Canonical Allele Identifier: CA377510022

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774079T>A (hg19) ; chr10:g.89014322T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014322T>A , CM000672.2:g.89014322T>A	GRCh38
NC_000010.10:g.90774079T>A , CM000672.1:g.90774079T>A	GRCh37
NC_000010.9:g.90764059T>A	NCBI36
NG_009089.2:g.28792T>A , LRG_134:g.28792T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1189T>A
ENST00000355740.8:c.*203T>A	ENSP00000347979.3:n.*203T>A
ENST00000357339.7:c.817T>A	ENSP00000349896.2:p.Leu273Met
ENST00000371857.8:n.2425T>A
ENST00000460510.6:c.163T>A	ENSP00000512812.1:p.Leu55Met
ENST00000466081.6:n.2529T>A
ENST00000477270.6:c.925T>A	ENSP00000512813.1:p.Leu309Met
ENST00000479522.6:c.*309T>A	ENSP00000424113.1:n.*309T>A
ENST00000484444.6:c.*321T>A	ENSP00000420975.1:n.*321T>A
ENST00000488877.6:c.771T>A	ENSP00000425159.1:n.771T>A
ENST00000492756.7:c.*309T>A	ENSP00000422453.1:n.*309T>A
ENST00000494799.6:c.163T>A	ENSP00000512834.1:p.Leu55Met
ENST00000562983.3:c.163T>A	ENSP00000512845.1:p.Leu55Met
ENST00000612663.6:c.*282T>A	ENSP00000477997.3:n.*282T>A
ENST00000640140.2:n.1025T>A
ENST00000640250.2:n.379T>A
ENST00000640681.2:n.984T>A
ENST00000696723.1:n.4513T>A
ENST00000696741.1:n.2518T>A
ENST00000696742.1:n.2245T>A
ENST00000696743.1:n.3648T>A
ENST00000696744.1:n.919T>A
ENST00000696767.1:n.1214T>A
ENST00000696768.1:c.*203T>A	ENSP00000512859.1:n.*203T>A
ENST00000696769.1:n.2569T>A
ENST00000696771.1:c.163T>A	ENSP00000512860.1:p.Leu55Met
ENST00000696772.1:n.2483T>A
ENST00000696773.1:n.2222T>A
ENST00000696774.1:n.5990T>A
ENST00000696776.1:c.973T>A	ENSP00000512861.1:p.Leu325Met
ENST00000696777.1:n.2288T>A
ENST00000696778.1:n.1316T>A
ENST00000696779.1:c.487T>A	ENSP00000512862.1:p.Leu163Met
ENST00000696780.1:c.910T>A	ENSP00000512863.1:p.Leu304Met
ENST00000696781.1:c.625T>A	ENSP00000512864.1:p.Leu209Met
ENST00000696782.1:c.*282T>A	ENSP00000512865.1:n.*282T>A
ENST00000696783.1:n.2748T>A
ENST00000696992.1:n.1997T>A
ENST00000696995.1:n.4409T>A
ENST00000696996.1:n.2322T>A
ENST00000696997.1:c.*510T>A	ENSP00000513028.1:n.*510T>A
ENST00000696998.1:n.2134T>A
ENST00000696999.1:c.163T>A	ENSP00000513029.1:p.Leu55Met
ENST00000697036.1:c.*296T>A	ENSP00000513060.1:n.*296T>A
ENST00000697037.1:n.915T>A
ENST00000697093.1:n.3116T>A
ENST00000697094.1:n.3463T>A
ENST00000697095.1:c.*2081T>A	ENSP00000513104.1:n.*2081T>A
ENST00000697096.1:n.2013T>A
ENST00000697097.1:c.163T>A	ENSP00000513105.1:p.Leu55Met
ENST00000562983.2:n.1066T>A
ENST00000690268.1:c.961T>A	ENSP00000509810.1:p.Leu321Met
ENST00000355740.7:c.*206T>A	ENSP00000347979.3:n.*206T>A
ENST00000612663.5:c.*282T>A	ENSP00000477997.3:n.*282T>A
ENST00000640140.1:n.1052T>A
ENST00000640250.1:n.379T>A
ENST00000640681.1:n.1001T>A
ENST00000652046.1:c.880T>A MANE Select	ENSP00000498466.1:p.Leu294Met
ENST00000352159.8:c.*197T>A	ENSP00000345601.4:n.*197T>A
ENST00000355279.2:c.855T>A	ENSP00000347426.2:n.855T>A
ENST00000355740.6:c.880T>A	ENSP00000347979.2:p.Leu294Met
ENST00000357339.6:c.817T>A	ENSP00000349896.2:p.Leu273Met
ENST00000479522.5:c.*309T>A	ENSP00000424113.1:n.*309T>A
ENST00000484444.5:c.*321T>A	ENSP00000420975.1:n.*321T>A
ENST00000488877.5:c.*321T>A	ENSP00000425159.1:n.*321T>A
ENST00000492756.5:c.708T>A	ENSP00000422453.1:n.708T>A
ENST00000494410.5:c.*238T>A	ENSP00000423755.1:n.*238T>A
ENST00000612663.4:c.*227T>A	ENSP00000477997.2:n.*227T>A
NM_000043.4:c.880T>A , LRG_134t1:c.880T>A	NP_000034.1:p.Leu294Met
NM_152871.2:c.817T>A	NP_690610.1:p.Leu273Met
NM_152872.2:c.*192T>A	NP_690611.1:n.*192T>A
NR_028033.2:n.1054T>A
NR_028034.2:n.916T>A
NR_028035.2:n.979T>A
NR_028036.2:n.1117T>A
XM_006717819.2:c.961T>A	XP_006717882.1:p.Leu321Met
XM_011539764.1:c.1042T>A	XP_011538066.1:p.Leu348Met
XM_011539765.1:c.979T>A	XP_011538067.1:p.Leu327Met
XM_011539766.1:c.961T>A	XP_011538068.1:p.Leu321Met
XM_011539767.1:c.925T>A	XP_011538069.1:p.Leu309Met
XR_945732.1:n.948T>A
XR_945733.1:n.885T>A
NM_000043.5:c.880T>A	NP_000034.1:p.Leu294Met
NM_001320619.1:c.*203T>A	NP_001307548.1:n.*203T>A
NM_152871.3:c.817T>A	NP_690610.1:p.Leu273Met
NM_152872.3:c.*192T>A	NP_690611.1:n.*192T>A
NR_028033.3:n.1026T>A
NR_028034.3:n.888T>A
NR_028035.3:n.951T>A
NR_028036.3:n.1089T>A
NR_135313.1:n.1006T>A
NR_135314.1:n.1189T>A
NR_135315.1:n.942T>A
XM_006717819.3:c.961T>A	XP_006717882.1:p.Leu321Met
XM_011539764.2:c.1042T>A	XP_011538066.1:p.Leu348Met
XM_011539765.2:c.979T>A	XP_011538067.1:p.Leu327Met
XM_011539766.2:c.961T>A	XP_011538068.1:p.Leu321Met
XM_011539767.3:c.925T>A	XP_011538069.1:p.Leu309Met
XR_945732.3:n.948T>A
XR_945733.2:n.885T>A
NM_000043.6:c.880T>A MANE Select	NP_000034.1:p.Leu294Met
NM_001320619.2:c.*203T>A	NP_001307548.1:n.*203T>A
NM_152871.4:c.817T>A	NP_690610.1:p.Leu273Met
NM_152872.4:c.*192T>A	NP_690611.1:n.*192T>A
NR_028033.4:n.787T>A
NR_028034.4:n.649T>A
NR_028035.4:n.712T>A
NR_028036.4:n.850T>A
NR_135313.2:n.767T>A
NR_135314.2:n.1046T>A
NR_135315.2:n.799T>A