Canonical Allele Identifier: CA1926639362
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014271C= , CM000672.2:g.89014271C= GRCh38
NC_000010.10:g.90774028C= , CM000672.1:g.90774028C= GRCh37
NC_000010.9:g.90764008C= NCBI36
NG_009089.2:g.28741C= , LRG_134:g.28741C=

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.1138C=
ENST00000355740.8:c.*152C= ENSP00000347979.3:n.*152C=
ENST00000357339.7:c.766C= ENSP00000349896.2:p.Leu256=
ENST00000371857.8:n.2374C=
ENST00000460510.6:c.112C= ENSP00000512812.1:p.Leu38=
ENST00000466081.6:n.2478C=
ENST00000477270.6:c.874C= ENSP00000512813.1:p.Leu292=
ENST00000479522.6:c.*258C= ENSP00000424113.1:n.*258C=
ENST00000484444.6:c.*270C= ENSP00000420975.1:n.*270C=
ENST00000488877.6:c.720C= ENSP00000425159.1:n.720C=
ENST00000492756.7:c.*258C= ENSP00000422453.1:n.*258C=
ENST00000494799.6:c.112C= ENSP00000512834.1:p.Leu38=
ENST00000562983.3:c.112C= ENSP00000512845.1:p.Leu38=
ENST00000612663.6:c.*231C= ENSP00000477997.3:n.*231C=
ENST00000640140.2:n.974C=
ENST00000640250.2:n.328C=
ENST00000640681.2:n.933C=
ENST00000696723.1:n.4462C=
ENST00000696741.1:n.2467C=
ENST00000696742.1:n.2194C=
ENST00000696743.1:n.3597C=
ENST00000696744.1:n.868C=
ENST00000696767.1:n.1163C=
ENST00000696768.1:c.*152C= ENSP00000512859.1:n.*152C=
ENST00000696769.1:n.2518C=
ENST00000696771.1:c.112C= ENSP00000512860.1:p.Leu38=
ENST00000696772.1:n.2432C=
ENST00000696773.1:n.2171C=
ENST00000696774.1:n.5939C=
ENST00000696776.1:c.922C= ENSP00000512861.1:p.Leu308=
ENST00000696777.1:n.2237C=
ENST00000696778.1:n.1265C=
ENST00000696779.1:c.436C= ENSP00000512862.1:p.Leu146=
ENST00000696780.1:c.859C= ENSP00000512863.1:p.Leu287=
ENST00000696781.1:c.574C= ENSP00000512864.1:p.Leu192=
ENST00000696782.1:c.*231C= ENSP00000512865.1:n.*231C=
ENST00000696783.1:n.2697C=
ENST00000696992.1:n.1946C=
ENST00000696995.1:n.4358C=
ENST00000696996.1:n.2271C=
ENST00000696997.1:c.*459C= ENSP00000513028.1:n.*459C=
ENST00000696998.1:n.2083C=
ENST00000696999.1:c.112C= ENSP00000513029.1:p.Leu38=
ENST00000697035.1:c.*162C= ENSP00000513059.1:n.*162C=
ENST00000697036.1:c.*245C= ENSP00000513060.1:n.*245C=
ENST00000697037.1:n.864C=
ENST00000697093.1:n.3065C=
ENST00000697094.1:n.3412C=
ENST00000697095.1:c.*2030C= ENSP00000513104.1:n.*2030C=
ENST00000697096.1:n.1962C=
ENST00000697097.1:c.112C= ENSP00000513105.1:p.Leu38=
ENST00000562983.2:n.1015C=
ENST00000690268.1:c.910C= ENSP00000509810.1:p.Leu304=
ENST00000355740.7:c.*155C= ENSP00000347979.3:n.*155C=
ENST00000612663.5:c.*231C= ENSP00000477997.3:n.*231C=
ENST00000640140.1:n.1001C=
ENST00000640250.1:n.328C=
ENST00000640681.1:n.950C=
ENST00000652046.1:c.829C= MANE Select ENSP00000498466.1:p.Leu277=
ENST00000352159.8:c.*146C= ENSP00000345601.4:n.*146C=
ENST00000355279.2:c.804C= ENSP00000347426.2:n.804C=
ENST00000355740.6:c.829C= ENSP00000347979.2:p.Leu277=
ENST00000357339.6:c.766C= ENSP00000349896.2:p.Leu256=
ENST00000479522.5:c.*258C= ENSP00000424113.1:n.*258C=
ENST00000484444.5:c.*270C= ENSP00000420975.1:n.*270C=
ENST00000488877.5:c.*270C= ENSP00000425159.1:n.*270C=
ENST00000492756.5:c.657C= ENSP00000422453.1:n.657C=
ENST00000494410.5:c.*187C= ENSP00000423755.1:n.*187C=
ENST00000612663.4:c.*176C= ENSP00000477997.2:n.*176C=
NM_000043.4:c.829C= , LRG_134t1:c.829C= NP_000034.1:p.Leu277=
NM_152871.2:c.766C= NP_690610.1:p.Leu256=
NM_152872.2:c.*141C= NP_690611.1:n.*141C=
NR_028033.2:n.1003C=
NR_028034.2:n.865C=
NR_028035.2:n.928C=
NR_028036.2:n.1066C=
XM_006717819.2:c.910C= XP_006717882.1:p.Leu304=
XM_011539764.1:c.991C= XP_011538066.1:p.Leu331=
XM_011539765.1:c.928C= XP_011538067.1:p.Leu310=
XM_011539766.1:c.910C= XP_011538068.1:p.Leu304=
XM_011539767.1:c.874C= XP_011538069.1:p.Leu292=
XR_945732.1:n.897C=
XR_945733.1:n.834C=
NM_000043.5:c.829C= NP_000034.1:p.Leu277=
NM_001320619.1:c.*152C= NP_001307548.1:n.*152C=
NM_152871.3:c.766C= NP_690610.1:p.Leu256=
NM_152872.3:c.*141C= NP_690611.1:n.*141C=
NR_028033.3:n.975C=
NR_028034.3:n.837C=
NR_028035.3:n.900C=
NR_028036.3:n.1038C=
NR_135313.1:n.955C=
NR_135314.1:n.1138C=
NR_135315.1:n.891C=
XM_006717819.3:c.910C= XP_006717882.1:p.Leu304=
XM_011539764.2:c.991C= XP_011538066.1:p.Leu331=
XM_011539765.2:c.928C= XP_011538067.1:p.Leu310=
XM_011539766.2:c.910C= XP_011538068.1:p.Leu304=
XM_011539767.3:c.874C= XP_011538069.1:p.Leu292=
XR_945732.3:n.897C=
XR_945733.2:n.834C=
NM_000043.6:c.829C= MANE Select NP_000034.1:p.Leu277=
NM_001320619.2:c.*152C= NP_001307548.1:n.*152C=
NM_152871.4:c.766C= NP_690610.1:p.Leu256=
NM_152872.4:c.*141C= NP_690611.1:n.*141C=
NR_028033.4:n.736C=
NR_028034.4:n.598C=
NR_028035.4:n.661C=
NR_028036.4:n.799C=
NR_135313.2:n.716C=
NR_135314.2:n.995C=
NR_135315.2:n.748C=