Canonical Allele Identifier: CA1926639350

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014245A= , CM000672.2:g.89014245A=	GRCh38
NC_000010.10:g.90774002A= , CM000672.1:g.90774002A=	GRCh37
NC_000010.9:g.90763982A=	NCBI36
NG_009089.2:g.28715A= , LRG_134:g.28715A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1112A=
ENST00000355740.8:c.*126A=	ENSP00000347979.3:n.*126A=
ENST00000357339.7:c.740A=	ENSP00000349896.2:p.Gln247=
ENST00000371857.8:n.2348A=
ENST00000460510.6:c.86A=	ENSP00000512812.1:p.Gln29=
ENST00000466081.6:n.2452A=
ENST00000477270.6:c.848A=	ENSP00000512813.1:p.Gln283=
ENST00000479522.6:c.*232A=	ENSP00000424113.1:n.*232A=
ENST00000484444.6:c.*244A=	ENSP00000420975.1:n.*244A=
ENST00000488877.6:c.694A=	ENSP00000425159.1:n.694A=
ENST00000492756.7:c.*232A=	ENSP00000422453.1:n.*232A=
ENST00000494799.6:c.86A=	ENSP00000512834.1:p.Gln29=
ENST00000562983.3:c.86A=	ENSP00000512845.1:p.Gln29=
ENST00000612663.6:c.*205A=	ENSP00000477997.3:n.*205A=
ENST00000640140.2:n.948A=
ENST00000640250.2:n.302A=
ENST00000640681.2:n.907A=
ENST00000696723.1:n.4436A=
ENST00000696741.1:n.2441A=
ENST00000696742.1:n.2168A=
ENST00000696743.1:n.3571A=
ENST00000696744.1:n.842A=
ENST00000696767.1:n.1137A=
ENST00000696768.1:c.*126A=	ENSP00000512859.1:n.*126A=
ENST00000696769.1:n.2492A=
ENST00000696771.1:c.86A=	ENSP00000512860.1:p.Gln29=
ENST00000696772.1:n.2406A=
ENST00000696773.1:n.2145A=
ENST00000696774.1:n.5913A=
ENST00000696776.1:c.896A=	ENSP00000512861.1:p.Gln299=
ENST00000696777.1:n.2211A=
ENST00000696778.1:n.1239A=
ENST00000696779.1:c.410A=	ENSP00000512862.1:p.Gln137=
ENST00000696780.1:c.833A=	ENSP00000512863.1:p.Gln278=
ENST00000696781.1:c.548A=	ENSP00000512864.1:p.Gln183=
ENST00000696782.1:c.*205A=	ENSP00000512865.1:n.*205A=
ENST00000696783.1:n.2671A=
ENST00000696992.1:n.1920A=
ENST00000696995.1:n.4332A=
ENST00000696996.1:n.2245A=
ENST00000696997.1:c.*433A=	ENSP00000513028.1:n.*433A=
ENST00000696998.1:n.2057A=
ENST00000696999.1:c.86A=	ENSP00000513029.1:p.Gln29=
ENST00000697035.1:c.*136A=	ENSP00000513059.1:n.*136A=
ENST00000697036.1:c.*219A=	ENSP00000513060.1:n.*219A=
ENST00000697037.1:n.838A=
ENST00000697093.1:n.3039A=
ENST00000697094.1:n.3386A=
ENST00000697095.1:c.*2004A=	ENSP00000513104.1:n.*2004A=
ENST00000697096.1:n.1936A=
ENST00000697097.1:c.86A=	ENSP00000513105.1:p.Gln29=
ENST00000562983.2:n.989A=
ENST00000690268.1:c.884A=	ENSP00000509810.1:p.Gln295=
ENST00000355740.7:c.*129A=	ENSP00000347979.3:n.*129A=
ENST00000612663.5:c.*205A=	ENSP00000477997.3:n.*205A=
ENST00000640140.1:n.975A=
ENST00000640250.1:n.302A=
ENST00000640681.1:n.924A=
ENST00000652046.1:c.803A= MANE Select	ENSP00000498466.1:p.Gln268=
ENST00000352159.8:c.*120A=	ENSP00000345601.4:n.*120A=
ENST00000355279.2:c.778A=	ENSP00000347426.2:n.778A=
ENST00000355740.6:c.803A=	ENSP00000347979.2:p.Gln268=
ENST00000357339.6:c.740A=	ENSP00000349896.2:p.Gln247=
ENST00000479522.5:c.*232A=	ENSP00000424113.1:n.*232A=
ENST00000484444.5:c.*244A=	ENSP00000420975.1:n.*244A=
ENST00000488877.5:c.*244A=	ENSP00000425159.1:n.*244A=
ENST00000492756.5:c.631A=	ENSP00000422453.1:n.631A=
ENST00000494410.5:c.*161A=	ENSP00000423755.1:n.*161A=
ENST00000612663.4:c.*150A=	ENSP00000477997.2:n.*150A=
NM_000043.4:c.803A= , LRG_134t1:c.803A=	NP_000034.1:p.Gln268=
NM_152871.2:c.740A=	NP_690610.1:p.Gln247=
NM_152872.2:c.*115A=	NP_690611.1:n.*115A=
NR_028033.2:n.977A=
NR_028034.2:n.839A=
NR_028035.2:n.902A=
NR_028036.2:n.1040A=
XM_006717819.2:c.884A=	XP_006717882.1:p.Gln295=
XM_011539764.1:c.965A=	XP_011538066.1:p.Gln322=
XM_011539765.1:c.902A=	XP_011538067.1:p.Gln301=
XM_011539766.1:c.884A=	XP_011538068.1:p.Gln295=
XM_011539767.1:c.848A=	XP_011538069.1:p.Gln283=
XR_945732.1:n.871A=
XR_945733.1:n.808A=
NM_000043.5:c.803A=	NP_000034.1:p.Gln268=
NM_001320619.1:c.*126A=	NP_001307548.1:n.*126A=
NM_152871.3:c.740A=	NP_690610.1:p.Gln247=
NM_152872.3:c.*115A=	NP_690611.1:n.*115A=
NR_028033.3:n.949A=
NR_028034.3:n.811A=
NR_028035.3:n.874A=
NR_028036.3:n.1012A=
NR_135313.1:n.929A=
NR_135314.1:n.1112A=
NR_135315.1:n.865A=
XM_006717819.3:c.884A=	XP_006717882.1:p.Gln295=
XM_011539764.2:c.965A=	XP_011538066.1:p.Gln322=
XM_011539765.2:c.902A=	XP_011538067.1:p.Gln301=
XM_011539766.2:c.884A=	XP_011538068.1:p.Gln295=
XM_011539767.3:c.848A=	XP_011538069.1:p.Gln283=
XR_945732.3:n.871A=
XR_945733.2:n.808A=
NM_000043.6:c.803A= MANE Select	NP_000034.1:p.Gln268=
NM_001320619.2:c.*126A=	NP_001307548.1:n.*126A=
NM_152871.4:c.740A=	NP_690610.1:p.Gln247=
NM_152872.4:c.*115A=	NP_690611.1:n.*115A=
NR_028033.4:n.710A=
NR_028034.4:n.572A=
NR_028035.4:n.635A=
NR_028036.4:n.773A=
NR_135313.2:n.690A=
NR_135314.2:n.969A=
NR_135315.2:n.722A=