Canonical Allele Identifier: CA377509902

Gene: FAS

Linked Data

• ClinVar Variation Id: 1701146
• ClinVar RCV Id: RCV002275482
• dbSNP Id: rs2119446558
• MyVariant Identifiers: chr10:g.90774026A>C (hg19) ; chr10:g.89014269A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014269A>C , CM000672.2:g.89014269A>C	GRCh38
NC_000010.10:g.90774026A>C , CM000672.1:g.90774026A>C	GRCh37
NC_000010.9:g.90764006A>C	NCBI36
NG_009089.2:g.28739A>C , LRG_134:g.28739A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1136A>C
ENST00000355740.8:c.*150A>C	ENSP00000347979.3:n.*150A>C
ENST00000357339.7:c.764A>C	ENSP00000349896.2:p.Gln255Pro
ENST00000371857.8:n.2372A>C
ENST00000460510.6:c.110A>C	ENSP00000512812.1:p.Gln37Pro
ENST00000466081.6:n.2476A>C
ENST00000477270.6:c.872A>C	ENSP00000512813.1:p.Gln291Pro
ENST00000479522.6:c.*256A>C	ENSP00000424113.1:n.*256A>C
ENST00000484444.6:c.*268A>C	ENSP00000420975.1:n.*268A>C
ENST00000488877.6:c.718A>C	ENSP00000425159.1:n.718A>C
ENST00000492756.7:c.*256A>C	ENSP00000422453.1:n.*256A>C
ENST00000494799.6:c.110A>C	ENSP00000512834.1:p.Gln37Pro
ENST00000562983.3:c.110A>C	ENSP00000512845.1:p.Gln37Pro
ENST00000612663.6:c.*229A>C	ENSP00000477997.3:n.*229A>C
ENST00000640140.2:n.972A>C
ENST00000640250.2:n.326A>C
ENST00000640681.2:n.931A>C
ENST00000696723.1:n.4460A>C
ENST00000696741.1:n.2465A>C
ENST00000696742.1:n.2192A>C
ENST00000696743.1:n.3595A>C
ENST00000696744.1:n.866A>C
ENST00000696767.1:n.1161A>C
ENST00000696768.1:c.*150A>C	ENSP00000512859.1:n.*150A>C
ENST00000696769.1:n.2516A>C
ENST00000696771.1:c.110A>C	ENSP00000512860.1:p.Gln37Pro
ENST00000696772.1:n.2430A>C
ENST00000696773.1:n.2169A>C
ENST00000696774.1:n.5937A>C
ENST00000696776.1:c.920A>C	ENSP00000512861.1:p.Gln307Pro
ENST00000696777.1:n.2235A>C
ENST00000696778.1:n.1263A>C
ENST00000696779.1:c.434A>C	ENSP00000512862.1:p.Gln145Pro
ENST00000696780.1:c.857A>C	ENSP00000512863.1:p.Gln286Pro
ENST00000696781.1:c.572A>C	ENSP00000512864.1:p.Gln191Pro
ENST00000696782.1:c.*229A>C	ENSP00000512865.1:n.*229A>C
ENST00000696783.1:n.2695A>C
ENST00000696992.1:n.1944A>C
ENST00000696995.1:n.4356A>C
ENST00000696996.1:n.2269A>C
ENST00000696997.1:c.*457A>C	ENSP00000513028.1:n.*457A>C
ENST00000696998.1:n.2081A>C
ENST00000696999.1:c.110A>C	ENSP00000513029.1:p.Gln37Pro
ENST00000697035.1:c.*160A>C	ENSP00000513059.1:n.*160A>C
ENST00000697036.1:c.*243A>C	ENSP00000513060.1:n.*243A>C
ENST00000697037.1:n.862A>C
ENST00000697093.1:n.3063A>C
ENST00000697094.1:n.3410A>C
ENST00000697095.1:c.*2028A>C	ENSP00000513104.1:n.*2028A>C
ENST00000697096.1:n.1960A>C
ENST00000697097.1:c.110A>C	ENSP00000513105.1:p.Gln37Pro
ENST00000562983.2:n.1013A>C
ENST00000690268.1:c.908A>C	ENSP00000509810.1:p.Gln303Pro
ENST00000355740.7:c.*153A>C	ENSP00000347979.3:n.*153A>C
ENST00000612663.5:c.*229A>C	ENSP00000477997.3:n.*229A>C
ENST00000640140.1:n.999A>C
ENST00000640250.1:n.326A>C
ENST00000640681.1:n.948A>C
ENST00000652046.1:c.827A>C MANE Select	ENSP00000498466.1:p.Gln276Pro
ENST00000352159.8:c.*144A>C	ENSP00000345601.4:n.*144A>C
ENST00000355279.2:c.802A>C	ENSP00000347426.2:n.802A>C
ENST00000355740.6:c.827A>C	ENSP00000347979.2:p.Gln276Pro
ENST00000357339.6:c.764A>C	ENSP00000349896.2:p.Gln255Pro
ENST00000479522.5:c.*256A>C	ENSP00000424113.1:n.*256A>C
ENST00000484444.5:c.*268A>C	ENSP00000420975.1:n.*268A>C
ENST00000488877.5:c.*268A>C	ENSP00000425159.1:n.*268A>C
ENST00000492756.5:c.655A>C	ENSP00000422453.1:n.655A>C
ENST00000494410.5:c.*185A>C	ENSP00000423755.1:n.*185A>C
ENST00000612663.4:c.*174A>C	ENSP00000477997.2:n.*174A>C
NM_000043.4:c.827A>C , LRG_134t1:c.827A>C	NP_000034.1:p.Gln276Pro
NM_152871.2:c.764A>C	NP_690610.1:p.Gln255Pro
NM_152872.2:c.*139A>C	NP_690611.1:n.*139A>C
NR_028033.2:n.1001A>C
NR_028034.2:n.863A>C
NR_028035.2:n.926A>C
NR_028036.2:n.1064A>C
XM_006717819.2:c.908A>C	XP_006717882.1:p.Gln303Pro
XM_011539764.1:c.989A>C	XP_011538066.1:p.Gln330Pro
XM_011539765.1:c.926A>C	XP_011538067.1:p.Gln309Pro
XM_011539766.1:c.908A>C	XP_011538068.1:p.Gln303Pro
XM_011539767.1:c.872A>C	XP_011538069.1:p.Gln291Pro
XR_945732.1:n.895A>C
XR_945733.1:n.832A>C
NM_000043.5:c.827A>C	NP_000034.1:p.Gln276Pro
NM_001320619.1:c.*150A>C	NP_001307548.1:n.*150A>C
NM_152871.3:c.764A>C	NP_690610.1:p.Gln255Pro
NM_152872.3:c.*139A>C	NP_690611.1:n.*139A>C
NR_028033.3:n.973A>C
NR_028034.3:n.835A>C
NR_028035.3:n.898A>C
NR_028036.3:n.1036A>C
NR_135313.1:n.953A>C
NR_135314.1:n.1136A>C
NR_135315.1:n.889A>C
XM_006717819.3:c.908A>C	XP_006717882.1:p.Gln303Pro
XM_011539764.2:c.989A>C	XP_011538066.1:p.Gln330Pro
XM_011539765.2:c.926A>C	XP_011538067.1:p.Gln309Pro
XM_011539766.2:c.908A>C	XP_011538068.1:p.Gln303Pro
XM_011539767.3:c.872A>C	XP_011538069.1:p.Gln291Pro
XR_945732.3:n.895A>C
XR_945733.2:n.832A>C
NM_000043.6:c.827A>C MANE Select	NP_000034.1:p.Gln276Pro
NM_001320619.2:c.*150A>C	NP_001307548.1:n.*150A>C
NM_152871.4:c.764A>C	NP_690610.1:p.Gln255Pro
NM_152872.4:c.*139A>C	NP_690611.1:n.*139A>C
NR_028033.4:n.734A>C
NR_028034.4:n.596A>C
NR_028035.4:n.659A>C
NR_028036.4:n.797A>C
NR_135313.2:n.714A>C
NR_135314.2:n.993A>C
NR_135315.2:n.746A>C