Canonical Allele Identifier: CA1926639327

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014176T= , CM000672.2:g.89014176T=	GRCh38
NC_000010.10:g.90773933T= , CM000672.1:g.90773933T=	GRCh37
NC_000010.9:g.90763913T=	NCBI36
NG_009089.2:g.28646T= , LRG_134:g.28646T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1043T=
ENST00000355740.8:c.*57T=	ENSP00000347979.3:n.*57T=
ENST00000357339.7:c.671T=	ENSP00000349896.2:p.Val224=
ENST00000371857.8:n.2279T=
ENST00000460510.6:c.17T=	ENSP00000512812.1:p.Val6=
ENST00000466081.6:n.2383T=
ENST00000477270.6:c.779T=	ENSP00000512813.1:p.Val260=
ENST00000479522.6:c.*163T=	ENSP00000424113.1:n.*163T=
ENST00000484444.6:c.*175T=	ENSP00000420975.1:n.*175T=
ENST00000488877.6:c.625T=	ENSP00000425159.1:n.625T=
ENST00000492756.7:c.*163T=	ENSP00000422453.1:n.*163T=
ENST00000494799.6:c.17T=	ENSP00000512834.1:p.Val6=
ENST00000562983.3:c.17T=	ENSP00000512845.1:p.Val6=
ENST00000612663.6:c.*136T=	ENSP00000477997.3:n.*136T=
ENST00000640140.2:n.879T=
ENST00000640250.2:n.233T=
ENST00000640681.2:n.838T=
ENST00000696723.1:n.4367T=
ENST00000696741.1:n.2372T=
ENST00000696742.1:n.2099T=
ENST00000696743.1:n.3502T=
ENST00000696744.1:n.773T=
ENST00000696767.1:n.1068T=
ENST00000696768.1:c.*57T=	ENSP00000512859.1:n.*57T=
ENST00000696769.1:n.2423T=
ENST00000696771.1:c.17T=	ENSP00000512860.1:p.Val6=
ENST00000696772.1:n.2337T=
ENST00000696773.1:n.2076T=
ENST00000696774.1:n.5844T=
ENST00000696776.1:c.827T=	ENSP00000512861.1:p.Val276=
ENST00000696777.1:n.2142T=
ENST00000696778.1:n.1170T=
ENST00000696779.1:c.341T=	ENSP00000512862.1:p.Val114=
ENST00000696780.1:c.764T=	ENSP00000512863.1:p.Val255=
ENST00000696781.1:c.479T=	ENSP00000512864.1:p.Val160=
ENST00000696782.1:c.*136T=	ENSP00000512865.1:n.*136T=
ENST00000696783.1:n.2602T=
ENST00000696992.1:n.1851T=
ENST00000696995.1:n.4263T=
ENST00000696996.1:n.2176T=
ENST00000696997.1:c.*364T=	ENSP00000513028.1:n.*364T=
ENST00000696998.1:n.1988T=
ENST00000696999.1:c.17T=	ENSP00000513029.1:p.Val6=
ENST00000697035.1:c.*67T=	ENSP00000513059.1:n.*67T=
ENST00000697036.1:c.*150T=	ENSP00000513060.1:n.*150T=
ENST00000697037.1:n.769T=
ENST00000697093.1:n.2970T=
ENST00000697094.1:n.3317T=
ENST00000697095.1:c.*1935T=	ENSP00000513104.1:n.*1935T=
ENST00000697096.1:n.1867T=
ENST00000697097.1:c.17T=	ENSP00000513105.1:p.Val6=
ENST00000562983.2:n.920T=
ENST00000690268.1:c.815T=	ENSP00000509810.1:p.Val272=
ENST00000355740.7:c.*60T=	ENSP00000347979.3:n.*60T=
ENST00000612663.5:c.*136T=	ENSP00000477997.3:n.*136T=
ENST00000640140.1:n.906T=
ENST00000640250.1:n.233T=
ENST00000640681.1:n.855T=
ENST00000652046.1:c.734T= MANE Select	ENSP00000498466.1:p.Val245=
ENST00000313771.9:n.1043T=
ENST00000352159.8:c.*51T=	ENSP00000345601.4:n.*51T=
ENST00000355279.2:c.709T=	ENSP00000347426.2:n.709T=
ENST00000355740.6:c.734T=	ENSP00000347979.2:p.Val245=
ENST00000357339.6:c.671T=	ENSP00000349896.2:p.Val224=
ENST00000479522.5:c.*163T=	ENSP00000424113.1:n.*163T=
ENST00000484444.5:c.*175T=	ENSP00000420975.1:n.*175T=
ENST00000488877.5:c.*175T=	ENSP00000425159.1:n.*175T=
ENST00000492756.5:c.562T=	ENSP00000422453.1:n.562T=
ENST00000494410.5:c.*92T=	ENSP00000423755.1:n.*92T=
ENST00000494799.5:n.641T=
ENST00000612663.4:c.*81T=	ENSP00000477997.2:n.*81T=
ENST00000615406.4:c.734T=	ENSP00000484575.1:p.Val245=
ENST00000626542.2:c.732T=	ENSP00000485876.1:p.Ser244=
NM_000043.4:c.734T= , LRG_134t1:c.734T=	NP_000034.1:p.Val245=
NM_152871.2:c.671T=	NP_690610.1:p.Val224=
NM_152872.2:c.*46T=	NP_690611.1:n.*46T=
NR_028033.2:n.908T=
NR_028034.2:n.770T=
NR_028035.2:n.833T=
NR_028036.2:n.971T=
XM_006717819.2:c.815T=	XP_006717882.1:p.Val272=
XM_011539764.1:c.896T=	XP_011538066.1:p.Val299=
XM_011539765.1:c.833T=	XP_011538067.1:p.Val278=
XM_011539766.1:c.815T=	XP_011538068.1:p.Val272=
XM_011539767.1:c.779T=	XP_011538069.1:p.Val260=
XR_945732.1:n.802T=
XR_945733.1:n.739T=
NM_000043.5:c.734T=	NP_000034.1:p.Val245=
NM_001320619.1:c.*57T=	NP_001307548.1:n.*57T=
NM_152871.3:c.671T=	NP_690610.1:p.Val224=
NM_152872.3:c.*46T=	NP_690611.1:n.*46T=
NR_028033.3:n.880T=
NR_028034.3:n.742T=
NR_028035.3:n.805T=
NR_028036.3:n.943T=
NR_135313.1:n.860T=
NR_135314.1:n.1043T=
NR_135315.1:n.796T=
XM_006717819.3:c.815T=	XP_006717882.1:p.Val272=
XM_011539764.2:c.896T=	XP_011538066.1:p.Val299=
XM_011539765.2:c.833T=	XP_011538067.1:p.Val278=
XM_011539766.2:c.815T=	XP_011538068.1:p.Val272=
XM_011539767.3:c.779T=	XP_011538069.1:p.Val260=
XR_945732.3:n.802T=
XR_945733.2:n.739T=
NM_000043.6:c.734T= MANE Select	NP_000034.1:p.Val245=
NM_001320619.2:c.*57T=	NP_001307548.1:n.*57T=
NM_152871.4:c.671T=	NP_690610.1:p.Val224=
NM_152872.4:c.*46T=	NP_690611.1:n.*46T=
NR_028033.4:n.641T=
NR_028034.4:n.503T=
NR_028035.4:n.566T=
NR_028036.4:n.704T=
NR_135313.2:n.621T=
NR_135314.2:n.900T=
NR_135315.2:n.653T=