Canonical Allele Identifier: CA1926639540
Gene: FAS HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014688C= , CM000672.2:g.89014688C= GRCh38
NC_000010.10:g.90774445C= , CM000672.1:g.90774445C= GRCh37
NC_000010.9:g.90764425C= NCBI36
NG_009089.2:g.29158C= , LRG_134:g.29158C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1555C=
ENST00000355740.8:c.*569C= ENSP00000347979.3:n.*569C=
ENST00000357339.7:c.*238C= ENSP00000349896.2:n.*238C=
ENST00000371857.8:n.2791C=
ENST00000460510.6:c.*238C= ENSP00000512812.1:n.*238C=
ENST00000466081.6:n.2895C=
ENST00000477270.6:c.*238C= ENSP00000512813.1:n.*238C=
ENST00000492756.7:c.*675C= ENSP00000422453.1:n.*675C=
ENST00000494799.6:c.*238C= ENSP00000512834.1:n.*238C=
ENST00000562983.3:c.*238C= ENSP00000512845.1:n.*238C=
ENST00000612663.6:c.*648C= ENSP00000477997.3:n.*648C=
ENST00000640140.2:n.1391C=
ENST00000640250.2:n.745C=
ENST00000640681.2:n.1350C=
ENST00000696723.1:n.4879C=
ENST00000696741.1:n.2884C=
ENST00000696742.1:n.2611C=
ENST00000696743.1:n.4014C=
ENST00000696744.1:n.1285C=
ENST00000696767.1:n.1580C=
ENST00000696768.1:c.*569C= ENSP00000512859.1:n.*569C=
ENST00000696771.1:c.*238C= ENSP00000512860.1:n.*238C=
ENST00000696772.1:n.2849C=
ENST00000696773.1:n.2588C=
ENST00000696774.1:n.6356C=
ENST00000696776.1:c.*238C= ENSP00000512861.1:n.*238C=
ENST00000696777.1:n.2654C=
ENST00000696778.1:n.1682C=
ENST00000696779.1:c.*238C= ENSP00000512862.1:n.*238C=
ENST00000696780.1:c.*238C= ENSP00000512863.1:n.*238C=
ENST00000696781.1:c.*238C= ENSP00000512864.1:n.*238C=
ENST00000696782.1:c.*648C= ENSP00000512865.1:n.*648C=
ENST00000696783.1:n.3114C=
ENST00000696992.1:n.2363C=
ENST00000696995.1:n.4775C=
ENST00000696996.1:n.2688C=
ENST00000696997.1:c.*876C= ENSP00000513028.1:n.*876C=
ENST00000696998.1:n.2500C=
ENST00000696999.1:c.*238C= ENSP00000513029.1:n.*238C=
ENST00000697036.1:c.*662C= ENSP00000513060.1:n.*662C=
ENST00000697037.1:n.1281C=
ENST00000697093.1:n.3482C=
ENST00000697094.1:n.3829C=
ENST00000697095.1:c.*2447C= ENSP00000513104.1:n.*2447C=
ENST00000697096.1:n.2379C=
ENST00000697097.1:c.*238C= ENSP00000513105.1:n.*238C=
ENST00000562983.2:n.1432C=
ENST00000690268.1:c.*238C= ENSP00000509810.1:n.*238C=
ENST00000355740.7:c.*572C= ENSP00000347979.3:n.*572C=
ENST00000640140.1:n.1418C=
ENST00000640250.1:n.745C=
ENST00000640681.1:n.1367C=
ENST00000652046.1:c.*238C= MANE Select ENSP00000498466.1:n.*238C=
ENST00000352159.8:c.*563C= ENSP00000345601.4:n.*563C=
ENST00000355740.6:c.*238C= ENSP00000347979.2:n.*238C=
NM_000043.4:c.*238C= , LRG_134t1:c.*238C= NP_000034.1:n.*238C=
NM_152871.2:c.*238C= NP_690610.1:n.*238C=
NM_152872.2:c.*558C= NP_690611.1:n.*558C=
NR_028033.2:n.1420C=
NR_028034.2:n.1282C=
NR_028035.2:n.1345C=
NR_028036.2:n.1483C=
XM_006717819.2:c.*238C= XP_006717882.1:n.*238C=
XM_011539764.1:c.*238C= XP_011538066.1:n.*238C=
XM_011539765.1:c.*238C= XP_011538067.1:n.*238C=
XM_011539766.1:c.*238C= XP_011538068.1:n.*238C=
XM_011539767.1:c.*238C= XP_011538069.1:n.*238C=
NM_000043.5:c.*238C= NP_000034.1:n.*238C=
NM_001320619.1:c.*569C= NP_001307548.1:n.*569C=
NM_152871.3:c.*238C= NP_690610.1:n.*238C=
NM_152872.3:c.*558C= NP_690611.1:n.*558C=
NR_028033.3:n.1392C=
NR_028034.3:n.1254C=
NR_028035.3:n.1317C=
NR_028036.3:n.1455C=
NR_135313.1:n.1372C=
NR_135314.1:n.1555C=
NR_135315.1:n.1308C=
XM_006717819.3:c.*238C= XP_006717882.1:n.*238C=
XM_011539764.2:c.*238C= XP_011538066.1:n.*238C=
XM_011539765.2:c.*238C= XP_011538067.1:n.*238C=
XM_011539766.2:c.*238C= XP_011538068.1:n.*238C=
XM_011539767.3:c.*238C= XP_011538069.1:n.*238C=
XR_945732.3:n.1314C=
XR_945733.2:n.1251C=
NM_000043.6:c.*238C= MANE Select NP_000034.1:n.*238C=
NM_001320619.2:c.*569C= NP_001307548.1:n.*569C=
NM_152871.4:c.*238C= NP_690610.1:n.*238C=
NM_152872.4:c.*558C= NP_690611.1:n.*558C=
NR_028033.4:n.1153C=
NR_028034.4:n.1015C=
NR_028035.4:n.1078C=
NR_028036.4:n.1216C=
NR_135313.2:n.1133C=
NR_135314.2:n.1412C=
NR_135315.2:n.1165C=