Canonical Allele Identifier: CA1926639389

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014340A= , CM000672.2:g.89014340A=	GRCh38
NC_000010.10:g.90774097A= , CM000672.1:g.90774097A=	GRCh37
NC_000010.9:g.90764077A=	NCBI36
NG_009089.2:g.28810A= , LRG_134:g.28810A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1207A=
ENST00000355740.8:c.*221A=	ENSP00000347979.3:n.*221A=
ENST00000357339.7:c.835A=	ENSP00000349896.2:p.Lys279=
ENST00000371857.8:n.2443A=
ENST00000460510.6:c.181A=	ENSP00000512812.1:p.Lys61=
ENST00000466081.6:n.2547A=
ENST00000477270.6:c.943A=	ENSP00000512813.1:p.Lys315=
ENST00000479522.6:c.*327A=	ENSP00000424113.1:n.*327A=
ENST00000484444.6:c.*339A=	ENSP00000420975.1:n.*339A=
ENST00000488877.6:c.789A=	ENSP00000425159.1:n.789A=
ENST00000492756.7:c.*327A=	ENSP00000422453.1:n.*327A=
ENST00000494799.6:c.181A=	ENSP00000512834.1:p.Lys61=
ENST00000562983.3:c.181A=	ENSP00000512845.1:p.Lys61=
ENST00000612663.6:c.*300A=	ENSP00000477997.3:n.*300A=
ENST00000640140.2:n.1043A=
ENST00000640250.2:n.397A=
ENST00000640681.2:n.1002A=
ENST00000696723.1:n.4531A=
ENST00000696741.1:n.2536A=
ENST00000696742.1:n.2263A=
ENST00000696743.1:n.3666A=
ENST00000696744.1:n.937A=
ENST00000696767.1:n.1232A=
ENST00000696768.1:c.*221A=	ENSP00000512859.1:n.*221A=
ENST00000696769.1:n.2587A=
ENST00000696771.1:c.181A=	ENSP00000512860.1:p.Lys61=
ENST00000696772.1:n.2501A=
ENST00000696773.1:n.2240A=
ENST00000696774.1:n.6008A=
ENST00000696776.1:c.991A=	ENSP00000512861.1:p.Lys331=
ENST00000696777.1:n.2306A=
ENST00000696778.1:n.1334A=
ENST00000696779.1:c.505A=	ENSP00000512862.1:p.Lys169=
ENST00000696780.1:c.928A=	ENSP00000512863.1:p.Lys310=
ENST00000696781.1:c.643A=	ENSP00000512864.1:p.Lys215=
ENST00000696782.1:c.*300A=	ENSP00000512865.1:n.*300A=
ENST00000696783.1:n.2766A=
ENST00000696992.1:n.2015A=
ENST00000696995.1:n.4427A=
ENST00000696996.1:n.2340A=
ENST00000696997.1:c.*528A=	ENSP00000513028.1:n.*528A=
ENST00000696998.1:n.2152A=
ENST00000696999.1:c.181A=	ENSP00000513029.1:p.Lys61=
ENST00000697036.1:c.*314A=	ENSP00000513060.1:n.*314A=
ENST00000697037.1:n.933A=
ENST00000697093.1:n.3134A=
ENST00000697094.1:n.3481A=
ENST00000697095.1:c.*2099A=	ENSP00000513104.1:n.*2099A=
ENST00000697096.1:n.2031A=
ENST00000697097.1:c.181A=	ENSP00000513105.1:p.Lys61=
ENST00000562983.2:n.1084A=
ENST00000690268.1:c.979A=	ENSP00000509810.1:p.Lys327=
ENST00000355740.7:c.*224A=	ENSP00000347979.3:n.*224A=
ENST00000612663.5:c.*300A=	ENSP00000477997.3:n.*300A=
ENST00000640140.1:n.1070A=
ENST00000640250.1:n.397A=
ENST00000640681.1:n.1019A=
ENST00000652046.1:c.898A= MANE Select	ENSP00000498466.1:p.Lys300=
ENST00000352159.8:c.*215A=	ENSP00000345601.4:n.*215A=
ENST00000355279.2:c.873A=	ENSP00000347426.2:n.873A=
ENST00000355740.6:c.898A=	ENSP00000347979.2:p.Lys300=
ENST00000357339.6:c.835A=	ENSP00000349896.2:p.Lys279=
ENST00000479522.5:c.*327A=	ENSP00000424113.1:n.*327A=
ENST00000484444.5:c.*339A=	ENSP00000420975.1:n.*339A=
ENST00000488877.5:c.*339A=	ENSP00000425159.1:n.*339A=
ENST00000492756.5:c.726A=	ENSP00000422453.1:n.726A=
ENST00000494410.5:c.*256A=	ENSP00000423755.1:n.*256A=
ENST00000612663.4:c.*245A=	ENSP00000477997.2:n.*245A=
NM_000043.4:c.898A= , LRG_134t1:c.898A=	NP_000034.1:p.Lys300=
NM_152871.2:c.835A=	NP_690610.1:p.Lys279=
NM_152872.2:c.*210A=	NP_690611.1:n.*210A=
NR_028033.2:n.1072A=
NR_028034.2:n.934A=
NR_028035.2:n.997A=
NR_028036.2:n.1135A=
XM_006717819.2:c.979A=	XP_006717882.1:p.Lys327=
XM_011539764.1:c.1060A=	XP_011538066.1:p.Lys354=
XM_011539765.1:c.997A=	XP_011538067.1:p.Lys333=
XM_011539766.1:c.979A=	XP_011538068.1:p.Lys327=
XM_011539767.1:c.943A=	XP_011538069.1:p.Lys315=
XR_945732.1:n.966A=
XR_945733.1:n.903A=
NM_000043.5:c.898A=	NP_000034.1:p.Lys300=
NM_001320619.1:c.*221A=	NP_001307548.1:n.*221A=
NM_152871.3:c.835A=	NP_690610.1:p.Lys279=
NM_152872.3:c.*210A=	NP_690611.1:n.*210A=
NR_028033.3:n.1044A=
NR_028034.3:n.906A=
NR_028035.3:n.969A=
NR_028036.3:n.1107A=
NR_135313.1:n.1024A=
NR_135314.1:n.1207A=
NR_135315.1:n.960A=
XM_006717819.3:c.979A=	XP_006717882.1:p.Lys327=
XM_011539764.2:c.1060A=	XP_011538066.1:p.Lys354=
XM_011539765.2:c.997A=	XP_011538067.1:p.Lys333=
XM_011539766.2:c.979A=	XP_011538068.1:p.Lys327=
XM_011539767.3:c.943A=	XP_011538069.1:p.Lys315=
XR_945732.3:n.966A=
XR_945733.2:n.903A=
NM_000043.6:c.898A= MANE Select	NP_000034.1:p.Lys300=
NM_001320619.2:c.*221A=	NP_001307548.1:n.*221A=
NM_152871.4:c.835A=	NP_690610.1:p.Lys279=
NM_152872.4:c.*210A=	NP_690611.1:n.*210A=
NR_028033.4:n.805A=
NR_028034.4:n.667A=
NR_028035.4:n.730A=
NR_028036.4:n.868A=
NR_135313.2:n.785A=
NR_135314.2:n.1064A=
NR_135315.2:n.817A=