Canonical Allele Identifier: CA470974961

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773949A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014192A>T , CM000672.2:g.89014192A>T	GRCh38
NC_000010.10:g.90773949A>T , CM000672.1:g.90773949A>T	GRCh37
NC_000010.9:g.90763929A>T	NCBI36
NG_009089.2:g.28662A>T , LRG_134:g.28662A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1059A>T
ENST00000355740.8:c.*73A>T	ENSP00000347979.3:n.*73A>T
ENST00000357339.7:c.687A>T	ENSP00000349896.2:p.Arg229=
ENST00000371857.8:n.2295A>T
ENST00000460510.6:c.33A>T	ENSP00000512812.1:p.Arg11=
ENST00000466081.6:n.2399A>T
ENST00000477270.6:c.795A>T	ENSP00000512813.1:p.Arg265=
ENST00000479522.6:c.*179A>T	ENSP00000424113.1:n.*179A>T
ENST00000484444.6:c.*191A>T	ENSP00000420975.1:n.*191A>T
ENST00000488877.6:c.641A>T	ENSP00000425159.1:n.641A>T
ENST00000492756.7:c.*179A>T	ENSP00000422453.1:n.*179A>T
ENST00000494799.6:c.33A>T	ENSP00000512834.1:p.Arg11=
ENST00000562983.3:c.33A>T	ENSP00000512845.1:p.Arg11=
ENST00000612663.6:c.*152A>T	ENSP00000477997.3:n.*152A>T
ENST00000640140.2:n.895A>T
ENST00000640250.2:n.249A>T
ENST00000640681.2:n.854A>T
ENST00000696723.1:n.4383A>T
ENST00000696741.1:n.2388A>T
ENST00000696742.1:n.2115A>T
ENST00000696743.1:n.3518A>T
ENST00000696744.1:n.789A>T
ENST00000696767.1:n.1084A>T
ENST00000696768.1:c.*73A>T	ENSP00000512859.1:n.*73A>T
ENST00000696769.1:n.2439A>T
ENST00000696771.1:c.33A>T	ENSP00000512860.1:p.Arg11=
ENST00000696772.1:n.2353A>T
ENST00000696773.1:n.2092A>T
ENST00000696774.1:n.5860A>T
ENST00000696776.1:c.843A>T	ENSP00000512861.1:p.Arg281=
ENST00000696777.1:n.2158A>T
ENST00000696778.1:n.1186A>T
ENST00000696779.1:c.357A>T	ENSP00000512862.1:p.Arg119=
ENST00000696780.1:c.780A>T	ENSP00000512863.1:p.Arg260=
ENST00000696781.1:c.495A>T	ENSP00000512864.1:p.Arg165=
ENST00000696782.1:c.*152A>T	ENSP00000512865.1:n.*152A>T
ENST00000696783.1:n.2618A>T
ENST00000696992.1:n.1867A>T
ENST00000696995.1:n.4279A>T
ENST00000696996.1:n.2192A>T
ENST00000696997.1:c.*380A>T	ENSP00000513028.1:n.*380A>T
ENST00000696998.1:n.2004A>T
ENST00000696999.1:c.33A>T	ENSP00000513029.1:p.Arg11=
ENST00000697035.1:c.*83A>T	ENSP00000513059.1:n.*83A>T
ENST00000697036.1:c.*166A>T	ENSP00000513060.1:n.*166A>T
ENST00000697037.1:n.785A>T
ENST00000697093.1:n.2986A>T
ENST00000697094.1:n.3333A>T
ENST00000697095.1:c.*1951A>T	ENSP00000513104.1:n.*1951A>T
ENST00000697096.1:n.1883A>T
ENST00000697097.1:c.33A>T	ENSP00000513105.1:p.Arg11=
ENST00000562983.2:n.936A>T
ENST00000690268.1:c.831A>T	ENSP00000509810.1:p.Arg277=
ENST00000355740.7:c.*76A>T	ENSP00000347979.3:n.*76A>T
ENST00000612663.5:c.*152A>T	ENSP00000477997.3:n.*152A>T
ENST00000640140.1:n.922A>T
ENST00000640250.1:n.249A>T
ENST00000640681.1:n.871A>T
ENST00000652046.1:c.750A>T MANE Select	ENSP00000498466.1:p.Arg250=
ENST00000352159.8:c.*67A>T	ENSP00000345601.4:n.*67A>T
ENST00000355279.2:c.725A>T	ENSP00000347426.2:n.725A>T
ENST00000355740.6:c.750A>T	ENSP00000347979.2:p.Arg250=
ENST00000357339.6:c.687A>T	ENSP00000349896.2:p.Arg229=
ENST00000479522.5:c.*179A>T	ENSP00000424113.1:n.*179A>T
ENST00000484444.5:c.*191A>T	ENSP00000420975.1:n.*191A>T
ENST00000488877.5:c.*191A>T	ENSP00000425159.1:n.*191A>T
ENST00000492756.5:c.578A>T	ENSP00000422453.1:n.578A>T
ENST00000494410.5:c.*108A>T	ENSP00000423755.1:n.*108A>T
ENST00000494799.5:n.657A>T
ENST00000612663.4:c.*97A>T	ENSP00000477997.2:n.*97A>T
ENST00000615406.4:c.750A>T	ENSP00000484575.1:p.Arg250=
NM_000043.4:c.750A>T , LRG_134t1:c.750A>T	NP_000034.1:p.Arg250=
NM_152871.2:c.687A>T	NP_690610.1:p.Arg229=
NM_152872.2:c.*62A>T	NP_690611.1:n.*62A>T
NR_028033.2:n.924A>T
NR_028034.2:n.786A>T
NR_028035.2:n.849A>T
NR_028036.2:n.987A>T
XM_006717819.2:c.831A>T	XP_006717882.1:p.Arg277=
XM_011539764.1:c.912A>T	XP_011538066.1:p.Arg304=
XM_011539765.1:c.849A>T	XP_011538067.1:p.Arg283=
XM_011539766.1:c.831A>T	XP_011538068.1:p.Arg277=
XM_011539767.1:c.795A>T	XP_011538069.1:p.Arg265=
XR_945732.1:n.818A>T
XR_945733.1:n.755A>T
NM_000043.5:c.750A>T	NP_000034.1:p.Arg250=
NM_001320619.1:c.*73A>T	NP_001307548.1:n.*73A>T
NM_152871.3:c.687A>T	NP_690610.1:p.Arg229=
NM_152872.3:c.*62A>T	NP_690611.1:n.*62A>T
NR_028033.3:n.896A>T
NR_028034.3:n.758A>T
NR_028035.3:n.821A>T
NR_028036.3:n.959A>T
NR_135313.1:n.876A>T
NR_135314.1:n.1059A>T
NR_135315.1:n.812A>T
XM_006717819.3:c.831A>T	XP_006717882.1:p.Arg277=
XM_011539764.2:c.912A>T	XP_011538066.1:p.Arg304=
XM_011539765.2:c.849A>T	XP_011538067.1:p.Arg283=
XM_011539766.2:c.831A>T	XP_011538068.1:p.Arg277=
XM_011539767.3:c.795A>T	XP_011538069.1:p.Arg265=
XR_945732.3:n.818A>T
XR_945733.2:n.755A>T
NM_000043.6:c.750A>T MANE Select	NP_000034.1:p.Arg250=
NM_001320619.2:c.*73A>T	NP_001307548.1:n.*73A>T
NM_152871.4:c.687A>T	NP_690610.1:p.Arg229=
NM_152872.4:c.*62A>T	NP_690611.1:n.*62A>T
NR_028033.4:n.657A>T
NR_028034.4:n.519A>T
NR_028035.4:n.582A>T
NR_028036.4:n.720A>T
NR_135313.2:n.637A>T
NR_135314.2:n.916A>T
NR_135315.2:n.669A>T