Canonical Allele Identifier: CA2610079807
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014670C>G , CM000672.2:g.89014670C>G GRCh38
NC_000010.10:g.90774427C>G , CM000672.1:g.90774427C>G GRCh37
NC_000010.9:g.90764407C>G NCBI36
NG_009089.2:g.29140C>G , LRG_134:g.29140C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1537C>G
ENST00000355740.8:c.*551C>G ENSP00000347979.3:n.*551C>G
ENST00000357339.7:c.*220C>G ENSP00000349896.2:n.*220C>G
ENST00000371857.8:n.2773C>G
ENST00000460510.6:c.*220C>G ENSP00000512812.1:n.*220C>G
ENST00000466081.6:n.2877C>G
ENST00000477270.6:c.*220C>G ENSP00000512813.1:n.*220C>G
ENST00000492756.7:c.*657C>G ENSP00000422453.1:n.*657C>G
ENST00000494799.6:c.*220C>G ENSP00000512834.1:n.*220C>G
ENST00000562983.3:c.*220C>G ENSP00000512845.1:n.*220C>G
ENST00000612663.6:c.*630C>G ENSP00000477997.3:n.*630C>G
ENST00000640140.2:n.1373C>G
ENST00000640250.2:n.727C>G
ENST00000640681.2:n.1332C>G
ENST00000696723.1:n.4861C>G
ENST00000696741.1:n.2866C>G
ENST00000696742.1:n.2593C>G
ENST00000696743.1:n.3996C>G
ENST00000696744.1:n.1267C>G
ENST00000696767.1:n.1562C>G
ENST00000696768.1:c.*551C>G ENSP00000512859.1:n.*551C>G
ENST00000696771.1:c.*220C>G ENSP00000512860.1:n.*220C>G
ENST00000696772.1:n.2831C>G
ENST00000696773.1:n.2570C>G
ENST00000696774.1:n.6338C>G
ENST00000696776.1:c.*220C>G ENSP00000512861.1:n.*220C>G
ENST00000696777.1:n.2636C>G
ENST00000696778.1:n.1664C>G
ENST00000696779.1:c.*220C>G ENSP00000512862.1:n.*220C>G
ENST00000696780.1:c.*220C>G ENSP00000512863.1:n.*220C>G
ENST00000696781.1:c.*220C>G ENSP00000512864.1:n.*220C>G
ENST00000696782.1:c.*630C>G ENSP00000512865.1:n.*630C>G
ENST00000696783.1:n.3096C>G
ENST00000696992.1:n.2345C>G
ENST00000696995.1:n.4757C>G
ENST00000696996.1:n.2670C>G
ENST00000696997.1:c.*858C>G ENSP00000513028.1:n.*858C>G
ENST00000696998.1:n.2482C>G
ENST00000696999.1:c.*220C>G ENSP00000513029.1:n.*220C>G
ENST00000697036.1:c.*644C>G ENSP00000513060.1:n.*644C>G
ENST00000697037.1:n.1263C>G
ENST00000697093.1:n.3464C>G
ENST00000697094.1:n.3811C>G
ENST00000697095.1:c.*2429C>G ENSP00000513104.1:n.*2429C>G
ENST00000697096.1:n.2361C>G
ENST00000697097.1:c.*220C>G ENSP00000513105.1:n.*220C>G
ENST00000562983.2:n.1414C>G
ENST00000690268.1:c.*220C>G ENSP00000509810.1:n.*220C>G
ENST00000355740.7:c.*554C>G ENSP00000347979.3:n.*554C>G
ENST00000640140.1:n.1400C>G
ENST00000640250.1:n.727C>G
ENST00000640681.1:n.1349C>G
ENST00000652046.1:c.*220C>G MANE Select ENSP00000498466.1:n.*220C>G
ENST00000352159.8:c.*545C>G ENSP00000345601.4:n.*545C>G
ENST00000355740.6:c.*220C>G ENSP00000347979.2:n.*220C>G
NM_000043.4:c.*220C>G , LRG_134t1:c.*220C>G NP_000034.1:n.*220C>G
NM_152871.2:c.*220C>G NP_690610.1:n.*220C>G
NM_152872.2:c.*540C>G NP_690611.1:n.*540C>G
NR_028033.2:n.1402C>G
NR_028034.2:n.1264C>G
NR_028035.2:n.1327C>G
NR_028036.2:n.1465C>G
XM_006717819.2:c.*220C>G XP_006717882.1:n.*220C>G
XM_011539764.1:c.*220C>G XP_011538066.1:n.*220C>G
XM_011539765.1:c.*220C>G XP_011538067.1:n.*220C>G
XM_011539766.1:c.*220C>G XP_011538068.1:n.*220C>G
XM_011539767.1:c.*220C>G XP_011538069.1:n.*220C>G
NM_000043.5:c.*220C>G NP_000034.1:n.*220C>G
NM_001320619.1:c.*551C>G NP_001307548.1:n.*551C>G
NM_152871.3:c.*220C>G NP_690610.1:n.*220C>G
NM_152872.3:c.*540C>G NP_690611.1:n.*540C>G
NR_028033.3:n.1374C>G
NR_028034.3:n.1236C>G
NR_028035.3:n.1299C>G
NR_028036.3:n.1437C>G
NR_135313.1:n.1354C>G
NR_135314.1:n.1537C>G
NR_135315.1:n.1290C>G
XM_006717819.3:c.*220C>G XP_006717882.1:n.*220C>G
XM_011539764.2:c.*220C>G XP_011538066.1:n.*220C>G
XM_011539765.2:c.*220C>G XP_011538067.1:n.*220C>G
XM_011539766.2:c.*220C>G XP_011538068.1:n.*220C>G
XM_011539767.3:c.*220C>G XP_011538069.1:n.*220C>G
XR_945732.3:n.1296C>G
XR_945733.2:n.1233C>G
NM_000043.6:c.*220C>G MANE Select NP_000034.1:n.*220C>G
NM_001320619.2:c.*551C>G NP_001307548.1:n.*551C>G
NM_152871.4:c.*220C>G NP_690610.1:n.*220C>G
NM_152872.4:c.*540C>G NP_690611.1:n.*540C>G
NR_028033.4:n.1135C>G
NR_028034.4:n.997C>G
NR_028035.4:n.1060C>G
NR_028036.4:n.1198C>G
NR_135313.2:n.1115C>G
NR_135314.2:n.1394C>G
NR_135315.2:n.1147C>G