Canonical Allele Identifier: CA377509646

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773920A>T (hg19) ; chr10:g.89014163A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014163A>T , CM000672.2:g.89014163A>T	GRCh38
NC_000010.10:g.90773920A>T , CM000672.1:g.90773920A>T	GRCh37
NC_000010.9:g.90763900A>T	NCBI36
NG_009089.2:g.28633A>T , LRG_134:g.28633A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1030A>T
ENST00000355740.8:c.*44A>T	ENSP00000347979.3:n.*44A>T
ENST00000357339.7:c.658A>T	ENSP00000349896.2:p.Thr220Ser
ENST00000371857.8:n.2266A>T
ENST00000460510.6:c.4A>T	ENSP00000512812.1:p.Thr2Ser
ENST00000466081.6:n.2370A>T
ENST00000477270.6:c.766A>T	ENSP00000512813.1:p.Thr256Ser
ENST00000479522.6:c.*150A>T	ENSP00000424113.1:n.*150A>T
ENST00000484444.6:c.*162A>T	ENSP00000420975.1:n.*162A>T
ENST00000488877.6:c.612A>T	ENSP00000425159.1:n.612A>T
ENST00000492756.7:c.*150A>T	ENSP00000422453.1:n.*150A>T
ENST00000494799.6:c.4A>T	ENSP00000512834.1:p.Thr2Ser
ENST00000562983.3:c.4A>T	ENSP00000512845.1:p.Thr2Ser
ENST00000612663.6:c.*123A>T	ENSP00000477997.3:n.*123A>T
ENST00000640140.2:n.866A>T
ENST00000640250.2:n.220A>T
ENST00000640681.2:n.825A>T
ENST00000696723.1:n.4354A>T
ENST00000696741.1:n.2359A>T
ENST00000696742.1:n.2086A>T
ENST00000696743.1:n.3489A>T
ENST00000696744.1:n.760A>T
ENST00000696767.1:n.1055A>T
ENST00000696768.1:c.*44A>T	ENSP00000512859.1:n.*44A>T
ENST00000696769.1:n.2410A>T
ENST00000696771.1:c.4A>T	ENSP00000512860.1:p.Thr2Ser
ENST00000696772.1:n.2324A>T
ENST00000696773.1:n.2063A>T
ENST00000696774.1:n.5831A>T
ENST00000696776.1:c.814A>T	ENSP00000512861.1:p.Thr272Ser
ENST00000696777.1:n.2129A>T
ENST00000696778.1:n.1157A>T
ENST00000696779.1:c.328A>T	ENSP00000512862.1:p.Thr110Ser
ENST00000696780.1:c.751A>T	ENSP00000512863.1:p.Thr251Ser
ENST00000696781.1:c.466A>T	ENSP00000512864.1:p.Thr156Ser
ENST00000696782.1:c.*123A>T	ENSP00000512865.1:n.*123A>T
ENST00000696783.1:n.2589A>T
ENST00000696992.1:n.1838A>T
ENST00000696995.1:n.4250A>T
ENST00000696996.1:n.2163A>T
ENST00000696997.1:c.*351A>T	ENSP00000513028.1:n.*351A>T
ENST00000696998.1:n.1975A>T
ENST00000696999.1:c.4A>T	ENSP00000513029.1:p.Thr2Ser
ENST00000697035.1:c.*54A>T	ENSP00000513059.1:n.*54A>T
ENST00000697036.1:c.*137A>T	ENSP00000513060.1:n.*137A>T
ENST00000697037.1:n.756A>T
ENST00000697093.1:n.2957A>T
ENST00000697094.1:n.3304A>T
ENST00000697095.1:c.*1922A>T	ENSP00000513104.1:n.*1922A>T
ENST00000697096.1:n.1854A>T
ENST00000697097.1:c.4A>T	ENSP00000513105.1:p.Thr2Ser
ENST00000562983.2:n.907A>T
ENST00000690268.1:c.802A>T	ENSP00000509810.1:p.Thr268Ser
ENST00000355740.7:c.*47A>T	ENSP00000347979.3:n.*47A>T
ENST00000612663.5:c.*123A>T	ENSP00000477997.3:n.*123A>T
ENST00000640140.1:n.893A>T
ENST00000640250.1:n.220A>T
ENST00000640681.1:n.842A>T
ENST00000652046.1:c.721A>T MANE Select	ENSP00000498466.1:p.Thr241Ser
ENST00000313771.9:n.1030A>T
ENST00000352159.8:c.*38A>T	ENSP00000345601.4:n.*38A>T
ENST00000355279.2:c.696A>T	ENSP00000347426.2:n.696A>T
ENST00000355740.6:c.721A>T	ENSP00000347979.2:p.Thr241Ser
ENST00000357339.6:c.658A>T	ENSP00000349896.2:p.Thr220Ser
ENST00000479522.5:c.*150A>T	ENSP00000424113.1:n.*150A>T
ENST00000484444.5:c.*162A>T	ENSP00000420975.1:n.*162A>T
ENST00000488877.5:c.*162A>T	ENSP00000425159.1:n.*162A>T
ENST00000492756.5:c.549A>T	ENSP00000422453.1:n.549A>T
ENST00000494410.5:c.*79A>T	ENSP00000423755.1:n.*79A>T
ENST00000494799.5:n.628A>T
ENST00000612663.4:c.*68A>T	ENSP00000477997.2:n.*68A>T
ENST00000615406.4:c.721A>T	ENSP00000484575.1:p.Thr241Ser
ENST00000626542.2:c.719A>T	ENSP00000485876.1:p.Asp240Val
NM_000043.4:c.721A>T , LRG_134t1:c.721A>T	NP_000034.1:p.Thr241Ser
NM_152871.2:c.658A>T	NP_690610.1:p.Thr220Ser
NM_152872.2:c.*33A>T	NP_690611.1:n.*33A>T
NR_028033.2:n.895A>T
NR_028034.2:n.757A>T
NR_028035.2:n.820A>T
NR_028036.2:n.958A>T
XM_006717819.2:c.802A>T	XP_006717882.1:p.Thr268Ser
XM_011539764.1:c.883A>T	XP_011538066.1:p.Thr295Ser
XM_011539765.1:c.820A>T	XP_011538067.1:p.Thr274Ser
XM_011539766.1:c.802A>T	XP_011538068.1:p.Thr268Ser
XM_011539767.1:c.766A>T	XP_011538069.1:p.Thr256Ser
XR_945732.1:n.789A>T
XR_945733.1:n.726A>T
NM_000043.5:c.721A>T	NP_000034.1:p.Thr241Ser
NM_001320619.1:c.*44A>T	NP_001307548.1:n.*44A>T
NM_152871.3:c.658A>T	NP_690610.1:p.Thr220Ser
NM_152872.3:c.*33A>T	NP_690611.1:n.*33A>T
NR_028033.3:n.867A>T
NR_028034.3:n.729A>T
NR_028035.3:n.792A>T
NR_028036.3:n.930A>T
NR_135313.1:n.847A>T
NR_135314.1:n.1030A>T
NR_135315.1:n.783A>T
XM_006717819.3:c.802A>T	XP_006717882.1:p.Thr268Ser
XM_011539764.2:c.883A>T	XP_011538066.1:p.Thr295Ser
XM_011539765.2:c.820A>T	XP_011538067.1:p.Thr274Ser
XM_011539766.2:c.802A>T	XP_011538068.1:p.Thr268Ser
XM_011539767.3:c.766A>T	XP_011538069.1:p.Thr256Ser
XR_945732.3:n.789A>T
XR_945733.2:n.726A>T
NM_000043.6:c.721A>T MANE Select	NP_000034.1:p.Thr241Ser
NM_001320619.2:c.*44A>T	NP_001307548.1:n.*44A>T
NM_152871.4:c.658A>T	NP_690610.1:p.Thr220Ser
NM_152872.4:c.*33A>T	NP_690611.1:n.*33A>T
NR_028033.4:n.628A>T
NR_028034.4:n.490A>T
NR_028035.4:n.553A>T
NR_028036.4:n.691A>T
NR_135313.2:n.608A>T
NR_135314.2:n.887A>T
NR_135315.2:n.640A>T