Canonical Allele Identifier: CA1926639337

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014198T= , CM000672.2:g.89014198T=	GRCh38
NC_000010.10:g.90773955T= , CM000672.1:g.90773955T=	GRCh37
NC_000010.9:g.90763935T=	NCBI36
NG_009089.2:g.28668T= , LRG_134:g.28668T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1065T=
ENST00000355740.8:c.*79T=	ENSP00000347979.3:n.*79T=
ENST00000357339.7:c.693T=	ENSP00000349896.2:p.Asn231=
ENST00000371857.8:n.2301T=
ENST00000460510.6:c.39T=	ENSP00000512812.1:p.Asn13=
ENST00000466081.6:n.2405T=
ENST00000477270.6:c.801T=	ENSP00000512813.1:p.Asn267=
ENST00000479522.6:c.*185T=	ENSP00000424113.1:n.*185T=
ENST00000484444.6:c.*197T=	ENSP00000420975.1:n.*197T=
ENST00000488877.6:c.647T=	ENSP00000425159.1:n.647T=
ENST00000492756.7:c.*185T=	ENSP00000422453.1:n.*185T=
ENST00000494799.6:c.39T=	ENSP00000512834.1:p.Asn13=
ENST00000562983.3:c.39T=	ENSP00000512845.1:p.Asn13=
ENST00000612663.6:c.*158T=	ENSP00000477997.3:n.*158T=
ENST00000640140.2:n.901T=
ENST00000640250.2:n.255T=
ENST00000640681.2:n.860T=
ENST00000696723.1:n.4389T=
ENST00000696741.1:n.2394T=
ENST00000696742.1:n.2121T=
ENST00000696743.1:n.3524T=
ENST00000696744.1:n.795T=
ENST00000696767.1:n.1090T=
ENST00000696768.1:c.*79T=	ENSP00000512859.1:n.*79T=
ENST00000696769.1:n.2445T=
ENST00000696771.1:c.39T=	ENSP00000512860.1:p.Asn13=
ENST00000696772.1:n.2359T=
ENST00000696773.1:n.2098T=
ENST00000696774.1:n.5866T=
ENST00000696776.1:c.849T=	ENSP00000512861.1:p.Asn283=
ENST00000696777.1:n.2164T=
ENST00000696778.1:n.1192T=
ENST00000696779.1:c.363T=	ENSP00000512862.1:p.Asn121=
ENST00000696780.1:c.786T=	ENSP00000512863.1:p.Asn262=
ENST00000696781.1:c.501T=	ENSP00000512864.1:p.Asn167=
ENST00000696782.1:c.*158T=	ENSP00000512865.1:n.*158T=
ENST00000696783.1:n.2624T=
ENST00000696992.1:n.1873T=
ENST00000696995.1:n.4285T=
ENST00000696996.1:n.2198T=
ENST00000696997.1:c.*386T=	ENSP00000513028.1:n.*386T=
ENST00000696998.1:n.2010T=
ENST00000696999.1:c.39T=	ENSP00000513029.1:p.Asn13=
ENST00000697035.1:c.*89T=	ENSP00000513059.1:n.*89T=
ENST00000697036.1:c.*172T=	ENSP00000513060.1:n.*172T=
ENST00000697037.1:n.791T=
ENST00000697093.1:n.2992T=
ENST00000697094.1:n.3339T=
ENST00000697095.1:c.*1957T=	ENSP00000513104.1:n.*1957T=
ENST00000697096.1:n.1889T=
ENST00000697097.1:c.39T=	ENSP00000513105.1:p.Asn13=
ENST00000562983.2:n.942T=
ENST00000690268.1:c.837T=	ENSP00000509810.1:p.Asn279=
ENST00000355740.7:c.*82T=	ENSP00000347979.3:n.*82T=
ENST00000612663.5:c.*158T=	ENSP00000477997.3:n.*158T=
ENST00000640140.1:n.928T=
ENST00000640250.1:n.255T=
ENST00000640681.1:n.877T=
ENST00000652046.1:c.756T= MANE Select	ENSP00000498466.1:p.Asn252=
ENST00000352159.8:c.*73T=	ENSP00000345601.4:n.*73T=
ENST00000355279.2:c.731T=	ENSP00000347426.2:n.731T=
ENST00000355740.6:c.756T=	ENSP00000347979.2:p.Asn252=
ENST00000357339.6:c.693T=	ENSP00000349896.2:p.Asn231=
ENST00000479522.5:c.*185T=	ENSP00000424113.1:n.*185T=
ENST00000484444.5:c.*197T=	ENSP00000420975.1:n.*197T=
ENST00000488877.5:c.*197T=	ENSP00000425159.1:n.*197T=
ENST00000492756.5:c.584T=	ENSP00000422453.1:n.584T=
ENST00000494410.5:c.*114T=	ENSP00000423755.1:n.*114T=
ENST00000494799.5:n.663T=
ENST00000612663.4:c.*103T=	ENSP00000477997.2:n.*103T=
ENST00000615406.4:c.754T=	ENSP00000484575.1:p.Trp252=
NM_000043.4:c.756T= , LRG_134t1:c.756T=	NP_000034.1:p.Asn252=
NM_152871.2:c.693T=	NP_690610.1:p.Asn231=
NM_152872.2:c.*68T=	NP_690611.1:n.*68T=
NR_028033.2:n.930T=
NR_028034.2:n.792T=
NR_028035.2:n.855T=
NR_028036.2:n.993T=
XM_006717819.2:c.837T=	XP_006717882.1:p.Asn279=
XM_011539764.1:c.918T=	XP_011538066.1:p.Asn306=
XM_011539765.1:c.855T=	XP_011538067.1:p.Asn285=
XM_011539766.1:c.837T=	XP_011538068.1:p.Asn279=
XM_011539767.1:c.801T=	XP_011538069.1:p.Asn267=
XR_945732.1:n.824T=
XR_945733.1:n.761T=
NM_000043.5:c.756T=	NP_000034.1:p.Asn252=
NM_001320619.1:c.*79T=	NP_001307548.1:n.*79T=
NM_152871.3:c.693T=	NP_690610.1:p.Asn231=
NM_152872.3:c.*68T=	NP_690611.1:n.*68T=
NR_028033.3:n.902T=
NR_028034.3:n.764T=
NR_028035.3:n.827T=
NR_028036.3:n.965T=
NR_135313.1:n.882T=
NR_135314.1:n.1065T=
NR_135315.1:n.818T=
XM_006717819.3:c.837T=	XP_006717882.1:p.Asn279=
XM_011539764.2:c.918T=	XP_011538066.1:p.Asn306=
XM_011539765.2:c.855T=	XP_011538067.1:p.Asn285=
XM_011539766.2:c.837T=	XP_011538068.1:p.Asn279=
XM_011539767.3:c.801T=	XP_011538069.1:p.Asn267=
XR_945732.3:n.824T=
XR_945733.2:n.761T=
NM_000043.6:c.756T= MANE Select	NP_000034.1:p.Asn252=
NM_001320619.2:c.*79T=	NP_001307548.1:n.*79T=
NM_152871.4:c.693T=	NP_690610.1:p.Asn231=
NM_152872.4:c.*68T=	NP_690611.1:n.*68T=
NR_028033.4:n.663T=
NR_028034.4:n.525T=
NR_028035.4:n.588T=
NR_028036.4:n.726T=
NR_135313.2:n.643T=
NR_135314.2:n.922T=
NR_135315.2:n.675T=