Canonical Allele Identifier: CA377509834

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773996A>C (hg19) ; chr10:g.89014239A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014239A>C , CM000672.2:g.89014239A>C	GRCh38
NC_000010.10:g.90773996A>C , CM000672.1:g.90773996A>C	GRCh37
NC_000010.9:g.90763976A>C	NCBI36
NG_009089.2:g.28709A>C , LRG_134:g.28709A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1106A>C
ENST00000355740.8:c.*120A>C	ENSP00000347979.3:n.*120A>C
ENST00000357339.7:c.734A>C	ENSP00000349896.2:p.Asn245Thr
ENST00000371857.8:n.2342A>C
ENST00000460510.6:c.80A>C	ENSP00000512812.1:p.Asn27Thr
ENST00000466081.6:n.2446A>C
ENST00000477270.6:c.842A>C	ENSP00000512813.1:p.Asn281Thr
ENST00000479522.6:c.*226A>C	ENSP00000424113.1:n.*226A>C
ENST00000484444.6:c.*238A>C	ENSP00000420975.1:n.*238A>C
ENST00000488877.6:c.688A>C	ENSP00000425159.1:n.688A>C
ENST00000492756.7:c.*226A>C	ENSP00000422453.1:n.*226A>C
ENST00000494799.6:c.80A>C	ENSP00000512834.1:p.Asn27Thr
ENST00000562983.3:c.80A>C	ENSP00000512845.1:p.Asn27Thr
ENST00000612663.6:c.*199A>C	ENSP00000477997.3:n.*199A>C
ENST00000640140.2:n.942A>C
ENST00000640250.2:n.296A>C
ENST00000640681.2:n.901A>C
ENST00000696723.1:n.4430A>C
ENST00000696741.1:n.2435A>C
ENST00000696742.1:n.2162A>C
ENST00000696743.1:n.3565A>C
ENST00000696744.1:n.836A>C
ENST00000696767.1:n.1131A>C
ENST00000696768.1:c.*120A>C	ENSP00000512859.1:n.*120A>C
ENST00000696769.1:n.2486A>C
ENST00000696771.1:c.80A>C	ENSP00000512860.1:p.Asn27Thr
ENST00000696772.1:n.2400A>C
ENST00000696773.1:n.2139A>C
ENST00000696774.1:n.5907A>C
ENST00000696776.1:c.890A>C	ENSP00000512861.1:p.Asn297Thr
ENST00000696777.1:n.2205A>C
ENST00000696778.1:n.1233A>C
ENST00000696779.1:c.404A>C	ENSP00000512862.1:p.Asn135Thr
ENST00000696780.1:c.827A>C	ENSP00000512863.1:p.Asn276Thr
ENST00000696781.1:c.542A>C	ENSP00000512864.1:p.Asn181Thr
ENST00000696782.1:c.*199A>C	ENSP00000512865.1:n.*199A>C
ENST00000696783.1:n.2665A>C
ENST00000696992.1:n.1914A>C
ENST00000696995.1:n.4326A>C
ENST00000696996.1:n.2239A>C
ENST00000696997.1:c.*427A>C	ENSP00000513028.1:n.*427A>C
ENST00000696998.1:n.2051A>C
ENST00000696999.1:c.80A>C	ENSP00000513029.1:p.Asn27Thr
ENST00000697035.1:c.*130A>C	ENSP00000513059.1:n.*130A>C
ENST00000697036.1:c.*213A>C	ENSP00000513060.1:n.*213A>C
ENST00000697037.1:n.832A>C
ENST00000697093.1:n.3033A>C
ENST00000697094.1:n.3380A>C
ENST00000697095.1:c.*1998A>C	ENSP00000513104.1:n.*1998A>C
ENST00000697096.1:n.1930A>C
ENST00000697097.1:c.80A>C	ENSP00000513105.1:p.Asn27Thr
ENST00000562983.2:n.983A>C
ENST00000690268.1:c.878A>C	ENSP00000509810.1:p.Asn293Thr
ENST00000355740.7:c.*123A>C	ENSP00000347979.3:n.*123A>C
ENST00000612663.5:c.*199A>C	ENSP00000477997.3:n.*199A>C
ENST00000640140.1:n.969A>C
ENST00000640250.1:n.296A>C
ENST00000640681.1:n.918A>C
ENST00000652046.1:c.797A>C MANE Select	ENSP00000498466.1:p.Asn266Thr
ENST00000352159.8:c.*114A>C	ENSP00000345601.4:n.*114A>C
ENST00000355279.2:c.772A>C	ENSP00000347426.2:n.772A>C
ENST00000355740.6:c.797A>C	ENSP00000347979.2:p.Asn266Thr
ENST00000357339.6:c.734A>C	ENSP00000349896.2:p.Asn245Thr
ENST00000479522.5:c.*226A>C	ENSP00000424113.1:n.*226A>C
ENST00000484444.5:c.*238A>C	ENSP00000420975.1:n.*238A>C
ENST00000488877.5:c.*238A>C	ENSP00000425159.1:n.*238A>C
ENST00000492756.5:c.625A>C	ENSP00000422453.1:n.625A>C
ENST00000494410.5:c.*155A>C	ENSP00000423755.1:n.*155A>C
ENST00000612663.4:c.*144A>C	ENSP00000477997.2:n.*144A>C
NM_000043.4:c.797A>C , LRG_134t1:c.797A>C	NP_000034.1:p.Asn266Thr
NM_152871.2:c.734A>C	NP_690610.1:p.Asn245Thr
NM_152872.2:c.*109A>C	NP_690611.1:n.*109A>C
NR_028033.2:n.971A>C
NR_028034.2:n.833A>C
NR_028035.2:n.896A>C
NR_028036.2:n.1034A>C
XM_006717819.2:c.878A>C	XP_006717882.1:p.Asn293Thr
XM_011539764.1:c.959A>C	XP_011538066.1:p.Asn320Thr
XM_011539765.1:c.896A>C	XP_011538067.1:p.Asn299Thr
XM_011539766.1:c.878A>C	XP_011538068.1:p.Asn293Thr
XM_011539767.1:c.842A>C	XP_011538069.1:p.Asn281Thr
XR_945732.1:n.865A>C
XR_945733.1:n.802A>C
NM_000043.5:c.797A>C	NP_000034.1:p.Asn266Thr
NM_001320619.1:c.*120A>C	NP_001307548.1:n.*120A>C
NM_152871.3:c.734A>C	NP_690610.1:p.Asn245Thr
NM_152872.3:c.*109A>C	NP_690611.1:n.*109A>C
NR_028033.3:n.943A>C
NR_028034.3:n.805A>C
NR_028035.3:n.868A>C
NR_028036.3:n.1006A>C
NR_135313.1:n.923A>C
NR_135314.1:n.1106A>C
NR_135315.1:n.859A>C
XM_006717819.3:c.878A>C	XP_006717882.1:p.Asn293Thr
XM_011539764.2:c.959A>C	XP_011538066.1:p.Asn320Thr
XM_011539765.2:c.896A>C	XP_011538067.1:p.Asn299Thr
XM_011539766.2:c.878A>C	XP_011538068.1:p.Asn293Thr
XM_011539767.3:c.842A>C	XP_011538069.1:p.Asn281Thr
XR_945732.3:n.865A>C
XR_945733.2:n.802A>C
NM_000043.6:c.797A>C MANE Select	NP_000034.1:p.Asn266Thr
NM_001320619.2:c.*120A>C	NP_001307548.1:n.*120A>C
NM_152871.4:c.734A>C	NP_690610.1:p.Asn245Thr
NM_152872.4:c.*109A>C	NP_690611.1:n.*109A>C
NR_028033.4:n.704A>C
NR_028034.4:n.566A>C
NR_028035.4:n.629A>C
NR_028036.4:n.767A>C
NR_135313.2:n.684A>C
NR_135314.2:n.963A>C
NR_135315.2:n.716A>C