Canonical Allele Identifier: CA1926637085
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89008908C= , CM000672.2:g.89008908C= GRCh38
NC_000010.10:g.90768665C= , CM000672.1:g.90768665C= GRCh37
NC_000010.9:g.90758645C= NCBI36
NG_009089.2:g.23378C= , LRG_134:g.23378C=

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.663C=
ENST00000355740.8:c.354C= ENSP00000347979.3:p.Asn118=
ENST00000357339.7:c.354C= ENSP00000349896.2:p.Asn118=
ENST00000371857.8:n.564C=
ENST00000460510.6:c.-364C= ENSP00000512812.1:n.-364C=
ENST00000466081.6:n.503+1071C=
ENST00000477270.6:c.399C= ENSP00000512813.1:p.Asn133=
ENST00000479522.6:c.197-1631C= ENSP00000424113.1:n.197-1631C=
ENST00000484444.6:c.197-1631C= ENSP00000420975.1:n.197-1631C=
ENST00000488877.6:c.334+1071C= ENSP00000425159.1:n.334+1071C=
ENST00000492756.7:c.334+1071C= ENSP00000422453.1:n.334+1071C=
ENST00000494799.6:c.-274-1631C= ENSP00000512834.1:n.-274-1631C=
ENST00000562983.3:c.-364C= ENSP00000512845.1:n.-364C=
ENST00000612663.6:c.354C= ENSP00000477997.3:p.Asn118=
ENST00000640140.2:n.499C=
ENST00000640681.2:n.458C=
ENST00000696723.1:n.3987C=
ENST00000696741.1:n.657C=
ENST00000696742.1:n.536C=
ENST00000696743.1:n.526C=
ENST00000696744.1:n.393C=
ENST00000696767.1:n.536C=
ENST00000696768.1:c.354C= ENSP00000512859.1:p.Asn118=
ENST00000696769.1:n.708C=
ENST00000696770.1:n.1588C=
ENST00000696771.1:c.-301C= ENSP00000512860.1:n.-301C=
ENST00000696772.1:n.520C=
ENST00000696773.1:n.513C=
ENST00000696774.1:n.576C=
ENST00000696775.1:n.629C=
ENST00000696776.1:c.447C= ENSP00000512861.1:p.Asn149=
ENST00000696777.1:n.516+1071C=
ENST00000696778.1:n.536C=
ENST00000696779.1:c.197-1631C= ENSP00000512862.1:n.197-1631C=
ENST00000696780.1:c.447C= ENSP00000512863.1:p.Asn149=
ENST00000696781.1:c.334+1071C= ENSP00000512864.1:n.334+1071C=
ENST00000696782.1:c.354C= ENSP00000512865.1:p.Asn118=
ENST00000696992.1:n.1471C=
ENST00000696995.1:n.536C=
ENST00000696996.1:n.535C=
ENST00000696997.1:c.354C= ENSP00000513028.1:p.Asn118=
ENST00000696998.1:n.363-1631C=
ENST00000696999.1:c.-212+1071C= ENSP00000513029.1:n.-212+1071C=
ENST00000697035.1:c.354C= ENSP00000513059.1:p.Asn118=
ENST00000697036.1:c.334+1071C= ENSP00000513060.1:n.334+1071C=
ENST00000697037.1:n.389C=
ENST00000697093.1:n.578C=
ENST00000697094.1:n.493C=
ENST00000697095.1:c.*14C= ENSP00000513104.1:n.*14C=
ENST00000697096.1:n.410C=
ENST00000697097.1:c.-364C= ENSP00000513105.1:n.-364C=
ENST00000562983.2:n.540C=
ENST00000690268.1:c.435C= ENSP00000509810.1:p.Asn145=
ENST00000355740.7:c.354C= ENSP00000347979.3:p.Asn118=
ENST00000612663.5:c.354C= ENSP00000477997.3:p.Asn118=
ENST00000640140.1:n.526C=
ENST00000640681.1:n.475C=
ENST00000652046.1:c.354C= MANE Select ENSP00000498466.1:p.Asn118=
ENST00000313771.9:n.663C=
ENST00000352159.8:c.354C= ENSP00000345601.4:p.Asn118=
ENST00000355279.2:c.354C= ENSP00000347426.2:p.Asn118=
ENST00000355740.6:c.354C= ENSP00000347979.2:p.Asn118=
ENST00000357339.6:c.354C= ENSP00000349896.2:p.Asn118=
ENST00000371857.7:n.520C=
ENST00000460510.5:n.721C=
ENST00000466081.5:n.503+1071C=
ENST00000477270.5:n.517C=
ENST00000479522.5:c.197-1631C= ENSP00000424113.1:n.197-1631C=
ENST00000484444.5:c.197-1631C= ENSP00000420975.1:n.197-1631C=
ENST00000487314.1:n.503C=
ENST00000488877.5:c.334+1071C= ENSP00000425159.1:n.334+1071C=
ENST00000492756.5:c.334+1071C= ENSP00000422453.1:n.334+1071C=
ENST00000494410.5:c.334+1071C= ENSP00000423755.1:n.334+1071C=
ENST00000494799.5:n.351-1631C=
ENST00000612663.4:c.354C= ENSP00000477997.2:p.Asn118=
ENST00000615406.4:c.354C= ENSP00000484575.1:p.Asn118=
ENST00000626542.2:c.354C= ENSP00000485876.1:p.Asn118=
NM_000043.4:c.354C= , LRG_134t1:c.354C= NP_000034.1:p.Asn118=
NM_152871.2:c.354C= NP_690610.1:p.Asn118=
NM_152872.2:c.354C= NP_690611.1:p.Asn118=
NR_028033.2:n.680+1071C=
NR_028034.2:n.543-1631C=
NR_028035.2:n.543-1631C=
NR_028036.2:n.680+1071C=
XM_006717819.2:c.435C= XP_006717882.1:p.Asn145=
XM_011539764.1:c.516C= XP_011538066.1:p.Asn172=
XM_011539765.1:c.516C= XP_011538067.1:p.Asn172=
XM_011539766.1:c.435C= XP_011538068.1:p.Asn145=
XM_011539767.1:c.399C= XP_011538069.1:p.Asn133=
XR_945732.1:n.511+1071C=
XR_945733.1:n.511+1071C=
NM_000043.5:c.354C= NP_000034.1:p.Asn118=
NM_001320619.1:c.354C= NP_001307548.1:p.Asn118=
NM_152871.3:c.354C= NP_690610.1:p.Asn118=
NM_152872.3:c.354C= NP_690611.1:p.Asn118=
NR_028033.3:n.652+1071C=
NR_028034.3:n.515-1631C=
NR_028035.3:n.515-1631C=
NR_028036.3:n.652+1071C=
NR_135313.1:n.652+1071C=
NR_135314.1:n.663C=
NR_135315.1:n.506-1631C=
XM_006717819.3:c.435C= XP_006717882.1:p.Asn145=
XM_011539764.2:c.516C= XP_011538066.1:p.Asn172=
XM_011539765.2:c.516C= XP_011538067.1:p.Asn172=
XM_011539766.2:c.435C= XP_011538068.1:p.Asn145=
XM_011539767.3:c.399C= XP_011538069.1:p.Asn133=
XR_945732.3:n.511+1071C=
XR_945733.2:n.511+1071C=
NM_000043.6:c.354C= MANE Select NP_000034.1:p.Asn118=
NM_001320619.2:c.354C= NP_001307548.1:p.Asn118=
NM_152871.4:c.354C= NP_690610.1:p.Asn118=
NM_152872.4:c.354C= NP_690611.1:p.Asn118=
NR_028033.4:n.413+1071C=
NR_028034.4:n.276-1631C=
NR_028035.4:n.276-1631C=
NR_028036.4:n.413+1071C=
NR_135313.2:n.413+1071C=
NR_135314.2:n.520C=
NR_135315.2:n.363-1631C=