Canonical Allele Identifier: CA377509759

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773966A>T (hg19) ; chr10:g.89014209A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014209A>T , CM000672.2:g.89014209A>T	GRCh38
NC_000010.10:g.90773966A>T , CM000672.1:g.90773966A>T	GRCh37
NC_000010.9:g.90763946A>T	NCBI36
NG_009089.2:g.28679A>T , LRG_134:g.28679A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1076A>T
ENST00000355740.8:c.*90A>T	ENSP00000347979.3:n.*90A>T
ENST00000357339.7:c.704A>T	ENSP00000349896.2:p.Glu235Val
ENST00000371857.8:n.2312A>T
ENST00000460510.6:c.50A>T	ENSP00000512812.1:p.Glu17Val
ENST00000466081.6:n.2416A>T
ENST00000477270.6:c.812A>T	ENSP00000512813.1:p.Glu271Val
ENST00000479522.6:c.*196A>T	ENSP00000424113.1:n.*196A>T
ENST00000484444.6:c.*208A>T	ENSP00000420975.1:n.*208A>T
ENST00000488877.6:c.658A>T	ENSP00000425159.1:n.658A>T
ENST00000492756.7:c.*196A>T	ENSP00000422453.1:n.*196A>T
ENST00000494799.6:c.50A>T	ENSP00000512834.1:p.Glu17Val
ENST00000562983.3:c.50A>T	ENSP00000512845.1:p.Glu17Val
ENST00000612663.6:c.*169A>T	ENSP00000477997.3:n.*169A>T
ENST00000640140.2:n.912A>T
ENST00000640250.2:n.266A>T
ENST00000640681.2:n.871A>T
ENST00000696723.1:n.4400A>T
ENST00000696741.1:n.2405A>T
ENST00000696742.1:n.2132A>T
ENST00000696743.1:n.3535A>T
ENST00000696744.1:n.806A>T
ENST00000696767.1:n.1101A>T
ENST00000696768.1:c.*90A>T	ENSP00000512859.1:n.*90A>T
ENST00000696769.1:n.2456A>T
ENST00000696771.1:c.50A>T	ENSP00000512860.1:p.Glu17Val
ENST00000696772.1:n.2370A>T
ENST00000696773.1:n.2109A>T
ENST00000696774.1:n.5877A>T
ENST00000696776.1:c.860A>T	ENSP00000512861.1:p.Glu287Val
ENST00000696777.1:n.2175A>T
ENST00000696778.1:n.1203A>T
ENST00000696779.1:c.374A>T	ENSP00000512862.1:p.Glu125Val
ENST00000696780.1:c.797A>T	ENSP00000512863.1:p.Glu266Val
ENST00000696781.1:c.512A>T	ENSP00000512864.1:p.Glu171Val
ENST00000696782.1:c.*169A>T	ENSP00000512865.1:n.*169A>T
ENST00000696783.1:n.2635A>T
ENST00000696992.1:n.1884A>T
ENST00000696995.1:n.4296A>T
ENST00000696996.1:n.2209A>T
ENST00000696997.1:c.*397A>T	ENSP00000513028.1:n.*397A>T
ENST00000696998.1:n.2021A>T
ENST00000696999.1:c.50A>T	ENSP00000513029.1:p.Glu17Val
ENST00000697035.1:c.*100A>T	ENSP00000513059.1:n.*100A>T
ENST00000697036.1:c.*183A>T	ENSP00000513060.1:n.*183A>T
ENST00000697037.1:n.802A>T
ENST00000697093.1:n.3003A>T
ENST00000697094.1:n.3350A>T
ENST00000697095.1:c.*1968A>T	ENSP00000513104.1:n.*1968A>T
ENST00000697096.1:n.1900A>T
ENST00000697097.1:c.50A>T	ENSP00000513105.1:p.Glu17Val
ENST00000562983.2:n.953A>T
ENST00000690268.1:c.848A>T	ENSP00000509810.1:p.Glu283Val
ENST00000355740.7:c.*93A>T	ENSP00000347979.3:n.*93A>T
ENST00000612663.5:c.*169A>T	ENSP00000477997.3:n.*169A>T
ENST00000640140.1:n.939A>T
ENST00000640250.1:n.266A>T
ENST00000640681.1:n.888A>T
ENST00000652046.1:c.767A>T MANE Select	ENSP00000498466.1:p.Glu256Val
ENST00000352159.8:c.*84A>T	ENSP00000345601.4:n.*84A>T
ENST00000355279.2:c.742A>T	ENSP00000347426.2:n.742A>T
ENST00000355740.6:c.767A>T	ENSP00000347979.2:p.Glu256Val
ENST00000357339.6:c.704A>T	ENSP00000349896.2:p.Glu235Val
ENST00000479522.5:c.*196A>T	ENSP00000424113.1:n.*196A>T
ENST00000484444.5:c.*208A>T	ENSP00000420975.1:n.*208A>T
ENST00000488877.5:c.*208A>T	ENSP00000425159.1:n.*208A>T
ENST00000492756.5:c.595A>T	ENSP00000422453.1:n.595A>T
ENST00000494410.5:c.*125A>T	ENSP00000423755.1:n.*125A>T
ENST00000494799.5:n.674A>T
ENST00000612663.4:c.*114A>T	ENSP00000477997.2:n.*114A>T
ENST00000615406.4:c.765A>T	ENSP00000484575.1:p.Ter255Cys
NM_000043.4:c.767A>T , LRG_134t1:c.767A>T	NP_000034.1:p.Glu256Val
NM_152871.2:c.704A>T	NP_690610.1:p.Glu235Val
NM_152872.2:c.*79A>T	NP_690611.1:n.*79A>T
NR_028033.2:n.941A>T
NR_028034.2:n.803A>T
NR_028035.2:n.866A>T
NR_028036.2:n.1004A>T
XM_006717819.2:c.848A>T	XP_006717882.1:p.Glu283Val
XM_011539764.1:c.929A>T	XP_011538066.1:p.Glu310Val
XM_011539765.1:c.866A>T	XP_011538067.1:p.Glu289Val
XM_011539766.1:c.848A>T	XP_011538068.1:p.Glu283Val
XM_011539767.1:c.812A>T	XP_011538069.1:p.Glu271Val
XR_945732.1:n.835A>T
XR_945733.1:n.772A>T
NM_000043.5:c.767A>T	NP_000034.1:p.Glu256Val
NM_001320619.1:c.*90A>T	NP_001307548.1:n.*90A>T
NM_152871.3:c.704A>T	NP_690610.1:p.Glu235Val
NM_152872.3:c.*79A>T	NP_690611.1:n.*79A>T
NR_028033.3:n.913A>T
NR_028034.3:n.775A>T
NR_028035.3:n.838A>T
NR_028036.3:n.976A>T
NR_135313.1:n.893A>T
NR_135314.1:n.1076A>T
NR_135315.1:n.829A>T
XM_006717819.3:c.848A>T	XP_006717882.1:p.Glu283Val
XM_011539764.2:c.929A>T	XP_011538066.1:p.Glu310Val
XM_011539765.2:c.866A>T	XP_011538067.1:p.Glu289Val
XM_011539766.2:c.848A>T	XP_011538068.1:p.Glu283Val
XM_011539767.3:c.812A>T	XP_011538069.1:p.Glu271Val
XR_945732.3:n.835A>T
XR_945733.2:n.772A>T
NM_000043.6:c.767A>T MANE Select	NP_000034.1:p.Glu256Val
NM_001320619.2:c.*90A>T	NP_001307548.1:n.*90A>T
NM_152871.4:c.704A>T	NP_690610.1:p.Glu235Val
NM_152872.4:c.*79A>T	NP_690611.1:n.*79A>T
NR_028033.4:n.674A>T
NR_028034.4:n.536A>T
NR_028035.4:n.599A>T
NR_028036.4:n.737A>T
NR_135313.2:n.654A>T
NR_135314.2:n.933A>T
NR_135315.2:n.686A>T