Canonical Allele Identifier: CA377509872

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774013G>T (hg19) ; chr10:g.89014256G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014256G>T , CM000672.2:g.89014256G>T	GRCh38
NC_000010.10:g.90774013G>T , CM000672.1:g.90774013G>T	GRCh37
NC_000010.9:g.90763993G>T	NCBI36
NG_009089.2:g.28726G>T , LRG_134:g.28726G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1123G>T
ENST00000355740.8:c.*137G>T	ENSP00000347979.3:n.*137G>T
ENST00000357339.7:c.751G>T	ENSP00000349896.2:p.Glu251Ter
ENST00000371857.8:n.2359G>T
ENST00000460510.6:c.97G>T	ENSP00000512812.1:p.Glu33Ter
ENST00000466081.6:n.2463G>T
ENST00000477270.6:c.859G>T	ENSP00000512813.1:p.Glu287Ter
ENST00000479522.6:c.*243G>T	ENSP00000424113.1:n.*243G>T
ENST00000484444.6:c.*255G>T	ENSP00000420975.1:n.*255G>T
ENST00000488877.6:c.705G>T	ENSP00000425159.1:n.705G>T
ENST00000492756.7:c.*243G>T	ENSP00000422453.1:n.*243G>T
ENST00000494799.6:c.97G>T	ENSP00000512834.1:p.Glu33Ter
ENST00000562983.3:c.97G>T	ENSP00000512845.1:p.Glu33Ter
ENST00000612663.6:c.*216G>T	ENSP00000477997.3:n.*216G>T
ENST00000640140.2:n.959G>T
ENST00000640250.2:n.313G>T
ENST00000640681.2:n.918G>T
ENST00000696723.1:n.4447G>T
ENST00000696741.1:n.2452G>T
ENST00000696742.1:n.2179G>T
ENST00000696743.1:n.3582G>T
ENST00000696744.1:n.853G>T
ENST00000696767.1:n.1148G>T
ENST00000696768.1:c.*137G>T	ENSP00000512859.1:n.*137G>T
ENST00000696769.1:n.2503G>T
ENST00000696771.1:c.97G>T	ENSP00000512860.1:p.Glu33Ter
ENST00000696772.1:n.2417G>T
ENST00000696773.1:n.2156G>T
ENST00000696774.1:n.5924G>T
ENST00000696776.1:c.907G>T	ENSP00000512861.1:p.Glu303Ter
ENST00000696777.1:n.2222G>T
ENST00000696778.1:n.1250G>T
ENST00000696779.1:c.421G>T	ENSP00000512862.1:p.Glu141Ter
ENST00000696780.1:c.844G>T	ENSP00000512863.1:p.Glu282Ter
ENST00000696781.1:c.559G>T	ENSP00000512864.1:p.Glu187Ter
ENST00000696782.1:c.*216G>T	ENSP00000512865.1:n.*216G>T
ENST00000696783.1:n.2682G>T
ENST00000696992.1:n.1931G>T
ENST00000696995.1:n.4343G>T
ENST00000696996.1:n.2256G>T
ENST00000696997.1:c.*444G>T	ENSP00000513028.1:n.*444G>T
ENST00000696998.1:n.2068G>T
ENST00000696999.1:c.97G>T	ENSP00000513029.1:p.Glu33Ter
ENST00000697035.1:c.*147G>T	ENSP00000513059.1:n.*147G>T
ENST00000697036.1:c.*230G>T	ENSP00000513060.1:n.*230G>T
ENST00000697037.1:n.849G>T
ENST00000697093.1:n.3050G>T
ENST00000697094.1:n.3397G>T
ENST00000697095.1:c.*2015G>T	ENSP00000513104.1:n.*2015G>T
ENST00000697096.1:n.1947G>T
ENST00000697097.1:c.97G>T	ENSP00000513105.1:p.Glu33Ter
ENST00000562983.2:n.1000G>T
ENST00000690268.1:c.895G>T	ENSP00000509810.1:p.Glu299Ter
ENST00000355740.7:c.*140G>T	ENSP00000347979.3:n.*140G>T
ENST00000612663.5:c.*216G>T	ENSP00000477997.3:n.*216G>T
ENST00000640140.1:n.986G>T
ENST00000640250.1:n.313G>T
ENST00000640681.1:n.935G>T
ENST00000652046.1:c.814G>T MANE Select	ENSP00000498466.1:p.Glu272Ter
ENST00000352159.8:c.*131G>T	ENSP00000345601.4:n.*131G>T
ENST00000355279.2:c.789G>T	ENSP00000347426.2:n.789G>T
ENST00000355740.6:c.814G>T	ENSP00000347979.2:p.Glu272Ter
ENST00000357339.6:c.751G>T	ENSP00000349896.2:p.Glu251Ter
ENST00000479522.5:c.*243G>T	ENSP00000424113.1:n.*243G>T
ENST00000484444.5:c.*255G>T	ENSP00000420975.1:n.*255G>T
ENST00000488877.5:c.*255G>T	ENSP00000425159.1:n.*255G>T
ENST00000492756.5:c.642G>T	ENSP00000422453.1:n.642G>T
ENST00000494410.5:c.*172G>T	ENSP00000423755.1:n.*172G>T
ENST00000612663.4:c.*161G>T	ENSP00000477997.2:n.*161G>T
NM_000043.4:c.814G>T , LRG_134t1:c.814G>T	NP_000034.1:p.Glu272Ter
NM_152871.2:c.751G>T	NP_690610.1:p.Glu251Ter
NM_152872.2:c.*126G>T	NP_690611.1:n.*126G>T
NR_028033.2:n.988G>T
NR_028034.2:n.850G>T
NR_028035.2:n.913G>T
NR_028036.2:n.1051G>T
XM_006717819.2:c.895G>T	XP_006717882.1:p.Glu299Ter
XM_011539764.1:c.976G>T	XP_011538066.1:p.Glu326Ter
XM_011539765.1:c.913G>T	XP_011538067.1:p.Glu305Ter
XM_011539766.1:c.895G>T	XP_011538068.1:p.Glu299Ter
XM_011539767.1:c.859G>T	XP_011538069.1:p.Glu287Ter
XR_945732.1:n.882G>T
XR_945733.1:n.819G>T
NM_000043.5:c.814G>T	NP_000034.1:p.Glu272Ter
NM_001320619.1:c.*137G>T	NP_001307548.1:n.*137G>T
NM_152871.3:c.751G>T	NP_690610.1:p.Glu251Ter
NM_152872.3:c.*126G>T	NP_690611.1:n.*126G>T
NR_028033.3:n.960G>T
NR_028034.3:n.822G>T
NR_028035.3:n.885G>T
NR_028036.3:n.1023G>T
NR_135313.1:n.940G>T
NR_135314.1:n.1123G>T
NR_135315.1:n.876G>T
XM_006717819.3:c.895G>T	XP_006717882.1:p.Glu299Ter
XM_011539764.2:c.976G>T	XP_011538066.1:p.Glu326Ter
XM_011539765.2:c.913G>T	XP_011538067.1:p.Glu305Ter
XM_011539766.2:c.895G>T	XP_011538068.1:p.Glu299Ter
XM_011539767.3:c.859G>T	XP_011538069.1:p.Glu287Ter
XR_945732.3:n.882G>T
XR_945733.2:n.819G>T
NM_000043.6:c.814G>T MANE Select	NP_000034.1:p.Glu272Ter
NM_001320619.2:c.*137G>T	NP_001307548.1:n.*137G>T
NM_152871.4:c.751G>T	NP_690610.1:p.Glu251Ter
NM_152872.4:c.*126G>T	NP_690611.1:n.*126G>T
NR_028033.4:n.721G>T
NR_028034.4:n.583G>T
NR_028035.4:n.646G>T
NR_028036.4:n.784G>T
NR_135313.2:n.701G>T
NR_135314.2:n.980G>T
NR_135315.2:n.733G>T