Canonical Allele Identifier: CA377509886

Gene: FAS

Linked Data

• ClinVar Variation Id: 2764356
• ClinVar RCV Id: RCV003517664
• MyVariant Identifiers: chr10:g.90774019A>G (hg19) ; chr10:g.89014262A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014262A>G , CM000672.2:g.89014262A>G	GRCh38
NC_000010.10:g.90774019A>G , CM000672.1:g.90774019A>G	GRCh37
NC_000010.9:g.90763999A>G	NCBI36
NG_009089.2:g.28732A>G , LRG_134:g.28732A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1129A>G
ENST00000355740.8:c.*143A>G	ENSP00000347979.3:n.*143A>G
ENST00000357339.7:c.757A>G	ENSP00000349896.2:p.Lys253Glu
ENST00000371857.8:n.2365A>G
ENST00000460510.6:c.103A>G	ENSP00000512812.1:p.Lys35Glu
ENST00000466081.6:n.2469A>G
ENST00000477270.6:c.865A>G	ENSP00000512813.1:p.Lys289Glu
ENST00000479522.6:c.*249A>G	ENSP00000424113.1:n.*249A>G
ENST00000484444.6:c.*261A>G	ENSP00000420975.1:n.*261A>G
ENST00000488877.6:c.711A>G	ENSP00000425159.1:n.711A>G
ENST00000492756.7:c.*249A>G	ENSP00000422453.1:n.*249A>G
ENST00000494799.6:c.103A>G	ENSP00000512834.1:p.Lys35Glu
ENST00000562983.3:c.103A>G	ENSP00000512845.1:p.Lys35Glu
ENST00000612663.6:c.*222A>G	ENSP00000477997.3:n.*222A>G
ENST00000640140.2:n.965A>G
ENST00000640250.2:n.319A>G
ENST00000640681.2:n.924A>G
ENST00000696723.1:n.4453A>G
ENST00000696741.1:n.2458A>G
ENST00000696742.1:n.2185A>G
ENST00000696743.1:n.3588A>G
ENST00000696744.1:n.859A>G
ENST00000696767.1:n.1154A>G
ENST00000696768.1:c.*143A>G	ENSP00000512859.1:n.*143A>G
ENST00000696769.1:n.2509A>G
ENST00000696771.1:c.103A>G	ENSP00000512860.1:p.Lys35Glu
ENST00000696772.1:n.2423A>G
ENST00000696773.1:n.2162A>G
ENST00000696774.1:n.5930A>G
ENST00000696776.1:c.913A>G	ENSP00000512861.1:p.Lys305Glu
ENST00000696777.1:n.2228A>G
ENST00000696778.1:n.1256A>G
ENST00000696779.1:c.427A>G	ENSP00000512862.1:p.Lys143Glu
ENST00000696780.1:c.850A>G	ENSP00000512863.1:p.Lys284Glu
ENST00000696781.1:c.565A>G	ENSP00000512864.1:p.Lys189Glu
ENST00000696782.1:c.*222A>G	ENSP00000512865.1:n.*222A>G
ENST00000696783.1:n.2688A>G
ENST00000696992.1:n.1937A>G
ENST00000696995.1:n.4349A>G
ENST00000696996.1:n.2262A>G
ENST00000696997.1:c.*450A>G	ENSP00000513028.1:n.*450A>G
ENST00000696998.1:n.2074A>G
ENST00000696999.1:c.103A>G	ENSP00000513029.1:p.Lys35Glu
ENST00000697035.1:c.*153A>G	ENSP00000513059.1:n.*153A>G
ENST00000697036.1:c.*236A>G	ENSP00000513060.1:n.*236A>G
ENST00000697037.1:n.855A>G
ENST00000697093.1:n.3056A>G
ENST00000697094.1:n.3403A>G
ENST00000697095.1:c.*2021A>G	ENSP00000513104.1:n.*2021A>G
ENST00000697096.1:n.1953A>G
ENST00000697097.1:c.103A>G	ENSP00000513105.1:p.Lys35Glu
ENST00000562983.2:n.1006A>G
ENST00000690268.1:c.901A>G	ENSP00000509810.1:p.Lys301Glu
ENST00000355740.7:c.*146A>G	ENSP00000347979.3:n.*146A>G
ENST00000612663.5:c.*222A>G	ENSP00000477997.3:n.*222A>G
ENST00000640140.1:n.992A>G
ENST00000640250.1:n.319A>G
ENST00000640681.1:n.941A>G
ENST00000652046.1:c.820A>G MANE Select	ENSP00000498466.1:p.Lys274Glu
ENST00000352159.8:c.*137A>G	ENSP00000345601.4:n.*137A>G
ENST00000355279.2:c.795A>G	ENSP00000347426.2:n.795A>G
ENST00000355740.6:c.820A>G	ENSP00000347979.2:p.Lys274Glu
ENST00000357339.6:c.757A>G	ENSP00000349896.2:p.Lys253Glu
ENST00000479522.5:c.*249A>G	ENSP00000424113.1:n.*249A>G
ENST00000484444.5:c.*261A>G	ENSP00000420975.1:n.*261A>G
ENST00000488877.5:c.*261A>G	ENSP00000425159.1:n.*261A>G
ENST00000492756.5:c.648A>G	ENSP00000422453.1:n.648A>G
ENST00000494410.5:c.*178A>G	ENSP00000423755.1:n.*178A>G
ENST00000612663.4:c.*167A>G	ENSP00000477997.2:n.*167A>G
NM_000043.4:c.820A>G , LRG_134t1:c.820A>G	NP_000034.1:p.Lys274Glu
NM_152871.2:c.757A>G	NP_690610.1:p.Lys253Glu
NM_152872.2:c.*132A>G	NP_690611.1:n.*132A>G
NR_028033.2:n.994A>G
NR_028034.2:n.856A>G
NR_028035.2:n.919A>G
NR_028036.2:n.1057A>G
XM_006717819.2:c.901A>G	XP_006717882.1:p.Lys301Glu
XM_011539764.1:c.982A>G	XP_011538066.1:p.Lys328Glu
XM_011539765.1:c.919A>G	XP_011538067.1:p.Lys307Glu
XM_011539766.1:c.901A>G	XP_011538068.1:p.Lys301Glu
XM_011539767.1:c.865A>G	XP_011538069.1:p.Lys289Glu
XR_945732.1:n.888A>G
XR_945733.1:n.825A>G
NM_000043.5:c.820A>G	NP_000034.1:p.Lys274Glu
NM_001320619.1:c.*143A>G	NP_001307548.1:n.*143A>G
NM_152871.3:c.757A>G	NP_690610.1:p.Lys253Glu
NM_152872.3:c.*132A>G	NP_690611.1:n.*132A>G
NR_028033.3:n.966A>G
NR_028034.3:n.828A>G
NR_028035.3:n.891A>G
NR_028036.3:n.1029A>G
NR_135313.1:n.946A>G
NR_135314.1:n.1129A>G
NR_135315.1:n.882A>G
XM_006717819.3:c.901A>G	XP_006717882.1:p.Lys301Glu
XM_011539764.2:c.982A>G	XP_011538066.1:p.Lys328Glu
XM_011539765.2:c.919A>G	XP_011538067.1:p.Lys307Glu
XM_011539766.2:c.901A>G	XP_011538068.1:p.Lys301Glu
XM_011539767.3:c.865A>G	XP_011538069.1:p.Lys289Glu
XR_945732.3:n.888A>G
XR_945733.2:n.825A>G
NM_000043.6:c.820A>G MANE Select	NP_000034.1:p.Lys274Glu
NM_001320619.2:c.*143A>G	NP_001307548.1:n.*143A>G
NM_152871.4:c.757A>G	NP_690610.1:p.Lys253Glu
NM_152872.4:c.*132A>G	NP_690611.1:n.*132A>G
NR_028033.4:n.727A>G
NR_028034.4:n.589A>G
NR_028035.4:n.652A>G
NR_028036.4:n.790A>G
NR_135313.2:n.707A>G
NR_135314.2:n.986A>G
NR_135315.2:n.739A>G