Canonical Allele Identifier: CA377509598

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773904T>C (hg19) ; chr10:g.89014147T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014147T>C , CM000672.2:g.89014147T>C	GRCh38
NC_000010.10:g.90773904T>C , CM000672.1:g.90773904T>C	GRCh37
NC_000010.9:g.90763884T>C	NCBI36
NG_009089.2:g.28617T>C , LRG_134:g.28617T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1014T>C
ENST00000355740.8:c.*28T>C	ENSP00000347979.3:n.*28T>C
ENST00000357339.7:c.642T>C	ENSP00000349896.2:p.Thr214=
ENST00000371857.8:n.2250T>C
ENST00000460510.6:c.-13T>C	ENSP00000512812.1:n.-13T>C
ENST00000466081.6:n.2354T>C
ENST00000477270.6:c.750T>C	ENSP00000512813.1:p.Thr250=
ENST00000479522.6:c.*134T>C	ENSP00000424113.1:n.*134T>C
ENST00000484444.6:c.*146T>C	ENSP00000420975.1:n.*146T>C
ENST00000488877.6:c.596T>C	ENSP00000425159.1:n.596T>C
ENST00000492756.7:c.*134T>C	ENSP00000422453.1:n.*134T>C
ENST00000494799.6:c.-13T>C	ENSP00000512834.1:n.-13T>C
ENST00000562983.3:c.-13T>C	ENSP00000512845.1:n.-13T>C
ENST00000612663.6:c.*107T>C	ENSP00000477997.3:n.*107T>C
ENST00000640140.2:n.850T>C
ENST00000640250.2:n.204T>C
ENST00000640681.2:n.809T>C
ENST00000696723.1:n.4338T>C
ENST00000696741.1:n.2343T>C
ENST00000696742.1:n.2070T>C
ENST00000696743.1:n.3473T>C
ENST00000696744.1:n.744T>C
ENST00000696767.1:n.1039T>C
ENST00000696768.1:c.*28T>C	ENSP00000512859.1:n.*28T>C
ENST00000696769.1:n.2394T>C
ENST00000696771.1:c.-13T>C	ENSP00000512860.1:n.-13T>C
ENST00000696772.1:n.2308T>C
ENST00000696773.1:n.2047T>C
ENST00000696774.1:n.5815T>C
ENST00000696776.1:c.798T>C	ENSP00000512861.1:p.Thr266=
ENST00000696777.1:n.2113T>C
ENST00000696778.1:n.1141T>C
ENST00000696779.1:c.312T>C	ENSP00000512862.1:p.Thr104=
ENST00000696780.1:c.735T>C	ENSP00000512863.1:p.Thr245=
ENST00000696781.1:c.450T>C	ENSP00000512864.1:p.Thr150=
ENST00000696782.1:c.*107T>C	ENSP00000512865.1:n.*107T>C
ENST00000696783.1:n.2573T>C
ENST00000696992.1:n.1822T>C
ENST00000696995.1:n.4234T>C
ENST00000696996.1:n.2147T>C
ENST00000696997.1:c.*335T>C	ENSP00000513028.1:n.*335T>C
ENST00000696998.1:n.1959T>C
ENST00000696999.1:c.-13T>C	ENSP00000513029.1:n.-13T>C
ENST00000697035.1:c.*38T>C	ENSP00000513059.1:n.*38T>C
ENST00000697036.1:c.*121T>C	ENSP00000513060.1:n.*121T>C
ENST00000697037.1:n.740T>C
ENST00000697093.1:n.2941T>C
ENST00000697094.1:n.3288T>C
ENST00000697095.1:c.*1906T>C	ENSP00000513104.1:n.*1906T>C
ENST00000697096.1:n.1838T>C
ENST00000697097.1:c.-13T>C	ENSP00000513105.1:n.-13T>C
ENST00000562983.2:n.891T>C
ENST00000690268.1:c.786T>C	ENSP00000509810.1:p.Thr262=
ENST00000355740.7:c.*31T>C	ENSP00000347979.3:n.*31T>C
ENST00000612663.5:c.*107T>C	ENSP00000477997.3:n.*107T>C
ENST00000640140.1:n.877T>C
ENST00000640250.1:n.204T>C
ENST00000640681.1:n.826T>C
ENST00000652046.1:c.705T>C MANE Select	ENSP00000498466.1:p.Thr235=
ENST00000313771.9:n.1014T>C
ENST00000352159.8:c.*22T>C	ENSP00000345601.4:n.*22T>C
ENST00000355279.2:c.680T>C	ENSP00000347426.2:n.680T>C
ENST00000355740.6:c.705T>C	ENSP00000347979.2:p.Thr235=
ENST00000357339.6:c.642T>C	ENSP00000349896.2:p.Thr214=
ENST00000479522.5:c.*134T>C	ENSP00000424113.1:n.*134T>C
ENST00000484444.5:c.*146T>C	ENSP00000420975.1:n.*146T>C
ENST00000488877.5:c.*146T>C	ENSP00000425159.1:n.*146T>C
ENST00000492756.5:c.533T>C	ENSP00000422453.1:n.533T>C
ENST00000494410.5:c.*63T>C	ENSP00000423755.1:n.*63T>C
ENST00000494799.5:n.612T>C
ENST00000612663.4:c.*52T>C	ENSP00000477997.2:n.*52T>C
ENST00000615406.4:c.705T>C	ENSP00000484575.1:p.Thr235=
ENST00000626542.2:c.703T>C	ENSP00000485876.1:p.Tyr235His
NM_000043.4:c.705T>C , LRG_134t1:c.705T>C	NP_000034.1:p.Thr235=
NM_152871.2:c.642T>C	NP_690610.1:p.Thr214=
NM_152872.2:c.*17T>C	NP_690611.1:n.*17T>C
NR_028033.2:n.879T>C
NR_028034.2:n.741T>C
NR_028035.2:n.804T>C
NR_028036.2:n.942T>C
XM_006717819.2:c.786T>C	XP_006717882.1:p.Thr262=
XM_011539764.1:c.867T>C	XP_011538066.1:p.Thr289=
XM_011539765.1:c.804T>C	XP_011538067.1:p.Thr268=
XM_011539766.1:c.786T>C	XP_011538068.1:p.Thr262=
XM_011539767.1:c.750T>C	XP_011538069.1:p.Thr250=
XR_945732.1:n.773T>C
XR_945733.1:n.710T>C
NM_000043.5:c.705T>C	NP_000034.1:p.Thr235=
NM_001320619.1:c.*28T>C	NP_001307548.1:n.*28T>C
NM_152871.3:c.642T>C	NP_690610.1:p.Thr214=
NM_152872.3:c.*17T>C	NP_690611.1:n.*17T>C
NR_028033.3:n.851T>C
NR_028034.3:n.713T>C
NR_028035.3:n.776T>C
NR_028036.3:n.914T>C
NR_135313.1:n.831T>C
NR_135314.1:n.1014T>C
NR_135315.1:n.767T>C
XM_006717819.3:c.786T>C	XP_006717882.1:p.Thr262=
XM_011539764.2:c.867T>C	XP_011538066.1:p.Thr289=
XM_011539765.2:c.804T>C	XP_011538067.1:p.Thr268=
XM_011539766.2:c.786T>C	XP_011538068.1:p.Thr262=
XM_011539767.3:c.750T>C	XP_011538069.1:p.Thr250=
XR_945732.3:n.773T>C
XR_945733.2:n.710T>C
NM_000043.6:c.705T>C MANE Select	NP_000034.1:p.Thr235=
NM_001320619.2:c.*28T>C	NP_001307548.1:n.*28T>C
NM_152871.4:c.642T>C	NP_690610.1:p.Thr214=
NM_152872.4:c.*17T>C	NP_690611.1:n.*17T>C
NR_028033.4:n.612T>C
NR_028034.4:n.474T>C
NR_028035.4:n.537T>C
NR_028036.4:n.675T>C
NR_135313.2:n.592T>C
NR_135314.2:n.871T>C
NR_135315.2:n.624T>C