Canonical Allele Identifier: CA1926639340

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014205A= , CM000672.2:g.89014205A=	GRCh38
NC_000010.10:g.90773962A= , CM000672.1:g.90773962A=	GRCh37
NC_000010.9:g.90763942A=	NCBI36
NG_009089.2:g.28675A= , LRG_134:g.28675A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1072A=
ENST00000355740.8:c.*86A=	ENSP00000347979.3:n.*86A=
ENST00000357339.7:c.700A=	ENSP00000349896.2:p.Asn234=
ENST00000371857.8:n.2308A=
ENST00000460510.6:c.46A=	ENSP00000512812.1:p.Asn16=
ENST00000466081.6:n.2412A=
ENST00000477270.6:c.808A=	ENSP00000512813.1:p.Asn270=
ENST00000479522.6:c.*192A=	ENSP00000424113.1:n.*192A=
ENST00000484444.6:c.*204A=	ENSP00000420975.1:n.*204A=
ENST00000488877.6:c.654A=	ENSP00000425159.1:n.654A=
ENST00000492756.7:c.*192A=	ENSP00000422453.1:n.*192A=
ENST00000494799.6:c.46A=	ENSP00000512834.1:p.Asn16=
ENST00000562983.3:c.46A=	ENSP00000512845.1:p.Asn16=
ENST00000612663.6:c.*165A=	ENSP00000477997.3:n.*165A=
ENST00000640140.2:n.908A=
ENST00000640250.2:n.262A=
ENST00000640681.2:n.867A=
ENST00000696723.1:n.4396A=
ENST00000696741.1:n.2401A=
ENST00000696742.1:n.2128A=
ENST00000696743.1:n.3531A=
ENST00000696744.1:n.802A=
ENST00000696767.1:n.1097A=
ENST00000696768.1:c.*86A=	ENSP00000512859.1:n.*86A=
ENST00000696769.1:n.2452A=
ENST00000696771.1:c.46A=	ENSP00000512860.1:p.Asn16=
ENST00000696772.1:n.2366A=
ENST00000696773.1:n.2105A=
ENST00000696774.1:n.5873A=
ENST00000696776.1:c.856A=	ENSP00000512861.1:p.Asn286=
ENST00000696777.1:n.2171A=
ENST00000696778.1:n.1199A=
ENST00000696779.1:c.370A=	ENSP00000512862.1:p.Asn124=
ENST00000696780.1:c.793A=	ENSP00000512863.1:p.Asn265=
ENST00000696781.1:c.508A=	ENSP00000512864.1:p.Asn170=
ENST00000696782.1:c.*165A=	ENSP00000512865.1:n.*165A=
ENST00000696783.1:n.2631A=
ENST00000696992.1:n.1880A=
ENST00000696995.1:n.4292A=
ENST00000696996.1:n.2205A=
ENST00000696997.1:c.*393A=	ENSP00000513028.1:n.*393A=
ENST00000696998.1:n.2017A=
ENST00000696999.1:c.46A=	ENSP00000513029.1:p.Asn16=
ENST00000697035.1:c.*96A=	ENSP00000513059.1:n.*96A=
ENST00000697036.1:c.*179A=	ENSP00000513060.1:n.*179A=
ENST00000697037.1:n.798A=
ENST00000697093.1:n.2999A=
ENST00000697094.1:n.3346A=
ENST00000697095.1:c.*1964A=	ENSP00000513104.1:n.*1964A=
ENST00000697096.1:n.1896A=
ENST00000697097.1:c.46A=	ENSP00000513105.1:p.Asn16=
ENST00000562983.2:n.949A=
ENST00000690268.1:c.844A=	ENSP00000509810.1:p.Asn282=
ENST00000355740.7:c.*89A=	ENSP00000347979.3:n.*89A=
ENST00000612663.5:c.*165A=	ENSP00000477997.3:n.*165A=
ENST00000640140.1:n.935A=
ENST00000640250.1:n.262A=
ENST00000640681.1:n.884A=
ENST00000652046.1:c.763A= MANE Select	ENSP00000498466.1:p.Asn255=
ENST00000352159.8:c.*80A=	ENSP00000345601.4:n.*80A=
ENST00000355279.2:c.738A=	ENSP00000347426.2:n.738A=
ENST00000355740.6:c.763A=	ENSP00000347979.2:p.Asn255=
ENST00000357339.6:c.700A=	ENSP00000349896.2:p.Asn234=
ENST00000479522.5:c.*192A=	ENSP00000424113.1:n.*192A=
ENST00000484444.5:c.*204A=	ENSP00000420975.1:n.*204A=
ENST00000488877.5:c.*204A=	ENSP00000425159.1:n.*204A=
ENST00000492756.5:c.591A=	ENSP00000422453.1:n.591A=
ENST00000494410.5:c.*121A=	ENSP00000423755.1:n.*121A=
ENST00000494799.5:n.670A=
ENST00000612663.4:c.*110A=	ENSP00000477997.2:n.*110A=
ENST00000615406.4:c.761A=	ENSP00000484575.1:p.Gln254=
NM_000043.4:c.763A= , LRG_134t1:c.763A=	NP_000034.1:p.Asn255=
NM_152871.2:c.700A=	NP_690610.1:p.Asn234=
NM_152872.2:c.*75A=	NP_690611.1:n.*75A=
NR_028033.2:n.937A=
NR_028034.2:n.799A=
NR_028035.2:n.862A=
NR_028036.2:n.1000A=
XM_006717819.2:c.844A=	XP_006717882.1:p.Asn282=
XM_011539764.1:c.925A=	XP_011538066.1:p.Asn309=
XM_011539765.1:c.862A=	XP_011538067.1:p.Asn288=
XM_011539766.1:c.844A=	XP_011538068.1:p.Asn282=
XM_011539767.1:c.808A=	XP_011538069.1:p.Asn270=
XR_945732.1:n.831A=
XR_945733.1:n.768A=
NM_000043.5:c.763A=	NP_000034.1:p.Asn255=
NM_001320619.1:c.*86A=	NP_001307548.1:n.*86A=
NM_152871.3:c.700A=	NP_690610.1:p.Asn234=
NM_152872.3:c.*75A=	NP_690611.1:n.*75A=
NR_028033.3:n.909A=
NR_028034.3:n.771A=
NR_028035.3:n.834A=
NR_028036.3:n.972A=
NR_135313.1:n.889A=
NR_135314.1:n.1072A=
NR_135315.1:n.825A=
XM_006717819.3:c.844A=	XP_006717882.1:p.Asn282=
XM_011539764.2:c.925A=	XP_011538066.1:p.Asn309=
XM_011539765.2:c.862A=	XP_011538067.1:p.Asn288=
XM_011539766.2:c.844A=	XP_011538068.1:p.Asn282=
XM_011539767.3:c.808A=	XP_011538069.1:p.Asn270=
XR_945732.3:n.831A=
XR_945733.2:n.768A=
NM_000043.6:c.763A= MANE Select	NP_000034.1:p.Asn255=
NM_001320619.2:c.*86A=	NP_001307548.1:n.*86A=
NM_152871.4:c.700A=	NP_690610.1:p.Asn234=
NM_152872.4:c.*75A=	NP_690611.1:n.*75A=
NR_028033.4:n.670A=
NR_028034.4:n.532A=
NR_028035.4:n.595A=
NR_028036.4:n.733A=
NR_135313.2:n.650A=
NR_135314.2:n.929A=
NR_135315.2:n.682A=