Canonical Allele Identifier: CA377509943

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774044A>T (hg19) ; chr10:g.89014287A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014287A>T , CM000672.2:g.89014287A>T	GRCh38
NC_000010.10:g.90774044A>T , CM000672.1:g.90774044A>T	GRCh37
NC_000010.9:g.90764024A>T	NCBI36
NG_009089.2:g.28757A>T , LRG_134:g.28757A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1154A>T
ENST00000355740.8:c.*168A>T	ENSP00000347979.3:n.*168A>T
ENST00000357339.7:c.782A>T	ENSP00000349896.2:p.His261Leu
ENST00000371857.8:n.2390A>T
ENST00000460510.6:c.128A>T	ENSP00000512812.1:p.His43Leu
ENST00000466081.6:n.2494A>T
ENST00000477270.6:c.890A>T	ENSP00000512813.1:p.His297Leu
ENST00000479522.6:c.*274A>T	ENSP00000424113.1:n.*274A>T
ENST00000484444.6:c.*286A>T	ENSP00000420975.1:n.*286A>T
ENST00000488877.6:c.736A>T	ENSP00000425159.1:n.736A>T
ENST00000492756.7:c.*274A>T	ENSP00000422453.1:n.*274A>T
ENST00000494799.6:c.128A>T	ENSP00000512834.1:p.His43Leu
ENST00000562983.3:c.128A>T	ENSP00000512845.1:p.His43Leu
ENST00000612663.6:c.*247A>T	ENSP00000477997.3:n.*247A>T
ENST00000640140.2:n.990A>T
ENST00000640250.2:n.344A>T
ENST00000640681.2:n.949A>T
ENST00000696723.1:n.4478A>T
ENST00000696741.1:n.2483A>T
ENST00000696742.1:n.2210A>T
ENST00000696743.1:n.3613A>T
ENST00000696744.1:n.884A>T
ENST00000696767.1:n.1179A>T
ENST00000696768.1:c.*168A>T	ENSP00000512859.1:n.*168A>T
ENST00000696769.1:n.2534A>T
ENST00000696771.1:c.128A>T	ENSP00000512860.1:p.His43Leu
ENST00000696772.1:n.2448A>T
ENST00000696773.1:n.2187A>T
ENST00000696774.1:n.5955A>T
ENST00000696776.1:c.938A>T	ENSP00000512861.1:p.His313Leu
ENST00000696777.1:n.2253A>T
ENST00000696778.1:n.1281A>T
ENST00000696779.1:c.452A>T	ENSP00000512862.1:p.His151Leu
ENST00000696780.1:c.875A>T	ENSP00000512863.1:p.His292Leu
ENST00000696781.1:c.590A>T	ENSP00000512864.1:p.His197Leu
ENST00000696782.1:c.*247A>T	ENSP00000512865.1:n.*247A>T
ENST00000696783.1:n.2713A>T
ENST00000696992.1:n.1962A>T
ENST00000696995.1:n.4374A>T
ENST00000696996.1:n.2287A>T
ENST00000696997.1:c.*475A>T	ENSP00000513028.1:n.*475A>T
ENST00000696998.1:n.2099A>T
ENST00000696999.1:c.128A>T	ENSP00000513029.1:p.His43Leu
ENST00000697035.1:c.*178A>T	ENSP00000513059.1:n.*178A>T
ENST00000697036.1:c.*261A>T	ENSP00000513060.1:n.*261A>T
ENST00000697037.1:n.880A>T
ENST00000697093.1:n.3081A>T
ENST00000697094.1:n.3428A>T
ENST00000697095.1:c.*2046A>T	ENSP00000513104.1:n.*2046A>T
ENST00000697096.1:n.1978A>T
ENST00000697097.1:c.128A>T	ENSP00000513105.1:p.His43Leu
ENST00000562983.2:n.1031A>T
ENST00000690268.1:c.926A>T	ENSP00000509810.1:p.His309Leu
ENST00000355740.7:c.*171A>T	ENSP00000347979.3:n.*171A>T
ENST00000612663.5:c.*247A>T	ENSP00000477997.3:n.*247A>T
ENST00000640140.1:n.1017A>T
ENST00000640250.1:n.344A>T
ENST00000640681.1:n.966A>T
ENST00000652046.1:c.845A>T MANE Select	ENSP00000498466.1:p.His282Leu
ENST00000352159.8:c.*162A>T	ENSP00000345601.4:n.*162A>T
ENST00000355279.2:c.820A>T	ENSP00000347426.2:n.820A>T
ENST00000355740.6:c.845A>T	ENSP00000347979.2:p.His282Leu
ENST00000357339.6:c.782A>T	ENSP00000349896.2:p.His261Leu
ENST00000479522.5:c.*274A>T	ENSP00000424113.1:n.*274A>T
ENST00000484444.5:c.*286A>T	ENSP00000420975.1:n.*286A>T
ENST00000488877.5:c.*286A>T	ENSP00000425159.1:n.*286A>T
ENST00000492756.5:c.673A>T	ENSP00000422453.1:n.673A>T
ENST00000494410.5:c.*203A>T	ENSP00000423755.1:n.*203A>T
ENST00000612663.4:c.*192A>T	ENSP00000477997.2:n.*192A>T
NM_000043.4:c.845A>T , LRG_134t1:c.845A>T	NP_000034.1:p.His282Leu
NM_152871.2:c.782A>T	NP_690610.1:p.His261Leu
NM_152872.2:c.*157A>T	NP_690611.1:n.*157A>T
NR_028033.2:n.1019A>T
NR_028034.2:n.881A>T
NR_028035.2:n.944A>T
NR_028036.2:n.1082A>T
XM_006717819.2:c.926A>T	XP_006717882.1:p.His309Leu
XM_011539764.1:c.1007A>T	XP_011538066.1:p.His336Leu
XM_011539765.1:c.944A>T	XP_011538067.1:p.His315Leu
XM_011539766.1:c.926A>T	XP_011538068.1:p.His309Leu
XM_011539767.1:c.890A>T	XP_011538069.1:p.His297Leu
XR_945732.1:n.913A>T
XR_945733.1:n.850A>T
NM_000043.5:c.845A>T	NP_000034.1:p.His282Leu
NM_001320619.1:c.*168A>T	NP_001307548.1:n.*168A>T
NM_152871.3:c.782A>T	NP_690610.1:p.His261Leu
NM_152872.3:c.*157A>T	NP_690611.1:n.*157A>T
NR_028033.3:n.991A>T
NR_028034.3:n.853A>T
NR_028035.3:n.916A>T
NR_028036.3:n.1054A>T
NR_135313.1:n.971A>T
NR_135314.1:n.1154A>T
NR_135315.1:n.907A>T
XM_006717819.3:c.926A>T	XP_006717882.1:p.His309Leu
XM_011539764.2:c.1007A>T	XP_011538066.1:p.His336Leu
XM_011539765.2:c.944A>T	XP_011538067.1:p.His315Leu
XM_011539766.2:c.926A>T	XP_011538068.1:p.His309Leu
XM_011539767.3:c.890A>T	XP_011538069.1:p.His297Leu
XR_945732.3:n.913A>T
XR_945733.2:n.850A>T
NM_000043.6:c.845A>T MANE Select	NP_000034.1:p.His282Leu
NM_001320619.2:c.*168A>T	NP_001307548.1:n.*168A>T
NM_152871.4:c.782A>T	NP_690610.1:p.His261Leu
NM_152872.4:c.*157A>T	NP_690611.1:n.*157A>T
NR_028033.4:n.752A>T
NR_028034.4:n.614A>T
NR_028035.4:n.677A>T
NR_028036.4:n.815A>T
NR_135313.2:n.732A>T
NR_135314.2:n.1011A>T
NR_135315.2:n.764A>T