Canonical Allele Identifier: CA377510028
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014325A>G , CM000672.2:g.89014325A>G GRCh38
NC_000010.10:g.90774082A>G , CM000672.1:g.90774082A>G GRCh37
NC_000010.9:g.90764062A>G NCBI36
NG_009089.2:g.28795A>G , LRG_134:g.28795A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1192A>G
ENST00000355740.8:c.*206A>G ENSP00000347979.3:n.*206A>G
ENST00000357339.7:c.820A>G ENSP00000349896.2:p.Ile274Val
ENST00000371857.8:n.2428A>G
ENST00000460510.6:c.166A>G ENSP00000512812.1:p.Ile56Val
ENST00000466081.6:n.2532A>G
ENST00000477270.6:c.928A>G ENSP00000512813.1:p.Ile310Val
ENST00000479522.6:c.*312A>G ENSP00000424113.1:n.*312A>G
ENST00000484444.6:c.*324A>G ENSP00000420975.1:n.*324A>G
ENST00000488877.6:c.774A>G ENSP00000425159.1:n.774A>G
ENST00000492756.7:c.*312A>G ENSP00000422453.1:n.*312A>G
ENST00000494799.6:c.166A>G ENSP00000512834.1:p.Ile56Val
ENST00000562983.3:c.166A>G ENSP00000512845.1:p.Ile56Val
ENST00000612663.6:c.*285A>G ENSP00000477997.3:n.*285A>G
ENST00000640140.2:n.1028A>G
ENST00000640250.2:n.382A>G
ENST00000640681.2:n.987A>G
ENST00000696723.1:n.4516A>G
ENST00000696741.1:n.2521A>G
ENST00000696742.1:n.2248A>G
ENST00000696743.1:n.3651A>G
ENST00000696744.1:n.922A>G
ENST00000696767.1:n.1217A>G
ENST00000696768.1:c.*206A>G ENSP00000512859.1:n.*206A>G
ENST00000696769.1:n.2572A>G
ENST00000696771.1:c.166A>G ENSP00000512860.1:p.Ile56Val
ENST00000696772.1:n.2486A>G
ENST00000696773.1:n.2225A>G
ENST00000696774.1:n.5993A>G
ENST00000696776.1:c.976A>G ENSP00000512861.1:p.Ile326Val
ENST00000696777.1:n.2291A>G
ENST00000696778.1:n.1319A>G
ENST00000696779.1:c.490A>G ENSP00000512862.1:p.Ile164Val
ENST00000696780.1:c.913A>G ENSP00000512863.1:p.Ile305Val
ENST00000696781.1:c.628A>G ENSP00000512864.1:p.Ile210Val
ENST00000696782.1:c.*285A>G ENSP00000512865.1:n.*285A>G
ENST00000696783.1:n.2751A>G
ENST00000696992.1:n.2000A>G
ENST00000696995.1:n.4412A>G
ENST00000696996.1:n.2325A>G
ENST00000696997.1:c.*513A>G ENSP00000513028.1:n.*513A>G
ENST00000696998.1:n.2137A>G
ENST00000696999.1:c.166A>G ENSP00000513029.1:p.Ile56Val
ENST00000697036.1:c.*299A>G ENSP00000513060.1:n.*299A>G
ENST00000697037.1:n.918A>G
ENST00000697093.1:n.3119A>G
ENST00000697094.1:n.3466A>G
ENST00000697095.1:c.*2084A>G ENSP00000513104.1:n.*2084A>G
ENST00000697096.1:n.2016A>G
ENST00000697097.1:c.166A>G ENSP00000513105.1:p.Ile56Val
ENST00000562983.2:n.1069A>G
ENST00000690268.1:c.964A>G ENSP00000509810.1:p.Ile322Val
ENST00000355740.7:c.*209A>G ENSP00000347979.3:n.*209A>G
ENST00000612663.5:c.*285A>G ENSP00000477997.3:n.*285A>G
ENST00000640140.1:n.1055A>G
ENST00000640250.1:n.382A>G
ENST00000640681.1:n.1004A>G
ENST00000652046.1:c.883A>G MANE Select ENSP00000498466.1:p.Ile295Val
ENST00000352159.8:c.*200A>G ENSP00000345601.4:n.*200A>G
ENST00000355279.2:c.858A>G ENSP00000347426.2:n.858A>G
ENST00000355740.6:c.883A>G ENSP00000347979.2:p.Ile295Val
ENST00000357339.6:c.820A>G ENSP00000349896.2:p.Ile274Val
ENST00000479522.5:c.*312A>G ENSP00000424113.1:n.*312A>G
ENST00000484444.5:c.*324A>G ENSP00000420975.1:n.*324A>G
ENST00000488877.5:c.*324A>G ENSP00000425159.1:n.*324A>G
ENST00000492756.5:c.711A>G ENSP00000422453.1:n.711A>G
ENST00000494410.5:c.*241A>G ENSP00000423755.1:n.*241A>G
ENST00000612663.4:c.*230A>G ENSP00000477997.2:n.*230A>G
NM_000043.4:c.883A>G , LRG_134t1:c.883A>G NP_000034.1:p.Ile295Val
NM_152871.2:c.820A>G NP_690610.1:p.Ile274Val
NM_152872.2:c.*195A>G NP_690611.1:n.*195A>G
NR_028033.2:n.1057A>G
NR_028034.2:n.919A>G
NR_028035.2:n.982A>G
NR_028036.2:n.1120A>G
XM_006717819.2:c.964A>G XP_006717882.1:p.Ile322Val
XM_011539764.1:c.1045A>G XP_011538066.1:p.Ile349Val
XM_011539765.1:c.982A>G XP_011538067.1:p.Ile328Val
XM_011539766.1:c.964A>G XP_011538068.1:p.Ile322Val
XM_011539767.1:c.928A>G XP_011538069.1:p.Ile310Val
XR_945732.1:n.951A>G
XR_945733.1:n.888A>G
NM_000043.5:c.883A>G NP_000034.1:p.Ile295Val
NM_001320619.1:c.*206A>G NP_001307548.1:n.*206A>G
NM_152871.3:c.820A>G NP_690610.1:p.Ile274Val
NM_152872.3:c.*195A>G NP_690611.1:n.*195A>G
NR_028033.3:n.1029A>G
NR_028034.3:n.891A>G
NR_028035.3:n.954A>G
NR_028036.3:n.1092A>G
NR_135313.1:n.1009A>G
NR_135314.1:n.1192A>G
NR_135315.1:n.945A>G
XM_006717819.3:c.964A>G XP_006717882.1:p.Ile322Val
XM_011539764.2:c.1045A>G XP_011538066.1:p.Ile349Val
XM_011539765.2:c.982A>G XP_011538067.1:p.Ile328Val
XM_011539766.2:c.964A>G XP_011538068.1:p.Ile322Val
XM_011539767.3:c.928A>G XP_011538069.1:p.Ile310Val
XR_945732.3:n.951A>G
XR_945733.2:n.888A>G
NM_000043.6:c.883A>G MANE Select NP_000034.1:p.Ile295Val
NM_001320619.2:c.*206A>G NP_001307548.1:n.*206A>G
NM_152871.4:c.820A>G NP_690610.1:p.Ile274Val
NM_152872.4:c.*195A>G NP_690611.1:n.*195A>G
NR_028033.4:n.790A>G
NR_028034.4:n.652A>G
NR_028035.4:n.715A>G
NR_028036.4:n.853A>G
NR_135313.2:n.770A>G
NR_135314.2:n.1049A>G
NR_135315.2:n.802A>G