Canonical Allele Identifier: CA377510023

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774080T>A (hg19) ; chr10:g.89014323T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014323T>A , CM000672.2:g.89014323T>A	GRCh38
NC_000010.10:g.90774080T>A , CM000672.1:g.90774080T>A	GRCh37
NC_000010.9:g.90764060T>A	NCBI36
NG_009089.2:g.28793T>A , LRG_134:g.28793T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1190T>A
ENST00000355740.8:c.*204T>A	ENSP00000347979.3:n.*204T>A
ENST00000357339.7:c.818T>A	ENSP00000349896.2:p.Leu273Ter
ENST00000371857.8:n.2426T>A
ENST00000460510.6:c.164T>A	ENSP00000512812.1:p.Leu55Ter
ENST00000466081.6:n.2530T>A
ENST00000477270.6:c.926T>A	ENSP00000512813.1:p.Leu309Ter
ENST00000479522.6:c.*310T>A	ENSP00000424113.1:n.*310T>A
ENST00000484444.6:c.*322T>A	ENSP00000420975.1:n.*322T>A
ENST00000488877.6:c.772T>A	ENSP00000425159.1:n.772T>A
ENST00000492756.7:c.*310T>A	ENSP00000422453.1:n.*310T>A
ENST00000494799.6:c.164T>A	ENSP00000512834.1:p.Leu55Ter
ENST00000562983.3:c.164T>A	ENSP00000512845.1:p.Leu55Ter
ENST00000612663.6:c.*283T>A	ENSP00000477997.3:n.*283T>A
ENST00000640140.2:n.1026T>A
ENST00000640250.2:n.380T>A
ENST00000640681.2:n.985T>A
ENST00000696723.1:n.4514T>A
ENST00000696741.1:n.2519T>A
ENST00000696742.1:n.2246T>A
ENST00000696743.1:n.3649T>A
ENST00000696744.1:n.920T>A
ENST00000696767.1:n.1215T>A
ENST00000696768.1:c.*204T>A	ENSP00000512859.1:n.*204T>A
ENST00000696769.1:n.2570T>A
ENST00000696771.1:c.164T>A	ENSP00000512860.1:p.Leu55Ter
ENST00000696772.1:n.2484T>A
ENST00000696773.1:n.2223T>A
ENST00000696774.1:n.5991T>A
ENST00000696776.1:c.974T>A	ENSP00000512861.1:p.Leu325Ter
ENST00000696777.1:n.2289T>A
ENST00000696778.1:n.1317T>A
ENST00000696779.1:c.488T>A	ENSP00000512862.1:p.Leu163Ter
ENST00000696780.1:c.911T>A	ENSP00000512863.1:p.Leu304Ter
ENST00000696781.1:c.626T>A	ENSP00000512864.1:p.Leu209Ter
ENST00000696782.1:c.*283T>A	ENSP00000512865.1:n.*283T>A
ENST00000696783.1:n.2749T>A
ENST00000696992.1:n.1998T>A
ENST00000696995.1:n.4410T>A
ENST00000696996.1:n.2323T>A
ENST00000696997.1:c.*511T>A	ENSP00000513028.1:n.*511T>A
ENST00000696998.1:n.2135T>A
ENST00000696999.1:c.164T>A	ENSP00000513029.1:p.Leu55Ter
ENST00000697036.1:c.*297T>A	ENSP00000513060.1:n.*297T>A
ENST00000697037.1:n.916T>A
ENST00000697093.1:n.3117T>A
ENST00000697094.1:n.3464T>A
ENST00000697095.1:c.*2082T>A	ENSP00000513104.1:n.*2082T>A
ENST00000697096.1:n.2014T>A
ENST00000697097.1:c.164T>A	ENSP00000513105.1:p.Leu55Ter
ENST00000562983.2:n.1067T>A
ENST00000690268.1:c.962T>A	ENSP00000509810.1:p.Leu321Ter
ENST00000355740.7:c.*207T>A	ENSP00000347979.3:n.*207T>A
ENST00000612663.5:c.*283T>A	ENSP00000477997.3:n.*283T>A
ENST00000640140.1:n.1053T>A
ENST00000640250.1:n.380T>A
ENST00000640681.1:n.1002T>A
ENST00000652046.1:c.881T>A MANE Select	ENSP00000498466.1:p.Leu294Ter
ENST00000352159.8:c.*198T>A	ENSP00000345601.4:n.*198T>A
ENST00000355279.2:c.856T>A	ENSP00000347426.2:n.856T>A
ENST00000355740.6:c.881T>A	ENSP00000347979.2:p.Leu294Ter
ENST00000357339.6:c.818T>A	ENSP00000349896.2:p.Leu273Ter
ENST00000479522.5:c.*310T>A	ENSP00000424113.1:n.*310T>A
ENST00000484444.5:c.*322T>A	ENSP00000420975.1:n.*322T>A
ENST00000488877.5:c.*322T>A	ENSP00000425159.1:n.*322T>A
ENST00000492756.5:c.709T>A	ENSP00000422453.1:n.709T>A
ENST00000494410.5:c.*239T>A	ENSP00000423755.1:n.*239T>A
ENST00000612663.4:c.*228T>A	ENSP00000477997.2:n.*228T>A
NM_000043.4:c.881T>A , LRG_134t1:c.881T>A	NP_000034.1:p.Leu294Ter
NM_152871.2:c.818T>A	NP_690610.1:p.Leu273Ter
NM_152872.2:c.*193T>A	NP_690611.1:n.*193T>A
NR_028033.2:n.1055T>A
NR_028034.2:n.917T>A
NR_028035.2:n.980T>A
NR_028036.2:n.1118T>A
XM_006717819.2:c.962T>A	XP_006717882.1:p.Leu321Ter
XM_011539764.1:c.1043T>A	XP_011538066.1:p.Leu348Ter
XM_011539765.1:c.980T>A	XP_011538067.1:p.Leu327Ter
XM_011539766.1:c.962T>A	XP_011538068.1:p.Leu321Ter
XM_011539767.1:c.926T>A	XP_011538069.1:p.Leu309Ter
XR_945732.1:n.949T>A
XR_945733.1:n.886T>A
NM_000043.5:c.881T>A	NP_000034.1:p.Leu294Ter
NM_001320619.1:c.*204T>A	NP_001307548.1:n.*204T>A
NM_152871.3:c.818T>A	NP_690610.1:p.Leu273Ter
NM_152872.3:c.*193T>A	NP_690611.1:n.*193T>A
NR_028033.3:n.1027T>A
NR_028034.3:n.889T>A
NR_028035.3:n.952T>A
NR_028036.3:n.1090T>A
NR_135313.1:n.1007T>A
NR_135314.1:n.1190T>A
NR_135315.1:n.943T>A
XM_006717819.3:c.962T>A	XP_006717882.1:p.Leu321Ter
XM_011539764.2:c.1043T>A	XP_011538066.1:p.Leu348Ter
XM_011539765.2:c.980T>A	XP_011538067.1:p.Leu327Ter
XM_011539766.2:c.962T>A	XP_011538068.1:p.Leu321Ter
XM_011539767.3:c.926T>A	XP_011538069.1:p.Leu309Ter
XR_945732.3:n.949T>A
XR_945733.2:n.886T>A
NM_000043.6:c.881T>A MANE Select	NP_000034.1:p.Leu294Ter
NM_001320619.2:c.*204T>A	NP_001307548.1:n.*204T>A
NM_152871.4:c.818T>A	NP_690610.1:p.Leu273Ter
NM_152872.4:c.*193T>A	NP_690611.1:n.*193T>A
NR_028033.4:n.788T>A
NR_028034.4:n.650T>A
NR_028035.4:n.713T>A
NR_028036.4:n.851T>A
NR_135313.2:n.768T>A
NR_135314.2:n.1047T>A
NR_135315.2:n.800T>A