Canonical Allele Identifier: CA377509526

Gene: FAS

Linked Data

• gnomAD v4: 10-89014119-A-T
• MyVariant Identifiers: chr10:g.90773876A>T (hg19) ; chr10:g.89014119A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014119A>T , CM000672.2:g.89014119A>T	GRCh38
NC_000010.10:g.90773876A>T , CM000672.1:g.90773876A>T	GRCh37
NC_000010.9:g.90763856A>T	NCBI36
NG_009089.2:g.28589A>T , LRG_134:g.28589A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.986A>T
ENST00000355740.8:c.594A>T	ENSP00000347979.3:p.Ter198Cys
ENST00000357339.7:c.614A>T	ENSP00000349896.2:p.Asp205Val
ENST00000371857.8:n.2222A>T
ENST00000460510.6:c.-41A>T	ENSP00000512812.1:n.-41A>T
ENST00000466081.6:n.2326A>T
ENST00000477270.6:c.722A>T	ENSP00000512813.1:p.Asp241Val
ENST00000479522.6:c.*106A>T	ENSP00000424113.1:n.*106A>T
ENST00000484444.6:c.*118A>T	ENSP00000420975.1:n.*118A>T
ENST00000488877.6:c.568A>T	ENSP00000425159.1:n.568A>T
ENST00000492756.7:c.*106A>T	ENSP00000422453.1:n.*106A>T
ENST00000494799.6:c.-41A>T	ENSP00000512834.1:n.-41A>T
ENST00000562983.3:c.-41A>T	ENSP00000512845.1:n.-41A>T
ENST00000612663.6:c.*79A>T	ENSP00000477997.3:n.*79A>T
ENST00000640140.2:n.822A>T
ENST00000640250.2:n.176A>T
ENST00000640681.2:n.781A>T
ENST00000696723.1:n.4310A>T
ENST00000696741.1:n.2315A>T
ENST00000696742.1:n.2042A>T
ENST00000696743.1:n.3445A>T
ENST00000696744.1:n.716A>T
ENST00000696767.1:n.1011A>T
ENST00000696768.1:c.531A>T	ENSP00000512859.1:p.Ter177Cys
ENST00000696769.1:n.2366A>T
ENST00000696771.1:c.-41A>T	ENSP00000512860.1:n.-41A>T
ENST00000696772.1:n.2280A>T
ENST00000696773.1:n.2019A>T
ENST00000696774.1:n.5787A>T
ENST00000696776.1:c.770A>T	ENSP00000512861.1:p.Asp257Val
ENST00000696777.1:n.2085A>T
ENST00000696778.1:n.1113A>T
ENST00000696779.1:c.284A>T	ENSP00000512862.1:p.Asp95Val
ENST00000696780.1:c.707A>T	ENSP00000512863.1:p.Asp236Val
ENST00000696781.1:c.422A>T	ENSP00000512864.1:p.Asp141Val
ENST00000696782.1:c.*79A>T	ENSP00000512865.1:n.*79A>T
ENST00000696783.1:n.2545A>T
ENST00000696992.1:n.1794A>T
ENST00000696995.1:n.4206A>T
ENST00000696996.1:n.2119A>T
ENST00000696997.1:c.*307A>T	ENSP00000513028.1:n.*307A>T
ENST00000696998.1:n.1931A>T
ENST00000696999.1:c.-41A>T	ENSP00000513029.1:n.-41A>T
ENST00000697035.1:c.*10A>T	ENSP00000513059.1:n.*10A>T
ENST00000697036.1:c.*93A>T	ENSP00000513060.1:n.*93A>T
ENST00000697037.1:n.712A>T
ENST00000697093.1:n.2913A>T
ENST00000697094.1:n.3260A>T
ENST00000697095.1:c.*1878A>T	ENSP00000513104.1:n.*1878A>T
ENST00000697096.1:n.1810A>T
ENST00000697097.1:c.-41A>T	ENSP00000513105.1:n.-41A>T
ENST00000562983.2:n.863A>T
ENST00000690268.1:c.758A>T	ENSP00000509810.1:p.Asp253Val
ENST00000355740.7:c.*3A>T	ENSP00000347979.3:n.*3A>T
ENST00000612663.5:c.*79A>T	ENSP00000477997.3:n.*79A>T
ENST00000640140.1:n.849A>T
ENST00000640250.1:n.176A>T
ENST00000640681.1:n.798A>T
ENST00000652046.1:c.677A>T MANE Select	ENSP00000498466.1:p.Asp226Val
ENST00000313771.9:n.986A>T
ENST00000352159.8:c.696A>T	ENSP00000345601.4:p.Arg232Ser
ENST00000355279.2:c.652A>T	ENSP00000347426.2:p.Met218Leu
ENST00000355740.6:c.677A>T	ENSP00000347979.2:p.Asp226Val
ENST00000357339.6:c.614A>T	ENSP00000349896.2:p.Asp205Val
ENST00000479522.5:c.*106A>T	ENSP00000424113.1:n.*106A>T
ENST00000484444.5:c.*118A>T	ENSP00000420975.1:n.*118A>T
ENST00000488877.5:c.*118A>T	ENSP00000425159.1:n.*118A>T
ENST00000492756.5:c.505A>T	ENSP00000422453.1:n.505A>T
ENST00000494410.5:c.*35A>T	ENSP00000423755.1:n.*35A>T
ENST00000494799.5:n.584A>T
ENST00000612663.4:c.*24A>T	ENSP00000477997.2:n.*24A>T
ENST00000615406.4:c.677A>T	ENSP00000484575.1:p.Asp226Val
ENST00000626542.2:c.677A>T	ENSP00000485876.1:p.Asp226Val
NM_000043.4:c.677A>T , LRG_134t1:c.677A>T	NP_000034.1:p.Asp226Val
NM_152871.2:c.614A>T	NP_690610.1:p.Asp205Val
NM_152872.2:c.652A>T	NP_690611.1:p.Met218Leu
NR_028033.2:n.851A>T
NR_028034.2:n.713A>T
NR_028035.2:n.776A>T
NR_028036.2:n.914A>T
XM_006717819.2:c.758A>T	XP_006717882.1:p.Asp253Val
XM_011539764.1:c.839A>T	XP_011538066.1:p.Asp280Val
XM_011539765.1:c.776A>T	XP_011538067.1:p.Asp259Val
XM_011539766.1:c.758A>T	XP_011538068.1:p.Asp253Val
XM_011539767.1:c.722A>T	XP_011538069.1:p.Asp241Val
XR_945732.1:n.745A>T
XR_945733.1:n.682A>T
NM_000043.5:c.677A>T	NP_000034.1:p.Asp226Val
NM_001320619.1:c.594A>T	NP_001307548.1:p.Ter198Cys
NM_152871.3:c.614A>T	NP_690610.1:p.Asp205Val
NM_152872.3:c.652A>T	NP_690611.1:p.Met218Leu
NR_028033.3:n.823A>T
NR_028034.3:n.685A>T
NR_028035.3:n.748A>T
NR_028036.3:n.886A>T
NR_135313.1:n.803A>T
NR_135314.1:n.986A>T
NR_135315.1:n.739A>T
XM_006717819.3:c.758A>T	XP_006717882.1:p.Asp253Val
XM_011539764.2:c.839A>T	XP_011538066.1:p.Asp280Val
XM_011539765.2:c.776A>T	XP_011538067.1:p.Asp259Val
XM_011539766.2:c.758A>T	XP_011538068.1:p.Asp253Val
XM_011539767.3:c.722A>T	XP_011538069.1:p.Asp241Val
XR_945732.3:n.745A>T
XR_945733.2:n.682A>T
NM_000043.6:c.677A>T MANE Select	NP_000034.1:p.Asp226Val
NM_001320619.2:c.594A>T	NP_001307548.1:p.Ter198Cys
NM_152871.4:c.614A>T	NP_690610.1:p.Asp205Val
NM_152872.4:c.652A>T	NP_690611.1:p.Met218Leu
NR_028033.4:n.584A>T
NR_028034.4:n.446A>T
NR_028035.4:n.509A>T
NR_028036.4:n.647A>T
NR_135313.2:n.564A>T
NR_135314.2:n.843A>T
NR_135315.2:n.596A>T