522.5:c.*311G=	ENSP00000424113.1:n.*311G=
ENST00000484444.5:c.*323G=	ENSP00000420975.1:n.*323G=
ENST00000488877.5:c.*323G=	ENSP00000425159.1:n.*323G=
ENST00000492756.5:c.710G=	ENSP00000422453.1:n.710G=
ENST00000494410.5:c.*240G=	ENSP00000423755.1:n.*240G=
ENST00000612663.4:c.*229G=	ENSP00000477997.2:n.*229G=
NM_000043.4:c.882G= , LRG_134t1:c.882G=	NP_000034.1:p.Leu294=
NM_152871.2:c.819G=	NP_690610.1:p.Leu273=
NM_152872.2:c.*194G=	NP_690611.1:n.*194G=
NR_028033.2:n.1056G=
NR_028034.2:n.918G=
NR_028035.2:n.981G=
NR_028036.2:n.1119G=
XM_006717819.2:c.963G=	XP_006717882.1:p.Leu321=
XM_011539764.1:c.1044G=	XP_011538066.1:p.Leu348=
XM_011539765.1:c.981G=	XP_011538067.1:p.Leu327=
XM_011539766.1:c.963G=	XP_011538068.1:p.Leu321=
XM_011539767.1:c.927G=	XP_011538069.1:p.Leu309=
XR_945732.1:n.950G=
XR_945733.1:n.887G=
NM_000043.5:c.882G=	NP_000034.1:p.Leu294=
NM_001320619.1:c.*205G=	NP_001307548.1:n.*205G=
NM_152871.3:c.819G=	NP_690610.1:p.Leu273=
NM_152872.3:c.*194G=	NP_690611.1:n.*194G=
NR_028033.3:n.1028G=
NR_028034.3:n.890G=
NR_028035.3:n.953G=
NR_028036.3:n.1091G=
NR_135313.1:n.1008G=
NR_135314.1:n.1191G=
NR_135315.1:n.944G=
XM_006717819.3:c.963G=	XP_006717882.1:p.Leu321=
XM_011539764.2:c.1044G=	XP_011538066.1:p.Leu348=
XM_011539765.2:c.981G=	XP_011538067.1:p.Leu327=
XM_011539766.2:c.963G=	XP_011538068.1:p.Leu321=
XM_011539767.3:c.927G=	XP_011538069.1:p.Leu309=
XR_945732.3:n.950G=
XR_945733.2:n.887G=
NM_000043.6:c.882G= MANE Select	NP_000034.1:p.Leu294=
NM_001320619.2:c.*205G=	NP_001307548.1:n.*205G=
NM_152871.4:c.819G=	NP_690610.1:p.Leu273=
NM_152872.4:c.*194G=	NP_690611.1:n.*194G=
NR_028033.4:n.789G=
NR_028034.4:n.651G=
NR_028035.4:n.714G=
NR_028036.4:n.852G=
NR_135313.2:n.769G=
NR_135314.2:n.1048G=
NR_135315.2:n.801G=