Canonical Allele Identifier: CA377509816

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773989A>T (hg19) ; chr10:g.89014232A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014232A>T , CM000672.2:g.89014232A>T	GRCh38
NC_000010.10:g.90773989A>T , CM000672.1:g.90773989A>T	GRCh37
NC_000010.9:g.90763969A>T	NCBI36
NG_009089.2:g.28702A>T , LRG_134:g.28702A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1099A>T
ENST00000355740.8:c.*113A>T	ENSP00000347979.3:n.*113A>T
ENST00000357339.7:c.727A>T	ENSP00000349896.2:p.Asn243Tyr
ENST00000371857.8:n.2335A>T
ENST00000460510.6:c.73A>T	ENSP00000512812.1:p.Asn25Tyr
ENST00000466081.6:n.2439A>T
ENST00000477270.6:c.835A>T	ENSP00000512813.1:p.Asn279Tyr
ENST00000479522.6:c.*219A>T	ENSP00000424113.1:n.*219A>T
ENST00000484444.6:c.*231A>T	ENSP00000420975.1:n.*231A>T
ENST00000488877.6:c.681A>T	ENSP00000425159.1:n.681A>T
ENST00000492756.7:c.*219A>T	ENSP00000422453.1:n.*219A>T
ENST00000494799.6:c.73A>T	ENSP00000512834.1:p.Asn25Tyr
ENST00000562983.3:c.73A>T	ENSP00000512845.1:p.Asn25Tyr
ENST00000612663.6:c.*192A>T	ENSP00000477997.3:n.*192A>T
ENST00000640140.2:n.935A>T
ENST00000640250.2:n.289A>T
ENST00000640681.2:n.894A>T
ENST00000696723.1:n.4423A>T
ENST00000696741.1:n.2428A>T
ENST00000696742.1:n.2155A>T
ENST00000696743.1:n.3558A>T
ENST00000696744.1:n.829A>T
ENST00000696767.1:n.1124A>T
ENST00000696768.1:c.*113A>T	ENSP00000512859.1:n.*113A>T
ENST00000696769.1:n.2479A>T
ENST00000696771.1:c.73A>T	ENSP00000512860.1:p.Asn25Tyr
ENST00000696772.1:n.2393A>T
ENST00000696773.1:n.2132A>T
ENST00000696774.1:n.5900A>T
ENST00000696776.1:c.883A>T	ENSP00000512861.1:p.Asn295Tyr
ENST00000696777.1:n.2198A>T
ENST00000696778.1:n.1226A>T
ENST00000696779.1:c.397A>T	ENSP00000512862.1:p.Asn133Tyr
ENST00000696780.1:c.820A>T	ENSP00000512863.1:p.Asn274Tyr
ENST00000696781.1:c.535A>T	ENSP00000512864.1:p.Asn179Tyr
ENST00000696782.1:c.*192A>T	ENSP00000512865.1:n.*192A>T
ENST00000696783.1:n.2658A>T
ENST00000696992.1:n.1907A>T
ENST00000696995.1:n.4319A>T
ENST00000696996.1:n.2232A>T
ENST00000696997.1:c.*420A>T	ENSP00000513028.1:n.*420A>T
ENST00000696998.1:n.2044A>T
ENST00000696999.1:c.73A>T	ENSP00000513029.1:p.Asn25Tyr
ENST00000697035.1:c.*123A>T	ENSP00000513059.1:n.*123A>T
ENST00000697036.1:c.*206A>T	ENSP00000513060.1:n.*206A>T
ENST00000697037.1:n.825A>T
ENST00000697093.1:n.3026A>T
ENST00000697094.1:n.3373A>T
ENST00000697095.1:c.*1991A>T	ENSP00000513104.1:n.*1991A>T
ENST00000697096.1:n.1923A>T
ENST00000697097.1:c.73A>T	ENSP00000513105.1:p.Asn25Tyr
ENST00000562983.2:n.976A>T
ENST00000690268.1:c.871A>T	ENSP00000509810.1:p.Asn291Tyr
ENST00000355740.7:c.*116A>T	ENSP00000347979.3:n.*116A>T
ENST00000612663.5:c.*192A>T	ENSP00000477997.3:n.*192A>T
ENST00000640140.1:n.962A>T
ENST00000640250.1:n.289A>T
ENST00000640681.1:n.911A>T
ENST00000652046.1:c.790A>T MANE Select	ENSP00000498466.1:p.Asn264Tyr
ENST00000352159.8:c.*107A>T	ENSP00000345601.4:n.*107A>T
ENST00000355279.2:c.765A>T	ENSP00000347426.2:n.765A>T
ENST00000355740.6:c.790A>T	ENSP00000347979.2:p.Asn264Tyr
ENST00000357339.6:c.727A>T	ENSP00000349896.2:p.Asn243Tyr
ENST00000479522.5:c.*219A>T	ENSP00000424113.1:n.*219A>T
ENST00000484444.5:c.*231A>T	ENSP00000420975.1:n.*231A>T
ENST00000488877.5:c.*231A>T	ENSP00000425159.1:n.*231A>T
ENST00000492756.5:c.618A>T	ENSP00000422453.1:n.618A>T
ENST00000494410.5:c.*148A>T	ENSP00000423755.1:n.*148A>T
ENST00000612663.4:c.*137A>T	ENSP00000477997.2:n.*137A>T
NM_000043.4:c.790A>T , LRG_134t1:c.790A>T	NP_000034.1:p.Asn264Tyr
NM_152871.2:c.727A>T	NP_690610.1:p.Asn243Tyr
NM_152872.2:c.*102A>T	NP_690611.1:n.*102A>T
NR_028033.2:n.964A>T
NR_028034.2:n.826A>T
NR_028035.2:n.889A>T
NR_028036.2:n.1027A>T
XM_006717819.2:c.871A>T	XP_006717882.1:p.Asn291Tyr
XM_011539764.1:c.952A>T	XP_011538066.1:p.Asn318Tyr
XM_011539765.1:c.889A>T	XP_011538067.1:p.Asn297Tyr
XM_011539766.1:c.871A>T	XP_011538068.1:p.Asn291Tyr
XM_011539767.1:c.835A>T	XP_011538069.1:p.Asn279Tyr
XR_945732.1:n.858A>T
XR_945733.1:n.795A>T
NM_000043.5:c.790A>T	NP_000034.1:p.Asn264Tyr
NM_001320619.1:c.*113A>T	NP_001307548.1:n.*113A>T
NM_152871.3:c.727A>T	NP_690610.1:p.Asn243Tyr
NM_152872.3:c.*102A>T	NP_690611.1:n.*102A>T
NR_028033.3:n.936A>T
NR_028034.3:n.798A>T
NR_028035.3:n.861A>T
NR_028036.3:n.999A>T
NR_135313.1:n.916A>T
NR_135314.1:n.1099A>T
NR_135315.1:n.852A>T
XM_006717819.3:c.871A>T	XP_006717882.1:p.Asn291Tyr
XM_011539764.2:c.952A>T	XP_011538066.1:p.Asn318Tyr
XM_011539765.2:c.889A>T	XP_011538067.1:p.Asn297Tyr
XM_011539766.2:c.871A>T	XP_011538068.1:p.Asn291Tyr
XM_011539767.3:c.835A>T	XP_011538069.1:p.Asn279Tyr
XR_945732.3:n.858A>T
XR_945733.2:n.795A>T
NM_000043.6:c.790A>T MANE Select	NP_000034.1:p.Asn264Tyr
NM_001320619.2:c.*113A>T	NP_001307548.1:n.*113A>T
NM_152871.4:c.727A>T	NP_690610.1:p.Asn243Tyr
NM_152872.4:c.*102A>T	NP_690611.1:n.*102A>T
NR_028033.4:n.697A>T
NR_028034.4:n.559A>T
NR_028035.4:n.622A>T
NR_028036.4:n.760A>T
NR_135313.2:n.677A>T
NR_135314.2:n.956A>T
NR_135315.2:n.709A>T