Canonical Allele Identifier: CA2610079650

Gene: FAS

Linked Data

• gnomAD v4: 10-89014491-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014491G>T , CM000672.2:g.89014491G>T	GRCh38
NC_000010.10:g.90774248G>T , CM000672.1:g.90774248G>T	GRCh37
NC_000010.9:g.90764228G>T	NCBI36
NG_009089.2:g.28961G>T , LRG_134:g.28961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1358G>T
ENST00000355740.8:c.*372G>T	ENSP00000347979.3:n.*372G>T
ENST00000357339.7:c.*41G>T	ENSP00000349896.2:n.*41G>T
ENST00000371857.8:n.2594G>T
ENST00000460510.6:c.*41G>T	ENSP00000512812.1:n.*41G>T
ENST00000466081.6:n.2698G>T
ENST00000477270.6:c.*41G>T	ENSP00000512813.1:n.*41G>T
ENST00000479522.6:c.*478G>T	ENSP00000424113.1:n.*478G>T
ENST00000484444.6:c.*490G>T	ENSP00000420975.1:n.*490G>T
ENST00000488877.6:c.940G>T	ENSP00000425159.1:n.940G>T
ENST00000492756.7:c.*478G>T	ENSP00000422453.1:n.*478G>T
ENST00000494799.6:c.*41G>T	ENSP00000512834.1:n.*41G>T
ENST00000562983.3:c.*41G>T	ENSP00000512845.1:n.*41G>T
ENST00000612663.6:c.*451G>T	ENSP00000477997.3:n.*451G>T
ENST00000640140.2:n.1194G>T
ENST00000640250.2:n.548G>T
ENST00000640681.2:n.1153G>T
ENST00000696723.1:n.4682G>T
ENST00000696741.1:n.2687G>T
ENST00000696742.1:n.2414G>T
ENST00000696743.1:n.3817G>T
ENST00000696744.1:n.1088G>T
ENST00000696767.1:n.1383G>T
ENST00000696768.1:c.*372G>T	ENSP00000512859.1:n.*372G>T
ENST00000696769.1:n.2738G>T
ENST00000696771.1:c.*41G>T	ENSP00000512860.1:n.*41G>T
ENST00000696772.1:n.2652G>T
ENST00000696773.1:n.2391G>T
ENST00000696774.1:n.6159G>T
ENST00000696776.1:c.*41G>T	ENSP00000512861.1:n.*41G>T
ENST00000696777.1:n.2457G>T
ENST00000696778.1:n.1485G>T
ENST00000696779.1:c.*41G>T	ENSP00000512862.1:n.*41G>T
ENST00000696780.1:c.*41G>T	ENSP00000512863.1:n.*41G>T
ENST00000696781.1:c.*41G>T	ENSP00000512864.1:n.*41G>T
ENST00000696782.1:c.*451G>T	ENSP00000512865.1:n.*451G>T
ENST00000696783.1:n.2917G>T
ENST00000696992.1:n.2166G>T
ENST00000696995.1:n.4578G>T
ENST00000696996.1:n.2491G>T
ENST00000696997.1:c.*679G>T	ENSP00000513028.1:n.*679G>T
ENST00000696998.1:n.2303G>T
ENST00000696999.1:c.*41G>T	ENSP00000513029.1:n.*41G>T
ENST00000697036.1:c.*465G>T	ENSP00000513060.1:n.*465G>T
ENST00000697037.1:n.1084G>T
ENST00000697093.1:n.3285G>T
ENST00000697094.1:n.3632G>T
ENST00000697095.1:c.*2250G>T	ENSP00000513104.1:n.*2250G>T
ENST00000697096.1:n.2182G>T
ENST00000697097.1:c.*41G>T	ENSP00000513105.1:n.*41G>T
ENST00000562983.2:n.1235G>T
ENST00000690268.1:c.*41G>T	ENSP00000509810.1:n.*41G>T
ENST00000355740.7:c.*375G>T	ENSP00000347979.3:n.*375G>T
ENST00000640140.1:n.1221G>T
ENST00000640250.1:n.548G>T
ENST00000640681.1:n.1170G>T
ENST00000652046.1:c.*41G>T MANE Select	ENSP00000498466.1:n.*41G>T
ENST00000352159.8:c.*366G>T	ENSP00000345601.4:n.*366G>T
ENST00000355740.6:c.*41G>T	ENSP00000347979.2:n.*41G>T
ENST00000479522.5:c.*478G>T	ENSP00000424113.1:n.*478G>T
ENST00000484444.5:c.*490G>T	ENSP00000420975.1:n.*490G>T
ENST00000494410.5:c.*407G>T	ENSP00000423755.1:n.*407G>T
NM_000043.4:c.*41G>T , LRG_134t1:c.*41G>T	NP_000034.1:n.*41G>T
NM_152871.2:c.*41G>T	NP_690610.1:n.*41G>T
NM_152872.2:c.*361G>T	NP_690611.1:n.*361G>T
NR_028033.2:n.1223G>T
NR_028034.2:n.1085G>T
NR_028035.2:n.1148G>T
NR_028036.2:n.1286G>T
XM_006717819.2:c.*41G>T	XP_006717882.1:n.*41G>T
XM_011539764.1:c.*41G>T	XP_011538066.1:n.*41G>T
XM_011539765.1:c.*41G>T	XP_011538067.1:n.*41G>T
XM_011539766.1:c.*41G>T	XP_011538068.1:n.*41G>T
XM_011539767.1:c.*41G>T	XP_011538069.1:n.*41G>T
XR_945733.1:n.1054G>T
NM_000043.5:c.*41G>T	NP_000034.1:n.*41G>T
NM_001320619.1:c.*372G>T	NP_001307548.1:n.*372G>T
NM_152871.3:c.*41G>T	NP_690610.1:n.*41G>T
NM_152872.3:c.*361G>T	NP_690611.1:n.*361G>T
NR_028033.3:n.1195G>T
NR_028034.3:n.1057G>T
NR_028035.3:n.1120G>T
NR_028036.3:n.1258G>T
NR_135313.1:n.1175G>T
NR_135314.1:n.1358G>T
NR_135315.1:n.1111G>T
XM_006717819.3:c.*41G>T	XP_006717882.1:n.*41G>T
XM_011539764.2:c.*41G>T	XP_011538066.1:n.*41G>T
XM_011539765.2:c.*41G>T	XP_011538067.1:n.*41G>T
XM_011539766.2:c.*41G>T	XP_011538068.1:n.*41G>T
XM_011539767.3:c.*41G>T	XP_011538069.1:n.*41G>T
XR_945732.3:n.1117G>T
XR_945733.2:n.1054G>T
NM_000043.6:c.*41G>T MANE Select	NP_000034.1:n.*41G>T
NM_001320619.2:c.*372G>T	NP_001307548.1:n.*372G>T
NM_152871.4:c.*41G>T	NP_690610.1:n.*41G>T
NM_152872.4:c.*361G>T	NP_690611.1:n.*361G>T
NR_028033.4:n.956G>T
NR_028034.4:n.818G>T
NR_028035.4:n.881G>T
NR_028036.4:n.1019G>T
NR_135313.2:n.936G>T
NR_135314.2:n.1215G>T
NR_135315.2:n.968G>T