Canonical Allele Identifier: CA377510094

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774110G>C (hg19) ; chr10:g.89014353G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014353G>C , CM000672.2:g.89014353G>C	GRCh38
NC_000010.10:g.90774110G>C , CM000672.1:g.90774110G>C	GRCh37
NC_000010.9:g.90764090G>C	NCBI36
NG_009089.2:g.28823G>C , LRG_134:g.28823G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1220G>C
ENST00000355740.8:c.*234G>C	ENSP00000347979.3:n.*234G>C
ENST00000357339.7:c.848G>C	ENSP00000349896.2:p.Cys283Ser
ENST00000371857.8:n.2456G>C
ENST00000460510.6:c.194G>C	ENSP00000512812.1:p.Cys65Ser
ENST00000466081.6:n.2560G>C
ENST00000477270.6:c.956G>C	ENSP00000512813.1:p.Cys319Ser
ENST00000479522.6:c.*340G>C	ENSP00000424113.1:n.*340G>C
ENST00000484444.6:c.*352G>C	ENSP00000420975.1:n.*352G>C
ENST00000488877.6:c.802G>C	ENSP00000425159.1:n.802G>C
ENST00000492756.7:c.*340G>C	ENSP00000422453.1:n.*340G>C
ENST00000494799.6:c.194G>C	ENSP00000512834.1:p.Cys65Ser
ENST00000562983.3:c.194G>C	ENSP00000512845.1:p.Cys65Ser
ENST00000612663.6:c.*313G>C	ENSP00000477997.3:n.*313G>C
ENST00000640140.2:n.1056G>C
ENST00000640250.2:n.410G>C
ENST00000640681.2:n.1015G>C
ENST00000696723.1:n.4544G>C
ENST00000696741.1:n.2549G>C
ENST00000696742.1:n.2276G>C
ENST00000696743.1:n.3679G>C
ENST00000696744.1:n.950G>C
ENST00000696767.1:n.1245G>C
ENST00000696768.1:c.*234G>C	ENSP00000512859.1:n.*234G>C
ENST00000696769.1:n.2600G>C
ENST00000696771.1:c.194G>C	ENSP00000512860.1:p.Cys65Ser
ENST00000696772.1:n.2514G>C
ENST00000696773.1:n.2253G>C
ENST00000696774.1:n.6021G>C
ENST00000696776.1:c.1004G>C	ENSP00000512861.1:p.Cys335Ser
ENST00000696777.1:n.2319G>C
ENST00000696778.1:n.1347G>C
ENST00000696779.1:c.518G>C	ENSP00000512862.1:p.Cys173Ser
ENST00000696780.1:c.941G>C	ENSP00000512863.1:p.Cys314Ser
ENST00000696781.1:c.656G>C	ENSP00000512864.1:p.Cys219Ser
ENST00000696782.1:c.*313G>C	ENSP00000512865.1:n.*313G>C
ENST00000696783.1:n.2779G>C
ENST00000696992.1:n.2028G>C
ENST00000696995.1:n.4440G>C
ENST00000696996.1:n.2353G>C
ENST00000696997.1:c.*541G>C	ENSP00000513028.1:n.*541G>C
ENST00000696998.1:n.2165G>C
ENST00000696999.1:c.194G>C	ENSP00000513029.1:p.Cys65Ser
ENST00000697036.1:c.*327G>C	ENSP00000513060.1:n.*327G>C
ENST00000697037.1:n.946G>C
ENST00000697093.1:n.3147G>C
ENST00000697094.1:n.3494G>C
ENST00000697095.1:c.*2112G>C	ENSP00000513104.1:n.*2112G>C
ENST00000697096.1:n.2044G>C
ENST00000697097.1:c.194G>C	ENSP00000513105.1:p.Cys65Ser
ENST00000562983.2:n.1097G>C
ENST00000690268.1:c.992G>C	ENSP00000509810.1:p.Cys331Ser
ENST00000355740.7:c.*237G>C	ENSP00000347979.3:n.*237G>C
ENST00000612663.5:c.*313G>C	ENSP00000477997.3:n.*313G>C
ENST00000640140.1:n.1083G>C
ENST00000640250.1:n.410G>C
ENST00000640681.1:n.1032G>C
ENST00000652046.1:c.911G>C MANE Select	ENSP00000498466.1:p.Cys304Ser
ENST00000352159.8:c.*228G>C	ENSP00000345601.4:n.*228G>C
ENST00000355279.2:c.886G>C	ENSP00000347426.2:n.886G>C
ENST00000355740.6:c.911G>C	ENSP00000347979.2:p.Cys304Ser
ENST00000357339.6:c.848G>C	ENSP00000349896.2:p.Cys283Ser
ENST00000479522.5:c.*340G>C	ENSP00000424113.1:n.*340G>C
ENST00000484444.5:c.*352G>C	ENSP00000420975.1:n.*352G>C
ENST00000488877.5:c.*352G>C	ENSP00000425159.1:n.*352G>C
ENST00000492756.5:c.739G>C	ENSP00000422453.1:n.739G>C
ENST00000494410.5:c.*269G>C	ENSP00000423755.1:n.*269G>C
ENST00000612663.4:c.*258G>C	ENSP00000477997.2:n.*258G>C
NM_000043.4:c.911G>C , LRG_134t1:c.911G>C	NP_000034.1:p.Cys304Ser
NM_152871.2:c.848G>C	NP_690610.1:p.Cys283Ser
NM_152872.2:c.*223G>C	NP_690611.1:n.*223G>C
NR_028033.2:n.1085G>C
NR_028034.2:n.947G>C
NR_028035.2:n.1010G>C
NR_028036.2:n.1148G>C
XM_006717819.2:c.992G>C	XP_006717882.1:p.Cys331Ser
XM_011539764.1:c.1073G>C	XP_011538066.1:p.Cys358Ser
XM_011539765.1:c.1010G>C	XP_011538067.1:p.Cys337Ser
XM_011539766.1:c.992G>C	XP_011538068.1:p.Cys331Ser
XM_011539767.1:c.956G>C	XP_011538069.1:p.Cys319Ser
XR_945732.1:n.979G>C
XR_945733.1:n.916G>C
NM_000043.5:c.911G>C	NP_000034.1:p.Cys304Ser
NM_001320619.1:c.*234G>C	NP_001307548.1:n.*234G>C
NM_152871.3:c.848G>C	NP_690610.1:p.Cys283Ser
NM_152872.3:c.*223G>C	NP_690611.1:n.*223G>C
NR_028033.3:n.1057G>C
NR_028034.3:n.919G>C
NR_028035.3:n.982G>C
NR_028036.3:n.1120G>C
NR_135313.1:n.1037G>C
NR_135314.1:n.1220G>C
NR_135315.1:n.973G>C
XM_006717819.3:c.992G>C	XP_006717882.1:p.Cys331Ser
XM_011539764.2:c.1073G>C	XP_011538066.1:p.Cys358Ser
XM_011539765.2:c.1010G>C	XP_011538067.1:p.Cys337Ser
XM_011539766.2:c.992G>C	XP_011538068.1:p.Cys331Ser
XM_011539767.3:c.956G>C	XP_011538069.1:p.Cys319Ser
XR_945732.3:n.979G>C
XR_945733.2:n.916G>C
NM_000043.6:c.911G>C MANE Select	NP_000034.1:p.Cys304Ser
NM_001320619.2:c.*234G>C	NP_001307548.1:n.*234G>C
NM_152871.4:c.848G>C	NP_690610.1:p.Cys283Ser
NM_152872.4:c.*223G>C	NP_690611.1:n.*223G>C
NR_028033.4:n.818G>C
NR_028034.4:n.680G>C
NR_028035.4:n.743G>C
NR_028036.4:n.881G>C
NR_135313.2:n.798G>C
NR_135314.2:n.1077G>C
NR_135315.2:n.830G>C