Canonical Allele Identifier: CA377509931

Gene: FAS

Linked Data

• ClinVar Variation Id: 2753226
• ClinVar RCV Id: RCV003516960
• MyVariant Identifiers: chr10:g.90774040T>A (hg19) ; chr10:g.89014283T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014283T>A , CM000672.2:g.89014283T>A	GRCh38
NC_000010.10:g.90774040T>A , CM000672.1:g.90774040T>A	GRCh37
NC_000010.9:g.90764020T>A	NCBI36
NG_009089.2:g.28753T>A , LRG_134:g.28753T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1150T>A
ENST00000355740.8:c.*164T>A	ENSP00000347979.3:n.*164T>A
ENST00000357339.7:c.778T>A	ENSP00000349896.2:p.Trp260Arg
ENST00000371857.8:n.2386T>A
ENST00000460510.6:c.124T>A	ENSP00000512812.1:p.Trp42Arg
ENST00000466081.6:n.2490T>A
ENST00000477270.6:c.886T>A	ENSP00000512813.1:p.Trp296Arg
ENST00000479522.6:c.*270T>A	ENSP00000424113.1:n.*270T>A
ENST00000484444.6:c.*282T>A	ENSP00000420975.1:n.*282T>A
ENST00000488877.6:c.732T>A	ENSP00000425159.1:n.732T>A
ENST00000492756.7:c.*270T>A	ENSP00000422453.1:n.*270T>A
ENST00000494799.6:c.124T>A	ENSP00000512834.1:p.Trp42Arg
ENST00000562983.3:c.124T>A	ENSP00000512845.1:p.Trp42Arg
ENST00000612663.6:c.*243T>A	ENSP00000477997.3:n.*243T>A
ENST00000640140.2:n.986T>A
ENST00000640250.2:n.340T>A
ENST00000640681.2:n.945T>A
ENST00000696723.1:n.4474T>A
ENST00000696741.1:n.2479T>A
ENST00000696742.1:n.2206T>A
ENST00000696743.1:n.3609T>A
ENST00000696744.1:n.880T>A
ENST00000696767.1:n.1175T>A
ENST00000696768.1:c.*164T>A	ENSP00000512859.1:n.*164T>A
ENST00000696769.1:n.2530T>A
ENST00000696771.1:c.124T>A	ENSP00000512860.1:p.Trp42Arg
ENST00000696772.1:n.2444T>A
ENST00000696773.1:n.2183T>A
ENST00000696774.1:n.5951T>A
ENST00000696776.1:c.934T>A	ENSP00000512861.1:p.Trp312Arg
ENST00000696777.1:n.2249T>A
ENST00000696778.1:n.1277T>A
ENST00000696779.1:c.448T>A	ENSP00000512862.1:p.Trp150Arg
ENST00000696780.1:c.871T>A	ENSP00000512863.1:p.Trp291Arg
ENST00000696781.1:c.586T>A	ENSP00000512864.1:p.Trp196Arg
ENST00000696782.1:c.*243T>A	ENSP00000512865.1:n.*243T>A
ENST00000696783.1:n.2709T>A
ENST00000696992.1:n.1958T>A
ENST00000696995.1:n.4370T>A
ENST00000696996.1:n.2283T>A
ENST00000696997.1:c.*471T>A	ENSP00000513028.1:n.*471T>A
ENST00000696998.1:n.2095T>A
ENST00000696999.1:c.124T>A	ENSP00000513029.1:p.Trp42Arg
ENST00000697035.1:c.*174T>A	ENSP00000513059.1:n.*174T>A
ENST00000697036.1:c.*257T>A	ENSP00000513060.1:n.*257T>A
ENST00000697037.1:n.876T>A
ENST00000697093.1:n.3077T>A
ENST00000697094.1:n.3424T>A
ENST00000697095.1:c.*2042T>A	ENSP00000513104.1:n.*2042T>A
ENST00000697096.1:n.1974T>A
ENST00000697097.1:c.124T>A	ENSP00000513105.1:p.Trp42Arg
ENST00000562983.2:n.1027T>A
ENST00000690268.1:c.922T>A	ENSP00000509810.1:p.Trp308Arg
ENST00000355740.7:c.*167T>A	ENSP00000347979.3:n.*167T>A
ENST00000612663.5:c.*243T>A	ENSP00000477997.3:n.*243T>A
ENST00000640140.1:n.1013T>A
ENST00000640250.1:n.340T>A
ENST00000640681.1:n.962T>A
ENST00000652046.1:c.841T>A MANE Select	ENSP00000498466.1:p.Trp281Arg
ENST00000352159.8:c.*158T>A	ENSP00000345601.4:n.*158T>A
ENST00000355279.2:c.816T>A	ENSP00000347426.2:n.816T>A
ENST00000355740.6:c.841T>A	ENSP00000347979.2:p.Trp281Arg
ENST00000357339.6:c.778T>A	ENSP00000349896.2:p.Trp260Arg
ENST00000479522.5:c.*270T>A	ENSP00000424113.1:n.*270T>A
ENST00000484444.5:c.*282T>A	ENSP00000420975.1:n.*282T>A
ENST00000488877.5:c.*282T>A	ENSP00000425159.1:n.*282T>A
ENST00000492756.5:c.669T>A	ENSP00000422453.1:n.669T>A
ENST00000494410.5:c.*199T>A	ENSP00000423755.1:n.*199T>A
ENST00000612663.4:c.*188T>A	ENSP00000477997.2:n.*188T>A
NM_000043.4:c.841T>A , LRG_134t1:c.841T>A	NP_000034.1:p.Trp281Arg
NM_152871.2:c.778T>A	NP_690610.1:p.Trp260Arg
NM_152872.2:c.*153T>A	NP_690611.1:n.*153T>A
NR_028033.2:n.1015T>A
NR_028034.2:n.877T>A
NR_028035.2:n.940T>A
NR_028036.2:n.1078T>A
XM_006717819.2:c.922T>A	XP_006717882.1:p.Trp308Arg
XM_011539764.1:c.1003T>A	XP_011538066.1:p.Trp335Arg
XM_011539765.1:c.940T>A	XP_011538067.1:p.Trp314Arg
XM_011539766.1:c.922T>A	XP_011538068.1:p.Trp308Arg
XM_011539767.1:c.886T>A	XP_011538069.1:p.Trp296Arg
XR_945732.1:n.909T>A
XR_945733.1:n.846T>A
NM_000043.5:c.841T>A	NP_000034.1:p.Trp281Arg
NM_001320619.1:c.*164T>A	NP_001307548.1:n.*164T>A
NM_152871.3:c.778T>A	NP_690610.1:p.Trp260Arg
NM_152872.3:c.*153T>A	NP_690611.1:n.*153T>A
NR_028033.3:n.987T>A
NR_028034.3:n.849T>A
NR_028035.3:n.912T>A
NR_028036.3:n.1050T>A
NR_135313.1:n.967T>A
NR_135314.1:n.1150T>A
NR_135315.1:n.903T>A
XM_006717819.3:c.922T>A	XP_006717882.1:p.Trp308Arg
XM_011539764.2:c.1003T>A	XP_011538066.1:p.Trp335Arg
XM_011539765.2:c.940T>A	XP_011538067.1:p.Trp314Arg
XM_011539766.2:c.922T>A	XP_011538068.1:p.Trp308Arg
XM_011539767.3:c.886T>A	XP_011538069.1:p.Trp296Arg
XR_945732.3:n.909T>A
XR_945733.2:n.846T>A
NM_000043.6:c.841T>A MANE Select	NP_000034.1:p.Trp281Arg
NM_001320619.2:c.*164T>A	NP_001307548.1:n.*164T>A
NM_152871.4:c.778T>A	NP_690610.1:p.Trp260Arg
NM_152872.4:c.*153T>A	NP_690611.1:n.*153T>A
NR_028033.4:n.748T>A
NR_028034.4:n.610T>A
NR_028035.4:n.673T>A
NR_028036.4:n.811T>A
NR_135313.2:n.728T>A
NR_135314.2:n.1007T>A
NR_135315.2:n.760T>A