Canonical Allele Identifier: CA2610079652

Gene: FAS

Linked Data

• gnomAD v4: 10-89014501-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014501A>T , CM000672.2:g.89014501A>T	GRCh38
NC_000010.10:g.90774258A>T , CM000672.1:g.90774258A>T	GRCh37
NC_000010.9:g.90764238A>T	NCBI36
NG_009089.2:g.28971A>T , LRG_134:g.28971A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1368A>T
ENST00000355740.8:c.*382A>T	ENSP00000347979.3:n.*382A>T
ENST00000357339.7:c.*51A>T	ENSP00000349896.2:n.*51A>T
ENST00000371857.8:n.2604A>T
ENST00000460510.6:c.*51A>T	ENSP00000512812.1:n.*51A>T
ENST00000466081.6:n.2708A>T
ENST00000477270.6:c.*51A>T	ENSP00000512813.1:n.*51A>T
ENST00000479522.6:c.*488A>T	ENSP00000424113.1:n.*488A>T
ENST00000484444.6:c.*500A>T	ENSP00000420975.1:n.*500A>T
ENST00000488877.6:c.950A>T	ENSP00000425159.1:n.950A>T
ENST00000492756.7:c.*488A>T	ENSP00000422453.1:n.*488A>T
ENST00000494799.6:c.*51A>T	ENSP00000512834.1:n.*51A>T
ENST00000562983.3:c.*51A>T	ENSP00000512845.1:n.*51A>T
ENST00000612663.6:c.*461A>T	ENSP00000477997.3:n.*461A>T
ENST00000640140.2:n.1204A>T
ENST00000640250.2:n.558A>T
ENST00000640681.2:n.1163A>T
ENST00000696723.1:n.4692A>T
ENST00000696741.1:n.2697A>T
ENST00000696742.1:n.2424A>T
ENST00000696743.1:n.3827A>T
ENST00000696744.1:n.1098A>T
ENST00000696767.1:n.1393A>T
ENST00000696768.1:c.*382A>T	ENSP00000512859.1:n.*382A>T
ENST00000696769.1:n.2748A>T
ENST00000696771.1:c.*51A>T	ENSP00000512860.1:n.*51A>T
ENST00000696772.1:n.2662A>T
ENST00000696773.1:n.2401A>T
ENST00000696774.1:n.6169A>T
ENST00000696776.1:c.*51A>T	ENSP00000512861.1:n.*51A>T
ENST00000696777.1:n.2467A>T
ENST00000696778.1:n.1495A>T
ENST00000696779.1:c.*51A>T	ENSP00000512862.1:n.*51A>T
ENST00000696780.1:c.*51A>T	ENSP00000512863.1:n.*51A>T
ENST00000696781.1:c.*51A>T	ENSP00000512864.1:n.*51A>T
ENST00000696782.1:c.*461A>T	ENSP00000512865.1:n.*461A>T
ENST00000696783.1:n.2927A>T
ENST00000696992.1:n.2176A>T
ENST00000696995.1:n.4588A>T
ENST00000696996.1:n.2501A>T
ENST00000696997.1:c.*689A>T	ENSP00000513028.1:n.*689A>T
ENST00000696998.1:n.2313A>T
ENST00000696999.1:c.*51A>T	ENSP00000513029.1:n.*51A>T
ENST00000697036.1:c.*475A>T	ENSP00000513060.1:n.*475A>T
ENST00000697037.1:n.1094A>T
ENST00000697093.1:n.3295A>T
ENST00000697094.1:n.3642A>T
ENST00000697095.1:c.*2260A>T	ENSP00000513104.1:n.*2260A>T
ENST00000697096.1:n.2192A>T
ENST00000697097.1:c.*51A>T	ENSP00000513105.1:n.*51A>T
ENST00000562983.2:n.1245A>T
ENST00000690268.1:c.*51A>T	ENSP00000509810.1:n.*51A>T
ENST00000355740.7:c.*385A>T	ENSP00000347979.3:n.*385A>T
ENST00000640140.1:n.1231A>T
ENST00000640250.1:n.558A>T
ENST00000640681.1:n.1180A>T
ENST00000652046.1:c.*51A>T MANE Select	ENSP00000498466.1:n.*51A>T
ENST00000352159.8:c.*376A>T	ENSP00000345601.4:n.*376A>T
ENST00000355740.6:c.*51A>T	ENSP00000347979.2:n.*51A>T
ENST00000479522.5:c.*488A>T	ENSP00000424113.1:n.*488A>T
ENST00000484444.5:c.*500A>T	ENSP00000420975.1:n.*500A>T
ENST00000494410.5:c.*417A>T	ENSP00000423755.1:n.*417A>T
NM_000043.4:c.*51A>T , LRG_134t1:c.*51A>T	NP_000034.1:n.*51A>T
NM_152871.2:c.*51A>T	NP_690610.1:n.*51A>T
NM_152872.2:c.*371A>T	NP_690611.1:n.*371A>T
NR_028033.2:n.1233A>T
NR_028034.2:n.1095A>T
NR_028035.2:n.1158A>T
NR_028036.2:n.1296A>T
XM_006717819.2:c.*51A>T	XP_006717882.1:n.*51A>T
XM_011539764.1:c.*51A>T	XP_011538066.1:n.*51A>T
XM_011539765.1:c.*51A>T	XP_011538067.1:n.*51A>T
XM_011539766.1:c.*51A>T	XP_011538068.1:n.*51A>T
XM_011539767.1:c.*51A>T	XP_011538069.1:n.*51A>T
XR_945733.1:n.1064A>T
NM_000043.5:c.*51A>T	NP_000034.1:n.*51A>T
NM_001320619.1:c.*382A>T	NP_001307548.1:n.*382A>T
NM_152871.3:c.*51A>T	NP_690610.1:n.*51A>T
NM_152872.3:c.*371A>T	NP_690611.1:n.*371A>T
NR_028033.3:n.1205A>T
NR_028034.3:n.1067A>T
NR_028035.3:n.1130A>T
NR_028036.3:n.1268A>T
NR_135313.1:n.1185A>T
NR_135314.1:n.1368A>T
NR_135315.1:n.1121A>T
XM_006717819.3:c.*51A>T	XP_006717882.1:n.*51A>T
XM_011539764.2:c.*51A>T	XP_011538066.1:n.*51A>T
XM_011539765.2:c.*51A>T	XP_011538067.1:n.*51A>T
XM_011539766.2:c.*51A>T	XP_011538068.1:n.*51A>T
XM_011539767.3:c.*51A>T	XP_011538069.1:n.*51A>T
XR_945732.3:n.1127A>T
XR_945733.2:n.1064A>T
NM_000043.6:c.*51A>T MANE Select	NP_000034.1:n.*51A>T
NM_001320619.2:c.*382A>T	NP_001307548.1:n.*382A>T
NM_152871.4:c.*51A>T	NP_690610.1:n.*51A>T
NM_152872.4:c.*371A>T	NP_690611.1:n.*371A>T
NR_028033.4:n.966A>T
NR_028034.4:n.828A>T
NR_028035.4:n.891A>T
NR_028036.4:n.1029A>T
NR_135313.2:n.946A>T
NR_135314.2:n.1225A>T
NR_135315.2:n.978A>T