Canonical Allele Identifier: CA377509535

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773880T>C (hg19) ; chr10:g.89014123T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014123T>C , CM000672.2:g.89014123T>C	GRCh38
NC_000010.10:g.90773880T>C , CM000672.1:g.90773880T>C	GRCh37
NC_000010.9:g.90763860T>C	NCBI36
NG_009089.2:g.28593T>C , LRG_134:g.28593T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.990T>C
ENST00000355740.8:c.*4T>C	ENSP00000347979.3:n.*4T>C
ENST00000357339.7:c.618T>C	ENSP00000349896.2:p.Val206=
ENST00000371857.8:n.2226T>C
ENST00000460510.6:c.-37T>C	ENSP00000512812.1:n.-37T>C
ENST00000466081.6:n.2330T>C
ENST00000477270.6:c.726T>C	ENSP00000512813.1:p.Val242=
ENST00000479522.6:c.*110T>C	ENSP00000424113.1:n.*110T>C
ENST00000484444.6:c.*122T>C	ENSP00000420975.1:n.*122T>C
ENST00000488877.6:c.572T>C	ENSP00000425159.1:n.572T>C
ENST00000492756.7:c.*110T>C	ENSP00000422453.1:n.*110T>C
ENST00000494799.6:c.-37T>C	ENSP00000512834.1:n.-37T>C
ENST00000562983.3:c.-37T>C	ENSP00000512845.1:n.-37T>C
ENST00000612663.6:c.*83T>C	ENSP00000477997.3:n.*83T>C
ENST00000640140.2:n.826T>C
ENST00000640250.2:n.180T>C
ENST00000640681.2:n.785T>C
ENST00000696723.1:n.4314T>C
ENST00000696741.1:n.2319T>C
ENST00000696742.1:n.2046T>C
ENST00000696743.1:n.3449T>C
ENST00000696744.1:n.720T>C
ENST00000696767.1:n.1015T>C
ENST00000696768.1:c.*4T>C	ENSP00000512859.1:n.*4T>C
ENST00000696769.1:n.2370T>C
ENST00000696771.1:c.-37T>C	ENSP00000512860.1:n.-37T>C
ENST00000696772.1:n.2284T>C
ENST00000696773.1:n.2023T>C
ENST00000696774.1:n.5791T>C
ENST00000696776.1:c.774T>C	ENSP00000512861.1:p.Val258=
ENST00000696777.1:n.2089T>C
ENST00000696778.1:n.1117T>C
ENST00000696779.1:c.288T>C	ENSP00000512862.1:p.Val96=
ENST00000696780.1:c.711T>C	ENSP00000512863.1:p.Val237=
ENST00000696781.1:c.426T>C	ENSP00000512864.1:p.Val142=
ENST00000696782.1:c.*83T>C	ENSP00000512865.1:n.*83T>C
ENST00000696783.1:n.2549T>C
ENST00000696992.1:n.1798T>C
ENST00000696995.1:n.4210T>C
ENST00000696996.1:n.2123T>C
ENST00000696997.1:c.*311T>C	ENSP00000513028.1:n.*311T>C
ENST00000696998.1:n.1935T>C
ENST00000696999.1:c.-37T>C	ENSP00000513029.1:n.-37T>C
ENST00000697035.1:c.*14T>C	ENSP00000513059.1:n.*14T>C
ENST00000697036.1:c.*97T>C	ENSP00000513060.1:n.*97T>C
ENST00000697037.1:n.716T>C
ENST00000697093.1:n.2917T>C
ENST00000697094.1:n.3264T>C
ENST00000697095.1:c.*1882T>C	ENSP00000513104.1:n.*1882T>C
ENST00000697096.1:n.1814T>C
ENST00000697097.1:c.-37T>C	ENSP00000513105.1:n.-37T>C
ENST00000562983.2:n.867T>C
ENST00000690268.1:c.762T>C	ENSP00000509810.1:p.Val254=
ENST00000355740.7:c.*7T>C	ENSP00000347979.3:n.*7T>C
ENST00000612663.5:c.*83T>C	ENSP00000477997.3:n.*83T>C
ENST00000640140.1:n.853T>C
ENST00000640250.1:n.180T>C
ENST00000640681.1:n.802T>C
ENST00000652046.1:c.681T>C MANE Select	ENSP00000498466.1:p.Val227=
ENST00000313771.9:n.990T>C
ENST00000352159.8:c.700T>C	ENSP00000345601.4:p.Ter234Arg
ENST00000355279.2:c.656T>C	ENSP00000347426.2:p.Leu219Ser
ENST00000355740.6:c.681T>C	ENSP00000347979.2:p.Val227=
ENST00000357339.6:c.618T>C	ENSP00000349896.2:p.Val206=
ENST00000479522.5:c.*110T>C	ENSP00000424113.1:n.*110T>C
ENST00000484444.5:c.*122T>C	ENSP00000420975.1:n.*122T>C
ENST00000488877.5:c.*122T>C	ENSP00000425159.1:n.*122T>C
ENST00000492756.5:c.509T>C	ENSP00000422453.1:n.509T>C
ENST00000494410.5:c.*39T>C	ENSP00000423755.1:n.*39T>C
ENST00000494799.5:n.588T>C
ENST00000612663.4:c.*28T>C	ENSP00000477997.2:n.*28T>C
ENST00000615406.4:c.681T>C	ENSP00000484575.1:p.Val227=
ENST00000626542.2:c.681T>C	ENSP00000485876.1:p.Val227=
NM_000043.4:c.681T>C , LRG_134t1:c.681T>C	NP_000034.1:p.Val227=
NM_152871.2:c.618T>C	NP_690610.1:p.Val206=
NM_152872.2:c.656T>C	NP_690611.1:p.Leu219Ser
NR_028033.2:n.855T>C
NR_028034.2:n.717T>C
NR_028035.2:n.780T>C
NR_028036.2:n.918T>C
XM_006717819.2:c.762T>C	XP_006717882.1:p.Val254=
XM_011539764.1:c.843T>C	XP_011538066.1:p.Val281=
XM_011539765.1:c.780T>C	XP_011538067.1:p.Val260=
XM_011539766.1:c.762T>C	XP_011538068.1:p.Val254=
XM_011539767.1:c.726T>C	XP_011538069.1:p.Val242=
XR_945732.1:n.749T>C
XR_945733.1:n.686T>C
NM_000043.5:c.681T>C	NP_000034.1:p.Val227=
NM_001320619.1:c.*4T>C	NP_001307548.1:n.*4T>C
NM_152871.3:c.618T>C	NP_690610.1:p.Val206=
NM_152872.3:c.656T>C	NP_690611.1:p.Leu219Ser
NR_028033.3:n.827T>C
NR_028034.3:n.689T>C
NR_028035.3:n.752T>C
NR_028036.3:n.890T>C
NR_135313.1:n.807T>C
NR_135314.1:n.990T>C
NR_135315.1:n.743T>C
XM_006717819.3:c.762T>C	XP_006717882.1:p.Val254=
XM_011539764.2:c.843T>C	XP_011538066.1:p.Val281=
XM_011539765.2:c.780T>C	XP_011538067.1:p.Val260=
XM_011539766.2:c.762T>C	XP_011538068.1:p.Val254=
XM_011539767.3:c.726T>C	XP_011538069.1:p.Val242=
XR_945732.3:n.749T>C
XR_945733.2:n.686T>C
NM_000043.6:c.681T>C MANE Select	NP_000034.1:p.Val227=
NM_001320619.2:c.*4T>C	NP_001307548.1:n.*4T>C
NM_152871.4:c.618T>C	NP_690610.1:p.Val206=
NM_152872.4:c.656T>C	NP_690611.1:p.Leu219Ser
NR_028033.4:n.588T>C
NR_028034.4:n.450T>C
NR_028035.4:n.513T>C
NR_028036.4:n.651T>C
NR_135313.2:n.568T>C
NR_135314.2:n.847T>C
NR_135315.2:n.600T>C