Canonical Allele Identifier: CA377509569

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773893T>G (hg19) ; chr10:g.89014136T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014136T>G , CM000672.2:g.89014136T>G	GRCh38
NC_000010.10:g.90773893T>G , CM000672.1:g.90773893T>G	GRCh37
NC_000010.9:g.90763873T>G	NCBI36
NG_009089.2:g.28606T>G , LRG_134:g.28606T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1003T>G
ENST00000355740.8:c.*17T>G	ENSP00000347979.3:n.*17T>G
ENST00000357339.7:c.631T>G	ENSP00000349896.2:p.Tyr211Asp
ENST00000371857.8:n.2239T>G
ENST00000460510.6:c.-24T>G	ENSP00000512812.1:n.-24T>G
ENST00000466081.6:n.2343T>G
ENST00000477270.6:c.739T>G	ENSP00000512813.1:p.Tyr247Asp
ENST00000479522.6:c.*123T>G	ENSP00000424113.1:n.*123T>G
ENST00000484444.6:c.*135T>G	ENSP00000420975.1:n.*135T>G
ENST00000488877.6:c.585T>G	ENSP00000425159.1:n.585T>G
ENST00000492756.7:c.*123T>G	ENSP00000422453.1:n.*123T>G
ENST00000494799.6:c.-24T>G	ENSP00000512834.1:n.-24T>G
ENST00000562983.3:c.-24T>G	ENSP00000512845.1:n.-24T>G
ENST00000612663.6:c.*96T>G	ENSP00000477997.3:n.*96T>G
ENST00000640140.2:n.839T>G
ENST00000640250.2:n.193T>G
ENST00000640681.2:n.798T>G
ENST00000696723.1:n.4327T>G
ENST00000696741.1:n.2332T>G
ENST00000696742.1:n.2059T>G
ENST00000696743.1:n.3462T>G
ENST00000696744.1:n.733T>G
ENST00000696767.1:n.1028T>G
ENST00000696768.1:c.*17T>G	ENSP00000512859.1:n.*17T>G
ENST00000696769.1:n.2383T>G
ENST00000696771.1:c.-24T>G	ENSP00000512860.1:n.-24T>G
ENST00000696772.1:n.2297T>G
ENST00000696773.1:n.2036T>G
ENST00000696774.1:n.5804T>G
ENST00000696776.1:c.787T>G	ENSP00000512861.1:p.Tyr263Asp
ENST00000696777.1:n.2102T>G
ENST00000696778.1:n.1130T>G
ENST00000696779.1:c.301T>G	ENSP00000512862.1:p.Tyr101Asp
ENST00000696780.1:c.724T>G	ENSP00000512863.1:p.Tyr242Asp
ENST00000696781.1:c.439T>G	ENSP00000512864.1:p.Tyr147Asp
ENST00000696782.1:c.*96T>G	ENSP00000512865.1:n.*96T>G
ENST00000696783.1:n.2562T>G
ENST00000696992.1:n.1811T>G
ENST00000696995.1:n.4223T>G
ENST00000696996.1:n.2136T>G
ENST00000696997.1:c.*324T>G	ENSP00000513028.1:n.*324T>G
ENST00000696998.1:n.1948T>G
ENST00000696999.1:c.-24T>G	ENSP00000513029.1:n.-24T>G
ENST00000697035.1:c.*27T>G	ENSP00000513059.1:n.*27T>G
ENST00000697036.1:c.*110T>G	ENSP00000513060.1:n.*110T>G
ENST00000697037.1:n.729T>G
ENST00000697093.1:n.2930T>G
ENST00000697094.1:n.3277T>G
ENST00000697095.1:c.*1895T>G	ENSP00000513104.1:n.*1895T>G
ENST00000697096.1:n.1827T>G
ENST00000697097.1:c.-24T>G	ENSP00000513105.1:n.-24T>G
ENST00000562983.2:n.880T>G
ENST00000690268.1:c.775T>G	ENSP00000509810.1:p.Tyr259Asp
ENST00000355740.7:c.*20T>G	ENSP00000347979.3:n.*20T>G
ENST00000612663.5:c.*96T>G	ENSP00000477997.3:n.*96T>G
ENST00000640140.1:n.866T>G
ENST00000640250.1:n.193T>G
ENST00000640681.1:n.815T>G
ENST00000652046.1:c.694T>G MANE Select	ENSP00000498466.1:p.Tyr232Asp
ENST00000313771.9:n.1003T>G
ENST00000352159.8:c.*11T>G	ENSP00000345601.4:n.*11T>G
ENST00000355279.2:c.669T>G	ENSP00000347426.2:n.669T>G
ENST00000355740.6:c.694T>G	ENSP00000347979.2:p.Tyr232Asp
ENST00000357339.6:c.631T>G	ENSP00000349896.2:p.Tyr211Asp
ENST00000479522.5:c.*123T>G	ENSP00000424113.1:n.*123T>G
ENST00000484444.5:c.*135T>G	ENSP00000420975.1:n.*135T>G
ENST00000488877.5:c.*135T>G	ENSP00000425159.1:n.*135T>G
ENST00000492756.5:c.522T>G	ENSP00000422453.1:n.522T>G
ENST00000494410.5:c.*52T>G	ENSP00000423755.1:n.*52T>G
ENST00000494799.5:n.601T>G
ENST00000612663.4:c.*41T>G	ENSP00000477997.2:n.*41T>G
ENST00000615406.4:c.694T>G	ENSP00000484575.1:p.Tyr232Asp
ENST00000626542.2:c.694T>G	ENSP00000485876.1:p.Tyr232Asp
NM_000043.4:c.694T>G , LRG_134t1:c.694T>G	NP_000034.1:p.Tyr232Asp
NM_152871.2:c.631T>G	NP_690610.1:p.Tyr211Asp
NM_152872.2:c.*6T>G	NP_690611.1:n.*6T>G
NR_028033.2:n.868T>G
NR_028034.2:n.730T>G
NR_028035.2:n.793T>G
NR_028036.2:n.931T>G
XM_006717819.2:c.775T>G	XP_006717882.1:p.Tyr259Asp
XM_011539764.1:c.856T>G	XP_011538066.1:p.Tyr286Asp
XM_011539765.1:c.793T>G	XP_011538067.1:p.Tyr265Asp
XM_011539766.1:c.775T>G	XP_011538068.1:p.Tyr259Asp
XM_011539767.1:c.739T>G	XP_011538069.1:p.Tyr247Asp
XR_945732.1:n.762T>G
XR_945733.1:n.699T>G
NM_000043.5:c.694T>G	NP_000034.1:p.Tyr232Asp
NM_001320619.1:c.*17T>G	NP_001307548.1:n.*17T>G
NM_152871.3:c.631T>G	NP_690610.1:p.Tyr211Asp
NM_152872.3:c.*6T>G	NP_690611.1:n.*6T>G
NR_028033.3:n.840T>G
NR_028034.3:n.702T>G
NR_028035.3:n.765T>G
NR_028036.3:n.903T>G
NR_135313.1:n.820T>G
NR_135314.1:n.1003T>G
NR_135315.1:n.756T>G
XM_006717819.3:c.775T>G	XP_006717882.1:p.Tyr259Asp
XM_011539764.2:c.856T>G	XP_011538066.1:p.Tyr286Asp
XM_011539765.2:c.793T>G	XP_011538067.1:p.Tyr265Asp
XM_011539766.2:c.775T>G	XP_011538068.1:p.Tyr259Asp
XM_011539767.3:c.739T>G	XP_011538069.1:p.Tyr247Asp
XR_945732.3:n.762T>G
XR_945733.2:n.699T>G
NM_000043.6:c.694T>G MANE Select	NP_000034.1:p.Tyr232Asp
NM_001320619.2:c.*17T>G	NP_001307548.1:n.*17T>G
NM_152871.4:c.631T>G	NP_690610.1:p.Tyr211Asp
NM_152872.4:c.*6T>G	NP_690611.1:n.*6T>G
NR_028033.4:n.601T>G
NR_028034.4:n.463T>G
NR_028035.4:n.526T>G
NR_028036.4:n.664T>G
NR_135313.2:n.581T>G
NR_135314.2:n.860T>G
NR_135315.2:n.613T>G