Canonical Allele Identifier: CA377509626

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773913A>T (hg19) ; chr10:g.89014156A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014156A>T , CM000672.2:g.89014156A>T	GRCh38
NC_000010.10:g.90773913A>T , CM000672.1:g.90773913A>T	GRCh37
NC_000010.9:g.90763893A>T	NCBI36
NG_009089.2:g.28626A>T , LRG_134:g.28626A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1023A>T
ENST00000355740.8:c.*37A>T	ENSP00000347979.3:n.*37A>T
ENST00000357339.7:c.651A>T	ENSP00000349896.2:p.Gly217=
ENST00000371857.8:n.2259A>T
ENST00000460510.6:c.-4A>T	ENSP00000512812.1:n.-4A>T
ENST00000466081.6:n.2363A>T
ENST00000477270.6:c.759A>T	ENSP00000512813.1:p.Gly253=
ENST00000479522.6:c.*143A>T	ENSP00000424113.1:n.*143A>T
ENST00000484444.6:c.*155A>T	ENSP00000420975.1:n.*155A>T
ENST00000488877.6:c.605A>T	ENSP00000425159.1:n.605A>T
ENST00000492756.7:c.*143A>T	ENSP00000422453.1:n.*143A>T
ENST00000494799.6:c.-4A>T	ENSP00000512834.1:n.-4A>T
ENST00000562983.3:c.-4A>T	ENSP00000512845.1:n.-4A>T
ENST00000612663.6:c.*116A>T	ENSP00000477997.3:n.*116A>T
ENST00000640140.2:n.859A>T
ENST00000640250.2:n.213A>T
ENST00000640681.2:n.818A>T
ENST00000696723.1:n.4347A>T
ENST00000696741.1:n.2352A>T
ENST00000696742.1:n.2079A>T
ENST00000696743.1:n.3482A>T
ENST00000696744.1:n.753A>T
ENST00000696767.1:n.1048A>T
ENST00000696768.1:c.*37A>T	ENSP00000512859.1:n.*37A>T
ENST00000696769.1:n.2403A>T
ENST00000696771.1:c.-4A>T	ENSP00000512860.1:n.-4A>T
ENST00000696772.1:n.2317A>T
ENST00000696773.1:n.2056A>T
ENST00000696774.1:n.5824A>T
ENST00000696776.1:c.807A>T	ENSP00000512861.1:p.Gly269=
ENST00000696777.1:n.2122A>T
ENST00000696778.1:n.1150A>T
ENST00000696779.1:c.321A>T	ENSP00000512862.1:p.Gly107=
ENST00000696780.1:c.744A>T	ENSP00000512863.1:p.Gly248=
ENST00000696781.1:c.459A>T	ENSP00000512864.1:p.Gly153=
ENST00000696782.1:c.*116A>T	ENSP00000512865.1:n.*116A>T
ENST00000696783.1:n.2582A>T
ENST00000696992.1:n.1831A>T
ENST00000696995.1:n.4243A>T
ENST00000696996.1:n.2156A>T
ENST00000696997.1:c.*344A>T	ENSP00000513028.1:n.*344A>T
ENST00000696998.1:n.1968A>T
ENST00000696999.1:c.-4A>T	ENSP00000513029.1:n.-4A>T
ENST00000697035.1:c.*47A>T	ENSP00000513059.1:n.*47A>T
ENST00000697036.1:c.*130A>T	ENSP00000513060.1:n.*130A>T
ENST00000697037.1:n.749A>T
ENST00000697093.1:n.2950A>T
ENST00000697094.1:n.3297A>T
ENST00000697095.1:c.*1915A>T	ENSP00000513104.1:n.*1915A>T
ENST00000697096.1:n.1847A>T
ENST00000697097.1:c.-4A>T	ENSP00000513105.1:n.-4A>T
ENST00000562983.2:n.900A>T
ENST00000690268.1:c.795A>T	ENSP00000509810.1:p.Gly265=
ENST00000355740.7:c.*40A>T	ENSP00000347979.3:n.*40A>T
ENST00000612663.5:c.*116A>T	ENSP00000477997.3:n.*116A>T
ENST00000640140.1:n.886A>T
ENST00000640250.1:n.213A>T
ENST00000640681.1:n.835A>T
ENST00000652046.1:c.714A>T MANE Select	ENSP00000498466.1:p.Gly238=
ENST00000313771.9:n.1023A>T
ENST00000352159.8:c.*31A>T	ENSP00000345601.4:n.*31A>T
ENST00000355279.2:c.689A>T	ENSP00000347426.2:n.689A>T
ENST00000355740.6:c.714A>T	ENSP00000347979.2:p.Gly238=
ENST00000357339.6:c.651A>T	ENSP00000349896.2:p.Gly217=
ENST00000479522.5:c.*143A>T	ENSP00000424113.1:n.*143A>T
ENST00000484444.5:c.*155A>T	ENSP00000420975.1:n.*155A>T
ENST00000488877.5:c.*155A>T	ENSP00000425159.1:n.*155A>T
ENST00000492756.5:c.542A>T	ENSP00000422453.1:n.542A>T
ENST00000494410.5:c.*72A>T	ENSP00000423755.1:n.*72A>T
ENST00000494799.5:n.621A>T
ENST00000612663.4:c.*61A>T	ENSP00000477997.2:n.*61A>T
ENST00000615406.4:c.714A>T	ENSP00000484575.1:p.Gly238=
ENST00000626542.2:c.712A>T	ENSP00000485876.1:p.Ser238Cys
NM_000043.4:c.714A>T , LRG_134t1:c.714A>T	NP_000034.1:p.Gly238=
NM_152871.2:c.651A>T	NP_690610.1:p.Gly217=
NM_152872.2:c.*26A>T	NP_690611.1:n.*26A>T
NR_028033.2:n.888A>T
NR_028034.2:n.750A>T
NR_028035.2:n.813A>T
NR_028036.2:n.951A>T
XM_006717819.2:c.795A>T	XP_006717882.1:p.Gly265=
XM_011539764.1:c.876A>T	XP_011538066.1:p.Gly292=
XM_011539765.1:c.813A>T	XP_011538067.1:p.Gly271=
XM_011539766.1:c.795A>T	XP_011538068.1:p.Gly265=
XM_011539767.1:c.759A>T	XP_011538069.1:p.Gly253=
XR_945732.1:n.782A>T
XR_945733.1:n.719A>T
NM_000043.5:c.714A>T	NP_000034.1:p.Gly238=
NM_001320619.1:c.*37A>T	NP_001307548.1:n.*37A>T
NM_152871.3:c.651A>T	NP_690610.1:p.Gly217=
NM_152872.3:c.*26A>T	NP_690611.1:n.*26A>T
NR_028033.3:n.860A>T
NR_028034.3:n.722A>T
NR_028035.3:n.785A>T
NR_028036.3:n.923A>T
NR_135313.1:n.840A>T
NR_135314.1:n.1023A>T
NR_135315.1:n.776A>T
XM_006717819.3:c.795A>T	XP_006717882.1:p.Gly265=
XM_011539764.2:c.876A>T	XP_011538066.1:p.Gly292=
XM_011539765.2:c.813A>T	XP_011538067.1:p.Gly271=
XM_011539766.2:c.795A>T	XP_011538068.1:p.Gly265=
XM_011539767.3:c.759A>T	XP_011538069.1:p.Gly253=
XR_945732.3:n.782A>T
XR_945733.2:n.719A>T
NM_000043.6:c.714A>T MANE Select	NP_000034.1:p.Gly238=
NM_001320619.2:c.*37A>T	NP_001307548.1:n.*37A>T
NM_152871.4:c.651A>T	NP_690610.1:p.Gly217=
NM_152872.4:c.*26A>T	NP_690611.1:n.*26A>T
NR_028033.4:n.621A>T
NR_028034.4:n.483A>T
NR_028035.4:n.546A>T
NR_028036.4:n.684A>T
NR_135313.2:n.601A>T
NR_135314.2:n.880A>T
NR_135315.2:n.633A>T