Canonical Allele Identifier: CA377509756

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773965G>T (hg19) ; chr10:g.89014208G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014208G>T , CM000672.2:g.89014208G>T	GRCh38
NC_000010.10:g.90773965G>T , CM000672.1:g.90773965G>T	GRCh37
NC_000010.9:g.90763945G>T	NCBI36
NG_009089.2:g.28678G>T , LRG_134:g.28678G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1075G>T
ENST00000355740.8:c.*89G>T	ENSP00000347979.3:n.*89G>T
ENST00000357339.7:c.703G>T	ENSP00000349896.2:p.Glu235Ter
ENST00000371857.8:n.2311G>T
ENST00000460510.6:c.49G>T	ENSP00000512812.1:p.Glu17Ter
ENST00000466081.6:n.2415G>T
ENST00000477270.6:c.811G>T	ENSP00000512813.1:p.Glu271Ter
ENST00000479522.6:c.*195G>T	ENSP00000424113.1:n.*195G>T
ENST00000484444.6:c.*207G>T	ENSP00000420975.1:n.*207G>T
ENST00000488877.6:c.657G>T	ENSP00000425159.1:n.657G>T
ENST00000492756.7:c.*195G>T	ENSP00000422453.1:n.*195G>T
ENST00000494799.6:c.49G>T	ENSP00000512834.1:p.Glu17Ter
ENST00000562983.3:c.49G>T	ENSP00000512845.1:p.Glu17Ter
ENST00000612663.6:c.*168G>T	ENSP00000477997.3:n.*168G>T
ENST00000640140.2:n.911G>T
ENST00000640250.2:n.265G>T
ENST00000640681.2:n.870G>T
ENST00000696723.1:n.4399G>T
ENST00000696741.1:n.2404G>T
ENST00000696742.1:n.2131G>T
ENST00000696743.1:n.3534G>T
ENST00000696744.1:n.805G>T
ENST00000696767.1:n.1100G>T
ENST00000696768.1:c.*89G>T	ENSP00000512859.1:n.*89G>T
ENST00000696769.1:n.2455G>T
ENST00000696771.1:c.49G>T	ENSP00000512860.1:p.Glu17Ter
ENST00000696772.1:n.2369G>T
ENST00000696773.1:n.2108G>T
ENST00000696774.1:n.5876G>T
ENST00000696776.1:c.859G>T	ENSP00000512861.1:p.Glu287Ter
ENST00000696777.1:n.2174G>T
ENST00000696778.1:n.1202G>T
ENST00000696779.1:c.373G>T	ENSP00000512862.1:p.Glu125Ter
ENST00000696780.1:c.796G>T	ENSP00000512863.1:p.Glu266Ter
ENST00000696781.1:c.511G>T	ENSP00000512864.1:p.Glu171Ter
ENST00000696782.1:c.*168G>T	ENSP00000512865.1:n.*168G>T
ENST00000696783.1:n.2634G>T
ENST00000696992.1:n.1883G>T
ENST00000696995.1:n.4295G>T
ENST00000696996.1:n.2208G>T
ENST00000696997.1:c.*396G>T	ENSP00000513028.1:n.*396G>T
ENST00000696998.1:n.2020G>T
ENST00000696999.1:c.49G>T	ENSP00000513029.1:p.Glu17Ter
ENST00000697035.1:c.*99G>T	ENSP00000513059.1:n.*99G>T
ENST00000697036.1:c.*182G>T	ENSP00000513060.1:n.*182G>T
ENST00000697037.1:n.801G>T
ENST00000697093.1:n.3002G>T
ENST00000697094.1:n.3349G>T
ENST00000697095.1:c.*1967G>T	ENSP00000513104.1:n.*1967G>T
ENST00000697096.1:n.1899G>T
ENST00000697097.1:c.49G>T	ENSP00000513105.1:p.Glu17Ter
ENST00000562983.2:n.952G>T
ENST00000690268.1:c.847G>T	ENSP00000509810.1:p.Glu283Ter
ENST00000355740.7:c.*92G>T	ENSP00000347979.3:n.*92G>T
ENST00000612663.5:c.*168G>T	ENSP00000477997.3:n.*168G>T
ENST00000640140.1:n.938G>T
ENST00000640250.1:n.265G>T
ENST00000640681.1:n.887G>T
ENST00000652046.1:c.766G>T MANE Select	ENSP00000498466.1:p.Glu256Ter
ENST00000352159.8:c.*83G>T	ENSP00000345601.4:n.*83G>T
ENST00000355279.2:c.741G>T	ENSP00000347426.2:n.741G>T
ENST00000355740.6:c.766G>T	ENSP00000347979.2:p.Glu256Ter
ENST00000357339.6:c.703G>T	ENSP00000349896.2:p.Glu235Ter
ENST00000479522.5:c.*195G>T	ENSP00000424113.1:n.*195G>T
ENST00000484444.5:c.*207G>T	ENSP00000420975.1:n.*207G>T
ENST00000488877.5:c.*207G>T	ENSP00000425159.1:n.*207G>T
ENST00000492756.5:c.594G>T	ENSP00000422453.1:n.594G>T
ENST00000494410.5:c.*124G>T	ENSP00000423755.1:n.*124G>T
ENST00000494799.5:n.673G>T
ENST00000612663.4:c.*113G>T	ENSP00000477997.2:n.*113G>T
ENST00000615406.4:c.764G>T	ENSP00000484575.1:p.Ter255Leu
NM_000043.4:c.766G>T , LRG_134t1:c.766G>T	NP_000034.1:p.Glu256Ter
NM_152871.2:c.703G>T	NP_690610.1:p.Glu235Ter
NM_152872.2:c.*78G>T	NP_690611.1:n.*78G>T
NR_028033.2:n.940G>T
NR_028034.2:n.802G>T
NR_028035.2:n.865G>T
NR_028036.2:n.1003G>T
XM_006717819.2:c.847G>T	XP_006717882.1:p.Glu283Ter
XM_011539764.1:c.928G>T	XP_011538066.1:p.Glu310Ter
XM_011539765.1:c.865G>T	XP_011538067.1:p.Glu289Ter
XM_011539766.1:c.847G>T	XP_011538068.1:p.Glu283Ter
XM_011539767.1:c.811G>T	XP_011538069.1:p.Glu271Ter
XR_945732.1:n.834G>T
XR_945733.1:n.771G>T
NM_000043.5:c.766G>T	NP_000034.1:p.Glu256Ter
NM_001320619.1:c.*89G>T	NP_001307548.1:n.*89G>T
NM_152871.3:c.703G>T	NP_690610.1:p.Glu235Ter
NM_152872.3:c.*78G>T	NP_690611.1:n.*78G>T
NR_028033.3:n.912G>T
NR_028034.3:n.774G>T
NR_028035.3:n.837G>T
NR_028036.3:n.975G>T
NR_135313.1:n.892G>T
NR_135314.1:n.1075G>T
NR_135315.1:n.828G>T
XM_006717819.3:c.847G>T	XP_006717882.1:p.Glu283Ter
XM_011539764.2:c.928G>T	XP_011538066.1:p.Glu310Ter
XM_011539765.2:c.865G>T	XP_011538067.1:p.Glu289Ter
XM_011539766.2:c.847G>T	XP_011538068.1:p.Glu283Ter
XM_011539767.3:c.811G>T	XP_011538069.1:p.Glu271Ter
XR_945732.3:n.834G>T
XR_945733.2:n.771G>T
NM_000043.6:c.766G>T MANE Select	NP_000034.1:p.Glu256Ter
NM_001320619.2:c.*89G>T	NP_001307548.1:n.*89G>T
NM_152871.4:c.703G>T	NP_690610.1:p.Glu235Ter
NM_152872.4:c.*78G>T	NP_690611.1:n.*78G>T
NR_028033.4:n.673G>T
NR_028034.4:n.535G>T
NR_028035.4:n.598G>T
NR_028036.4:n.736G>T
NR_135313.2:n.653G>T
NR_135314.2:n.932G>T
NR_135315.2:n.685G>T