Canonical Allele Identifier: CA1926639310

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014142A= , CM000672.2:g.89014142A=	GRCh38
NC_000010.10:g.90773899A= , CM000672.1:g.90773899A=	GRCh37
NC_000010.9:g.90763879A=	NCBI36
NG_009089.2:g.28612A= , LRG_134:g.28612A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1009A=
ENST00000355740.8:c.*23A=	ENSP00000347979.3:n.*23A=
ENST00000357339.7:c.637A=	ENSP00000349896.2:p.Thr213=
ENST00000371857.8:n.2245A=
ENST00000460510.6:c.-18A=	ENSP00000512812.1:n.-18A=
ENST00000466081.6:n.2349A=
ENST00000477270.6:c.745A=	ENSP00000512813.1:p.Thr249=
ENST00000479522.6:c.*129A=	ENSP00000424113.1:n.*129A=
ENST00000484444.6:c.*141A=	ENSP00000420975.1:n.*141A=
ENST00000488877.6:c.591A=	ENSP00000425159.1:n.591A=
ENST00000492756.7:c.*129A=	ENSP00000422453.1:n.*129A=
ENST00000494799.6:c.-18A=	ENSP00000512834.1:n.-18A=
ENST00000562983.3:c.-18A=	ENSP00000512845.1:n.-18A=
ENST00000612663.6:c.*102A=	ENSP00000477997.3:n.*102A=
ENST00000640140.2:n.845A=
ENST00000640250.2:n.199A=
ENST00000640681.2:n.804A=
ENST00000696723.1:n.4333A=
ENST00000696741.1:n.2338A=
ENST00000696742.1:n.2065A=
ENST00000696743.1:n.3468A=
ENST00000696744.1:n.739A=
ENST00000696767.1:n.1034A=
ENST00000696768.1:c.*23A=	ENSP00000512859.1:n.*23A=
ENST00000696769.1:n.2389A=
ENST00000696771.1:c.-18A=	ENSP00000512860.1:n.-18A=
ENST00000696772.1:n.2303A=
ENST00000696773.1:n.2042A=
ENST00000696774.1:n.5810A=
ENST00000696776.1:c.793A=	ENSP00000512861.1:p.Thr265=
ENST00000696777.1:n.2108A=
ENST00000696778.1:n.1136A=
ENST00000696779.1:c.307A=	ENSP00000512862.1:p.Thr103=
ENST00000696780.1:c.730A=	ENSP00000512863.1:p.Thr244=
ENST00000696781.1:c.445A=	ENSP00000512864.1:p.Thr149=
ENST00000696782.1:c.*102A=	ENSP00000512865.1:n.*102A=
ENST00000696783.1:n.2568A=
ENST00000696992.1:n.1817A=
ENST00000696995.1:n.4229A=
ENST00000696996.1:n.2142A=
ENST00000696997.1:c.*330A=	ENSP00000513028.1:n.*330A=
ENST00000696998.1:n.1954A=
ENST00000696999.1:c.-18A=	ENSP00000513029.1:n.-18A=
ENST00000697035.1:c.*33A=	ENSP00000513059.1:n.*33A=
ENST00000697036.1:c.*116A=	ENSP00000513060.1:n.*116A=
ENST00000697037.1:n.735A=
ENST00000697093.1:n.2936A=
ENST00000697094.1:n.3283A=
ENST00000697095.1:c.*1901A=	ENSP00000513104.1:n.*1901A=
ENST00000697096.1:n.1833A=
ENST00000697097.1:c.-18A=	ENSP00000513105.1:n.-18A=
ENST00000562983.2:n.886A=
ENST00000690268.1:c.781A=	ENSP00000509810.1:p.Thr261=
ENST00000355740.7:c.*26A=	ENSP00000347979.3:n.*26A=
ENST00000612663.5:c.*102A=	ENSP00000477997.3:n.*102A=
ENST00000640140.1:n.872A=
ENST00000640250.1:n.199A=
ENST00000640681.1:n.821A=
ENST00000652046.1:c.700A= MANE Select	ENSP00000498466.1:p.Thr234=
ENST00000313771.9:n.1009A=
ENST00000352159.8:c.*17A=	ENSP00000345601.4:n.*17A=
ENST00000355279.2:c.675A=	ENSP00000347426.2:n.675A=
ENST00000355740.6:c.700A=	ENSP00000347979.2:p.Thr234=
ENST00000357339.6:c.637A=	ENSP00000349896.2:p.Thr213=
ENST00000479522.5:c.*129A=	ENSP00000424113.1:n.*129A=
ENST00000484444.5:c.*141A=	ENSP00000420975.1:n.*141A=
ENST00000488877.5:c.*141A=	ENSP00000425159.1:n.*141A=
ENST00000492756.5:c.528A=	ENSP00000422453.1:n.528A=
ENST00000494410.5:c.*58A=	ENSP00000423755.1:n.*58A=
ENST00000494799.5:n.607A=
ENST00000612663.4:c.*47A=	ENSP00000477997.2:n.*47A=
ENST00000615406.4:c.700A=	ENSP00000484575.1:p.Thr234=
ENST00000626542.2:c.698A=	ENSP00000485876.1:p.His233=
NM_000043.4:c.700A= , LRG_134t1:c.700A=	NP_000034.1:p.Thr234=
NM_152871.2:c.637A=	NP_690610.1:p.Thr213=
NM_152872.2:c.*12A=	NP_690611.1:n.*12A=
NR_028033.2:n.874A=
NR_028034.2:n.736A=
NR_028035.2:n.799A=
NR_028036.2:n.937A=
XM_006717819.2:c.781A=	XP_006717882.1:p.Thr261=
XM_011539764.1:c.862A=	XP_011538066.1:p.Thr288=
XM_011539765.1:c.799A=	XP_011538067.1:p.Thr267=
XM_011539766.1:c.781A=	XP_011538068.1:p.Thr261=
XM_011539767.1:c.745A=	XP_011538069.1:p.Thr249=
XR_945732.1:n.768A=
XR_945733.1:n.705A=
NM_000043.5:c.700A=	NP_000034.1:p.Thr234=
NM_001320619.1:c.*23A=	NP_001307548.1:n.*23A=
NM_152871.3:c.637A=	NP_690610.1:p.Thr213=
NM_152872.3:c.*12A=	NP_690611.1:n.*12A=
NR_028033.3:n.846A=
NR_028034.3:n.708A=
NR_028035.3:n.771A=
NR_028036.3:n.909A=
NR_135313.1:n.826A=
NR_135314.1:n.1009A=
NR_135315.1:n.762A=
XM_006717819.3:c.781A=	XP_006717882.1:p.Thr261=
XM_011539764.2:c.862A=	XP_011538066.1:p.Thr288=
XM_011539765.2:c.799A=	XP_011538067.1:p.Thr267=
XM_011539766.2:c.781A=	XP_011538068.1:p.Thr261=
XM_011539767.3:c.745A=	XP_011538069.1:p.Thr249=
XR_945732.3:n.768A=
XR_945733.2:n.705A=
NM_000043.6:c.700A= MANE Select	NP_000034.1:p.Thr234=
NM_001320619.2:c.*23A=	NP_001307548.1:n.*23A=
NM_152871.4:c.637A=	NP_690610.1:p.Thr213=
NM_152872.4:c.*12A=	NP_690611.1:n.*12A=
NR_028033.4:n.607A=
NR_028034.4:n.469A=
NR_028035.4:n.532A=
NR_028036.4:n.670A=
NR_135313.2:n.587A=
NR_135314.2:n.866A=
NR_135315.2:n.619A=