Canonical Allele Identifier: CA2788920996

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014702A>G , CM000672.2:g.89014702A>G	GRCh38
NC_000010.10:g.90774459A>G , CM000672.1:g.90774459A>G	GRCh37
NC_000010.9:g.90764439A>G	NCBI36
NG_009089.2:g.29172A>G , LRG_134:g.29172A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1569A>G
ENST00000355740.8:c.*583A>G	ENSP00000347979.3:n.*583A>G
ENST00000357339.7:c.*252A>G	ENSP00000349896.2:n.*252A>G
ENST00000371857.8:n.2805A>G
ENST00000460510.6:c.*252A>G	ENSP00000512812.1:n.*252A>G
ENST00000466081.6:n.2909A>G
ENST00000477270.6:c.*252A>G	ENSP00000512813.1:n.*252A>G
ENST00000492756.7:c.*689A>G	ENSP00000422453.1:n.*689A>G
ENST00000494799.6:c.*252A>G	ENSP00000512834.1:n.*252A>G
ENST00000562983.3:c.*252A>G	ENSP00000512845.1:n.*252A>G
ENST00000612663.6:c.*662A>G	ENSP00000477997.3:n.*662A>G
ENST00000640140.2:n.1405A>G
ENST00000640250.2:n.759A>G
ENST00000640681.2:n.1364A>G
ENST00000696723.1:n.4893A>G
ENST00000696741.1:n.2898A>G
ENST00000696742.1:n.2625A>G
ENST00000696743.1:n.4028A>G
ENST00000696744.1:n.1299A>G
ENST00000696767.1:n.1594A>G
ENST00000696768.1:c.*583A>G	ENSP00000512859.1:n.*583A>G
ENST00000696771.1:c.*252A>G	ENSP00000512860.1:n.*252A>G
ENST00000696772.1:n.2863A>G
ENST00000696773.1:n.2602A>G
ENST00000696774.1:n.6370A>G
ENST00000696776.1:c.*252A>G	ENSP00000512861.1:n.*252A>G
ENST00000696777.1:n.2668A>G
ENST00000696778.1:n.1696A>G
ENST00000696779.1:c.*252A>G	ENSP00000512862.1:n.*252A>G
ENST00000696780.1:c.*252A>G	ENSP00000512863.1:n.*252A>G
ENST00000696781.1:c.*252A>G	ENSP00000512864.1:n.*252A>G
ENST00000696782.1:c.*662A>G	ENSP00000512865.1:n.*662A>G
ENST00000696783.1:n.3128A>G
ENST00000696992.1:n.2377A>G
ENST00000696995.1:n.4789A>G
ENST00000696996.1:n.2702A>G
ENST00000696997.1:c.*890A>G	ENSP00000513028.1:n.*890A>G
ENST00000696998.1:n.2514A>G
ENST00000696999.1:c.*252A>G	ENSP00000513029.1:n.*252A>G
ENST00000697036.1:c.*676A>G	ENSP00000513060.1:n.*676A>G
ENST00000697037.1:n.1295A>G
ENST00000697093.1:n.3496A>G
ENST00000697094.1:n.3843A>G
ENST00000697095.1:c.*2461A>G	ENSP00000513104.1:n.*2461A>G
ENST00000697096.1:n.2393A>G
ENST00000697097.1:c.*252A>G	ENSP00000513105.1:n.*252A>G
ENST00000562983.2:n.1446A>G
ENST00000690268.1:c.*252A>G	ENSP00000509810.1:n.*252A>G
ENST00000355740.7:c.*586A>G	ENSP00000347979.3:n.*586A>G
ENST00000640140.1:n.1432A>G
ENST00000640250.1:n.759A>G
ENST00000640681.1:n.1381A>G
ENST00000652046.1:c.*252A>G MANE Select	ENSP00000498466.1:n.*252A>G
ENST00000352159.8:c.*577A>G	ENSP00000345601.4:n.*577A>G
ENST00000355740.6:c.*252A>G	ENSP00000347979.2:n.*252A>G
NM_000043.4:c.*252A>G , LRG_134t1:c.*252A>G	NP_000034.1:n.*252A>G
NM_152871.2:c.*252A>G	NP_690610.1:n.*252A>G
NM_152872.2:c.*572A>G	NP_690611.1:n.*572A>G
NR_028033.2:n.1434A>G
NR_028034.2:n.1296A>G
NR_028035.2:n.1359A>G
NR_028036.2:n.1497A>G
XM_006717819.2:c.*252A>G	XP_006717882.1:n.*252A>G
XM_011539764.1:c.*252A>G	XP_011538066.1:n.*252A>G
XM_011539765.1:c.*252A>G	XP_011538067.1:n.*252A>G
XM_011539766.1:c.*252A>G	XP_011538068.1:n.*252A>G
XM_011539767.1:c.*252A>G	XP_011538069.1:n.*252A>G
NM_000043.5:c.*252A>G	NP_000034.1:n.*252A>G
NM_001320619.1:c.*583A>G	NP_001307548.1:n.*583A>G
NM_152871.3:c.*252A>G	NP_690610.1:n.*252A>G
NM_152872.3:c.*572A>G	NP_690611.1:n.*572A>G
NR_028033.3:n.1406A>G
NR_028034.3:n.1268A>G
NR_028035.3:n.1331A>G
NR_028036.3:n.1469A>G
NR_135313.1:n.1386A>G
NR_135314.1:n.1569A>G
NR_135315.1:n.1322A>G
XM_006717819.3:c.*252A>G	XP_006717882.1:n.*252A>G
XM_011539764.2:c.*252A>G	XP_011538066.1:n.*252A>G
XM_011539765.2:c.*252A>G	XP_011538067.1:n.*252A>G
XM_011539766.2:c.*252A>G	XP_011538068.1:n.*252A>G
XM_011539767.3:c.*252A>G	XP_011538069.1:n.*252A>G
XR_945732.3:n.1328A>G
XR_945733.2:n.1265A>G
NM_000043.6:c.*252A>G MANE Select	NP_000034.1:n.*252A>G
NM_001320619.2:c.*583A>G	NP_001307548.1:n.*583A>G
NM_152871.4:c.*252A>G	NP_690610.1:n.*252A>G
NM_152872.4:c.*572A>G	NP_690611.1:n.*572A>G
NR_028033.4:n.1167A>G
NR_028034.4:n.1029A>G
NR_028035.4:n.1092A>G
NR_028036.4:n.1230A>G
NR_135313.2:n.1147A>G
NR_135314.2:n.1426A>G
NR_135315.2:n.1179A>G