Canonical Allele Identifier: CA377509962

Gene: FAS

Linked Data

• COSMIC: COSM3441373
• MyVariant Identifiers: chr10:g.90774052C>T (hg19) ; chr10:g.89014295C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014295C>T , CM000672.2:g.89014295C>T	GRCh38
NC_000010.10:g.90774052C>T , CM000672.1:g.90774052C>T	GRCh37
NC_000010.9:g.90764032C>T	NCBI36
NG_009089.2:g.28765C>T , LRG_134:g.28765C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1162C>T
ENST00000355740.8:c.*176C>T	ENSP00000347979.3:n.*176C>T
ENST00000357339.7:c.790C>T	ENSP00000349896.2:p.His264Tyr
ENST00000371857.8:n.2398C>T
ENST00000460510.6:c.136C>T	ENSP00000512812.1:p.His46Tyr
ENST00000466081.6:n.2502C>T
ENST00000477270.6:c.898C>T	ENSP00000512813.1:p.His300Tyr
ENST00000479522.6:c.*282C>T	ENSP00000424113.1:n.*282C>T
ENST00000484444.6:c.*294C>T	ENSP00000420975.1:n.*294C>T
ENST00000488877.6:c.744C>T	ENSP00000425159.1:n.744C>T
ENST00000492756.7:c.*282C>T	ENSP00000422453.1:n.*282C>T
ENST00000494799.6:c.136C>T	ENSP00000512834.1:p.His46Tyr
ENST00000562983.3:c.136C>T	ENSP00000512845.1:p.His46Tyr
ENST00000612663.6:c.*255C>T	ENSP00000477997.3:n.*255C>T
ENST00000640140.2:n.998C>T
ENST00000640250.2:n.352C>T
ENST00000640681.2:n.957C>T
ENST00000696723.1:n.4486C>T
ENST00000696741.1:n.2491C>T
ENST00000696742.1:n.2218C>T
ENST00000696743.1:n.3621C>T
ENST00000696744.1:n.892C>T
ENST00000696767.1:n.1187C>T
ENST00000696768.1:c.*176C>T	ENSP00000512859.1:n.*176C>T
ENST00000696769.1:n.2542C>T
ENST00000696771.1:c.136C>T	ENSP00000512860.1:p.His46Tyr
ENST00000696772.1:n.2456C>T
ENST00000696773.1:n.2195C>T
ENST00000696774.1:n.5963C>T
ENST00000696776.1:c.946C>T	ENSP00000512861.1:p.His316Tyr
ENST00000696777.1:n.2261C>T
ENST00000696778.1:n.1289C>T
ENST00000696779.1:c.460C>T	ENSP00000512862.1:p.His154Tyr
ENST00000696780.1:c.883C>T	ENSP00000512863.1:p.His295Tyr
ENST00000696781.1:c.598C>T	ENSP00000512864.1:p.His200Tyr
ENST00000696782.1:c.*255C>T	ENSP00000512865.1:n.*255C>T
ENST00000696783.1:n.2721C>T
ENST00000696992.1:n.1970C>T
ENST00000696995.1:n.4382C>T
ENST00000696996.1:n.2295C>T
ENST00000696997.1:c.*483C>T	ENSP00000513028.1:n.*483C>T
ENST00000696998.1:n.2107C>T
ENST00000696999.1:c.136C>T	ENSP00000513029.1:p.His46Tyr
ENST00000697035.1:c.*186C>T	ENSP00000513059.1:n.*186C>T
ENST00000697036.1:c.*269C>T	ENSP00000513060.1:n.*269C>T
ENST00000697037.1:n.888C>T
ENST00000697093.1:n.3089C>T
ENST00000697094.1:n.3436C>T
ENST00000697095.1:c.*2054C>T	ENSP00000513104.1:n.*2054C>T
ENST00000697096.1:n.1986C>T
ENST00000697097.1:c.136C>T	ENSP00000513105.1:p.His46Tyr
ENST00000562983.2:n.1039C>T
ENST00000690268.1:c.934C>T	ENSP00000509810.1:p.His312Tyr
ENST00000355740.7:c.*179C>T	ENSP00000347979.3:n.*179C>T
ENST00000612663.5:c.*255C>T	ENSP00000477997.3:n.*255C>T
ENST00000640140.1:n.1025C>T
ENST00000640250.1:n.352C>T
ENST00000640681.1:n.974C>T
ENST00000652046.1:c.853C>T MANE Select	ENSP00000498466.1:p.His285Tyr
ENST00000352159.8:c.*170C>T	ENSP00000345601.4:n.*170C>T
ENST00000355279.2:c.828C>T	ENSP00000347426.2:n.828C>T
ENST00000355740.6:c.853C>T	ENSP00000347979.2:p.His285Tyr
ENST00000357339.6:c.790C>T	ENSP00000349896.2:p.His264Tyr
ENST00000479522.5:c.*282C>T	ENSP00000424113.1:n.*282C>T
ENST00000484444.5:c.*294C>T	ENSP00000420975.1:n.*294C>T
ENST00000488877.5:c.*294C>T	ENSP00000425159.1:n.*294C>T
ENST00000492756.5:c.681C>T	ENSP00000422453.1:n.681C>T
ENST00000494410.5:c.*211C>T	ENSP00000423755.1:n.*211C>T
ENST00000612663.4:c.*200C>T	ENSP00000477997.2:n.*200C>T
NM_000043.4:c.853C>T , LRG_134t1:c.853C>T	NP_000034.1:p.His285Tyr
NM_152871.2:c.790C>T	NP_690610.1:p.His264Tyr
NM_152872.2:c.*165C>T	NP_690611.1:n.*165C>T
NR_028033.2:n.1027C>T
NR_028034.2:n.889C>T
NR_028035.2:n.952C>T
NR_028036.2:n.1090C>T
XM_006717819.2:c.934C>T	XP_006717882.1:p.His312Tyr
XM_011539764.1:c.1015C>T	XP_011538066.1:p.His339Tyr
XM_011539765.1:c.952C>T	XP_011538067.1:p.His318Tyr
XM_011539766.1:c.934C>T	XP_011538068.1:p.His312Tyr
XM_011539767.1:c.898C>T	XP_011538069.1:p.His300Tyr
XR_945732.1:n.921C>T
XR_945733.1:n.858C>T
NM_000043.5:c.853C>T	NP_000034.1:p.His285Tyr
NM_001320619.1:c.*176C>T	NP_001307548.1:n.*176C>T
NM_152871.3:c.790C>T	NP_690610.1:p.His264Tyr
NM_152872.3:c.*165C>T	NP_690611.1:n.*165C>T
NR_028033.3:n.999C>T
NR_028034.3:n.861C>T
NR_028035.3:n.924C>T
NR_028036.3:n.1062C>T
NR_135313.1:n.979C>T
NR_135314.1:n.1162C>T
NR_135315.1:n.915C>T
XM_006717819.3:c.934C>T	XP_006717882.1:p.His312Tyr
XM_011539764.2:c.1015C>T	XP_011538066.1:p.His339Tyr
XM_011539765.2:c.952C>T	XP_011538067.1:p.His318Tyr
XM_011539766.2:c.934C>T	XP_011538068.1:p.His312Tyr
XM_011539767.3:c.898C>T	XP_011538069.1:p.His300Tyr
XR_945732.3:n.921C>T
XR_945733.2:n.858C>T
NM_000043.6:c.853C>T MANE Select	NP_000034.1:p.His285Tyr
NM_001320619.2:c.*176C>T	NP_001307548.1:n.*176C>T
NM_152871.4:c.790C>T	NP_690610.1:p.His264Tyr
NM_152872.4:c.*165C>T	NP_690611.1:n.*165C>T
NR_028033.4:n.760C>T
NR_028034.4:n.622C>T
NR_028035.4:n.685C>T
NR_028036.4:n.823C>T
NR_135313.2:n.740C>T
NR_135314.2:n.1019C>T
NR_135315.2:n.772C>T