Canonical Allele Identifier: CA2788920986

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014557C>T , CM000672.2:g.89014557C>T	GRCh38
NC_000010.10:g.90774314C>T , CM000672.1:g.90774314C>T	GRCh37
NC_000010.9:g.90764294C>T	NCBI36
NG_009089.2:g.29027C>T , LRG_134:g.29027C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1424C>T
ENST00000355740.8:c.*438C>T	ENSP00000347979.3:n.*438C>T
ENST00000357339.7:c.*107C>T	ENSP00000349896.2:n.*107C>T
ENST00000371857.8:n.2660C>T
ENST00000460510.6:c.*107C>T	ENSP00000512812.1:n.*107C>T
ENST00000466081.6:n.2764C>T
ENST00000477270.6:c.*107C>T	ENSP00000512813.1:n.*107C>T
ENST00000479522.6:c.*544C>T	ENSP00000424113.1:n.*544C>T
ENST00000484444.6:c.*556C>T	ENSP00000420975.1:n.*556C>T
ENST00000488877.6:c.1006C>T	ENSP00000425159.1:n.1006C>T
ENST00000492756.7:c.*544C>T	ENSP00000422453.1:n.*544C>T
ENST00000494799.6:c.*107C>T	ENSP00000512834.1:n.*107C>T
ENST00000562983.3:c.*107C>T	ENSP00000512845.1:n.*107C>T
ENST00000612663.6:c.*517C>T	ENSP00000477997.3:n.*517C>T
ENST00000640140.2:n.1260C>T
ENST00000640250.2:n.614C>T
ENST00000640681.2:n.1219C>T
ENST00000696723.1:n.4748C>T
ENST00000696741.1:n.2753C>T
ENST00000696742.1:n.2480C>T
ENST00000696743.1:n.3883C>T
ENST00000696744.1:n.1154C>T
ENST00000696767.1:n.1449C>T
ENST00000696768.1:c.*438C>T	ENSP00000512859.1:n.*438C>T
ENST00000696769.1:n.2804C>T
ENST00000696771.1:c.*107C>T	ENSP00000512860.1:n.*107C>T
ENST00000696772.1:n.2718C>T
ENST00000696773.1:n.2457C>T
ENST00000696774.1:n.6225C>T
ENST00000696776.1:c.*107C>T	ENSP00000512861.1:n.*107C>T
ENST00000696777.1:n.2523C>T
ENST00000696778.1:n.1551C>T
ENST00000696779.1:c.*107C>T	ENSP00000512862.1:n.*107C>T
ENST00000696780.1:c.*107C>T	ENSP00000512863.1:n.*107C>T
ENST00000696781.1:c.*107C>T	ENSP00000512864.1:n.*107C>T
ENST00000696782.1:c.*517C>T	ENSP00000512865.1:n.*517C>T
ENST00000696783.1:n.2983C>T
ENST00000696992.1:n.2232C>T
ENST00000696995.1:n.4644C>T
ENST00000696996.1:n.2557C>T
ENST00000696997.1:c.*745C>T	ENSP00000513028.1:n.*745C>T
ENST00000696998.1:n.2369C>T
ENST00000696999.1:c.*107C>T	ENSP00000513029.1:n.*107C>T
ENST00000697036.1:c.*531C>T	ENSP00000513060.1:n.*531C>T
ENST00000697037.1:n.1150C>T
ENST00000697093.1:n.3351C>T
ENST00000697094.1:n.3698C>T
ENST00000697095.1:c.*2316C>T	ENSP00000513104.1:n.*2316C>T
ENST00000697096.1:n.2248C>T
ENST00000697097.1:c.*107C>T	ENSP00000513105.1:n.*107C>T
ENST00000562983.2:n.1301C>T
ENST00000690268.1:c.*107C>T	ENSP00000509810.1:n.*107C>T
ENST00000355740.7:c.*441C>T	ENSP00000347979.3:n.*441C>T
ENST00000640140.1:n.1287C>T
ENST00000640250.1:n.614C>T
ENST00000640681.1:n.1236C>T
ENST00000652046.1:c.*107C>T MANE Select	ENSP00000498466.1:n.*107C>T
ENST00000352159.8:c.*432C>T	ENSP00000345601.4:n.*432C>T
ENST00000355740.6:c.*107C>T	ENSP00000347979.2:n.*107C>T
ENST00000479522.5:c.*544C>T	ENSP00000424113.1:n.*544C>T
ENST00000484444.5:c.*556C>T	ENSP00000420975.1:n.*556C>T
ENST00000494410.5:c.*473C>T	ENSP00000423755.1:n.*473C>T
NM_000043.4:c.*107C>T , LRG_134t1:c.*107C>T	NP_000034.1:n.*107C>T
NM_152871.2:c.*107C>T	NP_690610.1:n.*107C>T
NM_152872.2:c.*427C>T	NP_690611.1:n.*427C>T
NR_028033.2:n.1289C>T
NR_028034.2:n.1151C>T
NR_028035.2:n.1214C>T
NR_028036.2:n.1352C>T
XM_006717819.2:c.*107C>T	XP_006717882.1:n.*107C>T
XM_011539764.1:c.*107C>T	XP_011538066.1:n.*107C>T
XM_011539765.1:c.*107C>T	XP_011538067.1:n.*107C>T
XM_011539766.1:c.*107C>T	XP_011538068.1:n.*107C>T
XM_011539767.1:c.*107C>T	XP_011538069.1:n.*107C>T
NM_000043.5:c.*107C>T	NP_000034.1:n.*107C>T
NM_001320619.1:c.*438C>T	NP_001307548.1:n.*438C>T
NM_152871.3:c.*107C>T	NP_690610.1:n.*107C>T
NM_152872.3:c.*427C>T	NP_690611.1:n.*427C>T
NR_028033.3:n.1261C>T
NR_028034.3:n.1123C>T
NR_028035.3:n.1186C>T
NR_028036.3:n.1324C>T
NR_135313.1:n.1241C>T
NR_135314.1:n.1424C>T
NR_135315.1:n.1177C>T
XM_006717819.3:c.*107C>T	XP_006717882.1:n.*107C>T
XM_011539764.2:c.*107C>T	XP_011538066.1:n.*107C>T
XM_011539765.2:c.*107C>T	XP_011538067.1:n.*107C>T
XM_011539766.2:c.*107C>T	XP_011538068.1:n.*107C>T
XM_011539767.3:c.*107C>T	XP_011538069.1:n.*107C>T
XR_945732.3:n.1183C>T
XR_945733.2:n.1120C>T
NM_000043.6:c.*107C>T MANE Select	NP_000034.1:n.*107C>T
NM_001320619.2:c.*438C>T	NP_001307548.1:n.*438C>T
NM_152871.4:c.*107C>T	NP_690610.1:n.*107C>T
NM_152872.4:c.*427C>T	NP_690611.1:n.*427C>T
NR_028033.4:n.1022C>T
NR_028034.4:n.884C>T
NR_028035.4:n.947C>T
NR_028036.4:n.1085C>T
NR_135313.2:n.1002C>T
NR_135314.2:n.1281C>T
NR_135315.2:n.1034C>T