Canonical Allele Identifier: CA377509853

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774004G>T (hg19) ; chr10:g.89014247G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014247G>T , CM000672.2:g.89014247G>T	GRCh38
NC_000010.10:g.90774004G>T , CM000672.1:g.90774004G>T	GRCh37
NC_000010.9:g.90763984G>T	NCBI36
NG_009089.2:g.28717G>T , LRG_134:g.28717G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1114G>T
ENST00000355740.8:c.*128G>T	ENSP00000347979.3:n.*128G>T
ENST00000357339.7:c.742G>T	ENSP00000349896.2:p.Asp248Tyr
ENST00000371857.8:n.2350G>T
ENST00000460510.6:c.88G>T	ENSP00000512812.1:p.Asp30Tyr
ENST00000466081.6:n.2454G>T
ENST00000477270.6:c.850G>T	ENSP00000512813.1:p.Asp284Tyr
ENST00000479522.6:c.*234G>T	ENSP00000424113.1:n.*234G>T
ENST00000484444.6:c.*246G>T	ENSP00000420975.1:n.*246G>T
ENST00000488877.6:c.696G>T	ENSP00000425159.1:n.696G>T
ENST00000492756.7:c.*234G>T	ENSP00000422453.1:n.*234G>T
ENST00000494799.6:c.88G>T	ENSP00000512834.1:p.Asp30Tyr
ENST00000562983.3:c.88G>T	ENSP00000512845.1:p.Asp30Tyr
ENST00000612663.6:c.*207G>T	ENSP00000477997.3:n.*207G>T
ENST00000640140.2:n.950G>T
ENST00000640250.2:n.304G>T
ENST00000640681.2:n.909G>T
ENST00000696723.1:n.4438G>T
ENST00000696741.1:n.2443G>T
ENST00000696742.1:n.2170G>T
ENST00000696743.1:n.3573G>T
ENST00000696744.1:n.844G>T
ENST00000696767.1:n.1139G>T
ENST00000696768.1:c.*128G>T	ENSP00000512859.1:n.*128G>T
ENST00000696769.1:n.2494G>T
ENST00000696771.1:c.88G>T	ENSP00000512860.1:p.Asp30Tyr
ENST00000696772.1:n.2408G>T
ENST00000696773.1:n.2147G>T
ENST00000696774.1:n.5915G>T
ENST00000696776.1:c.898G>T	ENSP00000512861.1:p.Asp300Tyr
ENST00000696777.1:n.2213G>T
ENST00000696778.1:n.1241G>T
ENST00000696779.1:c.412G>T	ENSP00000512862.1:p.Asp138Tyr
ENST00000696780.1:c.835G>T	ENSP00000512863.1:p.Asp279Tyr
ENST00000696781.1:c.550G>T	ENSP00000512864.1:p.Asp184Tyr
ENST00000696782.1:c.*207G>T	ENSP00000512865.1:n.*207G>T
ENST00000696783.1:n.2673G>T
ENST00000696992.1:n.1922G>T
ENST00000696995.1:n.4334G>T
ENST00000696996.1:n.2247G>T
ENST00000696997.1:c.*435G>T	ENSP00000513028.1:n.*435G>T
ENST00000696998.1:n.2059G>T
ENST00000696999.1:c.88G>T	ENSP00000513029.1:p.Asp30Tyr
ENST00000697035.1:c.*138G>T	ENSP00000513059.1:n.*138G>T
ENST00000697036.1:c.*221G>T	ENSP00000513060.1:n.*221G>T
ENST00000697037.1:n.840G>T
ENST00000697093.1:n.3041G>T
ENST00000697094.1:n.3388G>T
ENST00000697095.1:c.*2006G>T	ENSP00000513104.1:n.*2006G>T
ENST00000697096.1:n.1938G>T
ENST00000697097.1:c.88G>T	ENSP00000513105.1:p.Asp30Tyr
ENST00000562983.2:n.991G>T
ENST00000690268.1:c.886G>T	ENSP00000509810.1:p.Asp296Tyr
ENST00000355740.7:c.*131G>T	ENSP00000347979.3:n.*131G>T
ENST00000612663.5:c.*207G>T	ENSP00000477997.3:n.*207G>T
ENST00000640140.1:n.977G>T
ENST00000640250.1:n.304G>T
ENST00000640681.1:n.926G>T
ENST00000652046.1:c.805G>T MANE Select	ENSP00000498466.1:p.Asp269Tyr
ENST00000352159.8:c.*122G>T	ENSP00000345601.4:n.*122G>T
ENST00000355279.2:c.780G>T	ENSP00000347426.2:n.780G>T
ENST00000355740.6:c.805G>T	ENSP00000347979.2:p.Asp269Tyr
ENST00000357339.6:c.742G>T	ENSP00000349896.2:p.Asp248Tyr
ENST00000479522.5:c.*234G>T	ENSP00000424113.1:n.*234G>T
ENST00000484444.5:c.*246G>T	ENSP00000420975.1:n.*246G>T
ENST00000488877.5:c.*246G>T	ENSP00000425159.1:n.*246G>T
ENST00000492756.5:c.633G>T	ENSP00000422453.1:n.633G>T
ENST00000494410.5:c.*163G>T	ENSP00000423755.1:n.*163G>T
ENST00000612663.4:c.*152G>T	ENSP00000477997.2:n.*152G>T
NM_000043.4:c.805G>T , LRG_134t1:c.805G>T	NP_000034.1:p.Asp269Tyr
NM_152871.2:c.742G>T	NP_690610.1:p.Asp248Tyr
NM_152872.2:c.*117G>T	NP_690611.1:n.*117G>T
NR_028033.2:n.979G>T
NR_028034.2:n.841G>T
NR_028035.2:n.904G>T
NR_028036.2:n.1042G>T
XM_006717819.2:c.886G>T	XP_006717882.1:p.Asp296Tyr
XM_011539764.1:c.967G>T	XP_011538066.1:p.Asp323Tyr
XM_011539765.1:c.904G>T	XP_011538067.1:p.Asp302Tyr
XM_011539766.1:c.886G>T	XP_011538068.1:p.Asp296Tyr
XM_011539767.1:c.850G>T	XP_011538069.1:p.Asp284Tyr
XR_945732.1:n.873G>T
XR_945733.1:n.810G>T
NM_000043.5:c.805G>T	NP_000034.1:p.Asp269Tyr
NM_001320619.1:c.*128G>T	NP_001307548.1:n.*128G>T
NM_152871.3:c.742G>T	NP_690610.1:p.Asp248Tyr
NM_152872.3:c.*117G>T	NP_690611.1:n.*117G>T
NR_028033.3:n.951G>T
NR_028034.3:n.813G>T
NR_028035.3:n.876G>T
NR_028036.3:n.1014G>T
NR_135313.1:n.931G>T
NR_135314.1:n.1114G>T
NR_135315.1:n.867G>T
XM_006717819.3:c.886G>T	XP_006717882.1:p.Asp296Tyr
XM_011539764.2:c.967G>T	XP_011538066.1:p.Asp323Tyr
XM_011539765.2:c.904G>T	XP_011538067.1:p.Asp302Tyr
XM_011539766.2:c.886G>T	XP_011538068.1:p.Asp296Tyr
XM_011539767.3:c.850G>T	XP_011538069.1:p.Asp284Tyr
XR_945732.3:n.873G>T
XR_945733.2:n.810G>T
NM_000043.6:c.805G>T MANE Select	NP_000034.1:p.Asp269Tyr
NM_001320619.2:c.*128G>T	NP_001307548.1:n.*128G>T
NM_152871.4:c.742G>T	NP_690610.1:p.Asp248Tyr
NM_152872.4:c.*117G>T	NP_690611.1:n.*117G>T
NR_028033.4:n.712G>T
NR_028034.4:n.574G>T
NR_028035.4:n.637G>T
NR_028036.4:n.775G>T
NR_135313.2:n.692G>T
NR_135314.2:n.971G>T
NR_135315.2:n.724G>T