Canonical Allele Identifier: CA5593221

Gene: FAS

Linked Data

• dbSNP Id: rs768620067
• ExAC: 10:90774009 A / G
• gnomAD v2: 10-90774009-A-G
• MyVariant Identifiers: chr10:g.90774009A>G (hg19) ; chr10:g.89014252A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014252A>G , CM000672.2:g.89014252A>G	GRCh38
NC_000010.10:g.90774009A>G , CM000672.1:g.90774009A>G	GRCh37
NC_000010.9:g.90763989A>G	NCBI36
NG_009089.2:g.28722A>G , LRG_134:g.28722A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1119A>G
ENST00000355740.8:c.*133A>G	ENSP00000347979.3:n.*133A>G
ENST00000357339.7:c.747A>G	ENSP00000349896.2:p.Thr249=
ENST00000371857.8:n.2355A>G
ENST00000460510.6:c.93A>G	ENSP00000512812.1:p.Thr31=
ENST00000466081.6:n.2459A>G
ENST00000477270.6:c.855A>G	ENSP00000512813.1:p.Thr285=
ENST00000479522.6:c.*239A>G	ENSP00000424113.1:n.*239A>G
ENST00000484444.6:c.*251A>G	ENSP00000420975.1:n.*251A>G
ENST00000488877.6:c.701A>G	ENSP00000425159.1:n.701A>G
ENST00000492756.7:c.*239A>G	ENSP00000422453.1:n.*239A>G
ENST00000494799.6:c.93A>G	ENSP00000512834.1:p.Thr31=
ENST00000562983.3:c.93A>G	ENSP00000512845.1:p.Thr31=
ENST00000612663.6:c.*212A>G	ENSP00000477997.3:n.*212A>G
ENST00000640140.2:n.955A>G
ENST00000640250.2:n.309A>G
ENST00000640681.2:n.914A>G
ENST00000696723.1:n.4443A>G
ENST00000696741.1:n.2448A>G
ENST00000696742.1:n.2175A>G
ENST00000696743.1:n.3578A>G
ENST00000696744.1:n.849A>G
ENST00000696767.1:n.1144A>G
ENST00000696768.1:c.*133A>G	ENSP00000512859.1:n.*133A>G
ENST00000696769.1:n.2499A>G
ENST00000696771.1:c.93A>G	ENSP00000512860.1:p.Thr31=
ENST00000696772.1:n.2413A>G
ENST00000696773.1:n.2152A>G
ENST00000696774.1:n.5920A>G
ENST00000696776.1:c.903A>G	ENSP00000512861.1:p.Thr301=
ENST00000696777.1:n.2218A>G
ENST00000696778.1:n.1246A>G
ENST00000696779.1:c.417A>G	ENSP00000512862.1:p.Thr139=
ENST00000696780.1:c.840A>G	ENSP00000512863.1:p.Thr280=
ENST00000696781.1:c.555A>G	ENSP00000512864.1:p.Thr185=
ENST00000696782.1:c.*212A>G	ENSP00000512865.1:n.*212A>G
ENST00000696783.1:n.2678A>G
ENST00000696992.1:n.1927A>G
ENST00000696995.1:n.4339A>G
ENST00000696996.1:n.2252A>G
ENST00000696997.1:c.*440A>G	ENSP00000513028.1:n.*440A>G
ENST00000696998.1:n.2064A>G
ENST00000696999.1:c.93A>G	ENSP00000513029.1:p.Thr31=
ENST00000697035.1:c.*143A>G	ENSP00000513059.1:n.*143A>G
ENST00000697036.1:c.*226A>G	ENSP00000513060.1:n.*226A>G
ENST00000697037.1:n.845A>G
ENST00000697093.1:n.3046A>G
ENST00000697094.1:n.3393A>G
ENST00000697095.1:c.*2011A>G	ENSP00000513104.1:n.*2011A>G
ENST00000697096.1:n.1943A>G
ENST00000697097.1:c.93A>G	ENSP00000513105.1:p.Thr31=
ENST00000562983.2:n.996A>G
ENST00000690268.1:c.891A>G	ENSP00000509810.1:p.Thr297=
ENST00000355740.7:c.*136A>G	ENSP00000347979.3:n.*136A>G
ENST00000612663.5:c.*212A>G	ENSP00000477997.3:n.*212A>G
ENST00000640140.1:n.982A>G
ENST00000640250.1:n.309A>G
ENST00000640681.1:n.931A>G
ENST00000652046.1:c.810A>G MANE Select	ENSP00000498466.1:p.Thr270=
ENST00000352159.8:c.*127A>G	ENSP00000345601.4:n.*127A>G
ENST00000355279.2:c.785A>G	ENSP00000347426.2:n.785A>G
ENST00000355740.6:c.810A>G	ENSP00000347979.2:p.Thr270=
ENST00000357339.6:c.747A>G	ENSP00000349896.2:p.Thr249=
ENST00000479522.5:c.*239A>G	ENSP00000424113.1:n.*239A>G
ENST00000484444.5:c.*251A>G	ENSP00000420975.1:n.*251A>G
ENST00000488877.5:c.*251A>G	ENSP00000425159.1:n.*251A>G
ENST00000492756.5:c.638A>G	ENSP00000422453.1:n.638A>G
ENST00000494410.5:c.*168A>G	ENSP00000423755.1:n.*168A>G
ENST00000612663.4:c.*157A>G	ENSP00000477997.2:n.*157A>G
NM_000043.4:c.810A>G , LRG_134t1:c.810A>G	NP_000034.1:p.Thr270=
NM_152871.2:c.747A>G	NP_690610.1:p.Thr249=
NM_152872.2:c.*122A>G	NP_690611.1:n.*122A>G
NR_028033.2:n.984A>G
NR_028034.2:n.846A>G
NR_028035.2:n.909A>G
NR_028036.2:n.1047A>G
XM_006717819.2:c.891A>G	XP_006717882.1:p.Thr297=
XM_011539764.1:c.972A>G	XP_011538066.1:p.Thr324=
XM_011539765.1:c.909A>G	XP_011538067.1:p.Thr303=
XM_011539766.1:c.891A>G	XP_011538068.1:p.Thr297=
XM_011539767.1:c.855A>G	XP_011538069.1:p.Thr285=
XR_945732.1:n.878A>G
XR_945733.1:n.815A>G
NM_000043.5:c.810A>G	NP_000034.1:p.Thr270=
NM_001320619.1:c.*133A>G	NP_001307548.1:n.*133A>G
NM_152871.3:c.747A>G	NP_690610.1:p.Thr249=
NM_152872.3:c.*122A>G	NP_690611.1:n.*122A>G
NR_028033.3:n.956A>G
NR_028034.3:n.818A>G
NR_028035.3:n.881A>G
NR_028036.3:n.1019A>G
NR_135313.1:n.936A>G
NR_135314.1:n.1119A>G
NR_135315.1:n.872A>G
XM_006717819.3:c.891A>G	XP_006717882.1:p.Thr297=
XM_011539764.2:c.972A>G	XP_011538066.1:p.Thr324=
XM_011539765.2:c.909A>G	XP_011538067.1:p.Thr303=
XM_011539766.2:c.891A>G	XP_011538068.1:p.Thr297=
XM_011539767.3:c.855A>G	XP_011538069.1:p.Thr285=
XR_945732.3:n.878A>G
XR_945733.2:n.815A>G
NM_000043.6:c.810A>G MANE Select	NP_000034.1:p.Thr270=
NM_001320619.2:c.*133A>G	NP_001307548.1:n.*133A>G
NM_152871.4:c.747A>G	NP_690610.1:p.Thr249=
NM_152872.4:c.*122A>G	NP_690611.1:n.*122A>G
NR_028033.4:n.717A>G
NR_028034.4:n.579A>G
NR_028035.4:n.642A>G
NR_028036.4:n.780A>G
NR_135313.2:n.697A>G
NR_135314.2:n.976A>G
NR_135315.2:n.729A>G