Canonical Allele Identifier: CA377509706

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773944G>T (hg19) ; chr10:g.89014187G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014187G>T , CM000672.2:g.89014187G>T	GRCh38
NC_000010.10:g.90773944G>T , CM000672.1:g.90773944G>T	GRCh37
NC_000010.9:g.90763924G>T	NCBI36
NG_009089.2:g.28657G>T , LRG_134:g.28657G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1054G>T
ENST00000355740.8:c.*68G>T	ENSP00000347979.3:n.*68G>T
ENST00000357339.7:c.682G>T	ENSP00000349896.2:p.Val228Phe
ENST00000371857.8:n.2290G>T
ENST00000460510.6:c.28G>T	ENSP00000512812.1:p.Val10Phe
ENST00000466081.6:n.2394G>T
ENST00000477270.6:c.790G>T	ENSP00000512813.1:p.Val264Phe
ENST00000479522.6:c.*174G>T	ENSP00000424113.1:n.*174G>T
ENST00000484444.6:c.*186G>T	ENSP00000420975.1:n.*186G>T
ENST00000488877.6:c.636G>T	ENSP00000425159.1:n.636G>T
ENST00000492756.7:c.*174G>T	ENSP00000422453.1:n.*174G>T
ENST00000494799.6:c.28G>T	ENSP00000512834.1:p.Val10Phe
ENST00000562983.3:c.28G>T	ENSP00000512845.1:p.Val10Phe
ENST00000612663.6:c.*147G>T	ENSP00000477997.3:n.*147G>T
ENST00000640140.2:n.890G>T
ENST00000640250.2:n.244G>T
ENST00000640681.2:n.849G>T
ENST00000696723.1:n.4378G>T
ENST00000696741.1:n.2383G>T
ENST00000696742.1:n.2110G>T
ENST00000696743.1:n.3513G>T
ENST00000696744.1:n.784G>T
ENST00000696767.1:n.1079G>T
ENST00000696768.1:c.*68G>T	ENSP00000512859.1:n.*68G>T
ENST00000696769.1:n.2434G>T
ENST00000696771.1:c.28G>T	ENSP00000512860.1:p.Val10Phe
ENST00000696772.1:n.2348G>T
ENST00000696773.1:n.2087G>T
ENST00000696774.1:n.5855G>T
ENST00000696776.1:c.838G>T	ENSP00000512861.1:p.Val280Phe
ENST00000696777.1:n.2153G>T
ENST00000696778.1:n.1181G>T
ENST00000696779.1:c.352G>T	ENSP00000512862.1:p.Val118Phe
ENST00000696780.1:c.775G>T	ENSP00000512863.1:p.Val259Phe
ENST00000696781.1:c.490G>T	ENSP00000512864.1:p.Val164Phe
ENST00000696782.1:c.*147G>T	ENSP00000512865.1:n.*147G>T
ENST00000696783.1:n.2613G>T
ENST00000696992.1:n.1862G>T
ENST00000696995.1:n.4274G>T
ENST00000696996.1:n.2187G>T
ENST00000696997.1:c.*375G>T	ENSP00000513028.1:n.*375G>T
ENST00000696998.1:n.1999G>T
ENST00000696999.1:c.28G>T	ENSP00000513029.1:p.Val10Phe
ENST00000697035.1:c.*78G>T	ENSP00000513059.1:n.*78G>T
ENST00000697036.1:c.*161G>T	ENSP00000513060.1:n.*161G>T
ENST00000697037.1:n.780G>T
ENST00000697093.1:n.2981G>T
ENST00000697094.1:n.3328G>T
ENST00000697095.1:c.*1946G>T	ENSP00000513104.1:n.*1946G>T
ENST00000697096.1:n.1878G>T
ENST00000697097.1:c.28G>T	ENSP00000513105.1:p.Val10Phe
ENST00000562983.2:n.931G>T
ENST00000690268.1:c.826G>T	ENSP00000509810.1:p.Val276Phe
ENST00000355740.7:c.*71G>T	ENSP00000347979.3:n.*71G>T
ENST00000612663.5:c.*147G>T	ENSP00000477997.3:n.*147G>T
ENST00000640140.1:n.917G>T
ENST00000640250.1:n.244G>T
ENST00000640681.1:n.866G>T
ENST00000652046.1:c.745G>T MANE Select	ENSP00000498466.1:p.Val249Phe
ENST00000352159.8:c.*62G>T	ENSP00000345601.4:n.*62G>T
ENST00000355279.2:c.720G>T	ENSP00000347426.2:n.720G>T
ENST00000355740.6:c.745G>T	ENSP00000347979.2:p.Val249Phe
ENST00000357339.6:c.682G>T	ENSP00000349896.2:p.Val228Phe
ENST00000479522.5:c.*174G>T	ENSP00000424113.1:n.*174G>T
ENST00000484444.5:c.*186G>T	ENSP00000420975.1:n.*186G>T
ENST00000488877.5:c.*186G>T	ENSP00000425159.1:n.*186G>T
ENST00000492756.5:c.573G>T	ENSP00000422453.1:n.573G>T
ENST00000494410.5:c.*103G>T	ENSP00000423755.1:n.*103G>T
ENST00000494799.5:n.652G>T
ENST00000612663.4:c.*92G>T	ENSP00000477997.2:n.*92G>T
ENST00000615406.4:c.745G>T	ENSP00000484575.1:p.Val249Phe
NM_000043.4:c.745G>T , LRG_134t1:c.745G>T	NP_000034.1:p.Val249Phe
NM_152871.2:c.682G>T	NP_690610.1:p.Val228Phe
NM_152872.2:c.*57G>T	NP_690611.1:n.*57G>T
NR_028033.2:n.919G>T
NR_028034.2:n.781G>T
NR_028035.2:n.844G>T
NR_028036.2:n.982G>T
XM_006717819.2:c.826G>T	XP_006717882.1:p.Val276Phe
XM_011539764.1:c.907G>T	XP_011538066.1:p.Val303Phe
XM_011539765.1:c.844G>T	XP_011538067.1:p.Val282Phe
XM_011539766.1:c.826G>T	XP_011538068.1:p.Val276Phe
XM_011539767.1:c.790G>T	XP_011538069.1:p.Val264Phe
XR_945732.1:n.813G>T
XR_945733.1:n.750G>T
NM_000043.5:c.745G>T	NP_000034.1:p.Val249Phe
NM_001320619.1:c.*68G>T	NP_001307548.1:n.*68G>T
NM_152871.3:c.682G>T	NP_690610.1:p.Val228Phe
NM_152872.3:c.*57G>T	NP_690611.1:n.*57G>T
NR_028033.3:n.891G>T
NR_028034.3:n.753G>T
NR_028035.3:n.816G>T
NR_028036.3:n.954G>T
NR_135313.1:n.871G>T
NR_135314.1:n.1054G>T
NR_135315.1:n.807G>T
XM_006717819.3:c.826G>T	XP_006717882.1:p.Val276Phe
XM_011539764.2:c.907G>T	XP_011538066.1:p.Val303Phe
XM_011539765.2:c.844G>T	XP_011538067.1:p.Val282Phe
XM_011539766.2:c.826G>T	XP_011538068.1:p.Val276Phe
XM_011539767.3:c.790G>T	XP_011538069.1:p.Val264Phe
XR_945732.3:n.813G>T
XR_945733.2:n.750G>T
NM_000043.6:c.745G>T MANE Select	NP_000034.1:p.Val249Phe
NM_001320619.2:c.*68G>T	NP_001307548.1:n.*68G>T
NM_152871.4:c.682G>T	NP_690610.1:p.Val228Phe
NM_152872.4:c.*57G>T	NP_690611.1:n.*57G>T
NR_028033.4:n.652G>T
NR_028034.4:n.514G>T
NR_028035.4:n.577G>T
NR_028036.4:n.715G>T
NR_135313.2:n.632G>T
NR_135314.2:n.911G>T
NR_135315.2:n.664G>T