Canonical Allele Identifier: CA377509774

Gene: FAS

Linked Data

• ClinVar Variation Id: 1715761
• ClinVar RCV Id: RCV002301488
• MyVariant Identifiers: chr10:g.90773971A>G (hg19) ; chr10:g.89014214A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014214A>G , CM000672.2:g.89014214A>G	GRCh38
NC_000010.10:g.90773971A>G , CM000672.1:g.90773971A>G	GRCh37
NC_000010.9:g.90763951A>G	NCBI36
NG_009089.2:g.28684A>G , LRG_134:g.28684A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1081A>G
ENST00000355740.8:c.*95A>G	ENSP00000347979.3:n.*95A>G
ENST00000357339.7:c.709A>G	ENSP00000349896.2:p.Lys237Glu
ENST00000371857.8:n.2317A>G
ENST00000460510.6:c.55A>G	ENSP00000512812.1:p.Lys19Glu
ENST00000466081.6:n.2421A>G
ENST00000477270.6:c.817A>G	ENSP00000512813.1:p.Lys273Glu
ENST00000479522.6:c.*201A>G	ENSP00000424113.1:n.*201A>G
ENST00000484444.6:c.*213A>G	ENSP00000420975.1:n.*213A>G
ENST00000488877.6:c.663A>G	ENSP00000425159.1:n.663A>G
ENST00000492756.7:c.*201A>G	ENSP00000422453.1:n.*201A>G
ENST00000494799.6:c.55A>G	ENSP00000512834.1:p.Lys19Glu
ENST00000562983.3:c.55A>G	ENSP00000512845.1:p.Lys19Glu
ENST00000612663.6:c.*174A>G	ENSP00000477997.3:n.*174A>G
ENST00000640140.2:n.917A>G
ENST00000640250.2:n.271A>G
ENST00000640681.2:n.876A>G
ENST00000696723.1:n.4405A>G
ENST00000696741.1:n.2410A>G
ENST00000696742.1:n.2137A>G
ENST00000696743.1:n.3540A>G
ENST00000696744.1:n.811A>G
ENST00000696767.1:n.1106A>G
ENST00000696768.1:c.*95A>G	ENSP00000512859.1:n.*95A>G
ENST00000696769.1:n.2461A>G
ENST00000696771.1:c.55A>G	ENSP00000512860.1:p.Lys19Glu
ENST00000696772.1:n.2375A>G
ENST00000696773.1:n.2114A>G
ENST00000696774.1:n.5882A>G
ENST00000696776.1:c.865A>G	ENSP00000512861.1:p.Lys289Glu
ENST00000696777.1:n.2180A>G
ENST00000696778.1:n.1208A>G
ENST00000696779.1:c.379A>G	ENSP00000512862.1:p.Lys127Glu
ENST00000696780.1:c.802A>G	ENSP00000512863.1:p.Lys268Glu
ENST00000696781.1:c.517A>G	ENSP00000512864.1:p.Lys173Glu
ENST00000696782.1:c.*174A>G	ENSP00000512865.1:n.*174A>G
ENST00000696783.1:n.2640A>G
ENST00000696992.1:n.1889A>G
ENST00000696995.1:n.4301A>G
ENST00000696996.1:n.2214A>G
ENST00000696997.1:c.*402A>G	ENSP00000513028.1:n.*402A>G
ENST00000696998.1:n.2026A>G
ENST00000696999.1:c.55A>G	ENSP00000513029.1:p.Lys19Glu
ENST00000697035.1:c.*105A>G	ENSP00000513059.1:n.*105A>G
ENST00000697036.1:c.*188A>G	ENSP00000513060.1:n.*188A>G
ENST00000697037.1:n.807A>G
ENST00000697093.1:n.3008A>G
ENST00000697094.1:n.3355A>G
ENST00000697095.1:c.*1973A>G	ENSP00000513104.1:n.*1973A>G
ENST00000697096.1:n.1905A>G
ENST00000697097.1:c.55A>G	ENSP00000513105.1:p.Lys19Glu
ENST00000562983.2:n.958A>G
ENST00000690268.1:c.853A>G	ENSP00000509810.1:p.Lys285Glu
ENST00000355740.7:c.*98A>G	ENSP00000347979.3:n.*98A>G
ENST00000612663.5:c.*174A>G	ENSP00000477997.3:n.*174A>G
ENST00000640140.1:n.944A>G
ENST00000640250.1:n.271A>G
ENST00000640681.1:n.893A>G
ENST00000652046.1:c.772A>G MANE Select	ENSP00000498466.1:p.Lys258Glu
ENST00000352159.8:c.*89A>G	ENSP00000345601.4:n.*89A>G
ENST00000355279.2:c.747A>G	ENSP00000347426.2:n.747A>G
ENST00000355740.6:c.772A>G	ENSP00000347979.2:p.Lys258Glu
ENST00000357339.6:c.709A>G	ENSP00000349896.2:p.Lys237Glu
ENST00000479522.5:c.*201A>G	ENSP00000424113.1:n.*201A>G
ENST00000484444.5:c.*213A>G	ENSP00000420975.1:n.*213A>G
ENST00000488877.5:c.*213A>G	ENSP00000425159.1:n.*213A>G
ENST00000492756.5:c.600A>G	ENSP00000422453.1:n.600A>G
ENST00000494410.5:c.*130A>G	ENSP00000423755.1:n.*130A>G
ENST00000494799.5:n.679A>G
ENST00000612663.4:c.*119A>G	ENSP00000477997.2:n.*119A>G
NM_000043.4:c.772A>G , LRG_134t1:c.772A>G	NP_000034.1:p.Lys258Glu
NM_152871.2:c.709A>G	NP_690610.1:p.Lys237Glu
NM_152872.2:c.*84A>G	NP_690611.1:n.*84A>G
NR_028033.2:n.946A>G
NR_028034.2:n.808A>G
NR_028035.2:n.871A>G
NR_028036.2:n.1009A>G
XM_006717819.2:c.853A>G	XP_006717882.1:p.Lys285Glu
XM_011539764.1:c.934A>G	XP_011538066.1:p.Lys312Glu
XM_011539765.1:c.871A>G	XP_011538067.1:p.Lys291Glu
XM_011539766.1:c.853A>G	XP_011538068.1:p.Lys285Glu
XM_011539767.1:c.817A>G	XP_011538069.1:p.Lys273Glu
XR_945732.1:n.840A>G
XR_945733.1:n.777A>G
NM_000043.5:c.772A>G	NP_000034.1:p.Lys258Glu
NM_001320619.1:c.*95A>G	NP_001307548.1:n.*95A>G
NM_152871.3:c.709A>G	NP_690610.1:p.Lys237Glu
NM_152872.3:c.*84A>G	NP_690611.1:n.*84A>G
NR_028033.3:n.918A>G
NR_028034.3:n.780A>G
NR_028035.3:n.843A>G
NR_028036.3:n.981A>G
NR_135313.1:n.898A>G
NR_135314.1:n.1081A>G
NR_135315.1:n.834A>G
XM_006717819.3:c.853A>G	XP_006717882.1:p.Lys285Glu
XM_011539764.2:c.934A>G	XP_011538066.1:p.Lys312Glu
XM_011539765.2:c.871A>G	XP_011538067.1:p.Lys291Glu
XM_011539766.2:c.853A>G	XP_011538068.1:p.Lys285Glu
XM_011539767.3:c.817A>G	XP_011538069.1:p.Lys273Glu
XR_945732.3:n.840A>G
XR_945733.2:n.777A>G
NM_000043.6:c.772A>G MANE Select	NP_000034.1:p.Lys258Glu
NM_001320619.2:c.*95A>G	NP_001307548.1:n.*95A>G
NM_152871.4:c.709A>G	NP_690610.1:p.Lys237Glu
NM_152872.4:c.*84A>G	NP_690611.1:n.*84A>G
NR_028033.4:n.679A>G
NR_028034.4:n.541A>G
NR_028035.4:n.604A>G
NR_028036.4:n.742A>G
NR_135313.2:n.659A>G
NR_135314.2:n.938A>G
NR_135315.2:n.691A>G