Canonical Allele Identifier: CA377509941

Gene: FAS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1154A>C
ENST00000355740.8:c.*168A>C	ENSP00000347979.3:n.*168A>C
ENST00000357339.7:c.782A>C	ENSP00000349896.2:p.His261Pro
ENST00000371857.8:n.2390A>C
ENST00000460510.6:c.128A>C	ENSP00000512812.1:p.His43Pro
ENST00000466081.6:n.2494A>C
ENST00000477270.6:c.890A>C	ENSP00000512813.1:p.His297Pro
ENST00000479522.6:c.*274A>C	ENSP00000424113.1:n.*274A>C
ENST00000484444.6:c.*286A>C	ENSP00000420975.1:n.*286A>C
ENST00000488877.6:c.736A>C	ENSP00000425159.1:n.736A>C
ENST00000492756.7:c.*274A>C	ENSP00000422453.1:n.*274A>C
ENST00000494799.6:c.128A>C	ENSP00000512834.1:p.His43Pro
ENST00000562983.3:c.128A>C	ENSP00000512845.1:p.His43Pro
ENST00000612663.6:c.*247A>C	ENSP00000477997.3:n.*247A>C
ENST00000640140.2:n.990A>C
ENST00000640250.2:n.344A>C
ENST00000640681.2:n.949A>C
ENST00000696723.1:n.4478A>C
ENST00000696741.1:n.2483A>C
ENST00000696742.1:n.2210A>C
ENST00000696743.1:n.3613A>C
ENST00000696744.1:n.884A>C
ENST00000696767.1:n.1179A>C
ENST00000696768.1:c.*168A>C	ENSP00000512859.1:n.*168A>C
ENST00000696769.1:n.2534A>C
ENST00000696771.1:c.128A>C	ENSP00000512860.1:p.His43Pro
ENST00000696772.1:n.2448A>C
ENST00000696773.1:n.2187A>C
ENST00000696774.1:n.5955A>C
ENST00000696776.1:c.938A>C	ENSP00000512861.1:p.His313Pro
ENST00000696777.1:n.2253A>C
ENST00000696778.1:n.1281A>C
ENST00000696779.1:c.452A>C	ENSP00000512862.1:p.His151Pro
ENST00000696780.1:c.875A>C	ENSP00000512863.1:p.His292Pro
ENST00000696781.1:c.590A>C	ENSP00000512864.1:p.His197Pro
ENST00000696782.1:c.*247A>C	ENSP00000512865.1:n.*247A>C
ENST00000696783.1:n.2713A>C
ENST00000696992.1:n.1962A>C
ENST00000696995.1:n.4374A>C
ENST00000696996.1:n.2287A>C
ENST00000696997.1:c.*475A>C	ENSP00000513028.1:n.*475A>C
ENST00000696998.1:n.2099A>C
ENST00000696999.1:c.128A>C	ENSP00000513029.1:p.His43Pro
ENST00000697035.1:c.*178A>C	ENSP00000513059.1:n.*178A>C
ENST00000697036.1:c.*261A>C	ENSP00000513060.1:n.*261A>C
ENST00000697037.1:n.880A>C
ENST00000697093.1:n.3081A>C
ENST00000697094.1:n.3428A>C
ENST00000697095.1:c.*2046A>C	ENSP00000513104.1:n.*2046A>C
ENST00000697096.1:n.1978A>C
ENST00000697097.1:c.128A>C	ENSP00000513105.1:p.His43Pro
ENST00000562983.2:n.1031A>C
ENST00000690268.1:c.926A>C	ENSP00000509810.1:p.His309Pro
ENST00000355740.7:c.*171A>C	ENSP00000347979.3:n.*171A>C
ENST00000612663.5:c.*247A>C	ENSP00000477997.3:n.*247A>C
ENST00000640140.1:n.1017A>C
ENST00000640250.1:n.344A>C
ENST00000640681.1:n.966A>C
ENST00000652046.1:c.845A>C MANE Select	ENSP00000498466.1:p.His282Pro
ENST00000352159.8:c.*162A>C	ENSP00000345601.4:n.*162A>C
ENST00000355279.2:c.820A>C	ENSP00000347426.2:n.820A>C
ENST00000355740.6:c.845A>C	ENSP00000347979.2:p.His282Pro
ENST00000357339.6:c.782A>C	ENSP00000349896.2:p.His261Pro
ENST00000479522.5:c.*274A>C	ENSP00000424113.1:n.*274A>C
ENST00000484444.5:c.*286A>C	ENSP00000420975.1:n.*286A>C
ENST00000488877.5:c.*286A>C	ENSP00000425159.1:n.*286A>C
ENST00000492756.5:c.673A>C	ENSP00000422453.1:n.673A>C
ENST00000494410.5:c.*203A>C	ENSP00000423755.1:n.*203A>C
ENST00000612663.4:c.*192A>C	ENSP00000477997.2:n.*192A>C
NM_000043.4:c.845A>C , LRG_134t1:c.845A>C	NP_000034.1:p.His282Pro
NM_152871.2:c.782A>C	NP_690610.1:p.His261Pro
NM_152872.2:c.*157A>C	NP_690611.1:n.*157A>C
NR_028033.2:n.1019A>C
NR_028034.2:n.881A>C
NR_028035.2:n.944A>C
NR_028036.2:n.1082A>C
XM_006717819.2:c.926A>C	XP_006717882.1:p.His309Pro
XM_011539764.1:c.1007A>C	XP_011538066.1:p.His336Pro
XM_011539765.1:c.944A>C	XP_011538067.1:p.His315Pro
XM_011539766.1:c.926A>C	XP_011538068.1:p.His309Pro
XM_011539767.1:c.890A>C	XP_011538069.1:p.His297Pro
XR_945732.1:n.913A>C
XR_945733.1:n.850A>C
NM_000043.5:c.845A>C	NP_000034.1:p.His282Pro
NM_001320619.1:c.*168A>C	NP_001307548.1:n.*168A>C
NM_152871.3:c.782A>C	NP_690610.1:p.His261Pro
NM_152872.3:c.*157A>C	NP_690611.1:n.*157A>C
NR_028033.3:n.991A>C
NR_028034.3:n.853A>C
NR_028035.3:n.916A>C
NR_028036.3:n.1054A>C
NR_135313.1:n.971A>C
NR_135314.1:n.1154A>C
NR_135315.1:n.907A>C
XM_006717819.3:c.926A>C	XP_006717882.1:p.His309Pro
XM_011539764.2:c.1007A>C	XP_011538066.1:p.His336Pro
XM_011539765.2:c.944A>C	XP_011538067.1:p.His315Pro
XM_011539766.2:c.926A>C	XP_011538068.1:p.His309Pro
XM_011539767.3:c.890A>C	XP_011538069.1:p.His297Pro
XR_945732.3:n.913A>C
XR_945733.2:n.850A>C
NM_000043.6:c.845A>C MANE Select	NP_000034.1:p.His282Pro
NM_001320619.2:c.*168A>C	NP_001307548.1:n.*168A>C
NM_152871.4:c.782A>C	NP_690610.1:p.His261Pro
NM_152872.4:c.*157A>C	NP_690611.1:n.*157A>C
NR_028033.4:n.752A>C
NR_028034.4:n.614A>C
NR_028035.4:n.677A>C
NR_028036.4:n.815A>C
NR_135313.2:n.732A>C
NR_135314.2:n.1011A>C
NR_135315.2:n.764A>C