Canonical Allele Identifier: CA470974980

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773976A>T (hg19)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1086A>T
ENST00000355740.8:c.*100A>T	ENSP00000347979.3:n.*100A>T
ENST00000357339.7:c.714A>T	ENSP00000349896.2:p.Ile238=
ENST00000371857.8:n.2322A>T
ENST00000460510.6:c.60A>T	ENSP00000512812.1:p.Ile20=
ENST00000466081.6:n.2426A>T
ENST00000477270.6:c.822A>T	ENSP00000512813.1:p.Ile274=
ENST00000479522.6:c.*206A>T	ENSP00000424113.1:n.*206A>T
ENST00000484444.6:c.*218A>T	ENSP00000420975.1:n.*218A>T
ENST00000488877.6:c.668A>T	ENSP00000425159.1:n.668A>T
ENST00000492756.7:c.*206A>T	ENSP00000422453.1:n.*206A>T
ENST00000494799.6:c.60A>T	ENSP00000512834.1:p.Ile20=
ENST00000562983.3:c.60A>T	ENSP00000512845.1:p.Ile20=
ENST00000612663.6:c.*179A>T	ENSP00000477997.3:n.*179A>T
ENST00000640140.2:n.922A>T
ENST00000640250.2:n.276A>T
ENST00000640681.2:n.881A>T
ENST00000696723.1:n.4410A>T
ENST00000696741.1:n.2415A>T
ENST00000696742.1:n.2142A>T
ENST00000696743.1:n.3545A>T
ENST00000696744.1:n.816A>T
ENST00000696767.1:n.1111A>T
ENST00000696768.1:c.*100A>T	ENSP00000512859.1:n.*100A>T
ENST00000696769.1:n.2466A>T
ENST00000696771.1:c.60A>T	ENSP00000512860.1:p.Ile20=
ENST00000696772.1:n.2380A>T
ENST00000696773.1:n.2119A>T
ENST00000696774.1:n.5887A>T
ENST00000696776.1:c.870A>T	ENSP00000512861.1:p.Ile290=
ENST00000696777.1:n.2185A>T
ENST00000696778.1:n.1213A>T
ENST00000696779.1:c.384A>T	ENSP00000512862.1:p.Ile128=
ENST00000696780.1:c.807A>T	ENSP00000512863.1:p.Ile269=
ENST00000696781.1:c.522A>T	ENSP00000512864.1:p.Ile174=
ENST00000696782.1:c.*179A>T	ENSP00000512865.1:n.*179A>T
ENST00000696783.1:n.2645A>T
ENST00000696992.1:n.1894A>T
ENST00000696995.1:n.4306A>T
ENST00000696996.1:n.2219A>T
ENST00000696997.1:c.*407A>T	ENSP00000513028.1:n.*407A>T
ENST00000696998.1:n.2031A>T
ENST00000696999.1:c.60A>T	ENSP00000513029.1:p.Ile20=
ENST00000697035.1:c.*110A>T	ENSP00000513059.1:n.*110A>T
ENST00000697036.1:c.*193A>T	ENSP00000513060.1:n.*193A>T
ENST00000697037.1:n.812A>T
ENST00000697093.1:n.3013A>T
ENST00000697094.1:n.3360A>T
ENST00000697095.1:c.*1978A>T	ENSP00000513104.1:n.*1978A>T
ENST00000697096.1:n.1910A>T
ENST00000697097.1:c.60A>T	ENSP00000513105.1:p.Ile20=
ENST00000562983.2:n.963A>T
ENST00000690268.1:c.858A>T	ENSP00000509810.1:p.Ile286=
ENST00000355740.7:c.*103A>T	ENSP00000347979.3:n.*103A>T
ENST00000612663.5:c.*179A>T	ENSP00000477997.3:n.*179A>T
ENST00000640140.1:n.949A>T
ENST00000640250.1:n.276A>T
ENST00000640681.1:n.898A>T
ENST00000652046.1:c.777A>T MANE Select	ENSP00000498466.1:p.Ile259=
ENST00000352159.8:c.*94A>T	ENSP00000345601.4:n.*94A>T
ENST00000355279.2:c.752A>T	ENSP00000347426.2:n.752A>T
ENST00000355740.6:c.777A>T	ENSP00000347979.2:p.Ile259=
ENST00000357339.6:c.714A>T	ENSP00000349896.2:p.Ile238=
ENST00000479522.5:c.*206A>T	ENSP00000424113.1:n.*206A>T
ENST00000484444.5:c.*218A>T	ENSP00000420975.1:n.*218A>T
ENST00000488877.5:c.*218A>T	ENSP00000425159.1:n.*218A>T
ENST00000492756.5:c.605A>T	ENSP00000422453.1:n.605A>T
ENST00000494410.5:c.*135A>T	ENSP00000423755.1:n.*135A>T
ENST00000612663.4:c.*124A>T	ENSP00000477997.2:n.*124A>T
NM_000043.4:c.777A>T , LRG_134t1:c.777A>T	NP_000034.1:p.Ile259=
NM_152871.2:c.714A>T	NP_690610.1:p.Ile238=
NM_152872.2:c.*89A>T	NP_690611.1:n.*89A>T
NR_028033.2:n.951A>T
NR_028034.2:n.813A>T
NR_028035.2:n.876A>T
NR_028036.2:n.1014A>T
XM_006717819.2:c.858A>T	XP_006717882.1:p.Ile286=
XM_011539764.1:c.939A>T	XP_011538066.1:p.Ile313=
XM_011539765.1:c.876A>T	XP_011538067.1:p.Ile292=
XM_011539766.1:c.858A>T	XP_011538068.1:p.Ile286=
XM_011539767.1:c.822A>T	XP_011538069.1:p.Ile274=
XR_945732.1:n.845A>T
XR_945733.1:n.782A>T
NM_000043.5:c.777A>T	NP_000034.1:p.Ile259=
NM_001320619.1:c.*100A>T	NP_001307548.1:n.*100A>T
NM_152871.3:c.714A>T	NP_690610.1:p.Ile238=
NM_152872.3:c.*89A>T	NP_690611.1:n.*89A>T
NR_028033.3:n.923A>T
NR_028034.3:n.785A>T
NR_028035.3:n.848A>T
NR_028036.3:n.986A>T
NR_135313.1:n.903A>T
NR_135314.1:n.1086A>T
NR_135315.1:n.839A>T
XM_006717819.3:c.858A>T	XP_006717882.1:p.Ile286=
XM_011539764.2:c.939A>T	XP_011538066.1:p.Ile313=
XM_011539765.2:c.876A>T	XP_011538067.1:p.Ile292=
XM_011539766.2:c.858A>T	XP_011538068.1:p.Ile286=
XM_011539767.3:c.822A>T	XP_011538069.1:p.Ile274=
XR_945732.3:n.845A>T
XR_945733.2:n.782A>T
NM_000043.6:c.777A>T MANE Select	NP_000034.1:p.Ile259=
NM_001320619.2:c.*100A>T	NP_001307548.1:n.*100A>T
NM_152871.4:c.714A>T	NP_690610.1:p.Ile238=
NM_152872.4:c.*89A>T	NP_690611.1:n.*89A>T
NR_028033.4:n.684A>T
NR_028034.4:n.546A>T
NR_028035.4:n.609A>T
NR_028036.4:n.747A>T
NR_135313.2:n.664A>T
NR_135314.2:n.943A>T
NR_135315.2:n.696A>T