Canonical Allele Identifier: CA377509804

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773983A>T (hg19) ; chr10:g.89014226A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014226A>T , CM000672.2:g.89014226A>T	GRCh38
NC_000010.10:g.90773983A>T , CM000672.1:g.90773983A>T	GRCh37
NC_000010.9:g.90763963A>T	NCBI36
NG_009089.2:g.28696A>T , LRG_134:g.28696A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1093A>T
ENST00000355740.8:c.*107A>T	ENSP00000347979.3:n.*107A>T
ENST00000357339.7:c.721A>T	ENSP00000349896.2:p.Ile241Phe
ENST00000371857.8:n.2329A>T
ENST00000460510.6:c.67A>T	ENSP00000512812.1:p.Ile23Phe
ENST00000466081.6:n.2433A>T
ENST00000477270.6:c.829A>T	ENSP00000512813.1:p.Ile277Phe
ENST00000479522.6:c.*213A>T	ENSP00000424113.1:n.*213A>T
ENST00000484444.6:c.*225A>T	ENSP00000420975.1:n.*225A>T
ENST00000488877.6:c.675A>T	ENSP00000425159.1:n.675A>T
ENST00000492756.7:c.*213A>T	ENSP00000422453.1:n.*213A>T
ENST00000494799.6:c.67A>T	ENSP00000512834.1:p.Ile23Phe
ENST00000562983.3:c.67A>T	ENSP00000512845.1:p.Ile23Phe
ENST00000612663.6:c.*186A>T	ENSP00000477997.3:n.*186A>T
ENST00000640140.2:n.929A>T
ENST00000640250.2:n.283A>T
ENST00000640681.2:n.888A>T
ENST00000696723.1:n.4417A>T
ENST00000696741.1:n.2422A>T
ENST00000696742.1:n.2149A>T
ENST00000696743.1:n.3552A>T
ENST00000696744.1:n.823A>T
ENST00000696767.1:n.1118A>T
ENST00000696768.1:c.*107A>T	ENSP00000512859.1:n.*107A>T
ENST00000696769.1:n.2473A>T
ENST00000696771.1:c.67A>T	ENSP00000512860.1:p.Ile23Phe
ENST00000696772.1:n.2387A>T
ENST00000696773.1:n.2126A>T
ENST00000696774.1:n.5894A>T
ENST00000696776.1:c.877A>T	ENSP00000512861.1:p.Ile293Phe
ENST00000696777.1:n.2192A>T
ENST00000696778.1:n.1220A>T
ENST00000696779.1:c.391A>T	ENSP00000512862.1:p.Ile131Phe
ENST00000696780.1:c.814A>T	ENSP00000512863.1:p.Ile272Phe
ENST00000696781.1:c.529A>T	ENSP00000512864.1:p.Ile177Phe
ENST00000696782.1:c.*186A>T	ENSP00000512865.1:n.*186A>T
ENST00000696783.1:n.2652A>T
ENST00000696992.1:n.1901A>T
ENST00000696995.1:n.4313A>T
ENST00000696996.1:n.2226A>T
ENST00000696997.1:c.*414A>T	ENSP00000513028.1:n.*414A>T
ENST00000696998.1:n.2038A>T
ENST00000696999.1:c.67A>T	ENSP00000513029.1:p.Ile23Phe
ENST00000697035.1:c.*117A>T	ENSP00000513059.1:n.*117A>T
ENST00000697036.1:c.*200A>T	ENSP00000513060.1:n.*200A>T
ENST00000697037.1:n.819A>T
ENST00000697093.1:n.3020A>T
ENST00000697094.1:n.3367A>T
ENST00000697095.1:c.*1985A>T	ENSP00000513104.1:n.*1985A>T
ENST00000697096.1:n.1917A>T
ENST00000697097.1:c.67A>T	ENSP00000513105.1:p.Ile23Phe
ENST00000562983.2:n.970A>T
ENST00000690268.1:c.865A>T	ENSP00000509810.1:p.Ile289Phe
ENST00000355740.7:c.*110A>T	ENSP00000347979.3:n.*110A>T
ENST00000612663.5:c.*186A>T	ENSP00000477997.3:n.*186A>T
ENST00000640140.1:n.956A>T
ENST00000640250.1:n.283A>T
ENST00000640681.1:n.905A>T
ENST00000652046.1:c.784A>T MANE Select	ENSP00000498466.1:p.Ile262Phe
ENST00000352159.8:c.*101A>T	ENSP00000345601.4:n.*101A>T
ENST00000355279.2:c.759A>T	ENSP00000347426.2:n.759A>T
ENST00000355740.6:c.784A>T	ENSP00000347979.2:p.Ile262Phe
ENST00000357339.6:c.721A>T	ENSP00000349896.2:p.Ile241Phe
ENST00000479522.5:c.*213A>T	ENSP00000424113.1:n.*213A>T
ENST00000484444.5:c.*225A>T	ENSP00000420975.1:n.*225A>T
ENST00000488877.5:c.*225A>T	ENSP00000425159.1:n.*225A>T
ENST00000492756.5:c.612A>T	ENSP00000422453.1:n.612A>T
ENST00000494410.5:c.*142A>T	ENSP00000423755.1:n.*142A>T
ENST00000612663.4:c.*131A>T	ENSP00000477997.2:n.*131A>T
NM_000043.4:c.784A>T , LRG_134t1:c.784A>T	NP_000034.1:p.Ile262Phe
NM_152871.2:c.721A>T	NP_690610.1:p.Ile241Phe
NM_152872.2:c.*96A>T	NP_690611.1:n.*96A>T
NR_028033.2:n.958A>T
NR_028034.2:n.820A>T
NR_028035.2:n.883A>T
NR_028036.2:n.1021A>T
XM_006717819.2:c.865A>T	XP_006717882.1:p.Ile289Phe
XM_011539764.1:c.946A>T	XP_011538066.1:p.Ile316Phe
XM_011539765.1:c.883A>T	XP_011538067.1:p.Ile295Phe
XM_011539766.1:c.865A>T	XP_011538068.1:p.Ile289Phe
XM_011539767.1:c.829A>T	XP_011538069.1:p.Ile277Phe
XR_945732.1:n.852A>T
XR_945733.1:n.789A>T
NM_000043.5:c.784A>T	NP_000034.1:p.Ile262Phe
NM_001320619.1:c.*107A>T	NP_001307548.1:n.*107A>T
NM_152871.3:c.721A>T	NP_690610.1:p.Ile241Phe
NM_152872.3:c.*96A>T	NP_690611.1:n.*96A>T
NR_028033.3:n.930A>T
NR_028034.3:n.792A>T
NR_028035.3:n.855A>T
NR_028036.3:n.993A>T
NR_135313.1:n.910A>T
NR_135314.1:n.1093A>T
NR_135315.1:n.846A>T
XM_006717819.3:c.865A>T	XP_006717882.1:p.Ile289Phe
XM_011539764.2:c.946A>T	XP_011538066.1:p.Ile316Phe
XM_011539765.2:c.883A>T	XP_011538067.1:p.Ile295Phe
XM_011539766.2:c.865A>T	XP_011538068.1:p.Ile289Phe
XM_011539767.3:c.829A>T	XP_011538069.1:p.Ile277Phe
XR_945732.3:n.852A>T
XR_945733.2:n.789A>T
NM_000043.6:c.784A>T MANE Select	NP_000034.1:p.Ile262Phe
NM_001320619.2:c.*107A>T	NP_001307548.1:n.*107A>T
NM_152871.4:c.721A>T	NP_690610.1:p.Ile241Phe
NM_152872.4:c.*96A>T	NP_690611.1:n.*96A>T
NR_028033.4:n.691A>T
NR_028034.4:n.553A>T
NR_028035.4:n.616A>T
NR_028036.4:n.754A>T
NR_135313.2:n.671A>T
NR_135314.2:n.950A>T
NR_135315.2:n.703A>T