Canonical Allele Identifier: CA2610079804
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014669G>A , CM000672.2:g.89014669G>A GRCh38
NC_000010.10:g.90774426G>A , CM000672.1:g.90774426G>A GRCh37
NC_000010.9:g.90764406G>A NCBI36
NG_009089.2:g.29139G>A , LRG_134:g.29139G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1536G>A
ENST00000355740.8:c.*550G>A ENSP00000347979.3:n.*550G>A
ENST00000357339.7:c.*219G>A ENSP00000349896.2:n.*219G>A
ENST00000371857.8:n.2772G>A
ENST00000460510.6:c.*219G>A ENSP00000512812.1:n.*219G>A
ENST00000466081.6:n.2876G>A
ENST00000477270.6:c.*219G>A ENSP00000512813.1:n.*219G>A
ENST00000492756.7:c.*656G>A ENSP00000422453.1:n.*656G>A
ENST00000494799.6:c.*219G>A ENSP00000512834.1:n.*219G>A
ENST00000562983.3:c.*219G>A ENSP00000512845.1:n.*219G>A
ENST00000612663.6:c.*629G>A ENSP00000477997.3:n.*629G>A
ENST00000640140.2:n.1372G>A
ENST00000640250.2:n.726G>A
ENST00000640681.2:n.1331G>A
ENST00000696723.1:n.4860G>A
ENST00000696741.1:n.2865G>A
ENST00000696742.1:n.2592G>A
ENST00000696743.1:n.3995G>A
ENST00000696744.1:n.1266G>A
ENST00000696767.1:n.1561G>A
ENST00000696768.1:c.*550G>A ENSP00000512859.1:n.*550G>A
ENST00000696771.1:c.*219G>A ENSP00000512860.1:n.*219G>A
ENST00000696772.1:n.2830G>A
ENST00000696773.1:n.2569G>A
ENST00000696774.1:n.6337G>A
ENST00000696776.1:c.*219G>A ENSP00000512861.1:n.*219G>A
ENST00000696777.1:n.2635G>A
ENST00000696778.1:n.1663G>A
ENST00000696779.1:c.*219G>A ENSP00000512862.1:n.*219G>A
ENST00000696780.1:c.*219G>A ENSP00000512863.1:n.*219G>A
ENST00000696781.1:c.*219G>A ENSP00000512864.1:n.*219G>A
ENST00000696782.1:c.*629G>A ENSP00000512865.1:n.*629G>A
ENST00000696783.1:n.3095G>A
ENST00000696992.1:n.2344G>A
ENST00000696995.1:n.4756G>A
ENST00000696996.1:n.2669G>A
ENST00000696997.1:c.*857G>A ENSP00000513028.1:n.*857G>A
ENST00000696998.1:n.2481G>A
ENST00000696999.1:c.*219G>A ENSP00000513029.1:n.*219G>A
ENST00000697036.1:c.*643G>A ENSP00000513060.1:n.*643G>A
ENST00000697037.1:n.1262G>A
ENST00000697093.1:n.3463G>A
ENST00000697094.1:n.3810G>A
ENST00000697095.1:c.*2428G>A ENSP00000513104.1:n.*2428G>A
ENST00000697096.1:n.2360G>A
ENST00000697097.1:c.*219G>A ENSP00000513105.1:n.*219G>A
ENST00000562983.2:n.1413G>A
ENST00000690268.1:c.*219G>A ENSP00000509810.1:n.*219G>A
ENST00000355740.7:c.*553G>A ENSP00000347979.3:n.*553G>A
ENST00000640140.1:n.1399G>A
ENST00000640250.1:n.726G>A
ENST00000640681.1:n.1348G>A
ENST00000652046.1:c.*219G>A MANE Select ENSP00000498466.1:n.*219G>A
ENST00000352159.8:c.*544G>A ENSP00000345601.4:n.*544G>A
ENST00000355740.6:c.*219G>A ENSP00000347979.2:n.*219G>A
NM_000043.4:c.*219G>A , LRG_134t1:c.*219G>A NP_000034.1:n.*219G>A
NM_152871.2:c.*219G>A NP_690610.1:n.*219G>A
NM_152872.2:c.*539G>A NP_690611.1:n.*539G>A
NR_028033.2:n.1401G>A
NR_028034.2:n.1263G>A
NR_028035.2:n.1326G>A
NR_028036.2:n.1464G>A
XM_006717819.2:c.*219G>A XP_006717882.1:n.*219G>A
XM_011539764.1:c.*219G>A XP_011538066.1:n.*219G>A
XM_011539765.1:c.*219G>A XP_011538067.1:n.*219G>A
XM_011539766.1:c.*219G>A XP_011538068.1:n.*219G>A
XM_011539767.1:c.*219G>A XP_011538069.1:n.*219G>A
NM_000043.5:c.*219G>A NP_000034.1:n.*219G>A
NM_001320619.1:c.*550G>A NP_001307548.1:n.*550G>A
NM_152871.3:c.*219G>A NP_690610.1:n.*219G>A
NM_152872.3:c.*539G>A NP_690611.1:n.*539G>A
NR_028033.3:n.1373G>A
NR_028034.3:n.1235G>A
NR_028035.3:n.1298G>A
NR_028036.3:n.1436G>A
NR_135313.1:n.1353G>A
NR_135314.1:n.1536G>A
NR_135315.1:n.1289G>A
XM_006717819.3:c.*219G>A XP_006717882.1:n.*219G>A
XM_011539764.2:c.*219G>A XP_011538066.1:n.*219G>A
XM_011539765.2:c.*219G>A XP_011538067.1:n.*219G>A
XM_011539766.2:c.*219G>A XP_011538068.1:n.*219G>A
XM_011539767.3:c.*219G>A XP_011538069.1:n.*219G>A
XR_945732.3:n.1295G>A
XR_945733.2:n.1232G>A
NM_000043.6:c.*219G>A MANE Select NP_000034.1:n.*219G>A
NM_001320619.2:c.*550G>A NP_001307548.1:n.*550G>A
NM_152871.4:c.*219G>A NP_690610.1:n.*219G>A
NM_152872.4:c.*539G>A NP_690611.1:n.*539G>A
NR_028033.4:n.1134G>A
NR_028034.4:n.996G>A
NR_028035.4:n.1059G>A
NR_028036.4:n.1197G>A
NR_135313.2:n.1114G>A
NR_135314.2:n.1393G>A
NR_135315.2:n.1146G>A