Canonical Allele Identifier: CA2610079795

Gene: FAS

Linked Data

• gnomAD v4: 10-89014662-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014662A>T , CM000672.2:g.89014662A>T	GRCh38
NC_000010.10:g.90774419A>T , CM000672.1:g.90774419A>T	GRCh37
NC_000010.9:g.90764399A>T	NCBI36
NG_009089.2:g.29132A>T , LRG_134:g.29132A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1529A>T
ENST00000355740.8:c.*543A>T	ENSP00000347979.3:n.*543A>T
ENST00000357339.7:c.*212A>T	ENSP00000349896.2:n.*212A>T
ENST00000371857.8:n.2765A>T
ENST00000460510.6:c.*212A>T	ENSP00000512812.1:n.*212A>T
ENST00000466081.6:n.2869A>T
ENST00000477270.6:c.*212A>T	ENSP00000512813.1:n.*212A>T
ENST00000492756.7:c.*649A>T	ENSP00000422453.1:n.*649A>T
ENST00000494799.6:c.*212A>T	ENSP00000512834.1:n.*212A>T
ENST00000562983.3:c.*212A>T	ENSP00000512845.1:n.*212A>T
ENST00000612663.6:c.*622A>T	ENSP00000477997.3:n.*622A>T
ENST00000640140.2:n.1365A>T
ENST00000640250.2:n.719A>T
ENST00000640681.2:n.1324A>T
ENST00000696723.1:n.4853A>T
ENST00000696741.1:n.2858A>T
ENST00000696742.1:n.2585A>T
ENST00000696743.1:n.3988A>T
ENST00000696744.1:n.1259A>T
ENST00000696767.1:n.1554A>T
ENST00000696768.1:c.*543A>T	ENSP00000512859.1:n.*543A>T
ENST00000696771.1:c.*212A>T	ENSP00000512860.1:n.*212A>T
ENST00000696772.1:n.2823A>T
ENST00000696773.1:n.2562A>T
ENST00000696774.1:n.6330A>T
ENST00000696776.1:c.*212A>T	ENSP00000512861.1:n.*212A>T
ENST00000696777.1:n.2628A>T
ENST00000696778.1:n.1656A>T
ENST00000696779.1:c.*212A>T	ENSP00000512862.1:n.*212A>T
ENST00000696780.1:c.*212A>T	ENSP00000512863.1:n.*212A>T
ENST00000696781.1:c.*212A>T	ENSP00000512864.1:n.*212A>T
ENST00000696782.1:c.*622A>T	ENSP00000512865.1:n.*622A>T
ENST00000696783.1:n.3088A>T
ENST00000696992.1:n.2337A>T
ENST00000696995.1:n.4749A>T
ENST00000696996.1:n.2662A>T
ENST00000696997.1:c.*850A>T	ENSP00000513028.1:n.*850A>T
ENST00000696998.1:n.2474A>T
ENST00000696999.1:c.*212A>T	ENSP00000513029.1:n.*212A>T
ENST00000697036.1:c.*636A>T	ENSP00000513060.1:n.*636A>T
ENST00000697037.1:n.1255A>T
ENST00000697093.1:n.3456A>T
ENST00000697094.1:n.3803A>T
ENST00000697095.1:c.*2421A>T	ENSP00000513104.1:n.*2421A>T
ENST00000697096.1:n.2353A>T
ENST00000697097.1:c.*212A>T	ENSP00000513105.1:n.*212A>T
ENST00000562983.2:n.1406A>T
ENST00000690268.1:c.*212A>T	ENSP00000509810.1:n.*212A>T
ENST00000355740.7:c.*546A>T	ENSP00000347979.3:n.*546A>T
ENST00000640140.1:n.1392A>T
ENST00000640250.1:n.719A>T
ENST00000640681.1:n.1341A>T
ENST00000652046.1:c.*212A>T MANE Select	ENSP00000498466.1:n.*212A>T
ENST00000352159.8:c.*537A>T	ENSP00000345601.4:n.*537A>T
ENST00000355740.6:c.*212A>T	ENSP00000347979.2:n.*212A>T
NM_000043.4:c.*212A>T , LRG_134t1:c.*212A>T	NP_000034.1:n.*212A>T
NM_152871.2:c.*212A>T	NP_690610.1:n.*212A>T
NM_152872.2:c.*532A>T	NP_690611.1:n.*532A>T
NR_028033.2:n.1394A>T
NR_028034.2:n.1256A>T
NR_028035.2:n.1319A>T
NR_028036.2:n.1457A>T
XM_006717819.2:c.*212A>T	XP_006717882.1:n.*212A>T
XM_011539764.1:c.*212A>T	XP_011538066.1:n.*212A>T
XM_011539765.1:c.*212A>T	XP_011538067.1:n.*212A>T
XM_011539766.1:c.*212A>T	XP_011538068.1:n.*212A>T
XM_011539767.1:c.*212A>T	XP_011538069.1:n.*212A>T
NM_000043.5:c.*212A>T	NP_000034.1:n.*212A>T
NM_001320619.1:c.*543A>T	NP_001307548.1:n.*543A>T
NM_152871.3:c.*212A>T	NP_690610.1:n.*212A>T
NM_152872.3:c.*532A>T	NP_690611.1:n.*532A>T
NR_028033.3:n.1366A>T
NR_028034.3:n.1228A>T
NR_028035.3:n.1291A>T
NR_028036.3:n.1429A>T
NR_135313.1:n.1346A>T
NR_135314.1:n.1529A>T
NR_135315.1:n.1282A>T
XM_006717819.3:c.*212A>T	XP_006717882.1:n.*212A>T
XM_011539764.2:c.*212A>T	XP_011538066.1:n.*212A>T
XM_011539765.2:c.*212A>T	XP_011538067.1:n.*212A>T
XM_011539766.2:c.*212A>T	XP_011538068.1:n.*212A>T
XM_011539767.3:c.*212A>T	XP_011538069.1:n.*212A>T
XR_945732.3:n.1288A>T
XR_945733.2:n.1225A>T
NM_000043.6:c.*212A>T MANE Select	NP_000034.1:n.*212A>T
NM_001320619.2:c.*543A>T	NP_001307548.1:n.*543A>T
NM_152871.4:c.*212A>T	NP_690610.1:n.*212A>T
NM_152872.4:c.*532A>T	NP_690611.1:n.*532A>T
NR_028033.4:n.1127A>T
NR_028034.4:n.989A>T
NR_028035.4:n.1052A>T
NR_028036.4:n.1190A>T
NR_135313.2:n.1107A>T
NR_135314.2:n.1386A>T
NR_135315.2:n.1139A>T