Canonical Allele Identifier: CA377510026

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774081G>T (hg19) ; chr10:g.89014324G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014324G>T , CM000672.2:g.89014324G>T	GRCh38
NC_000010.10:g.90774081G>T , CM000672.1:g.90774081G>T	GRCh37
NC_000010.9:g.90764061G>T	NCBI36
NG_009089.2:g.28794G>T , LRG_134:g.28794G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1191G>T
ENST00000355740.8:c.*205G>T	ENSP00000347979.3:n.*205G>T
ENST00000357339.7:c.819G>T	ENSP00000349896.2:p.Leu273Phe
ENST00000371857.8:n.2427G>T
ENST00000460510.6:c.165G>T	ENSP00000512812.1:p.Leu55Phe
ENST00000466081.6:n.2531G>T
ENST00000477270.6:c.927G>T	ENSP00000512813.1:p.Leu309Phe
ENST00000479522.6:c.*311G>T	ENSP00000424113.1:n.*311G>T
ENST00000484444.6:c.*323G>T	ENSP00000420975.1:n.*323G>T
ENST00000488877.6:c.773G>T	ENSP00000425159.1:n.773G>T
ENST00000492756.7:c.*311G>T	ENSP00000422453.1:n.*311G>T
ENST00000494799.6:c.165G>T	ENSP00000512834.1:p.Leu55Phe
ENST00000562983.3:c.165G>T	ENSP00000512845.1:p.Leu55Phe
ENST00000612663.6:c.*284G>T	ENSP00000477997.3:n.*284G>T
ENST00000640140.2:n.1027G>T
ENST00000640250.2:n.381G>T
ENST00000640681.2:n.986G>T
ENST00000696723.1:n.4515G>T
ENST00000696741.1:n.2520G>T
ENST00000696742.1:n.2247G>T
ENST00000696743.1:n.3650G>T
ENST00000696744.1:n.921G>T
ENST00000696767.1:n.1216G>T
ENST00000696768.1:c.*205G>T	ENSP00000512859.1:n.*205G>T
ENST00000696769.1:n.2571G>T
ENST00000696771.1:c.165G>T	ENSP00000512860.1:p.Leu55Phe
ENST00000696772.1:n.2485G>T
ENST00000696773.1:n.2224G>T
ENST00000696774.1:n.5992G>T
ENST00000696776.1:c.975G>T	ENSP00000512861.1:p.Leu325Phe
ENST00000696777.1:n.2290G>T
ENST00000696778.1:n.1318G>T
ENST00000696779.1:c.489G>T	ENSP00000512862.1:p.Leu163Phe
ENST00000696780.1:c.912G>T	ENSP00000512863.1:p.Leu304Phe
ENST00000696781.1:c.627G>T	ENSP00000512864.1:p.Leu209Phe
ENST00000696782.1:c.*284G>T	ENSP00000512865.1:n.*284G>T
ENST00000696783.1:n.2750G>T
ENST00000696992.1:n.1999G>T
ENST00000696995.1:n.4411G>T
ENST00000696996.1:n.2324G>T
ENST00000696997.1:c.*512G>T	ENSP00000513028.1:n.*512G>T
ENST00000696998.1:n.2136G>T
ENST00000696999.1:c.165G>T	ENSP00000513029.1:p.Leu55Phe
ENST00000697036.1:c.*298G>T	ENSP00000513060.1:n.*298G>T
ENST00000697037.1:n.917G>T
ENST00000697093.1:n.3118G>T
ENST00000697094.1:n.3465G>T
ENST00000697095.1:c.*2083G>T	ENSP00000513104.1:n.*2083G>T
ENST00000697096.1:n.2015G>T
ENST00000697097.1:c.165G>T	ENSP00000513105.1:p.Leu55Phe
ENST00000562983.2:n.1068G>T
ENST00000690268.1:c.963G>T	ENSP00000509810.1:p.Leu321Phe
ENST00000355740.7:c.*208G>T	ENSP00000347979.3:n.*208G>T
ENST00000612663.5:c.*284G>T	ENSP00000477997.3:n.*284G>T
ENST00000640140.1:n.1054G>T
ENST00000640250.1:n.381G>T
ENST00000640681.1:n.1003G>T
ENST00000652046.1:c.882G>T MANE Select	ENSP00000498466.1:p.Leu294Phe
ENST00000352159.8:c.*199G>T	ENSP00000345601.4:n.*199G>T
ENST00000355279.2:c.857G>T	ENSP00000347426.2:n.857G>T
ENST00000355740.6:c.882G>T	ENSP00000347979.2:p.Leu294Phe
ENST00000357339.6:c.819G>T	ENSP00000349896.2:p.Leu273Phe
ENST00000479522.5:c.*311G>T	ENSP00000424113.1:n.*311G>T
ENST00000484444.5:c.*323G>T	ENSP00000420975.1:n.*323G>T
ENST00000488877.5:c.*323G>T	ENSP00000425159.1:n.*323G>T
ENST00000492756.5:c.710G>T	ENSP00000422453.1:n.710G>T
ENST00000494410.5:c.*240G>T	ENSP00000423755.1:n.*240G>T
ENST00000612663.4:c.*229G>T	ENSP00000477997.2:n.*229G>T
NM_000043.4:c.882G>T , LRG_134t1:c.882G>T	NP_000034.1:p.Leu294Phe
NM_152871.2:c.819G>T	NP_690610.1:p.Leu273Phe
NM_152872.2:c.*194G>T	NP_690611.1:n.*194G>T
NR_028033.2:n.1056G>T
NR_028034.2:n.918G>T
NR_028035.2:n.981G>T
NR_028036.2:n.1119G>T
XM_006717819.2:c.963G>T	XP_006717882.1:p.Leu321Phe
XM_011539764.1:c.1044G>T	XP_011538066.1:p.Leu348Phe
XM_011539765.1:c.981G>T	XP_011538067.1:p.Leu327Phe
XM_011539766.1:c.963G>T	XP_011538068.1:p.Leu321Phe
XM_011539767.1:c.927G>T	XP_011538069.1:p.Leu309Phe
XR_945732.1:n.950G>T
XR_945733.1:n.887G>T
NM_000043.5:c.882G>T	NP_000034.1:p.Leu294Phe
NM_001320619.1:c.*205G>T	NP_001307548.1:n.*205G>T
NM_152871.3:c.819G>T	NP_690610.1:p.Leu273Phe
NM_152872.3:c.*194G>T	NP_690611.1:n.*194G>T
NR_028033.3:n.1028G>T
NR_028034.3:n.890G>T
NR_028035.3:n.953G>T
NR_028036.3:n.1091G>T
NR_135313.1:n.1008G>T
NR_135314.1:n.1191G>T
NR_135315.1:n.944G>T
XM_006717819.3:c.963G>T	XP_006717882.1:p.Leu321Phe
XM_011539764.2:c.1044G>T	XP_011538066.1:p.Leu348Phe
XM_011539765.2:c.981G>T	XP_011538067.1:p.Leu327Phe
XM_011539766.2:c.963G>T	XP_011538068.1:p.Leu321Phe
XM_011539767.3:c.927G>T	XP_011538069.1:p.Leu309Phe
XR_945732.3:n.950G>T
XR_945733.2:n.887G>T
NM_000043.6:c.882G>T MANE Select	NP_000034.1:p.Leu294Phe
NM_001320619.2:c.*205G>T	NP_001307548.1:n.*205G>T
NM_152871.4:c.819G>T	NP_690610.1:p.Leu273Phe
NM_152872.4:c.*194G>T	NP_690611.1:n.*194G>T
NR_028033.4:n.789G>T
NR_028034.4:n.651G>T
NR_028035.4:n.714G>T
NR_028036.4:n.852G>T
NR_135313.2:n.769G>T
NR_135314.2:n.1048G>T
NR_135315.2:n.801G>T