Canonical Allele Identifier: CA377509777

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773972A>G (hg19) ; chr10:g.89014215A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014215A>G , CM000672.2:g.89014215A>G	GRCh38
NC_000010.10:g.90773972A>G , CM000672.1:g.90773972A>G	GRCh37
NC_000010.9:g.90763952A>G	NCBI36
NG_009089.2:g.28685A>G , LRG_134:g.28685A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1082A>G
ENST00000355740.8:c.*96A>G	ENSP00000347979.3:n.*96A>G
ENST00000357339.7:c.710A>G	ENSP00000349896.2:p.Lys237Arg
ENST00000371857.8:n.2318A>G
ENST00000460510.6:c.56A>G	ENSP00000512812.1:p.Lys19Arg
ENST00000466081.6:n.2422A>G
ENST00000477270.6:c.818A>G	ENSP00000512813.1:p.Lys273Arg
ENST00000479522.6:c.*202A>G	ENSP00000424113.1:n.*202A>G
ENST00000484444.6:c.*214A>G	ENSP00000420975.1:n.*214A>G
ENST00000488877.6:c.664A>G	ENSP00000425159.1:n.664A>G
ENST00000492756.7:c.*202A>G	ENSP00000422453.1:n.*202A>G
ENST00000494799.6:c.56A>G	ENSP00000512834.1:p.Lys19Arg
ENST00000562983.3:c.56A>G	ENSP00000512845.1:p.Lys19Arg
ENST00000612663.6:c.*175A>G	ENSP00000477997.3:n.*175A>G
ENST00000640140.2:n.918A>G
ENST00000640250.2:n.272A>G
ENST00000640681.2:n.877A>G
ENST00000696723.1:n.4406A>G
ENST00000696741.1:n.2411A>G
ENST00000696742.1:n.2138A>G
ENST00000696743.1:n.3541A>G
ENST00000696744.1:n.812A>G
ENST00000696767.1:n.1107A>G
ENST00000696768.1:c.*96A>G	ENSP00000512859.1:n.*96A>G
ENST00000696769.1:n.2462A>G
ENST00000696771.1:c.56A>G	ENSP00000512860.1:p.Lys19Arg
ENST00000696772.1:n.2376A>G
ENST00000696773.1:n.2115A>G
ENST00000696774.1:n.5883A>G
ENST00000696776.1:c.866A>G	ENSP00000512861.1:p.Lys289Arg
ENST00000696777.1:n.2181A>G
ENST00000696778.1:n.1209A>G
ENST00000696779.1:c.380A>G	ENSP00000512862.1:p.Lys127Arg
ENST00000696780.1:c.803A>G	ENSP00000512863.1:p.Lys268Arg
ENST00000696781.1:c.518A>G	ENSP00000512864.1:p.Lys173Arg
ENST00000696782.1:c.*175A>G	ENSP00000512865.1:n.*175A>G
ENST00000696783.1:n.2641A>G
ENST00000696992.1:n.1890A>G
ENST00000696995.1:n.4302A>G
ENST00000696996.1:n.2215A>G
ENST00000696997.1:c.*403A>G	ENSP00000513028.1:n.*403A>G
ENST00000696998.1:n.2027A>G
ENST00000696999.1:c.56A>G	ENSP00000513029.1:p.Lys19Arg
ENST00000697035.1:c.*106A>G	ENSP00000513059.1:n.*106A>G
ENST00000697036.1:c.*189A>G	ENSP00000513060.1:n.*189A>G
ENST00000697037.1:n.808A>G
ENST00000697093.1:n.3009A>G
ENST00000697094.1:n.3356A>G
ENST00000697095.1:c.*1974A>G	ENSP00000513104.1:n.*1974A>G
ENST00000697096.1:n.1906A>G
ENST00000697097.1:c.56A>G	ENSP00000513105.1:p.Lys19Arg
ENST00000562983.2:n.959A>G
ENST00000690268.1:c.854A>G	ENSP00000509810.1:p.Lys285Arg
ENST00000355740.7:c.*99A>G	ENSP00000347979.3:n.*99A>G
ENST00000612663.5:c.*175A>G	ENSP00000477997.3:n.*175A>G
ENST00000640140.1:n.945A>G
ENST00000640250.1:n.272A>G
ENST00000640681.1:n.894A>G
ENST00000652046.1:c.773A>G MANE Select	ENSP00000498466.1:p.Lys258Arg
ENST00000352159.8:c.*90A>G	ENSP00000345601.4:n.*90A>G
ENST00000355279.2:c.748A>G	ENSP00000347426.2:n.748A>G
ENST00000355740.6:c.773A>G	ENSP00000347979.2:p.Lys258Arg
ENST00000357339.6:c.710A>G	ENSP00000349896.2:p.Lys237Arg
ENST00000479522.5:c.*202A>G	ENSP00000424113.1:n.*202A>G
ENST00000484444.5:c.*214A>G	ENSP00000420975.1:n.*214A>G
ENST00000488877.5:c.*214A>G	ENSP00000425159.1:n.*214A>G
ENST00000492756.5:c.601A>G	ENSP00000422453.1:n.601A>G
ENST00000494410.5:c.*131A>G	ENSP00000423755.1:n.*131A>G
ENST00000494799.5:n.680A>G
ENST00000612663.4:c.*120A>G	ENSP00000477997.2:n.*120A>G
NM_000043.4:c.773A>G , LRG_134t1:c.773A>G	NP_000034.1:p.Lys258Arg
NM_152871.2:c.710A>G	NP_690610.1:p.Lys237Arg
NM_152872.2:c.*85A>G	NP_690611.1:n.*85A>G
NR_028033.2:n.947A>G
NR_028034.2:n.809A>G
NR_028035.2:n.872A>G
NR_028036.2:n.1010A>G
XM_006717819.2:c.854A>G	XP_006717882.1:p.Lys285Arg
XM_011539764.1:c.935A>G	XP_011538066.1:p.Lys312Arg
XM_011539765.1:c.872A>G	XP_011538067.1:p.Lys291Arg
XM_011539766.1:c.854A>G	XP_011538068.1:p.Lys285Arg
XM_011539767.1:c.818A>G	XP_011538069.1:p.Lys273Arg
XR_945732.1:n.841A>G
XR_945733.1:n.778A>G
NM_000043.5:c.773A>G	NP_000034.1:p.Lys258Arg
NM_001320619.1:c.*96A>G	NP_001307548.1:n.*96A>G
NM_152871.3:c.710A>G	NP_690610.1:p.Lys237Arg
NM_152872.3:c.*85A>G	NP_690611.1:n.*85A>G
NR_028033.3:n.919A>G
NR_028034.3:n.781A>G
NR_028035.3:n.844A>G
NR_028036.3:n.982A>G
NR_135313.1:n.899A>G
NR_135314.1:n.1082A>G
NR_135315.1:n.835A>G
XM_006717819.3:c.854A>G	XP_006717882.1:p.Lys285Arg
XM_011539764.2:c.935A>G	XP_011538066.1:p.Lys312Arg
XM_011539765.2:c.872A>G	XP_011538067.1:p.Lys291Arg
XM_011539766.2:c.854A>G	XP_011538068.1:p.Lys285Arg
XM_011539767.3:c.818A>G	XP_011538069.1:p.Lys273Arg
XR_945732.3:n.841A>G
XR_945733.2:n.778A>G
NM_000043.6:c.773A>G MANE Select	NP_000034.1:p.Lys258Arg
NM_001320619.2:c.*96A>G	NP_001307548.1:n.*96A>G
NM_152871.4:c.710A>G	NP_690610.1:p.Lys237Arg
NM_152872.4:c.*85A>G	NP_690611.1:n.*85A>G
NR_028033.4:n.680A>G
NR_028034.4:n.542A>G
NR_028035.4:n.605A>G
NR_028036.4:n.743A>G
NR_135313.2:n.660A>G
NR_135314.2:n.939A>G
NR_135315.2:n.692A>G