Canonical Allele Identifier: CA1926639306

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014134A= , CM000672.2:g.89014134A=	GRCh38
NC_000010.10:g.90773891A= , CM000672.1:g.90773891A=	GRCh37
NC_000010.9:g.90763871A=	NCBI36
NG_009089.2:g.28604A= , LRG_134:g.28604A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1001A=
ENST00000355740.8:c.*15A=	ENSP00000347979.3:n.*15A=
ENST00000357339.7:c.629A=	ENSP00000349896.2:p.Lys210=
ENST00000371857.8:n.2237A=
ENST00000460510.6:c.-26A=	ENSP00000512812.1:n.-26A=
ENST00000466081.6:n.2341A=
ENST00000477270.6:c.737A=	ENSP00000512813.1:p.Lys246=
ENST00000479522.6:c.*121A=	ENSP00000424113.1:n.*121A=
ENST00000484444.6:c.*133A=	ENSP00000420975.1:n.*133A=
ENST00000488877.6:c.583A=	ENSP00000425159.1:n.583A=
ENST00000492756.7:c.*121A=	ENSP00000422453.1:n.*121A=
ENST00000494799.6:c.-26A=	ENSP00000512834.1:n.-26A=
ENST00000562983.3:c.-26A=	ENSP00000512845.1:n.-26A=
ENST00000612663.6:c.*94A=	ENSP00000477997.3:n.*94A=
ENST00000640140.2:n.837A=
ENST00000640250.2:n.191A=
ENST00000640681.2:n.796A=
ENST00000696723.1:n.4325A=
ENST00000696741.1:n.2330A=
ENST00000696742.1:n.2057A=
ENST00000696743.1:n.3460A=
ENST00000696744.1:n.731A=
ENST00000696767.1:n.1026A=
ENST00000696768.1:c.*15A=	ENSP00000512859.1:n.*15A=
ENST00000696769.1:n.2381A=
ENST00000696771.1:c.-26A=	ENSP00000512860.1:n.-26A=
ENST00000696772.1:n.2295A=
ENST00000696773.1:n.2034A=
ENST00000696774.1:n.5802A=
ENST00000696776.1:c.785A=	ENSP00000512861.1:p.Lys262=
ENST00000696777.1:n.2100A=
ENST00000696778.1:n.1128A=
ENST00000696779.1:c.299A=	ENSP00000512862.1:p.Lys100=
ENST00000696780.1:c.722A=	ENSP00000512863.1:p.Lys241=
ENST00000696781.1:c.437A=	ENSP00000512864.1:p.Lys146=
ENST00000696782.1:c.*94A=	ENSP00000512865.1:n.*94A=
ENST00000696783.1:n.2560A=
ENST00000696992.1:n.1809A=
ENST00000696995.1:n.4221A=
ENST00000696996.1:n.2134A=
ENST00000696997.1:c.*322A=	ENSP00000513028.1:n.*322A=
ENST00000696998.1:n.1946A=
ENST00000696999.1:c.-26A=	ENSP00000513029.1:n.-26A=
ENST00000697035.1:c.*25A=	ENSP00000513059.1:n.*25A=
ENST00000697036.1:c.*108A=	ENSP00000513060.1:n.*108A=
ENST00000697037.1:n.727A=
ENST00000697093.1:n.2928A=
ENST00000697094.1:n.3275A=
ENST00000697095.1:c.*1893A=	ENSP00000513104.1:n.*1893A=
ENST00000697096.1:n.1825A=
ENST00000697097.1:c.-26A=	ENSP00000513105.1:n.-26A=
ENST00000562983.2:n.878A=
ENST00000690268.1:c.773A=	ENSP00000509810.1:p.Lys258=
ENST00000355740.7:c.*18A=	ENSP00000347979.3:n.*18A=
ENST00000612663.5:c.*94A=	ENSP00000477997.3:n.*94A=
ENST00000640140.1:n.864A=
ENST00000640250.1:n.191A=
ENST00000640681.1:n.813A=
ENST00000652046.1:c.692A= MANE Select	ENSP00000498466.1:p.Lys231=
ENST00000313771.9:n.1001A=
ENST00000352159.8:c.*9A=	ENSP00000345601.4:n.*9A=
ENST00000355279.2:c.667A=	ENSP00000347426.2:n.667A=
ENST00000355740.6:c.692A=	ENSP00000347979.2:p.Lys231=
ENST00000357339.6:c.629A=	ENSP00000349896.2:p.Lys210=
ENST00000479522.5:c.*121A=	ENSP00000424113.1:n.*121A=
ENST00000484444.5:c.*133A=	ENSP00000420975.1:n.*133A=
ENST00000488877.5:c.*133A=	ENSP00000425159.1:n.*133A=
ENST00000492756.5:c.520A=	ENSP00000422453.1:n.520A=
ENST00000494410.5:c.*50A=	ENSP00000423755.1:n.*50A=
ENST00000494799.5:n.599A=
ENST00000612663.4:c.*39A=	ENSP00000477997.2:n.*39A=
ENST00000615406.4:c.692A=	ENSP00000484575.1:p.Lys231=
ENST00000626542.2:c.692A=	ENSP00000485876.1:p.Lys231=
NM_000043.4:c.692A= , LRG_134t1:c.692A=	NP_000034.1:p.Lys231=
NM_152871.2:c.629A=	NP_690610.1:p.Lys210=
NM_152872.2:c.*4A=	NP_690611.1:n.*4A=
NR_028033.2:n.866A=
NR_028034.2:n.728A=
NR_028035.2:n.791A=
NR_028036.2:n.929A=
XM_006717819.2:c.773A=	XP_006717882.1:p.Lys258=
XM_011539764.1:c.854A=	XP_011538066.1:p.Lys285=
XM_011539765.1:c.791A=	XP_011538067.1:p.Lys264=
XM_011539766.1:c.773A=	XP_011538068.1:p.Lys258=
XM_011539767.1:c.737A=	XP_011538069.1:p.Lys246=
XR_945732.1:n.760A=
XR_945733.1:n.697A=
NM_000043.5:c.692A=	NP_000034.1:p.Lys231=
NM_001320619.1:c.*15A=	NP_001307548.1:n.*15A=
NM_152871.3:c.629A=	NP_690610.1:p.Lys210=
NM_152872.3:c.*4A=	NP_690611.1:n.*4A=
NR_028033.3:n.838A=
NR_028034.3:n.700A=
NR_028035.3:n.763A=
NR_028036.3:n.901A=
NR_135313.1:n.818A=
NR_135314.1:n.1001A=
NR_135315.1:n.754A=
XM_006717819.3:c.773A=	XP_006717882.1:p.Lys258=
XM_011539764.2:c.854A=	XP_011538066.1:p.Lys285=
XM_011539765.2:c.791A=	XP_011538067.1:p.Lys264=
XM_011539766.2:c.773A=	XP_011538068.1:p.Lys258=
XM_011539767.3:c.737A=	XP_011538069.1:p.Lys246=
XR_945732.3:n.760A=
XR_945733.2:n.697A=
NM_000043.6:c.692A= MANE Select	NP_000034.1:p.Lys231=
NM_001320619.2:c.*15A=	NP_001307548.1:n.*15A=
NM_152871.4:c.629A=	NP_690610.1:p.Lys210=
NM_152872.4:c.*4A=	NP_690611.1:n.*4A=
NR_028033.4:n.599A=
NR_028034.4:n.461A=
NR_028035.4:n.524A=
NR_028036.4:n.662A=
NR_135313.2:n.579A=
NR_135314.2:n.858A=
NR_135315.2:n.611A=