Canonical Allele Identifier: CA377509877

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774015A>T (hg19) ; chr10:g.89014258A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014258A>T , CM000672.2:g.89014258A>T	GRCh38
NC_000010.10:g.90774015A>T , CM000672.1:g.90774015A>T	GRCh37
NC_000010.9:g.90763995A>T	NCBI36
NG_009089.2:g.28728A>T , LRG_134:g.28728A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1125A>T
ENST00000355740.8:c.*139A>T	ENSP00000347979.3:n.*139A>T
ENST00000357339.7:c.753A>T	ENSP00000349896.2:p.Glu251Asp
ENST00000371857.8:n.2361A>T
ENST00000460510.6:c.99A>T	ENSP00000512812.1:p.Glu33Asp
ENST00000466081.6:n.2465A>T
ENST00000477270.6:c.861A>T	ENSP00000512813.1:p.Glu287Asp
ENST00000479522.6:c.*245A>T	ENSP00000424113.1:n.*245A>T
ENST00000484444.6:c.*257A>T	ENSP00000420975.1:n.*257A>T
ENST00000488877.6:c.707A>T	ENSP00000425159.1:n.707A>T
ENST00000492756.7:c.*245A>T	ENSP00000422453.1:n.*245A>T
ENST00000494799.6:c.99A>T	ENSP00000512834.1:p.Glu33Asp
ENST00000562983.3:c.99A>T	ENSP00000512845.1:p.Glu33Asp
ENST00000612663.6:c.*218A>T	ENSP00000477997.3:n.*218A>T
ENST00000640140.2:n.961A>T
ENST00000640250.2:n.315A>T
ENST00000640681.2:n.920A>T
ENST00000696723.1:n.4449A>T
ENST00000696741.1:n.2454A>T
ENST00000696742.1:n.2181A>T
ENST00000696743.1:n.3584A>T
ENST00000696744.1:n.855A>T
ENST00000696767.1:n.1150A>T
ENST00000696768.1:c.*139A>T	ENSP00000512859.1:n.*139A>T
ENST00000696769.1:n.2505A>T
ENST00000696771.1:c.99A>T	ENSP00000512860.1:p.Glu33Asp
ENST00000696772.1:n.2419A>T
ENST00000696773.1:n.2158A>T
ENST00000696774.1:n.5926A>T
ENST00000696776.1:c.909A>T	ENSP00000512861.1:p.Glu303Asp
ENST00000696777.1:n.2224A>T
ENST00000696778.1:n.1252A>T
ENST00000696779.1:c.423A>T	ENSP00000512862.1:p.Glu141Asp
ENST00000696780.1:c.846A>T	ENSP00000512863.1:p.Glu282Asp
ENST00000696781.1:c.561A>T	ENSP00000512864.1:p.Glu187Asp
ENST00000696782.1:c.*218A>T	ENSP00000512865.1:n.*218A>T
ENST00000696783.1:n.2684A>T
ENST00000696992.1:n.1933A>T
ENST00000696995.1:n.4345A>T
ENST00000696996.1:n.2258A>T
ENST00000696997.1:c.*446A>T	ENSP00000513028.1:n.*446A>T
ENST00000696998.1:n.2070A>T
ENST00000696999.1:c.99A>T	ENSP00000513029.1:p.Glu33Asp
ENST00000697035.1:c.*149A>T	ENSP00000513059.1:n.*149A>T
ENST00000697036.1:c.*232A>T	ENSP00000513060.1:n.*232A>T
ENST00000697037.1:n.851A>T
ENST00000697093.1:n.3052A>T
ENST00000697094.1:n.3399A>T
ENST00000697095.1:c.*2017A>T	ENSP00000513104.1:n.*2017A>T
ENST00000697096.1:n.1949A>T
ENST00000697097.1:c.99A>T	ENSP00000513105.1:p.Glu33Asp
ENST00000562983.2:n.1002A>T
ENST00000690268.1:c.897A>T	ENSP00000509810.1:p.Glu299Asp
ENST00000355740.7:c.*142A>T	ENSP00000347979.3:n.*142A>T
ENST00000612663.5:c.*218A>T	ENSP00000477997.3:n.*218A>T
ENST00000640140.1:n.988A>T
ENST00000640250.1:n.315A>T
ENST00000640681.1:n.937A>T
ENST00000652046.1:c.816A>T MANE Select	ENSP00000498466.1:p.Glu272Asp
ENST00000352159.8:c.*133A>T	ENSP00000345601.4:n.*133A>T
ENST00000355279.2:c.791A>T	ENSP00000347426.2:n.791A>T
ENST00000355740.6:c.816A>T	ENSP00000347979.2:p.Glu272Asp
ENST00000357339.6:c.753A>T	ENSP00000349896.2:p.Glu251Asp
ENST00000479522.5:c.*245A>T	ENSP00000424113.1:n.*245A>T
ENST00000484444.5:c.*257A>T	ENSP00000420975.1:n.*257A>T
ENST00000488877.5:c.*257A>T	ENSP00000425159.1:n.*257A>T
ENST00000492756.5:c.644A>T	ENSP00000422453.1:n.644A>T
ENST00000494410.5:c.*174A>T	ENSP00000423755.1:n.*174A>T
ENST00000612663.4:c.*163A>T	ENSP00000477997.2:n.*163A>T
NM_000043.4:c.816A>T , LRG_134t1:c.816A>T	NP_000034.1:p.Glu272Asp
NM_152871.2:c.753A>T	NP_690610.1:p.Glu251Asp
NM_152872.2:c.*128A>T	NP_690611.1:n.*128A>T
NR_028033.2:n.990A>T
NR_028034.2:n.852A>T
NR_028035.2:n.915A>T
NR_028036.2:n.1053A>T
XM_006717819.2:c.897A>T	XP_006717882.1:p.Glu299Asp
XM_011539764.1:c.978A>T	XP_011538066.1:p.Glu326Asp
XM_011539765.1:c.915A>T	XP_011538067.1:p.Glu305Asp
XM_011539766.1:c.897A>T	XP_011538068.1:p.Glu299Asp
XM_011539767.1:c.861A>T	XP_011538069.1:p.Glu287Asp
XR_945732.1:n.884A>T
XR_945733.1:n.821A>T
NM_000043.5:c.816A>T	NP_000034.1:p.Glu272Asp
NM_001320619.1:c.*139A>T	NP_001307548.1:n.*139A>T
NM_152871.3:c.753A>T	NP_690610.1:p.Glu251Asp
NM_152872.3:c.*128A>T	NP_690611.1:n.*128A>T
NR_028033.3:n.962A>T
NR_028034.3:n.824A>T
NR_028035.3:n.887A>T
NR_028036.3:n.1025A>T
NR_135313.1:n.942A>T
NR_135314.1:n.1125A>T
NR_135315.1:n.878A>T
XM_006717819.3:c.897A>T	XP_006717882.1:p.Glu299Asp
XM_011539764.2:c.978A>T	XP_011538066.1:p.Glu326Asp
XM_011539765.2:c.915A>T	XP_011538067.1:p.Glu305Asp
XM_011539766.2:c.897A>T	XP_011538068.1:p.Glu299Asp
XM_011539767.3:c.861A>T	XP_011538069.1:p.Glu287Asp
XR_945732.3:n.884A>T
XR_945733.2:n.821A>T
NM_000043.6:c.816A>T MANE Select	NP_000034.1:p.Glu272Asp
NM_001320619.2:c.*139A>T	NP_001307548.1:n.*139A>T
NM_152871.4:c.753A>T	NP_690610.1:p.Glu251Asp
NM_152872.4:c.*128A>T	NP_690611.1:n.*128A>T
NR_028033.4:n.723A>T
NR_028034.4:n.585A>T
NR_028035.4:n.648A>T
NR_028036.4:n.786A>T
NR_135313.2:n.703A>T
NR_135314.2:n.982A>T
NR_135315.2:n.735A>T