Canonical Allele Identifier: CA377509825

Gene: FAS

Linked Data

• COSMIC: COSM4973184
• MyVariant Identifiers: chr10:g.90773992G>T (hg19) ; chr10:g.89014235G>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1102G>T
ENST00000355740.8:c.*116G>T	ENSP00000347979.3:n.*116G>T
ENST00000357339.7:c.730G>T	ENSP00000349896.2:p.Asp244Tyr
ENST00000371857.8:n.2338G>T
ENST00000460510.6:c.76G>T	ENSP00000512812.1:p.Asp26Tyr
ENST00000466081.6:n.2442G>T
ENST00000477270.6:c.838G>T	ENSP00000512813.1:p.Asp280Tyr
ENST00000479522.6:c.*222G>T	ENSP00000424113.1:n.*222G>T
ENST00000484444.6:c.*234G>T	ENSP00000420975.1:n.*234G>T
ENST00000488877.6:c.684G>T	ENSP00000425159.1:n.684G>T
ENST00000492756.7:c.*222G>T	ENSP00000422453.1:n.*222G>T
ENST00000494799.6:c.76G>T	ENSP00000512834.1:p.Asp26Tyr
ENST00000562983.3:c.76G>T	ENSP00000512845.1:p.Asp26Tyr
ENST00000612663.6:c.*195G>T	ENSP00000477997.3:n.*195G>T
ENST00000640140.2:n.938G>T
ENST00000640250.2:n.292G>T
ENST00000640681.2:n.897G>T
ENST00000696723.1:n.4426G>T
ENST00000696741.1:n.2431G>T
ENST00000696742.1:n.2158G>T
ENST00000696743.1:n.3561G>T
ENST00000696744.1:n.832G>T
ENST00000696767.1:n.1127G>T
ENST00000696768.1:c.*116G>T	ENSP00000512859.1:n.*116G>T
ENST00000696769.1:n.2482G>T
ENST00000696771.1:c.76G>T	ENSP00000512860.1:p.Asp26Tyr
ENST00000696772.1:n.2396G>T
ENST00000696773.1:n.2135G>T
ENST00000696774.1:n.5903G>T
ENST00000696776.1:c.886G>T	ENSP00000512861.1:p.Asp296Tyr
ENST00000696777.1:n.2201G>T
ENST00000696778.1:n.1229G>T
ENST00000696779.1:c.400G>T	ENSP00000512862.1:p.Asp134Tyr
ENST00000696780.1:c.823G>T	ENSP00000512863.1:p.Asp275Tyr
ENST00000696781.1:c.538G>T	ENSP00000512864.1:p.Asp180Tyr
ENST00000696782.1:c.*195G>T	ENSP00000512865.1:n.*195G>T
ENST00000696783.1:n.2661G>T
ENST00000696992.1:n.1910G>T
ENST00000696995.1:n.4322G>T
ENST00000696996.1:n.2235G>T
ENST00000696997.1:c.*423G>T	ENSP00000513028.1:n.*423G>T
ENST00000696998.1:n.2047G>T
ENST00000696999.1:c.76G>T	ENSP00000513029.1:p.Asp26Tyr
ENST00000697035.1:c.*126G>T	ENSP00000513059.1:n.*126G>T
ENST00000697036.1:c.*209G>T	ENSP00000513060.1:n.*209G>T
ENST00000697037.1:n.828G>T
ENST00000697093.1:n.3029G>T
ENST00000697094.1:n.3376G>T
ENST00000697095.1:c.*1994G>T	ENSP00000513104.1:n.*1994G>T
ENST00000697096.1:n.1926G>T
ENST00000697097.1:c.76G>T	ENSP00000513105.1:p.Asp26Tyr
ENST00000562983.2:n.979G>T
ENST00000690268.1:c.874G>T	ENSP00000509810.1:p.Asp292Tyr
ENST00000355740.7:c.*119G>T	ENSP00000347979.3:n.*119G>T
ENST00000612663.5:c.*195G>T	ENSP00000477997.3:n.*195G>T
ENST00000640140.1:n.965G>T
ENST00000640250.1:n.292G>T
ENST00000640681.1:n.914G>T
ENST00000652046.1:c.793G>T MANE Select	ENSP00000498466.1:p.Asp265Tyr
ENST00000352159.8:c.*110G>T	ENSP00000345601.4:n.*110G>T
ENST00000355279.2:c.768G>T	ENSP00000347426.2:n.768G>T
ENST00000355740.6:c.793G>T	ENSP00000347979.2:p.Asp265Tyr
ENST00000357339.6:c.730G>T	ENSP00000349896.2:p.Asp244Tyr
ENST00000479522.5:c.*222G>T	ENSP00000424113.1:n.*222G>T
ENST00000484444.5:c.*234G>T	ENSP00000420975.1:n.*234G>T
ENST00000488877.5:c.*234G>T	ENSP00000425159.1:n.*234G>T
ENST00000492756.5:c.621G>T	ENSP00000422453.1:n.621G>T
ENST00000494410.5:c.*151G>T	ENSP00000423755.1:n.*151G>T
ENST00000612663.4:c.*140G>T	ENSP00000477997.2:n.*140G>T
NM_000043.4:c.793G>T , LRG_134t1:c.793G>T	NP_000034.1:p.Asp265Tyr
NM_152871.2:c.730G>T	NP_690610.1:p.Asp244Tyr
NM_152872.2:c.*105G>T	NP_690611.1:n.*105G>T
NR_028033.2:n.967G>T
NR_028034.2:n.829G>T
NR_028035.2:n.892G>T
NR_028036.2:n.1030G>T
XM_006717819.2:c.874G>T	XP_006717882.1:p.Asp292Tyr
XM_011539764.1:c.955G>T	XP_011538066.1:p.Asp319Tyr
XM_011539765.1:c.892G>T	XP_011538067.1:p.Asp298Tyr
XM_011539766.1:c.874G>T	XP_011538068.1:p.Asp292Tyr
XM_011539767.1:c.838G>T	XP_011538069.1:p.Asp280Tyr
XR_945732.1:n.861G>T
XR_945733.1:n.798G>T
NM_000043.5:c.793G>T	NP_000034.1:p.Asp265Tyr
NM_001320619.1:c.*116G>T	NP_001307548.1:n.*116G>T
NM_152871.3:c.730G>T	NP_690610.1:p.Asp244Tyr
NM_152872.3:c.*105G>T	NP_690611.1:n.*105G>T
NR_028033.3:n.939G>T
NR_028034.3:n.801G>T
NR_028035.3:n.864G>T
NR_028036.3:n.1002G>T
NR_135313.1:n.919G>T
NR_135314.1:n.1102G>T
NR_135315.1:n.855G>T
XM_006717819.3:c.874G>T	XP_006717882.1:p.Asp292Tyr
XM_011539764.2:c.955G>T	XP_011538066.1:p.Asp319Tyr
XM_011539765.2:c.892G>T	XP_011538067.1:p.Asp298Tyr
XM_011539766.2:c.874G>T	XP_011538068.1:p.Asp292Tyr
XM_011539767.3:c.838G>T	XP_011538069.1:p.Asp280Tyr
XR_945732.3:n.861G>T
XR_945733.2:n.798G>T
NM_000043.6:c.793G>T MANE Select	NP_000034.1:p.Asp265Tyr
NM_001320619.2:c.*116G>T	NP_001307548.1:n.*116G>T
NM_152871.4:c.730G>T	NP_690610.1:p.Asp244Tyr
NM_152872.4:c.*105G>T	NP_690611.1:n.*105G>T
NR_028033.4:n.700G>T
NR_028034.4:n.562G>T
NR_028035.4:n.625G>T
NR_028036.4:n.763G>T
NR_135313.2:n.680G>T
NR_135314.2:n.959G>T
NR_135315.2:n.712G>T