Canonical Allele Identifier: CA377509548

Gene: FAS

Linked Data

• COSMIC: COSM6209711
• MyVariant Identifiers: chr10:g.90773885T>A (hg19) ; chr10:g.89014128T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014128T>A , CM000672.2:g.89014128T>A	GRCh38
NC_000010.10:g.90773885T>A , CM000672.1:g.90773885T>A	GRCh37
NC_000010.9:g.90763865T>A	NCBI36
NG_009089.2:g.28598T>A , LRG_134:g.28598T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.995T>A
ENST00000355740.8:c.*9T>A	ENSP00000347979.3:n.*9T>A
ENST00000357339.7:c.623T>A	ENSP00000349896.2:p.Leu208Ter
ENST00000371857.8:n.2231T>A
ENST00000460510.6:c.-32T>A	ENSP00000512812.1:n.-32T>A
ENST00000466081.6:n.2335T>A
ENST00000477270.6:c.731T>A	ENSP00000512813.1:p.Leu244Ter
ENST00000479522.6:c.*115T>A	ENSP00000424113.1:n.*115T>A
ENST00000484444.6:c.*127T>A	ENSP00000420975.1:n.*127T>A
ENST00000488877.6:c.577T>A	ENSP00000425159.1:n.577T>A
ENST00000492756.7:c.*115T>A	ENSP00000422453.1:n.*115T>A
ENST00000494799.6:c.-32T>A	ENSP00000512834.1:n.-32T>A
ENST00000562983.3:c.-32T>A	ENSP00000512845.1:n.-32T>A
ENST00000612663.6:c.*88T>A	ENSP00000477997.3:n.*88T>A
ENST00000640140.2:n.831T>A
ENST00000640250.2:n.185T>A
ENST00000640681.2:n.790T>A
ENST00000696723.1:n.4319T>A
ENST00000696741.1:n.2324T>A
ENST00000696742.1:n.2051T>A
ENST00000696743.1:n.3454T>A
ENST00000696744.1:n.725T>A
ENST00000696767.1:n.1020T>A
ENST00000696768.1:c.*9T>A	ENSP00000512859.1:n.*9T>A
ENST00000696769.1:n.2375T>A
ENST00000696771.1:c.-32T>A	ENSP00000512860.1:n.-32T>A
ENST00000696772.1:n.2289T>A
ENST00000696773.1:n.2028T>A
ENST00000696774.1:n.5796T>A
ENST00000696776.1:c.779T>A	ENSP00000512861.1:p.Leu260Ter
ENST00000696777.1:n.2094T>A
ENST00000696778.1:n.1122T>A
ENST00000696779.1:c.293T>A	ENSP00000512862.1:p.Leu98Ter
ENST00000696780.1:c.716T>A	ENSP00000512863.1:p.Leu239Ter
ENST00000696781.1:c.431T>A	ENSP00000512864.1:p.Leu144Ter
ENST00000696782.1:c.*88T>A	ENSP00000512865.1:n.*88T>A
ENST00000696783.1:n.2554T>A
ENST00000696992.1:n.1803T>A
ENST00000696995.1:n.4215T>A
ENST00000696996.1:n.2128T>A
ENST00000696997.1:c.*316T>A	ENSP00000513028.1:n.*316T>A
ENST00000696998.1:n.1940T>A
ENST00000696999.1:c.-32T>A	ENSP00000513029.1:n.-32T>A
ENST00000697035.1:c.*19T>A	ENSP00000513059.1:n.*19T>A
ENST00000697036.1:c.*102T>A	ENSP00000513060.1:n.*102T>A
ENST00000697037.1:n.721T>A
ENST00000697093.1:n.2922T>A
ENST00000697094.1:n.3269T>A
ENST00000697095.1:c.*1887T>A	ENSP00000513104.1:n.*1887T>A
ENST00000697096.1:n.1819T>A
ENST00000697097.1:c.-32T>A	ENSP00000513105.1:n.-32T>A
ENST00000562983.2:n.872T>A
ENST00000690268.1:c.767T>A	ENSP00000509810.1:p.Leu256Ter
ENST00000355740.7:c.*12T>A	ENSP00000347979.3:n.*12T>A
ENST00000612663.5:c.*88T>A	ENSP00000477997.3:n.*88T>A
ENST00000640140.1:n.858T>A
ENST00000640250.1:n.185T>A
ENST00000640681.1:n.807T>A
ENST00000652046.1:c.686T>A MANE Select	ENSP00000498466.1:p.Leu229Ter
ENST00000313771.9:n.995T>A
ENST00000352159.8:c.*3T>A	ENSP00000345601.4:n.*3T>A
ENST00000355279.2:c.661T>A	ENSP00000347426.2:p.Ter221Arg
ENST00000355740.6:c.686T>A	ENSP00000347979.2:p.Leu229Ter
ENST00000357339.6:c.623T>A	ENSP00000349896.2:p.Leu208Ter
ENST00000479522.5:c.*115T>A	ENSP00000424113.1:n.*115T>A
ENST00000484444.5:c.*127T>A	ENSP00000420975.1:n.*127T>A
ENST00000488877.5:c.*127T>A	ENSP00000425159.1:n.*127T>A
ENST00000492756.5:c.514T>A	ENSP00000422453.1:n.514T>A
ENST00000494410.5:c.*44T>A	ENSP00000423755.1:n.*44T>A
ENST00000494799.5:n.593T>A
ENST00000612663.4:c.*33T>A	ENSP00000477997.2:n.*33T>A
ENST00000615406.4:c.686T>A	ENSP00000484575.1:p.Leu229Ter
ENST00000626542.2:c.686T>A	ENSP00000485876.1:p.Leu229Ter
NM_000043.4:c.686T>A , LRG_134t1:c.686T>A	NP_000034.1:p.Leu229Ter
NM_152871.2:c.623T>A	NP_690610.1:p.Leu208Ter
NM_152872.2:c.661T>A	NP_690611.1:p.Ter221Arg
NR_028033.2:n.860T>A
NR_028034.2:n.722T>A
NR_028035.2:n.785T>A
NR_028036.2:n.923T>A
XM_006717819.2:c.767T>A	XP_006717882.1:p.Leu256Ter
XM_011539764.1:c.848T>A	XP_011538066.1:p.Leu283Ter
XM_011539765.1:c.785T>A	XP_011538067.1:p.Leu262Ter
XM_011539766.1:c.767T>A	XP_011538068.1:p.Leu256Ter
XM_011539767.1:c.731T>A	XP_011538069.1:p.Leu244Ter
XR_945732.1:n.754T>A
XR_945733.1:n.691T>A
NM_000043.5:c.686T>A	NP_000034.1:p.Leu229Ter
NM_001320619.1:c.*9T>A	NP_001307548.1:n.*9T>A
NM_152871.3:c.623T>A	NP_690610.1:p.Leu208Ter
NM_152872.3:c.661T>A	NP_690611.1:p.Ter221Arg
NR_028033.3:n.832T>A
NR_028034.3:n.694T>A
NR_028035.3:n.757T>A
NR_028036.3:n.895T>A
NR_135313.1:n.812T>A
NR_135314.1:n.995T>A
NR_135315.1:n.748T>A
XM_006717819.3:c.767T>A	XP_006717882.1:p.Leu256Ter
XM_011539764.2:c.848T>A	XP_011538066.1:p.Leu283Ter
XM_011539765.2:c.785T>A	XP_011538067.1:p.Leu262Ter
XM_011539766.2:c.767T>A	XP_011538068.1:p.Leu256Ter
XM_011539767.3:c.731T>A	XP_011538069.1:p.Leu244Ter
XR_945732.3:n.754T>A
XR_945733.2:n.691T>A
NM_000043.6:c.686T>A MANE Select	NP_000034.1:p.Leu229Ter
NM_001320619.2:c.*9T>A	NP_001307548.1:n.*9T>A
NM_152871.4:c.623T>A	NP_690610.1:p.Leu208Ter
NM_152872.4:c.661T>A	NP_690611.1:p.Ter221Arg
NR_028033.4:n.593T>A
NR_028034.4:n.455T>A
NR_028035.4:n.518T>A
NR_028036.4:n.656T>A
NR_135313.2:n.573T>A
NR_135314.2:n.852T>A
NR_135315.2:n.605T>A