Canonical Allele Identifier: CA1926636628

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89007876G= , CM000672.2:g.89007876G=	GRCh38
NC_000010.10:g.90767633G= , CM000672.1:g.90767633G=	GRCh37
NC_000010.9:g.90757613G=	NCBI36
NG_009089.2:g.22346G= , LRG_134:g.22346G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.643+39G=
ENST00000355740.8:c.334+39G=	ENSP00000347979.3:n.334+39G=
ENST00000357339.7:c.334+39G=	ENSP00000349896.2:n.334+39G=
ENST00000371857.8:n.544+39G=
ENST00000460510.6:c.-384+39G=	ENSP00000512812.1:n.-384+39G=
ENST00000466081.6:n.503+39G=
ENST00000477270.6:c.379+39G=	ENSP00000512813.1:n.379+39G=
ENST00000479522.6:c.197-2663G=	ENSP00000424113.1:n.197-2663G=
ENST00000484444.6:c.197-2663G=	ENSP00000420975.1:n.197-2663G=
ENST00000488877.6:c.334+39G=	ENSP00000425159.1:n.334+39G=
ENST00000492756.7:c.334+39G=	ENSP00000422453.1:n.334+39G=
ENST00000494799.6:c.-274-2663G=	ENSP00000512834.1:n.-274-2663G=
ENST00000562983.3:c.-384+39G=	ENSP00000512845.1:n.-384+39G=
ENST00000612663.6:c.334+39G=	ENSP00000477997.3:n.334+39G=
ENST00000640140.2:n.479+39G=
ENST00000640681.2:n.438+39G=
ENST00000696723.1:n.3967+39G=
ENST00000696741.1:n.637+39G=
ENST00000696742.1:n.516+39G=
ENST00000696743.1:n.506+39G=
ENST00000696744.1:n.373+39G=
ENST00000696767.1:n.516+39G=
ENST00000696768.1:c.334+39G=	ENSP00000512859.1:n.334+39G=
ENST00000696769.1:n.688+39G=
ENST00000696770.1:n.556G=
ENST00000696771.1:c.-321+39G=	ENSP00000512860.1:n.-321+39G=
ENST00000696772.1:n.500+39G=
ENST00000696773.1:n.493+39G=
ENST00000696774.1:n.556+39G=
ENST00000696775.1:n.609+39G=
ENST00000696776.1:c.427+39G=	ENSP00000512861.1:n.427+39G=
ENST00000696777.1:n.516+39G=
ENST00000696778.1:n.516+39G=
ENST00000696779.1:c.197-2663G=	ENSP00000512862.1:n.197-2663G=
ENST00000696780.1:c.427+39G=	ENSP00000512863.1:n.427+39G=
ENST00000696781.1:c.334+39G=	ENSP00000512864.1:n.334+39G=
ENST00000696782.1:c.334+39G=	ENSP00000512865.1:n.334+39G=
ENST00000696992.1:n.1451+39G=
ENST00000696994.1:n.555G=
ENST00000696995.1:n.516+39G=
ENST00000696996.1:n.515+39G=
ENST00000696997.1:c.334+39G=	ENSP00000513028.1:n.334+39G=
ENST00000696998.1:n.363-2663G=
ENST00000696999.1:c.-212+39G=	ENSP00000513029.1:n.-212+39G=
ENST00000697035.1:c.334+39G=	ENSP00000513059.1:n.334+39G=
ENST00000697036.1:c.334+39G=	ENSP00000513060.1:n.334+39G=
ENST00000697037.1:n.369+39G=
ENST00000697093.1:n.558+39G=
ENST00000697094.1:n.473+39G=
ENST00000697095.1:c.327+39G=	ENSP00000513104.1:n.327+39G=
ENST00000697096.1:n.390+39G=
ENST00000697097.1:c.-384+39G=	ENSP00000513105.1:n.-384+39G=
ENST00000562983.2:n.520+39G=
ENST00000690268.1:c.415+39G=	ENSP00000509810.1:n.415+39G=
ENST00000355740.7:c.334+39G=	ENSP00000347979.3:n.334+39G=
ENST00000612663.5:c.334+39G=	ENSP00000477997.3:n.334+39G=
ENST00000640140.1:n.506+39G=
ENST00000640681.1:n.455+39G=
ENST00000652046.1:c.334+39G= MANE Select	ENSP00000498466.1:n.334+39G=
ENST00000313771.9:n.643+39G=
ENST00000352159.8:c.334+39G=	ENSP00000345601.4:n.334+39G=
ENST00000355279.2:c.334+39G=	ENSP00000347426.2:n.334+39G=
ENST00000355740.6:c.334+39G=	ENSP00000347979.2:n.334+39G=
ENST00000357339.6:c.334+39G=	ENSP00000349896.2:n.334+39G=
ENST00000371857.7:n.500+39G=
ENST00000460510.5:n.701+39G=
ENST00000466081.5:n.503+39G=
ENST00000477270.5:n.497+39G=
ENST00000479522.5:c.197-2663G=	ENSP00000424113.1:n.197-2663G=
ENST00000484444.5:c.197-2663G=	ENSP00000420975.1:n.197-2663G=
ENST00000487314.1:n.483+39G=
ENST00000488877.5:c.334+39G=	ENSP00000425159.1:n.334+39G=
ENST00000492756.5:c.334+39G=	ENSP00000422453.1:n.334+39G=
ENST00000494410.5:c.334+39G=	ENSP00000423755.1:n.334+39G=
ENST00000494799.5:n.351-2663G=
ENST00000612663.4:c.334+39G=	ENSP00000477997.2:n.334+39G=
ENST00000615406.4:c.334+39G=	ENSP00000484575.1:n.334+39G=
ENST00000626542.2:c.334+39G=	ENSP00000485876.1:n.334+39G=
NM_000043.4:c.334+39G= , LRG_134t1:c.334+39G=	NP_000034.1:n.334+39G=
NM_152871.2:c.334+39G=	NP_690610.1:n.334+39G=
NM_152872.2:c.334+39G=	NP_690611.1:n.334+39G=
NR_028033.2:n.680+39G=
NR_028034.2:n.543-2663G=
NR_028035.2:n.543-2663G=
NR_028036.2:n.680+39G=
XM_006717819.2:c.415+39G=	XP_006717882.1:n.415+39G=
XM_011539764.1:c.496+39G=	XP_011538066.1:n.496+39G=
XM_011539765.1:c.496+39G=	XP_011538067.1:n.496+39G=
XM_011539766.1:c.415+39G=	XP_011538068.1:n.415+39G=
XM_011539767.1:c.379+39G=	XP_011538069.1:n.379+39G=
XR_945732.1:n.511+39G=
XR_945733.1:n.511+39G=
NM_000043.5:c.334+39G=	NP_000034.1:n.334+39G=
NM_001320619.1:c.334+39G=	NP_001307548.1:n.334+39G=
NM_152871.3:c.334+39G=	NP_690610.1:n.334+39G=
NM_152872.3:c.334+39G=	NP_690611.1:n.334+39G=
NR_028033.3:n.652+39G=
NR_028034.3:n.515-2663G=
NR_028035.3:n.515-2663G=
NR_028036.3:n.652+39G=
NR_135313.1:n.652+39G=
NR_135314.1:n.643+39G=
NR_135315.1:n.506-2663G=
XM_006717819.3:c.415+39G=	XP_006717882.1:n.415+39G=
XM_011539764.2:c.496+39G=	XP_011538066.1:n.496+39G=
XM_011539765.2:c.496+39G=	XP_011538067.1:n.496+39G=
XM_011539766.2:c.415+39G=	XP_011538068.1:n.415+39G=
XM_011539767.3:c.379+39G=	XP_011538069.1:n.379+39G=
XR_945732.3:n.511+39G=
XR_945733.2:n.511+39G=
NM_000043.6:c.334+39G= MANE Select	NP_000034.1:n.334+39G=
NM_001320619.2:c.334+39G=	NP_001307548.1:n.334+39G=
NM_152871.4:c.334+39G=	NP_690610.1:n.334+39G=
NM_152872.4:c.334+39G=	NP_690611.1:n.334+39G=
NR_028033.4:n.413+39G=
NR_028034.4:n.276-2663G=
NR_028035.4:n.276-2663G=
NR_028036.4:n.413+39G=
NR_135313.2:n.413+39G=
NR_135314.2:n.500+39G=
NR_135315.2:n.363-2663G=