Canonical Allele Identifier: CA377509659

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773926A>C (hg19) ; chr10:g.89014169A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014169A>C , CM000672.2:g.89014169A>C	GRCh38
NC_000010.10:g.90773926A>C , CM000672.1:g.90773926A>C	GRCh37
NC_000010.9:g.90763906A>C	NCBI36
NG_009089.2:g.28639A>C , LRG_134:g.28639A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1036A>C
ENST00000355740.8:c.*50A>C	ENSP00000347979.3:n.*50A>C
ENST00000357339.7:c.664A>C	ENSP00000349896.2:p.Ser222Arg
ENST00000371857.8:n.2272A>C
ENST00000460510.6:c.10A>C	ENSP00000512812.1:p.Ser4Arg
ENST00000466081.6:n.2376A>C
ENST00000477270.6:c.772A>C	ENSP00000512813.1:p.Ser258Arg
ENST00000479522.6:c.*156A>C	ENSP00000424113.1:n.*156A>C
ENST00000484444.6:c.*168A>C	ENSP00000420975.1:n.*168A>C
ENST00000488877.6:c.618A>C	ENSP00000425159.1:n.618A>C
ENST00000492756.7:c.*156A>C	ENSP00000422453.1:n.*156A>C
ENST00000494799.6:c.10A>C	ENSP00000512834.1:p.Ser4Arg
ENST00000562983.3:c.10A>C	ENSP00000512845.1:p.Ser4Arg
ENST00000612663.6:c.*129A>C	ENSP00000477997.3:n.*129A>C
ENST00000640140.2:n.872A>C
ENST00000640250.2:n.226A>C
ENST00000640681.2:n.831A>C
ENST00000696723.1:n.4360A>C
ENST00000696741.1:n.2365A>C
ENST00000696742.1:n.2092A>C
ENST00000696743.1:n.3495A>C
ENST00000696744.1:n.766A>C
ENST00000696767.1:n.1061A>C
ENST00000696768.1:c.*50A>C	ENSP00000512859.1:n.*50A>C
ENST00000696769.1:n.2416A>C
ENST00000696771.1:c.10A>C	ENSP00000512860.1:p.Ser4Arg
ENST00000696772.1:n.2330A>C
ENST00000696773.1:n.2069A>C
ENST00000696774.1:n.5837A>C
ENST00000696776.1:c.820A>C	ENSP00000512861.1:p.Ser274Arg
ENST00000696777.1:n.2135A>C
ENST00000696778.1:n.1163A>C
ENST00000696779.1:c.334A>C	ENSP00000512862.1:p.Ser112Arg
ENST00000696780.1:c.757A>C	ENSP00000512863.1:p.Ser253Arg
ENST00000696781.1:c.472A>C	ENSP00000512864.1:p.Ser158Arg
ENST00000696782.1:c.*129A>C	ENSP00000512865.1:n.*129A>C
ENST00000696783.1:n.2595A>C
ENST00000696992.1:n.1844A>C
ENST00000696995.1:n.4256A>C
ENST00000696996.1:n.2169A>C
ENST00000696997.1:c.*357A>C	ENSP00000513028.1:n.*357A>C
ENST00000696998.1:n.1981A>C
ENST00000696999.1:c.10A>C	ENSP00000513029.1:p.Ser4Arg
ENST00000697035.1:c.*60A>C	ENSP00000513059.1:n.*60A>C
ENST00000697036.1:c.*143A>C	ENSP00000513060.1:n.*143A>C
ENST00000697037.1:n.762A>C
ENST00000697093.1:n.2963A>C
ENST00000697094.1:n.3310A>C
ENST00000697095.1:c.*1928A>C	ENSP00000513104.1:n.*1928A>C
ENST00000697096.1:n.1860A>C
ENST00000697097.1:c.10A>C	ENSP00000513105.1:p.Ser4Arg
ENST00000562983.2:n.913A>C
ENST00000690268.1:c.808A>C	ENSP00000509810.1:p.Ser270Arg
ENST00000355740.7:c.*53A>C	ENSP00000347979.3:n.*53A>C
ENST00000612663.5:c.*129A>C	ENSP00000477997.3:n.*129A>C
ENST00000640140.1:n.899A>C
ENST00000640250.1:n.226A>C
ENST00000640681.1:n.848A>C
ENST00000652046.1:c.727A>C MANE Select	ENSP00000498466.1:p.Ser243Arg
ENST00000313771.9:n.1036A>C
ENST00000352159.8:c.*44A>C	ENSP00000345601.4:n.*44A>C
ENST00000355279.2:c.702A>C	ENSP00000347426.2:n.702A>C
ENST00000355740.6:c.727A>C	ENSP00000347979.2:p.Ser243Arg
ENST00000357339.6:c.664A>C	ENSP00000349896.2:p.Ser222Arg
ENST00000479522.5:c.*156A>C	ENSP00000424113.1:n.*156A>C
ENST00000484444.5:c.*168A>C	ENSP00000420975.1:n.*168A>C
ENST00000488877.5:c.*168A>C	ENSP00000425159.1:n.*168A>C
ENST00000492756.5:c.555A>C	ENSP00000422453.1:n.555A>C
ENST00000494410.5:c.*85A>C	ENSP00000423755.1:n.*85A>C
ENST00000494799.5:n.634A>C
ENST00000612663.4:c.*74A>C	ENSP00000477997.2:n.*74A>C
ENST00000615406.4:c.727A>C	ENSP00000484575.1:p.Ser243Arg
ENST00000626542.2:c.725A>C	ENSP00000485876.1:p.Lys242Thr
NM_000043.4:c.727A>C , LRG_134t1:c.727A>C	NP_000034.1:p.Ser243Arg
NM_152871.2:c.664A>C	NP_690610.1:p.Ser222Arg
NM_152872.2:c.*39A>C	NP_690611.1:n.*39A>C
NR_028033.2:n.901A>C
NR_028034.2:n.763A>C
NR_028035.2:n.826A>C
NR_028036.2:n.964A>C
XM_006717819.2:c.808A>C	XP_006717882.1:p.Ser270Arg
XM_011539764.1:c.889A>C	XP_011538066.1:p.Ser297Arg
XM_011539765.1:c.826A>C	XP_011538067.1:p.Ser276Arg
XM_011539766.1:c.808A>C	XP_011538068.1:p.Ser270Arg
XM_011539767.1:c.772A>C	XP_011538069.1:p.Ser258Arg
XR_945732.1:n.795A>C
XR_945733.1:n.732A>C
NM_000043.5:c.727A>C	NP_000034.1:p.Ser243Arg
NM_001320619.1:c.*50A>C	NP_001307548.1:n.*50A>C
NM_152871.3:c.664A>C	NP_690610.1:p.Ser222Arg
NM_152872.3:c.*39A>C	NP_690611.1:n.*39A>C
NR_028033.3:n.873A>C
NR_028034.3:n.735A>C
NR_028035.3:n.798A>C
NR_028036.3:n.936A>C
NR_135313.1:n.853A>C
NR_135314.1:n.1036A>C
NR_135315.1:n.789A>C
XM_006717819.3:c.808A>C	XP_006717882.1:p.Ser270Arg
XM_011539764.2:c.889A>C	XP_011538066.1:p.Ser297Arg
XM_011539765.2:c.826A>C	XP_011538067.1:p.Ser276Arg
XM_011539766.2:c.808A>C	XP_011538068.1:p.Ser270Arg
XM_011539767.3:c.772A>C	XP_011538069.1:p.Ser258Arg
XR_945732.3:n.795A>C
XR_945733.2:n.732A>C
NM_000043.6:c.727A>C MANE Select	NP_000034.1:p.Ser243Arg
NM_001320619.2:c.*50A>C	NP_001307548.1:n.*50A>C
NM_152871.4:c.664A>C	NP_690610.1:p.Ser222Arg
NM_152872.4:c.*39A>C	NP_690611.1:n.*39A>C
NR_028033.4:n.634A>C
NR_028034.4:n.496A>C
NR_028035.4:n.559A>C
NR_028036.4:n.697A>C
NR_135313.2:n.614A>C
NR_135314.2:n.893A>C
NR_135315.2:n.646A>C