Canonical Allele Identifier: CA2588960138

Gene: FAS

Linked Data

• gnomAD v3: 10-89014464-A-T
• gnomAD v4: 10-89014464-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014464A>T , CM000672.2:g.89014464A>T	GRCh38
NC_000010.10:g.90774221A>T , CM000672.1:g.90774221A>T	GRCh37
NC_000010.9:g.90764201A>T	NCBI36
NG_009089.2:g.28934A>T , LRG_134:g.28934A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1331A>T
ENST00000355740.8:c.*345A>T	ENSP00000347979.3:n.*345A>T
ENST00000357339.7:c.*14A>T	ENSP00000349896.2:n.*14A>T
ENST00000371857.8:n.2567A>T
ENST00000460510.6:c.*14A>T	ENSP00000512812.1:n.*14A>T
ENST00000466081.6:n.2671A>T
ENST00000477270.6:c.*14A>T	ENSP00000512813.1:n.*14A>T
ENST00000479522.6:c.*451A>T	ENSP00000424113.1:n.*451A>T
ENST00000484444.6:c.*463A>T	ENSP00000420975.1:n.*463A>T
ENST00000488877.6:c.913A>T	ENSP00000425159.1:n.913A>T
ENST00000492756.7:c.*451A>T	ENSP00000422453.1:n.*451A>T
ENST00000494799.6:c.*14A>T	ENSP00000512834.1:n.*14A>T
ENST00000562983.3:c.*14A>T	ENSP00000512845.1:n.*14A>T
ENST00000612663.6:c.*424A>T	ENSP00000477997.3:n.*424A>T
ENST00000640140.2:n.1167A>T
ENST00000640250.2:n.521A>T
ENST00000640681.2:n.1126A>T
ENST00000696723.1:n.4655A>T
ENST00000696741.1:n.2660A>T
ENST00000696742.1:n.2387A>T
ENST00000696743.1:n.3790A>T
ENST00000696744.1:n.1061A>T
ENST00000696767.1:n.1356A>T
ENST00000696768.1:c.*345A>T	ENSP00000512859.1:n.*345A>T
ENST00000696769.1:n.2711A>T
ENST00000696771.1:c.*14A>T	ENSP00000512860.1:n.*14A>T
ENST00000696772.1:n.2625A>T
ENST00000696773.1:n.2364A>T
ENST00000696774.1:n.6132A>T
ENST00000696776.1:c.*14A>T	ENSP00000512861.1:n.*14A>T
ENST00000696777.1:n.2430A>T
ENST00000696778.1:n.1458A>T
ENST00000696779.1:c.*14A>T	ENSP00000512862.1:n.*14A>T
ENST00000696780.1:c.*14A>T	ENSP00000512863.1:n.*14A>T
ENST00000696781.1:c.*14A>T	ENSP00000512864.1:n.*14A>T
ENST00000696782.1:c.*424A>T	ENSP00000512865.1:n.*424A>T
ENST00000696783.1:n.2890A>T
ENST00000696992.1:n.2139A>T
ENST00000696995.1:n.4551A>T
ENST00000696996.1:n.2464A>T
ENST00000696997.1:c.*652A>T	ENSP00000513028.1:n.*652A>T
ENST00000696998.1:n.2276A>T
ENST00000696999.1:c.*14A>T	ENSP00000513029.1:n.*14A>T
ENST00000697036.1:c.*438A>T	ENSP00000513060.1:n.*438A>T
ENST00000697037.1:n.1057A>T
ENST00000697093.1:n.3258A>T
ENST00000697094.1:n.3605A>T
ENST00000697095.1:c.*2223A>T	ENSP00000513104.1:n.*2223A>T
ENST00000697096.1:n.2155A>T
ENST00000697097.1:c.*14A>T	ENSP00000513105.1:n.*14A>T
ENST00000562983.2:n.1208A>T
ENST00000690268.1:c.*14A>T	ENSP00000509810.1:n.*14A>T
ENST00000355740.7:c.*348A>T	ENSP00000347979.3:n.*348A>T
ENST00000612663.5:c.*424A>T	ENSP00000477997.3:n.*424A>T
ENST00000640140.1:n.1194A>T
ENST00000640250.1:n.521A>T
ENST00000640681.1:n.1143A>T
ENST00000652046.1:c.*14A>T MANE Select	ENSP00000498466.1:n.*14A>T
ENST00000352159.8:c.*339A>T	ENSP00000345601.4:n.*339A>T
ENST00000355740.6:c.*14A>T	ENSP00000347979.2:n.*14A>T
ENST00000479522.5:c.*451A>T	ENSP00000424113.1:n.*451A>T
ENST00000484444.5:c.*463A>T	ENSP00000420975.1:n.*463A>T
ENST00000494410.5:c.*380A>T	ENSP00000423755.1:n.*380A>T
NM_000043.4:c.*14A>T , LRG_134t1:c.*14A>T	NP_000034.1:n.*14A>T
NM_152871.2:c.*14A>T	NP_690610.1:n.*14A>T
NM_152872.2:c.*334A>T	NP_690611.1:n.*334A>T
NR_028033.2:n.1196A>T
NR_028034.2:n.1058A>T
NR_028035.2:n.1121A>T
NR_028036.2:n.1259A>T
XM_006717819.2:c.*14A>T	XP_006717882.1:n.*14A>T
XM_011539764.1:c.*14A>T	XP_011538066.1:n.*14A>T
XM_011539765.1:c.*14A>T	XP_011538067.1:n.*14A>T
XM_011539766.1:c.*14A>T	XP_011538068.1:n.*14A>T
XM_011539767.1:c.*14A>T	XP_011538069.1:n.*14A>T
XR_945733.1:n.1027A>T
NM_000043.5:c.*14A>T	NP_000034.1:n.*14A>T
NM_001320619.1:c.*345A>T	NP_001307548.1:n.*345A>T
NM_152871.3:c.*14A>T	NP_690610.1:n.*14A>T
NM_152872.3:c.*334A>T	NP_690611.1:n.*334A>T
NR_028033.3:n.1168A>T
NR_028034.3:n.1030A>T
NR_028035.3:n.1093A>T
NR_028036.3:n.1231A>T
NR_135313.1:n.1148A>T
NR_135314.1:n.1331A>T
NR_135315.1:n.1084A>T
XM_006717819.3:c.*14A>T	XP_006717882.1:n.*14A>T
XM_011539764.2:c.*14A>T	XP_011538066.1:n.*14A>T
XM_011539765.2:c.*14A>T	XP_011538067.1:n.*14A>T
XM_011539766.2:c.*14A>T	XP_011538068.1:n.*14A>T
XM_011539767.3:c.*14A>T	XP_011538069.1:n.*14A>T
XR_945732.3:n.1090A>T
XR_945733.2:n.1027A>T
NM_000043.6:c.*14A>T MANE Select	NP_000034.1:n.*14A>T
NM_001320619.2:c.*345A>T	NP_001307548.1:n.*345A>T
NM_152871.4:c.*14A>T	NP_690610.1:n.*14A>T
NM_152872.4:c.*334A>T	NP_690611.1:n.*334A>T
NR_028033.4:n.929A>T
NR_028034.4:n.791A>T
NR_028035.4:n.854A>T
NR_028036.4:n.992A>T
NR_135313.2:n.909A>T
NR_135314.2:n.1188A>T
NR_135315.2:n.941A>T