Canonical Allele Identifier: CA377509905

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774027A>T (hg19) ; chr10:g.89014270A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014270A>T , CM000672.2:g.89014270A>T	GRCh38
NC_000010.10:g.90774027A>T , CM000672.1:g.90774027A>T	GRCh37
NC_000010.9:g.90764007A>T	NCBI36
NG_009089.2:g.28740A>T , LRG_134:g.28740A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1137A>T
ENST00000355740.8:c.*151A>T	ENSP00000347979.3:n.*151A>T
ENST00000357339.7:c.765A>T	ENSP00000349896.2:p.Gln255His
ENST00000371857.8:n.2373A>T
ENST00000460510.6:c.111A>T	ENSP00000512812.1:p.Gln37His
ENST00000466081.6:n.2477A>T
ENST00000477270.6:c.873A>T	ENSP00000512813.1:p.Gln291His
ENST00000479522.6:c.*257A>T	ENSP00000424113.1:n.*257A>T
ENST00000484444.6:c.*269A>T	ENSP00000420975.1:n.*269A>T
ENST00000488877.6:c.719A>T	ENSP00000425159.1:n.719A>T
ENST00000492756.7:c.*257A>T	ENSP00000422453.1:n.*257A>T
ENST00000494799.6:c.111A>T	ENSP00000512834.1:p.Gln37His
ENST00000562983.3:c.111A>T	ENSP00000512845.1:p.Gln37His
ENST00000612663.6:c.*230A>T	ENSP00000477997.3:n.*230A>T
ENST00000640140.2:n.973A>T
ENST00000640250.2:n.327A>T
ENST00000640681.2:n.932A>T
ENST00000696723.1:n.4461A>T
ENST00000696741.1:n.2466A>T
ENST00000696742.1:n.2193A>T
ENST00000696743.1:n.3596A>T
ENST00000696744.1:n.867A>T
ENST00000696767.1:n.1162A>T
ENST00000696768.1:c.*151A>T	ENSP00000512859.1:n.*151A>T
ENST00000696769.1:n.2517A>T
ENST00000696771.1:c.111A>T	ENSP00000512860.1:p.Gln37His
ENST00000696772.1:n.2431A>T
ENST00000696773.1:n.2170A>T
ENST00000696774.1:n.5938A>T
ENST00000696776.1:c.921A>T	ENSP00000512861.1:p.Gln307His
ENST00000696777.1:n.2236A>T
ENST00000696778.1:n.1264A>T
ENST00000696779.1:c.435A>T	ENSP00000512862.1:p.Gln145His
ENST00000696780.1:c.858A>T	ENSP00000512863.1:p.Gln286His
ENST00000696781.1:c.573A>T	ENSP00000512864.1:p.Gln191His
ENST00000696782.1:c.*230A>T	ENSP00000512865.1:n.*230A>T
ENST00000696783.1:n.2696A>T
ENST00000696992.1:n.1945A>T
ENST00000696995.1:n.4357A>T
ENST00000696996.1:n.2270A>T
ENST00000696997.1:c.*458A>T	ENSP00000513028.1:n.*458A>T
ENST00000696998.1:n.2082A>T
ENST00000696999.1:c.111A>T	ENSP00000513029.1:p.Gln37His
ENST00000697035.1:c.*161A>T	ENSP00000513059.1:n.*161A>T
ENST00000697036.1:c.*244A>T	ENSP00000513060.1:n.*244A>T
ENST00000697037.1:n.863A>T
ENST00000697093.1:n.3064A>T
ENST00000697094.1:n.3411A>T
ENST00000697095.1:c.*2029A>T	ENSP00000513104.1:n.*2029A>T
ENST00000697096.1:n.1961A>T
ENST00000697097.1:c.111A>T	ENSP00000513105.1:p.Gln37His
ENST00000562983.2:n.1014A>T
ENST00000690268.1:c.909A>T	ENSP00000509810.1:p.Gln303His
ENST00000355740.7:c.*154A>T	ENSP00000347979.3:n.*154A>T
ENST00000612663.5:c.*230A>T	ENSP00000477997.3:n.*230A>T
ENST00000640140.1:n.1000A>T
ENST00000640250.1:n.327A>T
ENST00000640681.1:n.949A>T
ENST00000652046.1:c.828A>T MANE Select	ENSP00000498466.1:p.Gln276His
ENST00000352159.8:c.*145A>T	ENSP00000345601.4:n.*145A>T
ENST00000355279.2:c.803A>T	ENSP00000347426.2:n.803A>T
ENST00000355740.6:c.828A>T	ENSP00000347979.2:p.Gln276His
ENST00000357339.6:c.765A>T	ENSP00000349896.2:p.Gln255His
ENST00000479522.5:c.*257A>T	ENSP00000424113.1:n.*257A>T
ENST00000484444.5:c.*269A>T	ENSP00000420975.1:n.*269A>T
ENST00000488877.5:c.*269A>T	ENSP00000425159.1:n.*269A>T
ENST00000492756.5:c.656A>T	ENSP00000422453.1:n.656A>T
ENST00000494410.5:c.*186A>T	ENSP00000423755.1:n.*186A>T
ENST00000612663.4:c.*175A>T	ENSP00000477997.2:n.*175A>T
NM_000043.4:c.828A>T , LRG_134t1:c.828A>T	NP_000034.1:p.Gln276His
NM_152871.2:c.765A>T	NP_690610.1:p.Gln255His
NM_152872.2:c.*140A>T	NP_690611.1:n.*140A>T
NR_028033.2:n.1002A>T
NR_028034.2:n.864A>T
NR_028035.2:n.927A>T
NR_028036.2:n.1065A>T
XM_006717819.2:c.909A>T	XP_006717882.1:p.Gln303His
XM_011539764.1:c.990A>T	XP_011538066.1:p.Gln330His
XM_011539765.1:c.927A>T	XP_011538067.1:p.Gln309His
XM_011539766.1:c.909A>T	XP_011538068.1:p.Gln303His
XM_011539767.1:c.873A>T	XP_011538069.1:p.Gln291His
XR_945732.1:n.896A>T
XR_945733.1:n.833A>T
NM_000043.5:c.828A>T	NP_000034.1:p.Gln276His
NM_001320619.1:c.*151A>T	NP_001307548.1:n.*151A>T
NM_152871.3:c.765A>T	NP_690610.1:p.Gln255His
NM_152872.3:c.*140A>T	NP_690611.1:n.*140A>T
NR_028033.3:n.974A>T
NR_028034.3:n.836A>T
NR_028035.3:n.899A>T
NR_028036.3:n.1037A>T
NR_135313.1:n.954A>T
NR_135314.1:n.1137A>T
NR_135315.1:n.890A>T
XM_006717819.3:c.909A>T	XP_006717882.1:p.Gln303His
XM_011539764.2:c.990A>T	XP_011538066.1:p.Gln330His
XM_011539765.2:c.927A>T	XP_011538067.1:p.Gln309His
XM_011539766.2:c.909A>T	XP_011538068.1:p.Gln303His
XM_011539767.3:c.873A>T	XP_011538069.1:p.Gln291His
XR_945732.3:n.896A>T
XR_945733.2:n.833A>T
NM_000043.6:c.828A>T MANE Select	NP_000034.1:p.Gln276His
NM_001320619.2:c.*151A>T	NP_001307548.1:n.*151A>T
NM_152871.4:c.765A>T	NP_690610.1:p.Gln255His
NM_152872.4:c.*140A>T	NP_690611.1:n.*140A>T
NR_028033.4:n.735A>T
NR_028034.4:n.597A>T
NR_028035.4:n.660A>T
NR_028036.4:n.798A>T
NR_135313.2:n.715A>T
NR_135314.2:n.994A>T
NR_135315.2:n.747A>T