Canonical Allele Identifier: CA377509952

Gene: FAS

Linked Data

• COSMIC: COSM5703787
• MyVariant Identifiers: chr10:g.90774048A>C (hg19) ; chr10:g.89014291A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014291A>C , CM000672.2:g.89014291A>C	GRCh38
NC_000010.10:g.90774048A>C , CM000672.1:g.90774048A>C	GRCh37
NC_000010.9:g.90764028A>C	NCBI36
NG_009089.2:g.28761A>C , LRG_134:g.28761A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1158A>C
ENST00000355740.8:c.*172A>C	ENSP00000347979.3:n.*172A>C
ENST00000357339.7:c.786A>C	ENSP00000349896.2:p.Gln262His
ENST00000371857.8:n.2394A>C
ENST00000460510.6:c.132A>C	ENSP00000512812.1:p.Gln44His
ENST00000466081.6:n.2498A>C
ENST00000477270.6:c.894A>C	ENSP00000512813.1:p.Gln298His
ENST00000479522.6:c.*278A>C	ENSP00000424113.1:n.*278A>C
ENST00000484444.6:c.*290A>C	ENSP00000420975.1:n.*290A>C
ENST00000488877.6:c.740A>C	ENSP00000425159.1:n.740A>C
ENST00000492756.7:c.*278A>C	ENSP00000422453.1:n.*278A>C
ENST00000494799.6:c.132A>C	ENSP00000512834.1:p.Gln44His
ENST00000562983.3:c.132A>C	ENSP00000512845.1:p.Gln44His
ENST00000612663.6:c.*251A>C	ENSP00000477997.3:n.*251A>C
ENST00000640140.2:n.994A>C
ENST00000640250.2:n.348A>C
ENST00000640681.2:n.953A>C
ENST00000696723.1:n.4482A>C
ENST00000696741.1:n.2487A>C
ENST00000696742.1:n.2214A>C
ENST00000696743.1:n.3617A>C
ENST00000696744.1:n.888A>C
ENST00000696767.1:n.1183A>C
ENST00000696768.1:c.*172A>C	ENSP00000512859.1:n.*172A>C
ENST00000696769.1:n.2538A>C
ENST00000696771.1:c.132A>C	ENSP00000512860.1:p.Gln44His
ENST00000696772.1:n.2452A>C
ENST00000696773.1:n.2191A>C
ENST00000696774.1:n.5959A>C
ENST00000696776.1:c.942A>C	ENSP00000512861.1:p.Gln314His
ENST00000696777.1:n.2257A>C
ENST00000696778.1:n.1285A>C
ENST00000696779.1:c.456A>C	ENSP00000512862.1:p.Gln152His
ENST00000696780.1:c.879A>C	ENSP00000512863.1:p.Gln293His
ENST00000696781.1:c.594A>C	ENSP00000512864.1:p.Gln198His
ENST00000696782.1:c.*251A>C	ENSP00000512865.1:n.*251A>C
ENST00000696783.1:n.2717A>C
ENST00000696992.1:n.1966A>C
ENST00000696995.1:n.4378A>C
ENST00000696996.1:n.2291A>C
ENST00000696997.1:c.*479A>C	ENSP00000513028.1:n.*479A>C
ENST00000696998.1:n.2103A>C
ENST00000696999.1:c.132A>C	ENSP00000513029.1:p.Gln44His
ENST00000697035.1:c.*182A>C	ENSP00000513059.1:n.*182A>C
ENST00000697036.1:c.*265A>C	ENSP00000513060.1:n.*265A>C
ENST00000697037.1:n.884A>C
ENST00000697093.1:n.3085A>C
ENST00000697094.1:n.3432A>C
ENST00000697095.1:c.*2050A>C	ENSP00000513104.1:n.*2050A>C
ENST00000697096.1:n.1982A>C
ENST00000697097.1:c.132A>C	ENSP00000513105.1:p.Gln44His
ENST00000562983.2:n.1035A>C
ENST00000690268.1:c.930A>C	ENSP00000509810.1:p.Gln310His
ENST00000355740.7:c.*175A>C	ENSP00000347979.3:n.*175A>C
ENST00000612663.5:c.*251A>C	ENSP00000477997.3:n.*251A>C
ENST00000640140.1:n.1021A>C
ENST00000640250.1:n.348A>C
ENST00000640681.1:n.970A>C
ENST00000652046.1:c.849A>C MANE Select	ENSP00000498466.1:p.Gln283His
ENST00000352159.8:c.*166A>C	ENSP00000345601.4:n.*166A>C
ENST00000355279.2:c.824A>C	ENSP00000347426.2:n.824A>C
ENST00000355740.6:c.849A>C	ENSP00000347979.2:p.Gln283His
ENST00000357339.6:c.786A>C	ENSP00000349896.2:p.Gln262His
ENST00000479522.5:c.*278A>C	ENSP00000424113.1:n.*278A>C
ENST00000484444.5:c.*290A>C	ENSP00000420975.1:n.*290A>C
ENST00000488877.5:c.*290A>C	ENSP00000425159.1:n.*290A>C
ENST00000492756.5:c.677A>C	ENSP00000422453.1:n.677A>C
ENST00000494410.5:c.*207A>C	ENSP00000423755.1:n.*207A>C
ENST00000612663.4:c.*196A>C	ENSP00000477997.2:n.*196A>C
NM_000043.4:c.849A>C , LRG_134t1:c.849A>C	NP_000034.1:p.Gln283His
NM_152871.2:c.786A>C	NP_690610.1:p.Gln262His
NM_152872.2:c.*161A>C	NP_690611.1:n.*161A>C
NR_028033.2:n.1023A>C
NR_028034.2:n.885A>C
NR_028035.2:n.948A>C
NR_028036.2:n.1086A>C
XM_006717819.2:c.930A>C	XP_006717882.1:p.Gln310His
XM_011539764.1:c.1011A>C	XP_011538066.1:p.Gln337His
XM_011539765.1:c.948A>C	XP_011538067.1:p.Gln316His
XM_011539766.1:c.930A>C	XP_011538068.1:p.Gln310His
XM_011539767.1:c.894A>C	XP_011538069.1:p.Gln298His
XR_945732.1:n.917A>C
XR_945733.1:n.854A>C
NM_000043.5:c.849A>C	NP_000034.1:p.Gln283His
NM_001320619.1:c.*172A>C	NP_001307548.1:n.*172A>C
NM_152871.3:c.786A>C	NP_690610.1:p.Gln262His
NM_152872.3:c.*161A>C	NP_690611.1:n.*161A>C
NR_028033.3:n.995A>C
NR_028034.3:n.857A>C
NR_028035.3:n.920A>C
NR_028036.3:n.1058A>C
NR_135313.1:n.975A>C
NR_135314.1:n.1158A>C
NR_135315.1:n.911A>C
XM_006717819.3:c.930A>C	XP_006717882.1:p.Gln310His
XM_011539764.2:c.1011A>C	XP_011538066.1:p.Gln337His
XM_011539765.2:c.948A>C	XP_011538067.1:p.Gln316His
XM_011539766.2:c.930A>C	XP_011538068.1:p.Gln310His
XM_011539767.3:c.894A>C	XP_011538069.1:p.Gln298His
XR_945732.3:n.917A>C
XR_945733.2:n.854A>C
NM_000043.6:c.849A>C MANE Select	NP_000034.1:p.Gln283His
NM_001320619.2:c.*172A>C	NP_001307548.1:n.*172A>C
NM_152871.4:c.786A>C	NP_690610.1:p.Gln262His
NM_152872.4:c.*161A>C	NP_690611.1:n.*161A>C
NR_028033.4:n.756A>C
NR_028034.4:n.618A>C
NR_028035.4:n.681A>C
NR_028036.4:n.819A>C
NR_135313.2:n.736A>C
NR_135314.2:n.1015A>C
NR_135315.2:n.768A>C