Canonical Allele Identifier: CA2610079687
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014540dup , CM000672.2:g.89014540dup GRCh38
NC_000010.10:g.90774297dup , CM000672.1:g.90774297dup GRCh37
NC_000010.9:g.90764277dup NCBI36
NG_009089.2:g.29010dup , LRG_134:g.29010dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1407dup
ENST00000355740.8:c.*421dup ENSP00000347979.3:n.*421dup
ENST00000357339.7:c.*90dup ENSP00000349896.2:n.*90dup
ENST00000371857.8:n.2643dup
ENST00000460510.6:c.*90dup ENSP00000512812.1:n.*90dup
ENST00000466081.6:n.2747dup
ENST00000477270.6:c.*90dup ENSP00000512813.1:n.*90dup
ENST00000479522.6:c.*527dup ENSP00000424113.1:n.*527dup
ENST00000484444.6:c.*539dup ENSP00000420975.1:n.*539dup
ENST00000488877.6:c.989dup ENSP00000425159.1:n.989dup
ENST00000492756.7:c.*527dup ENSP00000422453.1:n.*527dup
ENST00000494799.6:c.*90dup ENSP00000512834.1:n.*90dup
ENST00000562983.3:c.*90dup ENSP00000512845.1:n.*90dup
ENST00000612663.6:c.*500dup ENSP00000477997.3:n.*500dup
ENST00000640140.2:n.1243dup
ENST00000640250.2:n.597dup
ENST00000640681.2:n.1202dup
ENST00000696723.1:n.4731dup
ENST00000696741.1:n.2736dup
ENST00000696742.1:n.2463dup
ENST00000696743.1:n.3866dup
ENST00000696744.1:n.1137dup
ENST00000696767.1:n.1432dup
ENST00000696768.1:c.*421dup ENSP00000512859.1:n.*421dup
ENST00000696769.1:n.2787dup
ENST00000696771.1:c.*90dup ENSP00000512860.1:n.*90dup
ENST00000696772.1:n.2701dup
ENST00000696773.1:n.2440dup
ENST00000696774.1:n.6208dup
ENST00000696776.1:c.*90dup ENSP00000512861.1:n.*90dup
ENST00000696777.1:n.2506dup
ENST00000696778.1:n.1534dup
ENST00000696779.1:c.*90dup ENSP00000512862.1:n.*90dup
ENST00000696780.1:c.*90dup ENSP00000512863.1:n.*90dup
ENST00000696781.1:c.*90dup ENSP00000512864.1:n.*90dup
ENST00000696782.1:c.*500dup ENSP00000512865.1:n.*500dup
ENST00000696783.1:n.2966dup
ENST00000696992.1:n.2215dup
ENST00000696995.1:n.4627dup
ENST00000696996.1:n.2540dup
ENST00000696997.1:c.*728dup ENSP00000513028.1:n.*728dup
ENST00000696998.1:n.2352dup
ENST00000696999.1:c.*90dup ENSP00000513029.1:n.*90dup
ENST00000697036.1:c.*514dup ENSP00000513060.1:n.*514dup
ENST00000697037.1:n.1133dup
ENST00000697093.1:n.3334dup
ENST00000697094.1:n.3681dup
ENST00000697095.1:c.*2299dup ENSP00000513104.1:n.*2299dup
ENST00000697096.1:n.2231dup
ENST00000697097.1:c.*90dup ENSP00000513105.1:n.*90dup
ENST00000562983.2:n.1284dup
ENST00000690268.1:c.*90dup ENSP00000509810.1:n.*90dup
ENST00000355740.7:c.*424dup ENSP00000347979.3:n.*424dup
ENST00000640140.1:n.1270dup
ENST00000640250.1:n.597dup
ENST00000640681.1:n.1219dup
ENST00000652046.1:c.*90dup MANE Select ENSP00000498466.1:n.*90dup
ENST00000352159.8:c.*415dup ENSP00000345601.4:n.*415dup
ENST00000355740.6:c.*90dup ENSP00000347979.2:n.*90dup
ENST00000479522.5:c.*527dup ENSP00000424113.1:n.*527dup
ENST00000484444.5:c.*539dup ENSP00000420975.1:n.*539dup
ENST00000494410.5:c.*456dup ENSP00000423755.1:n.*456dup
NM_000043.4:c.*90dup , LRG_134t1:c.*90dup NP_000034.1:n.*90dup
NM_152871.2:c.*90dup NP_690610.1:n.*90dup
NM_152872.2:c.*410dup NP_690611.1:n.*410dup
NR_028033.2:n.1272dup
NR_028034.2:n.1134dup
NR_028035.2:n.1197dup
NR_028036.2:n.1335dup
XM_006717819.2:c.*90dup XP_006717882.1:n.*90dup
XM_011539764.1:c.*90dup XP_011538066.1:n.*90dup
XM_011539765.1:c.*90dup XP_011538067.1:n.*90dup
XM_011539766.1:c.*90dup XP_011538068.1:n.*90dup
XM_011539767.1:c.*90dup XP_011538069.1:n.*90dup
NM_000043.5:c.*90dup NP_000034.1:n.*90dup
NM_001320619.1:c.*421dup NP_001307548.1:n.*421dup
NM_152871.3:c.*90dup NP_690610.1:n.*90dup
NM_152872.3:c.*410dup NP_690611.1:n.*410dup
NR_028033.3:n.1244dup
NR_028034.3:n.1106dup
NR_028035.3:n.1169dup
NR_028036.3:n.1307dup
NR_135313.1:n.1224dup
NR_135314.1:n.1407dup
NR_135315.1:n.1160dup
XM_006717819.3:c.*90dup XP_006717882.1:n.*90dup
XM_011539764.2:c.*90dup XP_011538066.1:n.*90dup
XM_011539765.2:c.*90dup XP_011538067.1:n.*90dup
XM_011539766.2:c.*90dup XP_011538068.1:n.*90dup
XM_011539767.3:c.*90dup XP_011538069.1:n.*90dup
XR_945732.3:n.1166dup
XR_945733.2:n.1103dup
NM_000043.6:c.*90dup MANE Select NP_000034.1:n.*90dup
NM_001320619.2:c.*421dup NP_001307548.1:n.*421dup
NM_152871.4:c.*90dup NP_690610.1:n.*90dup
NM_152872.4:c.*410dup NP_690611.1:n.*410dup
NR_028033.4:n.1005dup
NR_028034.4:n.867dup
NR_028035.4:n.930dup
NR_028036.4:n.1068dup
NR_135313.2:n.985dup
NR_135314.2:n.1264dup
NR_135315.2:n.1017dup