Canonical Allele Identifier: CA5593233

Gene: FAS

Linked Data

• dbSNP Id: rs765240013
• ExAC: 10:90774099 A / G
• gnomAD v2: 10-90774099-A-G
• gnomAD v4: 10-89014342-A-G
• MyVariant Identifiers: chr10:g.90774099A>G (hg19) ; chr10:g.89014342A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014342A>G , CM000672.2:g.89014342A>G	GRCh38
NC_000010.10:g.90774099A>G , CM000672.1:g.90774099A>G	GRCh37
NC_000010.9:g.90764079A>G	NCBI36
NG_009089.2:g.28812A>G , LRG_134:g.28812A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1209A>G
ENST00000355740.8:c.*223A>G	ENSP00000347979.3:n.*223A>G
ENST00000357339.7:c.837A>G	ENSP00000349896.2:p.Lys279=
ENST00000371857.8:n.2445A>G
ENST00000460510.6:c.183A>G	ENSP00000512812.1:p.Lys61=
ENST00000466081.6:n.2549A>G
ENST00000477270.6:c.945A>G	ENSP00000512813.1:p.Lys315=
ENST00000479522.6:c.*329A>G	ENSP00000424113.1:n.*329A>G
ENST00000484444.6:c.*341A>G	ENSP00000420975.1:n.*341A>G
ENST00000488877.6:c.791A>G	ENSP00000425159.1:n.791A>G
ENST00000492756.7:c.*329A>G	ENSP00000422453.1:n.*329A>G
ENST00000494799.6:c.183A>G	ENSP00000512834.1:p.Lys61=
ENST00000562983.3:c.183A>G	ENSP00000512845.1:p.Lys61=
ENST00000612663.6:c.*302A>G	ENSP00000477997.3:n.*302A>G
ENST00000640140.2:n.1045A>G
ENST00000640250.2:n.399A>G
ENST00000640681.2:n.1004A>G
ENST00000696723.1:n.4533A>G
ENST00000696741.1:n.2538A>G
ENST00000696742.1:n.2265A>G
ENST00000696743.1:n.3668A>G
ENST00000696744.1:n.939A>G
ENST00000696767.1:n.1234A>G
ENST00000696768.1:c.*223A>G	ENSP00000512859.1:n.*223A>G
ENST00000696769.1:n.2589A>G
ENST00000696771.1:c.183A>G	ENSP00000512860.1:p.Lys61=
ENST00000696772.1:n.2503A>G
ENST00000696773.1:n.2242A>G
ENST00000696774.1:n.6010A>G
ENST00000696776.1:c.993A>G	ENSP00000512861.1:p.Lys331=
ENST00000696777.1:n.2308A>G
ENST00000696778.1:n.1336A>G
ENST00000696779.1:c.507A>G	ENSP00000512862.1:p.Lys169=
ENST00000696780.1:c.930A>G	ENSP00000512863.1:p.Lys310=
ENST00000696781.1:c.645A>G	ENSP00000512864.1:p.Lys215=
ENST00000696782.1:c.*302A>G	ENSP00000512865.1:n.*302A>G
ENST00000696783.1:n.2768A>G
ENST00000696992.1:n.2017A>G
ENST00000696995.1:n.4429A>G
ENST00000696996.1:n.2342A>G
ENST00000696997.1:c.*530A>G	ENSP00000513028.1:n.*530A>G
ENST00000696998.1:n.2154A>G
ENST00000696999.1:c.183A>G	ENSP00000513029.1:p.Lys61=
ENST00000697036.1:c.*316A>G	ENSP00000513060.1:n.*316A>G
ENST00000697037.1:n.935A>G
ENST00000697093.1:n.3136A>G
ENST00000697094.1:n.3483A>G
ENST00000697095.1:c.*2101A>G	ENSP00000513104.1:n.*2101A>G
ENST00000697096.1:n.2033A>G
ENST00000697097.1:c.183A>G	ENSP00000513105.1:p.Lys61=
ENST00000562983.2:n.1086A>G
ENST00000690268.1:c.981A>G	ENSP00000509810.1:p.Lys327=
ENST00000355740.7:c.*226A>G	ENSP00000347979.3:n.*226A>G
ENST00000612663.5:c.*302A>G	ENSP00000477997.3:n.*302A>G
ENST00000640140.1:n.1072A>G
ENST00000640250.1:n.399A>G
ENST00000640681.1:n.1021A>G
ENST00000652046.1:c.900A>G MANE Select	ENSP00000498466.1:p.Lys300=
ENST00000352159.8:c.*217A>G	ENSP00000345601.4:n.*217A>G
ENST00000355279.2:c.875A>G	ENSP00000347426.2:n.875A>G
ENST00000355740.6:c.900A>G	ENSP00000347979.2:p.Lys300=
ENST00000357339.6:c.837A>G	ENSP00000349896.2:p.Lys279=
ENST00000479522.5:c.*329A>G	ENSP00000424113.1:n.*329A>G
ENST00000484444.5:c.*341A>G	ENSP00000420975.1:n.*341A>G
ENST00000488877.5:c.*341A>G	ENSP00000425159.1:n.*341A>G
ENST00000492756.5:c.728A>G	ENSP00000422453.1:n.728A>G
ENST00000494410.5:c.*258A>G	ENSP00000423755.1:n.*258A>G
ENST00000612663.4:c.*247A>G	ENSP00000477997.2:n.*247A>G
NM_000043.4:c.900A>G , LRG_134t1:c.900A>G	NP_000034.1:p.Lys300=
NM_152871.2:c.837A>G	NP_690610.1:p.Lys279=
NM_152872.2:c.*212A>G	NP_690611.1:n.*212A>G
NR_028033.2:n.1074A>G
NR_028034.2:n.936A>G
NR_028035.2:n.999A>G
NR_028036.2:n.1137A>G
XM_006717819.2:c.981A>G	XP_006717882.1:p.Lys327=
XM_011539764.1:c.1062A>G	XP_011538066.1:p.Lys354=
XM_011539765.1:c.999A>G	XP_011538067.1:p.Lys333=
XM_011539766.1:c.981A>G	XP_011538068.1:p.Lys327=
XM_011539767.1:c.945A>G	XP_011538069.1:p.Lys315=
XR_945732.1:n.968A>G
XR_945733.1:n.905A>G
NM_000043.5:c.900A>G	NP_000034.1:p.Lys300=
NM_001320619.1:c.*223A>G	NP_001307548.1:n.*223A>G
NM_152871.3:c.837A>G	NP_690610.1:p.Lys279=
NM_152872.3:c.*212A>G	NP_690611.1:n.*212A>G
NR_028033.3:n.1046A>G
NR_028034.3:n.908A>G
NR_028035.3:n.971A>G
NR_028036.3:n.1109A>G
NR_135313.1:n.1026A>G
NR_135314.1:n.1209A>G
NR_135315.1:n.962A>G
XM_006717819.3:c.981A>G	XP_006717882.1:p.Lys327=
XM_011539764.2:c.1062A>G	XP_011538066.1:p.Lys354=
XM_011539765.2:c.999A>G	XP_011538067.1:p.Lys333=
XM_011539766.2:c.981A>G	XP_011538068.1:p.Lys327=
XM_011539767.3:c.945A>G	XP_011538069.1:p.Lys315=
XR_945732.3:n.968A>G
XR_945733.2:n.905A>G
NM_000043.6:c.900A>G MANE Select	NP_000034.1:p.Lys300=
NM_001320619.2:c.*223A>G	NP_001307548.1:n.*223A>G
NM_152871.4:c.837A>G	NP_690610.1:p.Lys279=
NM_152872.4:c.*212A>G	NP_690611.1:n.*212A>G
NR_028033.4:n.807A>G
NR_028034.4:n.669A>G
NR_028035.4:n.732A>G
NR_028036.4:n.870A>G
NR_135313.2:n.787A>G
NR_135314.2:n.1066A>G
NR_135315.2:n.819A>G