Canonical Allele Identifier: CA377510053

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774092T>G (hg19) ; chr10:g.89014335T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014335T>G , CM000672.2:g.89014335T>G	GRCh38
NC_000010.10:g.90774092T>G , CM000672.1:g.90774092T>G	GRCh37
NC_000010.9:g.90764072T>G	NCBI36
NG_009089.2:g.28805T>G , LRG_134:g.28805T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1202T>G
ENST00000355740.8:c.*216T>G	ENSP00000347979.3:n.*216T>G
ENST00000357339.7:c.830T>G	ENSP00000349896.2:p.Leu277Arg
ENST00000371857.8:n.2438T>G
ENST00000460510.6:c.176T>G	ENSP00000512812.1:p.Leu59Arg
ENST00000466081.6:n.2542T>G
ENST00000477270.6:c.938T>G	ENSP00000512813.1:p.Leu313Arg
ENST00000479522.6:c.*322T>G	ENSP00000424113.1:n.*322T>G
ENST00000484444.6:c.*334T>G	ENSP00000420975.1:n.*334T>G
ENST00000488877.6:c.784T>G	ENSP00000425159.1:n.784T>G
ENST00000492756.7:c.*322T>G	ENSP00000422453.1:n.*322T>G
ENST00000494799.6:c.176T>G	ENSP00000512834.1:p.Leu59Arg
ENST00000562983.3:c.176T>G	ENSP00000512845.1:p.Leu59Arg
ENST00000612663.6:c.*295T>G	ENSP00000477997.3:n.*295T>G
ENST00000640140.2:n.1038T>G
ENST00000640250.2:n.392T>G
ENST00000640681.2:n.997T>G
ENST00000696723.1:n.4526T>G
ENST00000696741.1:n.2531T>G
ENST00000696742.1:n.2258T>G
ENST00000696743.1:n.3661T>G
ENST00000696744.1:n.932T>G
ENST00000696767.1:n.1227T>G
ENST00000696768.1:c.*216T>G	ENSP00000512859.1:n.*216T>G
ENST00000696769.1:n.2582T>G
ENST00000696771.1:c.176T>G	ENSP00000512860.1:p.Leu59Arg
ENST00000696772.1:n.2496T>G
ENST00000696773.1:n.2235T>G
ENST00000696774.1:n.6003T>G
ENST00000696776.1:c.986T>G	ENSP00000512861.1:p.Leu329Arg
ENST00000696777.1:n.2301T>G
ENST00000696778.1:n.1329T>G
ENST00000696779.1:c.500T>G	ENSP00000512862.1:p.Leu167Arg
ENST00000696780.1:c.923T>G	ENSP00000512863.1:p.Leu308Arg
ENST00000696781.1:c.638T>G	ENSP00000512864.1:p.Leu213Arg
ENST00000696782.1:c.*295T>G	ENSP00000512865.1:n.*295T>G
ENST00000696783.1:n.2761T>G
ENST00000696992.1:n.2010T>G
ENST00000696995.1:n.4422T>G
ENST00000696996.1:n.2335T>G
ENST00000696997.1:c.*523T>G	ENSP00000513028.1:n.*523T>G
ENST00000696998.1:n.2147T>G
ENST00000696999.1:c.176T>G	ENSP00000513029.1:p.Leu59Arg
ENST00000697036.1:c.*309T>G	ENSP00000513060.1:n.*309T>G
ENST00000697037.1:n.928T>G
ENST00000697093.1:n.3129T>G
ENST00000697094.1:n.3476T>G
ENST00000697095.1:c.*2094T>G	ENSP00000513104.1:n.*2094T>G
ENST00000697096.1:n.2026T>G
ENST00000697097.1:c.176T>G	ENSP00000513105.1:p.Leu59Arg
ENST00000562983.2:n.1079T>G
ENST00000690268.1:c.974T>G	ENSP00000509810.1:p.Leu325Arg
ENST00000355740.7:c.*219T>G	ENSP00000347979.3:n.*219T>G
ENST00000612663.5:c.*295T>G	ENSP00000477997.3:n.*295T>G
ENST00000640140.1:n.1065T>G
ENST00000640250.1:n.392T>G
ENST00000640681.1:n.1014T>G
ENST00000652046.1:c.893T>G MANE Select	ENSP00000498466.1:p.Leu298Arg
ENST00000352159.8:c.*210T>G	ENSP00000345601.4:n.*210T>G
ENST00000355279.2:c.868T>G	ENSP00000347426.2:n.868T>G
ENST00000355740.6:c.893T>G	ENSP00000347979.2:p.Leu298Arg
ENST00000357339.6:c.830T>G	ENSP00000349896.2:p.Leu277Arg
ENST00000479522.5:c.*322T>G	ENSP00000424113.1:n.*322T>G
ENST00000484444.5:c.*334T>G	ENSP00000420975.1:n.*334T>G
ENST00000488877.5:c.*334T>G	ENSP00000425159.1:n.*334T>G
ENST00000492756.5:c.721T>G	ENSP00000422453.1:n.721T>G
ENST00000494410.5:c.*251T>G	ENSP00000423755.1:n.*251T>G
ENST00000612663.4:c.*240T>G	ENSP00000477997.2:n.*240T>G
NM_000043.4:c.893T>G , LRG_134t1:c.893T>G	NP_000034.1:p.Leu298Arg
NM_152871.2:c.830T>G	NP_690610.1:p.Leu277Arg
NM_152872.2:c.*205T>G	NP_690611.1:n.*205T>G
NR_028033.2:n.1067T>G
NR_028034.2:n.929T>G
NR_028035.2:n.992T>G
NR_028036.2:n.1130T>G
XM_006717819.2:c.974T>G	XP_006717882.1:p.Leu325Arg
XM_011539764.1:c.1055T>G	XP_011538066.1:p.Leu352Arg
XM_011539765.1:c.992T>G	XP_011538067.1:p.Leu331Arg
XM_011539766.1:c.974T>G	XP_011538068.1:p.Leu325Arg
XM_011539767.1:c.938T>G	XP_011538069.1:p.Leu313Arg
XR_945732.1:n.961T>G
XR_945733.1:n.898T>G
NM_000043.5:c.893T>G	NP_000034.1:p.Leu298Arg
NM_001320619.1:c.*216T>G	NP_001307548.1:n.*216T>G
NM_152871.3:c.830T>G	NP_690610.1:p.Leu277Arg
NM_152872.3:c.*205T>G	NP_690611.1:n.*205T>G
NR_028033.3:n.1039T>G
NR_028034.3:n.901T>G
NR_028035.3:n.964T>G
NR_028036.3:n.1102T>G
NR_135313.1:n.1019T>G
NR_135314.1:n.1202T>G
NR_135315.1:n.955T>G
XM_006717819.3:c.974T>G	XP_006717882.1:p.Leu325Arg
XM_011539764.2:c.1055T>G	XP_011538066.1:p.Leu352Arg
XM_011539765.2:c.992T>G	XP_011538067.1:p.Leu331Arg
XM_011539766.2:c.974T>G	XP_011538068.1:p.Leu325Arg
XM_011539767.3:c.938T>G	XP_011538069.1:p.Leu313Arg
XR_945732.3:n.961T>G
XR_945733.2:n.898T>G
NM_000043.6:c.893T>G MANE Select	NP_000034.1:p.Leu298Arg
NM_001320619.2:c.*216T>G	NP_001307548.1:n.*216T>G
NM_152871.4:c.830T>G	NP_690610.1:p.Leu277Arg
NM_152872.4:c.*205T>G	NP_690611.1:n.*205T>G
NR_028033.4:n.800T>G
NR_028034.4:n.662T>G
NR_028035.4:n.725T>G
NR_028036.4:n.863T>G
NR_135313.2:n.780T>G
NR_135314.2:n.1059T>G
NR_135315.2:n.812T>G