Canonical Allele Identifier: CA377509847

Gene: FAS

Linked Data

• dbSNP Id: rs1848676365
• MyVariant Identifiers: chr10:g.90774002A>G (hg19) ; chr10:g.89014245A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1112A>G
ENST00000355740.8:c.*126A>G	ENSP00000347979.3:n.*126A>G
ENST00000357339.7:c.740A>G	ENSP00000349896.2:p.Gln247Arg
ENST00000371857.8:n.2348A>G
ENST00000460510.6:c.86A>G	ENSP00000512812.1:p.Gln29Arg
ENST00000466081.6:n.2452A>G
ENST00000477270.6:c.848A>G	ENSP00000512813.1:p.Gln283Arg
ENST00000479522.6:c.*232A>G	ENSP00000424113.1:n.*232A>G
ENST00000484444.6:c.*244A>G	ENSP00000420975.1:n.*244A>G
ENST00000488877.6:c.694A>G	ENSP00000425159.1:n.694A>G
ENST00000492756.7:c.*232A>G	ENSP00000422453.1:n.*232A>G
ENST00000494799.6:c.86A>G	ENSP00000512834.1:p.Gln29Arg
ENST00000562983.3:c.86A>G	ENSP00000512845.1:p.Gln29Arg
ENST00000612663.6:c.*205A>G	ENSP00000477997.3:n.*205A>G
ENST00000640140.2:n.948A>G
ENST00000640250.2:n.302A>G
ENST00000640681.2:n.907A>G
ENST00000696723.1:n.4436A>G
ENST00000696741.1:n.2441A>G
ENST00000696742.1:n.2168A>G
ENST00000696743.1:n.3571A>G
ENST00000696744.1:n.842A>G
ENST00000696767.1:n.1137A>G
ENST00000696768.1:c.*126A>G	ENSP00000512859.1:n.*126A>G
ENST00000696769.1:n.2492A>G
ENST00000696771.1:c.86A>G	ENSP00000512860.1:p.Gln29Arg
ENST00000696772.1:n.2406A>G
ENST00000696773.1:n.2145A>G
ENST00000696774.1:n.5913A>G
ENST00000696776.1:c.896A>G	ENSP00000512861.1:p.Gln299Arg
ENST00000696777.1:n.2211A>G
ENST00000696778.1:n.1239A>G
ENST00000696779.1:c.410A>G	ENSP00000512862.1:p.Gln137Arg
ENST00000696780.1:c.833A>G	ENSP00000512863.1:p.Gln278Arg
ENST00000696781.1:c.548A>G	ENSP00000512864.1:p.Gln183Arg
ENST00000696782.1:c.*205A>G	ENSP00000512865.1:n.*205A>G
ENST00000696783.1:n.2671A>G
ENST00000696992.1:n.1920A>G
ENST00000696995.1:n.4332A>G
ENST00000696996.1:n.2245A>G
ENST00000696997.1:c.*433A>G	ENSP00000513028.1:n.*433A>G
ENST00000696998.1:n.2057A>G
ENST00000696999.1:c.86A>G	ENSP00000513029.1:p.Gln29Arg
ENST00000697035.1:c.*136A>G	ENSP00000513059.1:n.*136A>G
ENST00000697036.1:c.*219A>G	ENSP00000513060.1:n.*219A>G
ENST00000697037.1:n.838A>G
ENST00000697093.1:n.3039A>G
ENST00000697094.1:n.3386A>G
ENST00000697095.1:c.*2004A>G	ENSP00000513104.1:n.*2004A>G
ENST00000697096.1:n.1936A>G
ENST00000697097.1:c.86A>G	ENSP00000513105.1:p.Gln29Arg
ENST00000562983.2:n.989A>G
ENST00000690268.1:c.884A>G	ENSP00000509810.1:p.Gln295Arg
ENST00000355740.7:c.*129A>G	ENSP00000347979.3:n.*129A>G
ENST00000612663.5:c.*205A>G	ENSP00000477997.3:n.*205A>G
ENST00000640140.1:n.975A>G
ENST00000640250.1:n.302A>G
ENST00000640681.1:n.924A>G
ENST00000652046.1:c.803A>G MANE Select	ENSP00000498466.1:p.Gln268Arg
ENST00000352159.8:c.*120A>G	ENSP00000345601.4:n.*120A>G
ENST00000355279.2:c.778A>G	ENSP00000347426.2:n.778A>G
ENST00000355740.6:c.803A>G	ENSP00000347979.2:p.Gln268Arg
ENST00000357339.6:c.740A>G	ENSP00000349896.2:p.Gln247Arg
ENST00000479522.5:c.*232A>G	ENSP00000424113.1:n.*232A>G
ENST00000484444.5:c.*244A>G	ENSP00000420975.1:n.*244A>G
ENST00000488877.5:c.*244A>G	ENSP00000425159.1:n.*244A>G
ENST00000492756.5:c.631A>G	ENSP00000422453.1:n.631A>G
ENST00000494410.5:c.*161A>G	ENSP00000423755.1:n.*161A>G
ENST00000612663.4:c.*150A>G	ENSP00000477997.2:n.*150A>G
NM_000043.4:c.803A>G , LRG_134t1:c.803A>G	NP_000034.1:p.Gln268Arg
NM_152871.2:c.740A>G	NP_690610.1:p.Gln247Arg
NM_152872.2:c.*115A>G	NP_690611.1:n.*115A>G
NR_028033.2:n.977A>G
NR_028034.2:n.839A>G
NR_028035.2:n.902A>G
NR_028036.2:n.1040A>G
XM_006717819.2:c.884A>G	XP_006717882.1:p.Gln295Arg
XM_011539764.1:c.965A>G	XP_011538066.1:p.Gln322Arg
XM_011539765.1:c.902A>G	XP_011538067.1:p.Gln301Arg
XM_011539766.1:c.884A>G	XP_011538068.1:p.Gln295Arg
XM_011539767.1:c.848A>G	XP_011538069.1:p.Gln283Arg
XR_945732.1:n.871A>G
XR_945733.1:n.808A>G
NM_000043.5:c.803A>G	NP_000034.1:p.Gln268Arg
NM_001320619.1:c.*126A>G	NP_001307548.1:n.*126A>G
NM_152871.3:c.740A>G	NP_690610.1:p.Gln247Arg
NM_152872.3:c.*115A>G	NP_690611.1:n.*115A>G
NR_028033.3:n.949A>G
NR_028034.3:n.811A>G
NR_028035.3:n.874A>G
NR_028036.3:n.1012A>G
NR_135313.1:n.929A>G
NR_135314.1:n.1112A>G
NR_135315.1:n.865A>G
XM_006717819.3:c.884A>G	XP_006717882.1:p.Gln295Arg
XM_011539764.2:c.965A>G	XP_011538066.1:p.Gln322Arg
XM_011539765.2:c.902A>G	XP_011538067.1:p.Gln301Arg
XM_011539766.2:c.884A>G	XP_011538068.1:p.Gln295Arg
XM_011539767.3:c.848A>G	XP_011538069.1:p.Gln283Arg
XR_945732.3:n.871A>G
XR_945733.2:n.808A>G
NM_000043.6:c.803A>G MANE Select	NP_000034.1:p.Gln268Arg
NM_001320619.2:c.*126A>G	NP_001307548.1:n.*126A>G
NM_152871.4:c.740A>G	NP_690610.1:p.Gln247Arg
NM_152872.4:c.*115A>G	NP_690611.1:n.*115A>G
NR_028033.4:n.710A>G
NR_028034.4:n.572A>G
NR_028035.4:n.635A>G
NR_028036.4:n.773A>G
NR_135313.2:n.690A>G
NR_135314.2:n.969A>G
NR_135315.2:n.722A>G