Canonical Allele Identifier: CA377509800

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773982G>C (hg19) ; chr10:g.89014225G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014225G>C , CM000672.2:g.89014225G>C	GRCh38
NC_000010.10:g.90773982G>C , CM000672.1:g.90773982G>C	GRCh37
NC_000010.9:g.90763962G>C	NCBI36
NG_009089.2:g.28695G>C , LRG_134:g.28695G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1092G>C
ENST00000355740.8:c.*106G>C	ENSP00000347979.3:n.*106G>C
ENST00000357339.7:c.720G>C	ENSP00000349896.2:p.Glu240Asp
ENST00000371857.8:n.2328G>C
ENST00000460510.6:c.66G>C	ENSP00000512812.1:p.Glu22Asp
ENST00000466081.6:n.2432G>C
ENST00000477270.6:c.828G>C	ENSP00000512813.1:p.Glu276Asp
ENST00000479522.6:c.*212G>C	ENSP00000424113.1:n.*212G>C
ENST00000484444.6:c.*224G>C	ENSP00000420975.1:n.*224G>C
ENST00000488877.6:c.674G>C	ENSP00000425159.1:n.674G>C
ENST00000492756.7:c.*212G>C	ENSP00000422453.1:n.*212G>C
ENST00000494799.6:c.66G>C	ENSP00000512834.1:p.Glu22Asp
ENST00000562983.3:c.66G>C	ENSP00000512845.1:p.Glu22Asp
ENST00000612663.6:c.*185G>C	ENSP00000477997.3:n.*185G>C
ENST00000640140.2:n.928G>C
ENST00000640250.2:n.282G>C
ENST00000640681.2:n.887G>C
ENST00000696723.1:n.4416G>C
ENST00000696741.1:n.2421G>C
ENST00000696742.1:n.2148G>C
ENST00000696743.1:n.3551G>C
ENST00000696744.1:n.822G>C
ENST00000696767.1:n.1117G>C
ENST00000696768.1:c.*106G>C	ENSP00000512859.1:n.*106G>C
ENST00000696769.1:n.2472G>C
ENST00000696771.1:c.66G>C	ENSP00000512860.1:p.Glu22Asp
ENST00000696772.1:n.2386G>C
ENST00000696773.1:n.2125G>C
ENST00000696774.1:n.5893G>C
ENST00000696776.1:c.876G>C	ENSP00000512861.1:p.Glu292Asp
ENST00000696777.1:n.2191G>C
ENST00000696778.1:n.1219G>C
ENST00000696779.1:c.390G>C	ENSP00000512862.1:p.Glu130Asp
ENST00000696780.1:c.813G>C	ENSP00000512863.1:p.Glu271Asp
ENST00000696781.1:c.528G>C	ENSP00000512864.1:p.Glu176Asp
ENST00000696782.1:c.*185G>C	ENSP00000512865.1:n.*185G>C
ENST00000696783.1:n.2651G>C
ENST00000696992.1:n.1900G>C
ENST00000696995.1:n.4312G>C
ENST00000696996.1:n.2225G>C
ENST00000696997.1:c.*413G>C	ENSP00000513028.1:n.*413G>C
ENST00000696998.1:n.2037G>C
ENST00000696999.1:c.66G>C	ENSP00000513029.1:p.Glu22Asp
ENST00000697035.1:c.*116G>C	ENSP00000513059.1:n.*116G>C
ENST00000697036.1:c.*199G>C	ENSP00000513060.1:n.*199G>C
ENST00000697037.1:n.818G>C
ENST00000697093.1:n.3019G>C
ENST00000697094.1:n.3366G>C
ENST00000697095.1:c.*1984G>C	ENSP00000513104.1:n.*1984G>C
ENST00000697096.1:n.1916G>C
ENST00000697097.1:c.66G>C	ENSP00000513105.1:p.Glu22Asp
ENST00000562983.2:n.969G>C
ENST00000690268.1:c.864G>C	ENSP00000509810.1:p.Glu288Asp
ENST00000355740.7:c.*109G>C	ENSP00000347979.3:n.*109G>C
ENST00000612663.5:c.*185G>C	ENSP00000477997.3:n.*185G>C
ENST00000640140.1:n.955G>C
ENST00000640250.1:n.282G>C
ENST00000640681.1:n.904G>C
ENST00000652046.1:c.783G>C MANE Select	ENSP00000498466.1:p.Glu261Asp
ENST00000352159.8:c.*100G>C	ENSP00000345601.4:n.*100G>C
ENST00000355279.2:c.758G>C	ENSP00000347426.2:n.758G>C
ENST00000355740.6:c.783G>C	ENSP00000347979.2:p.Glu261Asp
ENST00000357339.6:c.720G>C	ENSP00000349896.2:p.Glu240Asp
ENST00000479522.5:c.*212G>C	ENSP00000424113.1:n.*212G>C
ENST00000484444.5:c.*224G>C	ENSP00000420975.1:n.*224G>C
ENST00000488877.5:c.*224G>C	ENSP00000425159.1:n.*224G>C
ENST00000492756.5:c.611G>C	ENSP00000422453.1:n.611G>C
ENST00000494410.5:c.*141G>C	ENSP00000423755.1:n.*141G>C
ENST00000612663.4:c.*130G>C	ENSP00000477997.2:n.*130G>C
NM_000043.4:c.783G>C , LRG_134t1:c.783G>C	NP_000034.1:p.Glu261Asp
NM_152871.2:c.720G>C	NP_690610.1:p.Glu240Asp
NM_152872.2:c.*95G>C	NP_690611.1:n.*95G>C
NR_028033.2:n.957G>C
NR_028034.2:n.819G>C
NR_028035.2:n.882G>C
NR_028036.2:n.1020G>C
XM_006717819.2:c.864G>C	XP_006717882.1:p.Glu288Asp
XM_011539764.1:c.945G>C	XP_011538066.1:p.Glu315Asp
XM_011539765.1:c.882G>C	XP_011538067.1:p.Glu294Asp
XM_011539766.1:c.864G>C	XP_011538068.1:p.Glu288Asp
XM_011539767.1:c.828G>C	XP_011538069.1:p.Glu276Asp
XR_945732.1:n.851G>C
XR_945733.1:n.788G>C
NM_000043.5:c.783G>C	NP_000034.1:p.Glu261Asp
NM_001320619.1:c.*106G>C	NP_001307548.1:n.*106G>C
NM_152871.3:c.720G>C	NP_690610.1:p.Glu240Asp
NM_152872.3:c.*95G>C	NP_690611.1:n.*95G>C
NR_028033.3:n.929G>C
NR_028034.3:n.791G>C
NR_028035.3:n.854G>C
NR_028036.3:n.992G>C
NR_135313.1:n.909G>C
NR_135314.1:n.1092G>C
NR_135315.1:n.845G>C
XM_006717819.3:c.864G>C	XP_006717882.1:p.Glu288Asp
XM_011539764.2:c.945G>C	XP_011538066.1:p.Glu315Asp
XM_011539765.2:c.882G>C	XP_011538067.1:p.Glu294Asp
XM_011539766.2:c.864G>C	XP_011538068.1:p.Glu288Asp
XM_011539767.3:c.828G>C	XP_011538069.1:p.Glu276Asp
XR_945732.3:n.851G>C
XR_945733.2:n.788G>C
NM_000043.6:c.783G>C MANE Select	NP_000034.1:p.Glu261Asp
NM_001320619.2:c.*106G>C	NP_001307548.1:n.*106G>C
NM_152871.4:c.720G>C	NP_690610.1:p.Glu240Asp
NM_152872.4:c.*95G>C	NP_690611.1:n.*95G>C
NR_028033.4:n.690G>C
NR_028034.4:n.552G>C
NR_028035.4:n.615G>C
NR_028036.4:n.753G>C
NR_135313.2:n.670G>C
NR_135314.2:n.949G>C
NR_135315.2:n.702G>C