Canonical Allele Identifier: CA377509787

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773976A>G (hg19) ; chr10:g.89014219A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014219A>G , CM000672.2:g.89014219A>G	GRCh38
NC_000010.10:g.90773976A>G , CM000672.1:g.90773976A>G	GRCh37
NC_000010.9:g.90763956A>G	NCBI36
NG_009089.2:g.28689A>G , LRG_134:g.28689A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1086A>G
ENST00000355740.8:c.*100A>G	ENSP00000347979.3:n.*100A>G
ENST00000357339.7:c.714A>G	ENSP00000349896.2:p.Ile238Met
ENST00000371857.8:n.2322A>G
ENST00000460510.6:c.60A>G	ENSP00000512812.1:p.Ile20Met
ENST00000466081.6:n.2426A>G
ENST00000477270.6:c.822A>G	ENSP00000512813.1:p.Ile274Met
ENST00000479522.6:c.*206A>G	ENSP00000424113.1:n.*206A>G
ENST00000484444.6:c.*218A>G	ENSP00000420975.1:n.*218A>G
ENST00000488877.6:c.668A>G	ENSP00000425159.1:n.668A>G
ENST00000492756.7:c.*206A>G	ENSP00000422453.1:n.*206A>G
ENST00000494799.6:c.60A>G	ENSP00000512834.1:p.Ile20Met
ENST00000562983.3:c.60A>G	ENSP00000512845.1:p.Ile20Met
ENST00000612663.6:c.*179A>G	ENSP00000477997.3:n.*179A>G
ENST00000640140.2:n.922A>G
ENST00000640250.2:n.276A>G
ENST00000640681.2:n.881A>G
ENST00000696723.1:n.4410A>G
ENST00000696741.1:n.2415A>G
ENST00000696742.1:n.2142A>G
ENST00000696743.1:n.3545A>G
ENST00000696744.1:n.816A>G
ENST00000696767.1:n.1111A>G
ENST00000696768.1:c.*100A>G	ENSP00000512859.1:n.*100A>G
ENST00000696769.1:n.2466A>G
ENST00000696771.1:c.60A>G	ENSP00000512860.1:p.Ile20Met
ENST00000696772.1:n.2380A>G
ENST00000696773.1:n.2119A>G
ENST00000696774.1:n.5887A>G
ENST00000696776.1:c.870A>G	ENSP00000512861.1:p.Ile290Met
ENST00000696777.1:n.2185A>G
ENST00000696778.1:n.1213A>G
ENST00000696779.1:c.384A>G	ENSP00000512862.1:p.Ile128Met
ENST00000696780.1:c.807A>G	ENSP00000512863.1:p.Ile269Met
ENST00000696781.1:c.522A>G	ENSP00000512864.1:p.Ile174Met
ENST00000696782.1:c.*179A>G	ENSP00000512865.1:n.*179A>G
ENST00000696783.1:n.2645A>G
ENST00000696992.1:n.1894A>G
ENST00000696995.1:n.4306A>G
ENST00000696996.1:n.2219A>G
ENST00000696997.1:c.*407A>G	ENSP00000513028.1:n.*407A>G
ENST00000696998.1:n.2031A>G
ENST00000696999.1:c.60A>G	ENSP00000513029.1:p.Ile20Met
ENST00000697035.1:c.*110A>G	ENSP00000513059.1:n.*110A>G
ENST00000697036.1:c.*193A>G	ENSP00000513060.1:n.*193A>G
ENST00000697037.1:n.812A>G
ENST00000697093.1:n.3013A>G
ENST00000697094.1:n.3360A>G
ENST00000697095.1:c.*1978A>G	ENSP00000513104.1:n.*1978A>G
ENST00000697096.1:n.1910A>G
ENST00000697097.1:c.60A>G	ENSP00000513105.1:p.Ile20Met
ENST00000562983.2:n.963A>G
ENST00000690268.1:c.858A>G	ENSP00000509810.1:p.Ile286Met
ENST00000355740.7:c.*103A>G	ENSP00000347979.3:n.*103A>G
ENST00000612663.5:c.*179A>G	ENSP00000477997.3:n.*179A>G
ENST00000640140.1:n.949A>G
ENST00000640250.1:n.276A>G
ENST00000640681.1:n.898A>G
ENST00000652046.1:c.777A>G MANE Select	ENSP00000498466.1:p.Ile259Met
ENST00000352159.8:c.*94A>G	ENSP00000345601.4:n.*94A>G
ENST00000355279.2:c.752A>G	ENSP00000347426.2:n.752A>G
ENST00000355740.6:c.777A>G	ENSP00000347979.2:p.Ile259Met
ENST00000357339.6:c.714A>G	ENSP00000349896.2:p.Ile238Met
ENST00000479522.5:c.*206A>G	ENSP00000424113.1:n.*206A>G
ENST00000484444.5:c.*218A>G	ENSP00000420975.1:n.*218A>G
ENST00000488877.5:c.*218A>G	ENSP00000425159.1:n.*218A>G
ENST00000492756.5:c.605A>G	ENSP00000422453.1:n.605A>G
ENST00000494410.5:c.*135A>G	ENSP00000423755.1:n.*135A>G
ENST00000612663.4:c.*124A>G	ENSP00000477997.2:n.*124A>G
NM_000043.4:c.777A>G , LRG_134t1:c.777A>G	NP_000034.1:p.Ile259Met
NM_152871.2:c.714A>G	NP_690610.1:p.Ile238Met
NM_152872.2:c.*89A>G	NP_690611.1:n.*89A>G
NR_028033.2:n.951A>G
NR_028034.2:n.813A>G
NR_028035.2:n.876A>G
NR_028036.2:n.1014A>G
XM_006717819.2:c.858A>G	XP_006717882.1:p.Ile286Met
XM_011539764.1:c.939A>G	XP_011538066.1:p.Ile313Met
XM_011539765.1:c.876A>G	XP_011538067.1:p.Ile292Met
XM_011539766.1:c.858A>G	XP_011538068.1:p.Ile286Met
XM_011539767.1:c.822A>G	XP_011538069.1:p.Ile274Met
XR_945732.1:n.845A>G
XR_945733.1:n.782A>G
NM_000043.5:c.777A>G	NP_000034.1:p.Ile259Met
NM_001320619.1:c.*100A>G	NP_001307548.1:n.*100A>G
NM_152871.3:c.714A>G	NP_690610.1:p.Ile238Met
NM_152872.3:c.*89A>G	NP_690611.1:n.*89A>G
NR_028033.3:n.923A>G
NR_028034.3:n.785A>G
NR_028035.3:n.848A>G
NR_028036.3:n.986A>G
NR_135313.1:n.903A>G
NR_135314.1:n.1086A>G
NR_135315.1:n.839A>G
XM_006717819.3:c.858A>G	XP_006717882.1:p.Ile286Met
XM_011539764.2:c.939A>G	XP_011538066.1:p.Ile313Met
XM_011539765.2:c.876A>G	XP_011538067.1:p.Ile292Met
XM_011539766.2:c.858A>G	XP_011538068.1:p.Ile286Met
XM_011539767.3:c.822A>G	XP_011538069.1:p.Ile274Met
XR_945732.3:n.845A>G
XR_945733.2:n.782A>G
NM_000043.6:c.777A>G MANE Select	NP_000034.1:p.Ile259Met
NM_001320619.2:c.*100A>G	NP_001307548.1:n.*100A>G
NM_152871.4:c.714A>G	NP_690610.1:p.Ile238Met
NM_152872.4:c.*89A>G	NP_690611.1:n.*89A>G
NR_028033.4:n.684A>G
NR_028034.4:n.546A>G
NR_028035.4:n.609A>G
NR_028036.4:n.747A>G
NR_135313.2:n.664A>G
NR_135314.2:n.943A>G
NR_135315.2:n.696A>G