Canonical Allele Identifier: CA470974889

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774057A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014300A>G , CM000672.2:g.89014300A>G	GRCh38
NC_000010.10:g.90774057A>G , CM000672.1:g.90774057A>G	GRCh37
NC_000010.9:g.90764037A>G	NCBI36
NG_009089.2:g.28770A>G , LRG_134:g.28770A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1167A>G
ENST00000355740.8:c.*181A>G	ENSP00000347979.3:n.*181A>G
ENST00000357339.7:c.795A>G	ENSP00000349896.2:p.Gly265=
ENST00000371857.8:n.2403A>G
ENST00000460510.6:c.141A>G	ENSP00000512812.1:p.Gly47=
ENST00000466081.6:n.2507A>G
ENST00000477270.6:c.903A>G	ENSP00000512813.1:p.Gly301=
ENST00000479522.6:c.*287A>G	ENSP00000424113.1:n.*287A>G
ENST00000484444.6:c.*299A>G	ENSP00000420975.1:n.*299A>G
ENST00000488877.6:c.749A>G	ENSP00000425159.1:n.749A>G
ENST00000492756.7:c.*287A>G	ENSP00000422453.1:n.*287A>G
ENST00000494799.6:c.141A>G	ENSP00000512834.1:p.Gly47=
ENST00000562983.3:c.141A>G	ENSP00000512845.1:p.Gly47=
ENST00000612663.6:c.*260A>G	ENSP00000477997.3:n.*260A>G
ENST00000640140.2:n.1003A>G
ENST00000640250.2:n.357A>G
ENST00000640681.2:n.962A>G
ENST00000696723.1:n.4491A>G
ENST00000696741.1:n.2496A>G
ENST00000696742.1:n.2223A>G
ENST00000696743.1:n.3626A>G
ENST00000696744.1:n.897A>G
ENST00000696767.1:n.1192A>G
ENST00000696768.1:c.*181A>G	ENSP00000512859.1:n.*181A>G
ENST00000696769.1:n.2547A>G
ENST00000696771.1:c.141A>G	ENSP00000512860.1:p.Gly47=
ENST00000696772.1:n.2461A>G
ENST00000696773.1:n.2200A>G
ENST00000696774.1:n.5968A>G
ENST00000696776.1:c.951A>G	ENSP00000512861.1:p.Gly317=
ENST00000696777.1:n.2266A>G
ENST00000696778.1:n.1294A>G
ENST00000696779.1:c.465A>G	ENSP00000512862.1:p.Gly155=
ENST00000696780.1:c.888A>G	ENSP00000512863.1:p.Gly296=
ENST00000696781.1:c.603A>G	ENSP00000512864.1:p.Gly201=
ENST00000696782.1:c.*260A>G	ENSP00000512865.1:n.*260A>G
ENST00000696783.1:n.2726A>G
ENST00000696992.1:n.1975A>G
ENST00000696995.1:n.4387A>G
ENST00000696996.1:n.2300A>G
ENST00000696997.1:c.*488A>G	ENSP00000513028.1:n.*488A>G
ENST00000696998.1:n.2112A>G
ENST00000696999.1:c.141A>G	ENSP00000513029.1:p.Gly47=
ENST00000697035.1:c.*191A>G	ENSP00000513059.1:n.*191A>G
ENST00000697036.1:c.*274A>G	ENSP00000513060.1:n.*274A>G
ENST00000697037.1:n.893A>G
ENST00000697093.1:n.3094A>G
ENST00000697094.1:n.3441A>G
ENST00000697095.1:c.*2059A>G	ENSP00000513104.1:n.*2059A>G
ENST00000697096.1:n.1991A>G
ENST00000697097.1:c.141A>G	ENSP00000513105.1:p.Gly47=
ENST00000562983.2:n.1044A>G
ENST00000690268.1:c.939A>G	ENSP00000509810.1:p.Gly313=
ENST00000355740.7:c.*184A>G	ENSP00000347979.3:n.*184A>G
ENST00000612663.5:c.*260A>G	ENSP00000477997.3:n.*260A>G
ENST00000640140.1:n.1030A>G
ENST00000640250.1:n.357A>G
ENST00000640681.1:n.979A>G
ENST00000652046.1:c.858A>G MANE Select	ENSP00000498466.1:p.Gly286=
ENST00000352159.8:c.*175A>G	ENSP00000345601.4:n.*175A>G
ENST00000355279.2:c.833A>G	ENSP00000347426.2:n.833A>G
ENST00000355740.6:c.858A>G	ENSP00000347979.2:p.Gly286=
ENST00000357339.6:c.795A>G	ENSP00000349896.2:p.Gly265=
ENST00000479522.5:c.*287A>G	ENSP00000424113.1:n.*287A>G
ENST00000484444.5:c.*299A>G	ENSP00000420975.1:n.*299A>G
ENST00000488877.5:c.*299A>G	ENSP00000425159.1:n.*299A>G
ENST00000492756.5:c.686A>G	ENSP00000422453.1:n.686A>G
ENST00000494410.5:c.*216A>G	ENSP00000423755.1:n.*216A>G
ENST00000612663.4:c.*205A>G	ENSP00000477997.2:n.*205A>G
NM_000043.4:c.858A>G , LRG_134t1:c.858A>G	NP_000034.1:p.Gly286=
NM_152871.2:c.795A>G	NP_690610.1:p.Gly265=
NM_152872.2:c.*170A>G	NP_690611.1:n.*170A>G
NR_028033.2:n.1032A>G
NR_028034.2:n.894A>G
NR_028035.2:n.957A>G
NR_028036.2:n.1095A>G
XM_006717819.2:c.939A>G	XP_006717882.1:p.Gly313=
XM_011539764.1:c.1020A>G	XP_011538066.1:p.Gly340=
XM_011539765.1:c.957A>G	XP_011538067.1:p.Gly319=
XM_011539766.1:c.939A>G	XP_011538068.1:p.Gly313=
XM_011539767.1:c.903A>G	XP_011538069.1:p.Gly301=
XR_945732.1:n.926A>G
XR_945733.1:n.863A>G
NM_000043.5:c.858A>G	NP_000034.1:p.Gly286=
NM_001320619.1:c.*181A>G	NP_001307548.1:n.*181A>G
NM_152871.3:c.795A>G	NP_690610.1:p.Gly265=
NM_152872.3:c.*170A>G	NP_690611.1:n.*170A>G
NR_028033.3:n.1004A>G
NR_028034.3:n.866A>G
NR_028035.3:n.929A>G
NR_028036.3:n.1067A>G
NR_135313.1:n.984A>G
NR_135314.1:n.1167A>G
NR_135315.1:n.920A>G
XM_006717819.3:c.939A>G	XP_006717882.1:p.Gly313=
XM_011539764.2:c.1020A>G	XP_011538066.1:p.Gly340=
XM_011539765.2:c.957A>G	XP_011538067.1:p.Gly319=
XM_011539766.2:c.939A>G	XP_011538068.1:p.Gly313=
XM_011539767.3:c.903A>G	XP_011538069.1:p.Gly301=
XR_945732.3:n.926A>G
XR_945733.2:n.863A>G
NM_000043.6:c.858A>G MANE Select	NP_000034.1:p.Gly286=
NM_001320619.2:c.*181A>G	NP_001307548.1:n.*181A>G
NM_152871.4:c.795A>G	NP_690610.1:p.Gly265=
NM_152872.4:c.*170A>G	NP_690611.1:n.*170A>G
NR_028033.4:n.765A>G
NR_028034.4:n.627A>G
NR_028035.4:n.690A>G
NR_028036.4:n.828A>G
NR_135313.2:n.745A>G
NR_135314.2:n.1024A>G
NR_135315.2:n.777A>G