Canonical Allele Identifier: CA1926639316

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014154G= , CM000672.2:g.89014154G=	GRCh38
NC_000010.10:g.90773911G= , CM000672.1:g.90773911G=	GRCh37
NC_000010.9:g.90763891G=	NCBI36
NG_009089.2:g.28624G= , LRG_134:g.28624G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1021G=
ENST00000355740.8:c.*35G=	ENSP00000347979.3:n.*35G=
ENST00000357339.7:c.649G=	ENSP00000349896.2:p.Gly217=
ENST00000371857.8:n.2257G=
ENST00000460510.6:c.-6G=	ENSP00000512812.1:n.-6G=
ENST00000466081.6:n.2361G=
ENST00000477270.6:c.757G=	ENSP00000512813.1:p.Gly253=
ENST00000479522.6:c.*141G=	ENSP00000424113.1:n.*141G=
ENST00000484444.6:c.*153G=	ENSP00000420975.1:n.*153G=
ENST00000488877.6:c.603G=	ENSP00000425159.1:n.603G=
ENST00000492756.7:c.*141G=	ENSP00000422453.1:n.*141G=
ENST00000494799.6:c.-6G=	ENSP00000512834.1:n.-6G=
ENST00000562983.3:c.-6G=	ENSP00000512845.1:n.-6G=
ENST00000612663.6:c.*114G=	ENSP00000477997.3:n.*114G=
ENST00000640140.2:n.857G=
ENST00000640250.2:n.211G=
ENST00000640681.2:n.816G=
ENST00000696723.1:n.4345G=
ENST00000696741.1:n.2350G=
ENST00000696742.1:n.2077G=
ENST00000696743.1:n.3480G=
ENST00000696744.1:n.751G=
ENST00000696767.1:n.1046G=
ENST00000696768.1:c.*35G=	ENSP00000512859.1:n.*35G=
ENST00000696769.1:n.2401G=
ENST00000696771.1:c.-6G=	ENSP00000512860.1:n.-6G=
ENST00000696772.1:n.2315G=
ENST00000696773.1:n.2054G=
ENST00000696774.1:n.5822G=
ENST00000696776.1:c.805G=	ENSP00000512861.1:p.Gly269=
ENST00000696777.1:n.2120G=
ENST00000696778.1:n.1148G=
ENST00000696779.1:c.319G=	ENSP00000512862.1:p.Gly107=
ENST00000696780.1:c.742G=	ENSP00000512863.1:p.Gly248=
ENST00000696781.1:c.457G=	ENSP00000512864.1:p.Gly153=
ENST00000696782.1:c.*114G=	ENSP00000512865.1:n.*114G=
ENST00000696783.1:n.2580G=
ENST00000696992.1:n.1829G=
ENST00000696995.1:n.4241G=
ENST00000696996.1:n.2154G=
ENST00000696997.1:c.*342G=	ENSP00000513028.1:n.*342G=
ENST00000696998.1:n.1966G=
ENST00000696999.1:c.-6G=	ENSP00000513029.1:n.-6G=
ENST00000697035.1:c.*45G=	ENSP00000513059.1:n.*45G=
ENST00000697036.1:c.*128G=	ENSP00000513060.1:n.*128G=
ENST00000697037.1:n.747G=
ENST00000697093.1:n.2948G=
ENST00000697094.1:n.3295G=
ENST00000697095.1:c.*1913G=	ENSP00000513104.1:n.*1913G=
ENST00000697096.1:n.1845G=
ENST00000697097.1:c.-6G=	ENSP00000513105.1:n.-6G=
ENST00000562983.2:n.898G=
ENST00000690268.1:c.793G=	ENSP00000509810.1:p.Gly265=
ENST00000355740.7:c.*38G=	ENSP00000347979.3:n.*38G=
ENST00000612663.5:c.*114G=	ENSP00000477997.3:n.*114G=
ENST00000640140.1:n.884G=
ENST00000640250.1:n.211G=
ENST00000640681.1:n.833G=
ENST00000652046.1:c.712G= MANE Select	ENSP00000498466.1:p.Gly238=
ENST00000313771.9:n.1021G=
ENST00000352159.8:c.*29G=	ENSP00000345601.4:n.*29G=
ENST00000355279.2:c.687G=	ENSP00000347426.2:n.687G=
ENST00000355740.6:c.712G=	ENSP00000347979.2:p.Gly238=
ENST00000357339.6:c.649G=	ENSP00000349896.2:p.Gly217=
ENST00000479522.5:c.*141G=	ENSP00000424113.1:n.*141G=
ENST00000484444.5:c.*153G=	ENSP00000420975.1:n.*153G=
ENST00000488877.5:c.*153G=	ENSP00000425159.1:n.*153G=
ENST00000492756.5:c.540G=	ENSP00000422453.1:n.540G=
ENST00000494410.5:c.*70G=	ENSP00000423755.1:n.*70G=
ENST00000494799.5:n.619G=
ENST00000612663.4:c.*59G=	ENSP00000477997.2:n.*59G=
ENST00000615406.4:c.712G=	ENSP00000484575.1:p.Gly238=
ENST00000626542.2:c.710G=	ENSP00000485876.1:p.Trp237=
NM_000043.4:c.712G= , LRG_134t1:c.712G=	NP_000034.1:p.Gly238=
NM_152871.2:c.649G=	NP_690610.1:p.Gly217=
NM_152872.2:c.*24G=	NP_690611.1:n.*24G=
NR_028033.2:n.886G=
NR_028034.2:n.748G=
NR_028035.2:n.811G=
NR_028036.2:n.949G=
XM_006717819.2:c.793G=	XP_006717882.1:p.Gly265=
XM_011539764.1:c.874G=	XP_011538066.1:p.Gly292=
XM_011539765.1:c.811G=	XP_011538067.1:p.Gly271=
XM_011539766.1:c.793G=	XP_011538068.1:p.Gly265=
XM_011539767.1:c.757G=	XP_011538069.1:p.Gly253=
XR_945732.1:n.780G=
XR_945733.1:n.717G=
NM_000043.5:c.712G=	NP_000034.1:p.Gly238=
NM_001320619.1:c.*35G=	NP_001307548.1:n.*35G=
NM_152871.3:c.649G=	NP_690610.1:p.Gly217=
NM_152872.3:c.*24G=	NP_690611.1:n.*24G=
NR_028033.3:n.858G=
NR_028034.3:n.720G=
NR_028035.3:n.783G=
NR_028036.3:n.921G=
NR_135313.1:n.838G=
NR_135314.1:n.1021G=
NR_135315.1:n.774G=
XM_006717819.3:c.793G=	XP_006717882.1:p.Gly265=
XM_011539764.2:c.874G=	XP_011538066.1:p.Gly292=
XM_011539765.2:c.811G=	XP_011538067.1:p.Gly271=
XM_011539766.2:c.793G=	XP_011538068.1:p.Gly265=
XM_011539767.3:c.757G=	XP_011538069.1:p.Gly253=
XR_945732.3:n.780G=
XR_945733.2:n.717G=
NM_000043.6:c.712G= MANE Select	NP_000034.1:p.Gly238=
NM_001320619.2:c.*35G=	NP_001307548.1:n.*35G=
NM_152871.4:c.649G=	NP_690610.1:p.Gly217=
NM_152872.4:c.*24G=	NP_690611.1:n.*24G=
NR_028033.4:n.619G=
NR_028034.4:n.481G=
NR_028035.4:n.544G=
NR_028036.4:n.682G=
NR_135313.2:n.599G=
NR_135314.2:n.878G=
NR_135315.2:n.631G=