Canonical Allele Identifier: CA377509824

Gene: FAS

Linked Data

• COSMIC: COSM3807929
• MyVariant Identifiers: chr10:g.90773992G>C (hg19) ; chr10:g.89014235G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014235G>C , CM000672.2:g.89014235G>C	GRCh38
NC_000010.10:g.90773992G>C , CM000672.1:g.90773992G>C	GRCh37
NC_000010.9:g.90763972G>C	NCBI36
NG_009089.2:g.28705G>C , LRG_134:g.28705G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1102G>C
ENST00000355740.8:c.*116G>C	ENSP00000347979.3:n.*116G>C
ENST00000357339.7:c.730G>C	ENSP00000349896.2:p.Asp244His
ENST00000371857.8:n.2338G>C
ENST00000460510.6:c.76G>C	ENSP00000512812.1:p.Asp26His
ENST00000466081.6:n.2442G>C
ENST00000477270.6:c.838G>C	ENSP00000512813.1:p.Asp280His
ENST00000479522.6:c.*222G>C	ENSP00000424113.1:n.*222G>C
ENST00000484444.6:c.*234G>C	ENSP00000420975.1:n.*234G>C
ENST00000488877.6:c.684G>C	ENSP00000425159.1:n.684G>C
ENST00000492756.7:c.*222G>C	ENSP00000422453.1:n.*222G>C
ENST00000494799.6:c.76G>C	ENSP00000512834.1:p.Asp26His
ENST00000562983.3:c.76G>C	ENSP00000512845.1:p.Asp26His
ENST00000612663.6:c.*195G>C	ENSP00000477997.3:n.*195G>C
ENST00000640140.2:n.938G>C
ENST00000640250.2:n.292G>C
ENST00000640681.2:n.897G>C
ENST00000696723.1:n.4426G>C
ENST00000696741.1:n.2431G>C
ENST00000696742.1:n.2158G>C
ENST00000696743.1:n.3561G>C
ENST00000696744.1:n.832G>C
ENST00000696767.1:n.1127G>C
ENST00000696768.1:c.*116G>C	ENSP00000512859.1:n.*116G>C
ENST00000696769.1:n.2482G>C
ENST00000696771.1:c.76G>C	ENSP00000512860.1:p.Asp26His
ENST00000696772.1:n.2396G>C
ENST00000696773.1:n.2135G>C
ENST00000696774.1:n.5903G>C
ENST00000696776.1:c.886G>C	ENSP00000512861.1:p.Asp296His
ENST00000696777.1:n.2201G>C
ENST00000696778.1:n.1229G>C
ENST00000696779.1:c.400G>C	ENSP00000512862.1:p.Asp134His
ENST00000696780.1:c.823G>C	ENSP00000512863.1:p.Asp275His
ENST00000696781.1:c.538G>C	ENSP00000512864.1:p.Asp180His
ENST00000696782.1:c.*195G>C	ENSP00000512865.1:n.*195G>C
ENST00000696783.1:n.2661G>C
ENST00000696992.1:n.1910G>C
ENST00000696995.1:n.4322G>C
ENST00000696996.1:n.2235G>C
ENST00000696997.1:c.*423G>C	ENSP00000513028.1:n.*423G>C
ENST00000696998.1:n.2047G>C
ENST00000696999.1:c.76G>C	ENSP00000513029.1:p.Asp26His
ENST00000697035.1:c.*126G>C	ENSP00000513059.1:n.*126G>C
ENST00000697036.1:c.*209G>C	ENSP00000513060.1:n.*209G>C
ENST00000697037.1:n.828G>C
ENST00000697093.1:n.3029G>C
ENST00000697094.1:n.3376G>C
ENST00000697095.1:c.*1994G>C	ENSP00000513104.1:n.*1994G>C
ENST00000697096.1:n.1926G>C
ENST00000697097.1:c.76G>C	ENSP00000513105.1:p.Asp26His
ENST00000562983.2:n.979G>C
ENST00000690268.1:c.874G>C	ENSP00000509810.1:p.Asp292His
ENST00000355740.7:c.*119G>C	ENSP00000347979.3:n.*119G>C
ENST00000612663.5:c.*195G>C	ENSP00000477997.3:n.*195G>C
ENST00000640140.1:n.965G>C
ENST00000640250.1:n.292G>C
ENST00000640681.1:n.914G>C
ENST00000652046.1:c.793G>C MANE Select	ENSP00000498466.1:p.Asp265His
ENST00000352159.8:c.*110G>C	ENSP00000345601.4:n.*110G>C
ENST00000355279.2:c.768G>C	ENSP00000347426.2:n.768G>C
ENST00000355740.6:c.793G>C	ENSP00000347979.2:p.Asp265His
ENST00000357339.6:c.730G>C	ENSP00000349896.2:p.Asp244His
ENST00000479522.5:c.*222G>C	ENSP00000424113.1:n.*222G>C
ENST00000484444.5:c.*234G>C	ENSP00000420975.1:n.*234G>C
ENST00000488877.5:c.*234G>C	ENSP00000425159.1:n.*234G>C
ENST00000492756.5:c.621G>C	ENSP00000422453.1:n.621G>C
ENST00000494410.5:c.*151G>C	ENSP00000423755.1:n.*151G>C
ENST00000612663.4:c.*140G>C	ENSP00000477997.2:n.*140G>C
NM_000043.4:c.793G>C , LRG_134t1:c.793G>C	NP_000034.1:p.Asp265His
NM_152871.2:c.730G>C	NP_690610.1:p.Asp244His
NM_152872.2:c.*105G>C	NP_690611.1:n.*105G>C
NR_028033.2:n.967G>C
NR_028034.2:n.829G>C
NR_028035.2:n.892G>C
NR_028036.2:n.1030G>C
XM_006717819.2:c.874G>C	XP_006717882.1:p.Asp292His
XM_011539764.1:c.955G>C	XP_011538066.1:p.Asp319His
XM_011539765.1:c.892G>C	XP_011538067.1:p.Asp298His
XM_011539766.1:c.874G>C	XP_011538068.1:p.Asp292His
XM_011539767.1:c.838G>C	XP_011538069.1:p.Asp280His
XR_945732.1:n.861G>C
XR_945733.1:n.798G>C
NM_000043.5:c.793G>C	NP_000034.1:p.Asp265His
NM_001320619.1:c.*116G>C	NP_001307548.1:n.*116G>C
NM_152871.3:c.730G>C	NP_690610.1:p.Asp244His
NM_152872.3:c.*105G>C	NP_690611.1:n.*105G>C
NR_028033.3:n.939G>C
NR_028034.3:n.801G>C
NR_028035.3:n.864G>C
NR_028036.3:n.1002G>C
NR_135313.1:n.919G>C
NR_135314.1:n.1102G>C
NR_135315.1:n.855G>C
XM_006717819.3:c.874G>C	XP_006717882.1:p.Asp292His
XM_011539764.2:c.955G>C	XP_011538066.1:p.Asp319His
XM_011539765.2:c.892G>C	XP_011538067.1:p.Asp298His
XM_011539766.2:c.874G>C	XP_011538068.1:p.Asp292His
XM_011539767.3:c.838G>C	XP_011538069.1:p.Asp280His
XR_945732.3:n.861G>C
XR_945733.2:n.798G>C
NM_000043.6:c.793G>C MANE Select	NP_000034.1:p.Asp265His
NM_001320619.2:c.*116G>C	NP_001307548.1:n.*116G>C
NM_152871.4:c.730G>C	NP_690610.1:p.Asp244His
NM_152872.4:c.*105G>C	NP_690611.1:n.*105G>C
NR_028033.4:n.700G>C
NR_028034.4:n.562G>C
NR_028035.4:n.625G>C
NR_028036.4:n.763G>C
NR_135313.2:n.680G>C
NR_135314.2:n.959G>C
NR_135315.2:n.712G>C