Canonical Allele Identifier: CA377509556

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773888G>C (hg19) ; chr10:g.89014131G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014131G>C , CM000672.2:g.89014131G>C	GRCh38
NC_000010.10:g.90773888G>C , CM000672.1:g.90773888G>C	GRCh37
NC_000010.9:g.90763868G>C	NCBI36
NG_009089.2:g.28601G>C , LRG_134:g.28601G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.998G>C
ENST00000355740.8:c.*12G>C	ENSP00000347979.3:n.*12G>C
ENST00000357339.7:c.626G>C	ENSP00000349896.2:p.Ser209Thr
ENST00000371857.8:n.2234G>C
ENST00000460510.6:c.-29G>C	ENSP00000512812.1:n.-29G>C
ENST00000466081.6:n.2338G>C
ENST00000477270.6:c.734G>C	ENSP00000512813.1:p.Ser245Thr
ENST00000479522.6:c.*118G>C	ENSP00000424113.1:n.*118G>C
ENST00000484444.6:c.*130G>C	ENSP00000420975.1:n.*130G>C
ENST00000488877.6:c.580G>C	ENSP00000425159.1:n.580G>C
ENST00000492756.7:c.*118G>C	ENSP00000422453.1:n.*118G>C
ENST00000494799.6:c.-29G>C	ENSP00000512834.1:n.-29G>C
ENST00000562983.3:c.-29G>C	ENSP00000512845.1:n.-29G>C
ENST00000612663.6:c.*91G>C	ENSP00000477997.3:n.*91G>C
ENST00000640140.2:n.834G>C
ENST00000640250.2:n.188G>C
ENST00000640681.2:n.793G>C
ENST00000696723.1:n.4322G>C
ENST00000696741.1:n.2327G>C
ENST00000696742.1:n.2054G>C
ENST00000696743.1:n.3457G>C
ENST00000696744.1:n.728G>C
ENST00000696767.1:n.1023G>C
ENST00000696768.1:c.*12G>C	ENSP00000512859.1:n.*12G>C
ENST00000696769.1:n.2378G>C
ENST00000696771.1:c.-29G>C	ENSP00000512860.1:n.-29G>C
ENST00000696772.1:n.2292G>C
ENST00000696773.1:n.2031G>C
ENST00000696774.1:n.5799G>C
ENST00000696776.1:c.782G>C	ENSP00000512861.1:p.Ser261Thr
ENST00000696777.1:n.2097G>C
ENST00000696778.1:n.1125G>C
ENST00000696779.1:c.296G>C	ENSP00000512862.1:p.Ser99Thr
ENST00000696780.1:c.719G>C	ENSP00000512863.1:p.Ser240Thr
ENST00000696781.1:c.434G>C	ENSP00000512864.1:p.Ser145Thr
ENST00000696782.1:c.*91G>C	ENSP00000512865.1:n.*91G>C
ENST00000696783.1:n.2557G>C
ENST00000696992.1:n.1806G>C
ENST00000696995.1:n.4218G>C
ENST00000696996.1:n.2131G>C
ENST00000696997.1:c.*319G>C	ENSP00000513028.1:n.*319G>C
ENST00000696998.1:n.1943G>C
ENST00000696999.1:c.-29G>C	ENSP00000513029.1:n.-29G>C
ENST00000697035.1:c.*22G>C	ENSP00000513059.1:n.*22G>C
ENST00000697036.1:c.*105G>C	ENSP00000513060.1:n.*105G>C
ENST00000697037.1:n.724G>C
ENST00000697093.1:n.2925G>C
ENST00000697094.1:n.3272G>C
ENST00000697095.1:c.*1890G>C	ENSP00000513104.1:n.*1890G>C
ENST00000697096.1:n.1822G>C
ENST00000697097.1:c.-29G>C	ENSP00000513105.1:n.-29G>C
ENST00000562983.2:n.875G>C
ENST00000690268.1:c.770G>C	ENSP00000509810.1:p.Ser257Thr
ENST00000355740.7:c.*15G>C	ENSP00000347979.3:n.*15G>C
ENST00000612663.5:c.*91G>C	ENSP00000477997.3:n.*91G>C
ENST00000640140.1:n.861G>C
ENST00000640250.1:n.188G>C
ENST00000640681.1:n.810G>C
ENST00000652046.1:c.689G>C MANE Select	ENSP00000498466.1:p.Ser230Thr
ENST00000313771.9:n.998G>C
ENST00000352159.8:c.*6G>C	ENSP00000345601.4:n.*6G>C
ENST00000355279.2:c.664G>C	ENSP00000347426.2:n.664G>C
ENST00000355740.6:c.689G>C	ENSP00000347979.2:p.Ser230Thr
ENST00000357339.6:c.626G>C	ENSP00000349896.2:p.Ser209Thr
ENST00000479522.5:c.*118G>C	ENSP00000424113.1:n.*118G>C
ENST00000484444.5:c.*130G>C	ENSP00000420975.1:n.*130G>C
ENST00000488877.5:c.*130G>C	ENSP00000425159.1:n.*130G>C
ENST00000492756.5:c.517G>C	ENSP00000422453.1:n.517G>C
ENST00000494410.5:c.*47G>C	ENSP00000423755.1:n.*47G>C
ENST00000494799.5:n.596G>C
ENST00000612663.4:c.*36G>C	ENSP00000477997.2:n.*36G>C
ENST00000615406.4:c.689G>C	ENSP00000484575.1:p.Ser230Thr
ENST00000626542.2:c.689G>C	ENSP00000485876.1:p.Ser230Thr
NM_000043.4:c.689G>C , LRG_134t1:c.689G>C	NP_000034.1:p.Ser230Thr
NM_152871.2:c.626G>C	NP_690610.1:p.Ser209Thr
NM_152872.2:c.*1G>C	NP_690611.1:n.*1G>C
NR_028033.2:n.863G>C
NR_028034.2:n.725G>C
NR_028035.2:n.788G>C
NR_028036.2:n.926G>C
XM_006717819.2:c.770G>C	XP_006717882.1:p.Ser257Thr
XM_011539764.1:c.851G>C	XP_011538066.1:p.Ser284Thr
XM_011539765.1:c.788G>C	XP_011538067.1:p.Ser263Thr
XM_011539766.1:c.770G>C	XP_011538068.1:p.Ser257Thr
XM_011539767.1:c.734G>C	XP_011538069.1:p.Ser245Thr
XR_945732.1:n.757G>C
XR_945733.1:n.694G>C
NM_000043.5:c.689G>C	NP_000034.1:p.Ser230Thr
NM_001320619.1:c.*12G>C	NP_001307548.1:n.*12G>C
NM_152871.3:c.626G>C	NP_690610.1:p.Ser209Thr
NM_152872.3:c.*1G>C	NP_690611.1:n.*1G>C
NR_028033.3:n.835G>C
NR_028034.3:n.697G>C
NR_028035.3:n.760G>C
NR_028036.3:n.898G>C
NR_135313.1:n.815G>C
NR_135314.1:n.998G>C
NR_135315.1:n.751G>C
XM_006717819.3:c.770G>C	XP_006717882.1:p.Ser257Thr
XM_011539764.2:c.851G>C	XP_011538066.1:p.Ser284Thr
XM_011539765.2:c.788G>C	XP_011538067.1:p.Ser263Thr
XM_011539766.2:c.770G>C	XP_011538068.1:p.Ser257Thr
XM_011539767.3:c.734G>C	XP_011538069.1:p.Ser245Thr
XR_945732.3:n.757G>C
XR_945733.2:n.694G>C
NM_000043.6:c.689G>C MANE Select	NP_000034.1:p.Ser230Thr
NM_001320619.2:c.*12G>C	NP_001307548.1:n.*12G>C
NM_152871.4:c.626G>C	NP_690610.1:p.Ser209Thr
NM_152872.4:c.*1G>C	NP_690611.1:n.*1G>C
NR_028033.4:n.596G>C
NR_028034.4:n.458G>C
NR_028035.4:n.521G>C
NR_028036.4:n.659G>C
NR_135313.2:n.576G>C
NR_135314.2:n.855G>C
NR_135315.2:n.608G>C