Canonical Allele Identifier: CA5593227

Gene: FAS

Linked Data

• dbSNP Id: rs770556399
• ExAC: 10:90774053 A / G
• gnomAD v2: 10-90774053-A-G
• gnomAD v4: 10-89014296-A-G
• MyVariant Identifiers: chr10:g.90774053A>G (hg19) ; chr10:g.89014296A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014296A>G , CM000672.2:g.89014296A>G	GRCh38
NC_000010.10:g.90774053A>G , CM000672.1:g.90774053A>G	GRCh37
NC_000010.9:g.90764033A>G	NCBI36
NG_009089.2:g.28766A>G , LRG_134:g.28766A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1163A>G
ENST00000355740.8:c.*177A>G	ENSP00000347979.3:n.*177A>G
ENST00000357339.7:c.791A>G	ENSP00000349896.2:p.His264Arg
ENST00000371857.8:n.2399A>G
ENST00000460510.6:c.137A>G	ENSP00000512812.1:p.His46Arg
ENST00000466081.6:n.2503A>G
ENST00000477270.6:c.899A>G	ENSP00000512813.1:p.His300Arg
ENST00000479522.6:c.*283A>G	ENSP00000424113.1:n.*283A>G
ENST00000484444.6:c.*295A>G	ENSP00000420975.1:n.*295A>G
ENST00000488877.6:c.745A>G	ENSP00000425159.1:n.745A>G
ENST00000492756.7:c.*283A>G	ENSP00000422453.1:n.*283A>G
ENST00000494799.6:c.137A>G	ENSP00000512834.1:p.His46Arg
ENST00000562983.3:c.137A>G	ENSP00000512845.1:p.His46Arg
ENST00000612663.6:c.*256A>G	ENSP00000477997.3:n.*256A>G
ENST00000640140.2:n.999A>G
ENST00000640250.2:n.353A>G
ENST00000640681.2:n.958A>G
ENST00000696723.1:n.4487A>G
ENST00000696741.1:n.2492A>G
ENST00000696742.1:n.2219A>G
ENST00000696743.1:n.3622A>G
ENST00000696744.1:n.893A>G
ENST00000696767.1:n.1188A>G
ENST00000696768.1:c.*177A>G	ENSP00000512859.1:n.*177A>G
ENST00000696769.1:n.2543A>G
ENST00000696771.1:c.137A>G	ENSP00000512860.1:p.His46Arg
ENST00000696772.1:n.2457A>G
ENST00000696773.1:n.2196A>G
ENST00000696774.1:n.5964A>G
ENST00000696776.1:c.947A>G	ENSP00000512861.1:p.His316Arg
ENST00000696777.1:n.2262A>G
ENST00000696778.1:n.1290A>G
ENST00000696779.1:c.461A>G	ENSP00000512862.1:p.His154Arg
ENST00000696780.1:c.884A>G	ENSP00000512863.1:p.His295Arg
ENST00000696781.1:c.599A>G	ENSP00000512864.1:p.His200Arg
ENST00000696782.1:c.*256A>G	ENSP00000512865.1:n.*256A>G
ENST00000696783.1:n.2722A>G
ENST00000696992.1:n.1971A>G
ENST00000696995.1:n.4383A>G
ENST00000696996.1:n.2296A>G
ENST00000696997.1:c.*484A>G	ENSP00000513028.1:n.*484A>G
ENST00000696998.1:n.2108A>G
ENST00000696999.1:c.137A>G	ENSP00000513029.1:p.His46Arg
ENST00000697035.1:c.*187A>G	ENSP00000513059.1:n.*187A>G
ENST00000697036.1:c.*270A>G	ENSP00000513060.1:n.*270A>G
ENST00000697037.1:n.889A>G
ENST00000697093.1:n.3090A>G
ENST00000697094.1:n.3437A>G
ENST00000697095.1:c.*2055A>G	ENSP00000513104.1:n.*2055A>G
ENST00000697096.1:n.1987A>G
ENST00000697097.1:c.137A>G	ENSP00000513105.1:p.His46Arg
ENST00000562983.2:n.1040A>G
ENST00000690268.1:c.935A>G	ENSP00000509810.1:p.His312Arg
ENST00000355740.7:c.*180A>G	ENSP00000347979.3:n.*180A>G
ENST00000612663.5:c.*256A>G	ENSP00000477997.3:n.*256A>G
ENST00000640140.1:n.1026A>G
ENST00000640250.1:n.353A>G
ENST00000640681.1:n.975A>G
ENST00000652046.1:c.854A>G MANE Select	ENSP00000498466.1:p.His285Arg
ENST00000352159.8:c.*171A>G	ENSP00000345601.4:n.*171A>G
ENST00000355279.2:c.829A>G	ENSP00000347426.2:n.829A>G
ENST00000355740.6:c.854A>G	ENSP00000347979.2:p.His285Arg
ENST00000357339.6:c.791A>G	ENSP00000349896.2:p.His264Arg
ENST00000479522.5:c.*283A>G	ENSP00000424113.1:n.*283A>G
ENST00000484444.5:c.*295A>G	ENSP00000420975.1:n.*295A>G
ENST00000488877.5:c.*295A>G	ENSP00000425159.1:n.*295A>G
ENST00000492756.5:c.682A>G	ENSP00000422453.1:n.682A>G
ENST00000494410.5:c.*212A>G	ENSP00000423755.1:n.*212A>G
ENST00000612663.4:c.*201A>G	ENSP00000477997.2:n.*201A>G
NM_000043.4:c.854A>G , LRG_134t1:c.854A>G	NP_000034.1:p.His285Arg
NM_152871.2:c.791A>G	NP_690610.1:p.His264Arg
NM_152872.2:c.*166A>G	NP_690611.1:n.*166A>G
NR_028033.2:n.1028A>G
NR_028034.2:n.890A>G
NR_028035.2:n.953A>G
NR_028036.2:n.1091A>G
XM_006717819.2:c.935A>G	XP_006717882.1:p.His312Arg
XM_011539764.1:c.1016A>G	XP_011538066.1:p.His339Arg
XM_011539765.1:c.953A>G	XP_011538067.1:p.His318Arg
XM_011539766.1:c.935A>G	XP_011538068.1:p.His312Arg
XM_011539767.1:c.899A>G	XP_011538069.1:p.His300Arg
XR_945732.1:n.922A>G
XR_945733.1:n.859A>G
NM_000043.5:c.854A>G	NP_000034.1:p.His285Arg
NM_001320619.1:c.*177A>G	NP_001307548.1:n.*177A>G
NM_152871.3:c.791A>G	NP_690610.1:p.His264Arg
NM_152872.3:c.*166A>G	NP_690611.1:n.*166A>G
NR_028033.3:n.1000A>G
NR_028034.3:n.862A>G
NR_028035.3:n.925A>G
NR_028036.3:n.1063A>G
NR_135313.1:n.980A>G
NR_135314.1:n.1163A>G
NR_135315.1:n.916A>G
XM_006717819.3:c.935A>G	XP_006717882.1:p.His312Arg
XM_011539764.2:c.1016A>G	XP_011538066.1:p.His339Arg
XM_011539765.2:c.953A>G	XP_011538067.1:p.His318Arg
XM_011539766.2:c.935A>G	XP_011538068.1:p.His312Arg
XM_011539767.3:c.899A>G	XP_011538069.1:p.His300Arg
XR_945732.3:n.922A>G
XR_945733.2:n.859A>G
NM_000043.6:c.854A>G MANE Select	NP_000034.1:p.His285Arg
NM_001320619.2:c.*177A>G	NP_001307548.1:n.*177A>G
NM_152871.4:c.791A>G	NP_690610.1:p.His264Arg
NM_152872.4:c.*166A>G	NP_690611.1:n.*166A>G
NR_028033.4:n.761A>G
NR_028034.4:n.623A>G
NR_028035.4:n.686A>G
NR_028036.4:n.824A>G
NR_135313.2:n.741A>G
NR_135314.2:n.1020A>G
NR_135315.2:n.773A>G