Canonical Allele Identifier: CA1926639311

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014143C= , CM000672.2:g.89014143C=	GRCh38
NC_000010.10:g.90773900C= , CM000672.1:g.90773900C=	GRCh37
NC_000010.9:g.90763880C=	NCBI36
NG_009089.2:g.28613C= , LRG_134:g.28613C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1010C=
ENST00000355740.8:c.*24C=	ENSP00000347979.3:n.*24C=
ENST00000357339.7:c.638C=	ENSP00000349896.2:p.Thr213=
ENST00000371857.8:n.2246C=
ENST00000460510.6:c.-17C=	ENSP00000512812.1:n.-17C=
ENST00000466081.6:n.2350C=
ENST00000477270.6:c.746C=	ENSP00000512813.1:p.Thr249=
ENST00000479522.6:c.*130C=	ENSP00000424113.1:n.*130C=
ENST00000484444.6:c.*142C=	ENSP00000420975.1:n.*142C=
ENST00000488877.6:c.592C=	ENSP00000425159.1:n.592C=
ENST00000492756.7:c.*130C=	ENSP00000422453.1:n.*130C=
ENST00000494799.6:c.-17C=	ENSP00000512834.1:n.-17C=
ENST00000562983.3:c.-17C=	ENSP00000512845.1:n.-17C=
ENST00000612663.6:c.*103C=	ENSP00000477997.3:n.*103C=
ENST00000640140.2:n.846C=
ENST00000640250.2:n.200C=
ENST00000640681.2:n.805C=
ENST00000696723.1:n.4334C=
ENST00000696741.1:n.2339C=
ENST00000696742.1:n.2066C=
ENST00000696743.1:n.3469C=
ENST00000696744.1:n.740C=
ENST00000696767.1:n.1035C=
ENST00000696768.1:c.*24C=	ENSP00000512859.1:n.*24C=
ENST00000696769.1:n.2390C=
ENST00000696771.1:c.-17C=	ENSP00000512860.1:n.-17C=
ENST00000696772.1:n.2304C=
ENST00000696773.1:n.2043C=
ENST00000696774.1:n.5811C=
ENST00000696776.1:c.794C=	ENSP00000512861.1:p.Thr265=
ENST00000696777.1:n.2109C=
ENST00000696778.1:n.1137C=
ENST00000696779.1:c.308C=	ENSP00000512862.1:p.Thr103=
ENST00000696780.1:c.731C=	ENSP00000512863.1:p.Thr244=
ENST00000696781.1:c.446C=	ENSP00000512864.1:p.Thr149=
ENST00000696782.1:c.*103C=	ENSP00000512865.1:n.*103C=
ENST00000696783.1:n.2569C=
ENST00000696992.1:n.1818C=
ENST00000696995.1:n.4230C=
ENST00000696996.1:n.2143C=
ENST00000696997.1:c.*331C=	ENSP00000513028.1:n.*331C=
ENST00000696998.1:n.1955C=
ENST00000696999.1:c.-17C=	ENSP00000513029.1:n.-17C=
ENST00000697035.1:c.*34C=	ENSP00000513059.1:n.*34C=
ENST00000697036.1:c.*117C=	ENSP00000513060.1:n.*117C=
ENST00000697037.1:n.736C=
ENST00000697093.1:n.2937C=
ENST00000697094.1:n.3284C=
ENST00000697095.1:c.*1902C=	ENSP00000513104.1:n.*1902C=
ENST00000697096.1:n.1834C=
ENST00000697097.1:c.-17C=	ENSP00000513105.1:n.-17C=
ENST00000562983.2:n.887C=
ENST00000690268.1:c.782C=	ENSP00000509810.1:p.Thr261=
ENST00000355740.7:c.*27C=	ENSP00000347979.3:n.*27C=
ENST00000612663.5:c.*103C=	ENSP00000477997.3:n.*103C=
ENST00000640140.1:n.873C=
ENST00000640250.1:n.200C=
ENST00000640681.1:n.822C=
ENST00000652046.1:c.701C= MANE Select	ENSP00000498466.1:p.Thr234=
ENST00000313771.9:n.1010C=
ENST00000352159.8:c.*18C=	ENSP00000345601.4:n.*18C=
ENST00000355279.2:c.676C=	ENSP00000347426.2:n.676C=
ENST00000355740.6:c.701C=	ENSP00000347979.2:p.Thr234=
ENST00000357339.6:c.638C=	ENSP00000349896.2:p.Thr213=
ENST00000479522.5:c.*130C=	ENSP00000424113.1:n.*130C=
ENST00000484444.5:c.*142C=	ENSP00000420975.1:n.*142C=
ENST00000488877.5:c.*142C=	ENSP00000425159.1:n.*142C=
ENST00000492756.5:c.529C=	ENSP00000422453.1:n.529C=
ENST00000494410.5:c.*59C=	ENSP00000423755.1:n.*59C=
ENST00000494799.5:n.608C=
ENST00000612663.4:c.*48C=	ENSP00000477997.2:n.*48C=
ENST00000615406.4:c.701C=	ENSP00000484575.1:p.Thr234=
ENST00000626542.2:c.699C=	ENSP00000485876.1:p.His233=
NM_000043.4:c.701C= , LRG_134t1:c.701C=	NP_000034.1:p.Thr234=
NM_152871.2:c.638C=	NP_690610.1:p.Thr213=
NM_152872.2:c.*13C=	NP_690611.1:n.*13C=
NR_028033.2:n.875C=
NR_028034.2:n.737C=
NR_028035.2:n.800C=
NR_028036.2:n.938C=
XM_006717819.2:c.782C=	XP_006717882.1:p.Thr261=
XM_011539764.1:c.863C=	XP_011538066.1:p.Thr288=
XM_011539765.1:c.800C=	XP_011538067.1:p.Thr267=
XM_011539766.1:c.782C=	XP_011538068.1:p.Thr261=
XM_011539767.1:c.746C=	XP_011538069.1:p.Thr249=
XR_945732.1:n.769C=
XR_945733.1:n.706C=
NM_000043.5:c.701C=	NP_000034.1:p.Thr234=
NM_001320619.1:c.*24C=	NP_001307548.1:n.*24C=
NM_152871.3:c.638C=	NP_690610.1:p.Thr213=
NM_152872.3:c.*13C=	NP_690611.1:n.*13C=
NR_028033.3:n.847C=
NR_028034.3:n.709C=
NR_028035.3:n.772C=
NR_028036.3:n.910C=
NR_135313.1:n.827C=
NR_135314.1:n.1010C=
NR_135315.1:n.763C=
XM_006717819.3:c.782C=	XP_006717882.1:p.Thr261=
XM_011539764.2:c.863C=	XP_011538066.1:p.Thr288=
XM_011539765.2:c.800C=	XP_011538067.1:p.Thr267=
XM_011539766.2:c.782C=	XP_011538068.1:p.Thr261=
XM_011539767.3:c.746C=	XP_011538069.1:p.Thr249=
XR_945732.3:n.769C=
XR_945733.2:n.706C=
NM_000043.6:c.701C= MANE Select	NP_000034.1:p.Thr234=
NM_001320619.2:c.*24C=	NP_001307548.1:n.*24C=
NM_152871.4:c.638C=	NP_690610.1:p.Thr213=
NM_152872.4:c.*13C=	NP_690611.1:n.*13C=
NR_028033.4:n.608C=
NR_028034.4:n.470C=
NR_028035.4:n.533C=
NR_028036.4:n.671C=
NR_135313.2:n.588C=
NR_135314.2:n.867C=
NR_135315.2:n.620C=