Canonical Allele Identifier: CA470974917

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773895T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014138T>C , CM000672.2:g.89014138T>C	GRCh38
NC_000010.10:g.90773895T>C , CM000672.1:g.90773895T>C	GRCh37
NC_000010.9:g.90763875T>C	NCBI36
NG_009089.2:g.28608T>C , LRG_134:g.28608T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1005T>C
ENST00000355740.8:c.*19T>C	ENSP00000347979.3:n.*19T>C
ENST00000357339.7:c.633T>C	ENSP00000349896.2:p.Tyr211=
ENST00000371857.8:n.2241T>C
ENST00000460510.6:c.-22T>C	ENSP00000512812.1:n.-22T>C
ENST00000466081.6:n.2345T>C
ENST00000477270.6:c.741T>C	ENSP00000512813.1:p.Tyr247=
ENST00000479522.6:c.*125T>C	ENSP00000424113.1:n.*125T>C
ENST00000484444.6:c.*137T>C	ENSP00000420975.1:n.*137T>C
ENST00000488877.6:c.587T>C	ENSP00000425159.1:n.587T>C
ENST00000492756.7:c.*125T>C	ENSP00000422453.1:n.*125T>C
ENST00000494799.6:c.-22T>C	ENSP00000512834.1:n.-22T>C
ENST00000562983.3:c.-22T>C	ENSP00000512845.1:n.-22T>C
ENST00000612663.6:c.*98T>C	ENSP00000477997.3:n.*98T>C
ENST00000640140.2:n.841T>C
ENST00000640250.2:n.195T>C
ENST00000640681.2:n.800T>C
ENST00000696723.1:n.4329T>C
ENST00000696741.1:n.2334T>C
ENST00000696742.1:n.2061T>C
ENST00000696743.1:n.3464T>C
ENST00000696744.1:n.735T>C
ENST00000696767.1:n.1030T>C
ENST00000696768.1:c.*19T>C	ENSP00000512859.1:n.*19T>C
ENST00000696769.1:n.2385T>C
ENST00000696771.1:c.-22T>C	ENSP00000512860.1:n.-22T>C
ENST00000696772.1:n.2299T>C
ENST00000696773.1:n.2038T>C
ENST00000696774.1:n.5806T>C
ENST00000696776.1:c.789T>C	ENSP00000512861.1:p.Tyr263=
ENST00000696777.1:n.2104T>C
ENST00000696778.1:n.1132T>C
ENST00000696779.1:c.303T>C	ENSP00000512862.1:p.Tyr101=
ENST00000696780.1:c.726T>C	ENSP00000512863.1:p.Tyr242=
ENST00000696781.1:c.441T>C	ENSP00000512864.1:p.Tyr147=
ENST00000696782.1:c.*98T>C	ENSP00000512865.1:n.*98T>C
ENST00000696783.1:n.2564T>C
ENST00000696992.1:n.1813T>C
ENST00000696995.1:n.4225T>C
ENST00000696996.1:n.2138T>C
ENST00000696997.1:c.*326T>C	ENSP00000513028.1:n.*326T>C
ENST00000696998.1:n.1950T>C
ENST00000696999.1:c.-22T>C	ENSP00000513029.1:n.-22T>C
ENST00000697035.1:c.*29T>C	ENSP00000513059.1:n.*29T>C
ENST00000697036.1:c.*112T>C	ENSP00000513060.1:n.*112T>C
ENST00000697037.1:n.731T>C
ENST00000697093.1:n.2932T>C
ENST00000697094.1:n.3279T>C
ENST00000697095.1:c.*1897T>C	ENSP00000513104.1:n.*1897T>C
ENST00000697096.1:n.1829T>C
ENST00000697097.1:c.-22T>C	ENSP00000513105.1:n.-22T>C
ENST00000562983.2:n.882T>C
ENST00000690268.1:c.777T>C	ENSP00000509810.1:p.Tyr259=
ENST00000355740.7:c.*22T>C	ENSP00000347979.3:n.*22T>C
ENST00000612663.5:c.*98T>C	ENSP00000477997.3:n.*98T>C
ENST00000640140.1:n.868T>C
ENST00000640250.1:n.195T>C
ENST00000640681.1:n.817T>C
ENST00000652046.1:c.696T>C MANE Select	ENSP00000498466.1:p.Tyr232=
ENST00000313771.9:n.1005T>C
ENST00000352159.8:c.*13T>C	ENSP00000345601.4:n.*13T>C
ENST00000355279.2:c.671T>C	ENSP00000347426.2:n.671T>C
ENST00000355740.6:c.696T>C	ENSP00000347979.2:p.Tyr232=
ENST00000357339.6:c.633T>C	ENSP00000349896.2:p.Tyr211=
ENST00000479522.5:c.*125T>C	ENSP00000424113.1:n.*125T>C
ENST00000484444.5:c.*137T>C	ENSP00000420975.1:n.*137T>C
ENST00000488877.5:c.*137T>C	ENSP00000425159.1:n.*137T>C
ENST00000492756.5:c.524T>C	ENSP00000422453.1:n.524T>C
ENST00000494410.5:c.*54T>C	ENSP00000423755.1:n.*54T>C
ENST00000494799.5:n.603T>C
ENST00000612663.4:c.*43T>C	ENSP00000477997.2:n.*43T>C
ENST00000615406.4:c.696T>C	ENSP00000484575.1:p.Tyr232=
ENST00000626542.2:c.696T>C	ENSP00000485876.1:p.Tyr232=
NM_000043.4:c.696T>C , LRG_134t1:c.696T>C	NP_000034.1:p.Tyr232=
NM_152871.2:c.633T>C	NP_690610.1:p.Tyr211=
NM_152872.2:c.*8T>C	NP_690611.1:n.*8T>C
NR_028033.2:n.870T>C
NR_028034.2:n.732T>C
NR_028035.2:n.795T>C
NR_028036.2:n.933T>C
XM_006717819.2:c.777T>C	XP_006717882.1:p.Tyr259=
XM_011539764.1:c.858T>C	XP_011538066.1:p.Tyr286=
XM_011539765.1:c.795T>C	XP_011538067.1:p.Tyr265=
XM_011539766.1:c.777T>C	XP_011538068.1:p.Tyr259=
XM_011539767.1:c.741T>C	XP_011538069.1:p.Tyr247=
XR_945732.1:n.764T>C
XR_945733.1:n.701T>C
NM_000043.5:c.696T>C	NP_000034.1:p.Tyr232=
NM_001320619.1:c.*19T>C	NP_001307548.1:n.*19T>C
NM_152871.3:c.633T>C	NP_690610.1:p.Tyr211=
NM_152872.3:c.*8T>C	NP_690611.1:n.*8T>C
NR_028033.3:n.842T>C
NR_028034.3:n.704T>C
NR_028035.3:n.767T>C
NR_028036.3:n.905T>C
NR_135313.1:n.822T>C
NR_135314.1:n.1005T>C
NR_135315.1:n.758T>C
XM_006717819.3:c.777T>C	XP_006717882.1:p.Tyr259=
XM_011539764.2:c.858T>C	XP_011538066.1:p.Tyr286=
XM_011539765.2:c.795T>C	XP_011538067.1:p.Tyr265=
XM_011539766.2:c.777T>C	XP_011538068.1:p.Tyr259=
XM_011539767.3:c.741T>C	XP_011538069.1:p.Tyr247=
XR_945732.3:n.764T>C
XR_945733.2:n.701T>C
NM_000043.6:c.696T>C MANE Select	NP_000034.1:p.Tyr232=
NM_001320619.2:c.*19T>C	NP_001307548.1:n.*19T>C
NM_152871.4:c.633T>C	NP_690610.1:p.Tyr211=
NM_152872.4:c.*8T>C	NP_690611.1:n.*8T>C
NR_028033.4:n.603T>C
NR_028034.4:n.465T>C
NR_028035.4:n.528T>C
NR_028036.4:n.666T>C
NR_135313.2:n.583T>C
NR_135314.2:n.862T>C
NR_135315.2:n.615T>C