Canonical Allele Identifier: CA2610079706

Gene: FAS

Linked Data

• gnomAD v4: 10-89014558-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014558A>G , CM000672.2:g.89014558A>G	GRCh38
NC_000010.10:g.90774315A>G , CM000672.1:g.90774315A>G	GRCh37
NC_000010.9:g.90764295A>G	NCBI36
NG_009089.2:g.29028A>G , LRG_134:g.29028A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1425A>G
ENST00000355740.8:c.*439A>G	ENSP00000347979.3:n.*439A>G
ENST00000357339.7:c.*108A>G	ENSP00000349896.2:n.*108A>G
ENST00000371857.8:n.2661A>G
ENST00000460510.6:c.*108A>G	ENSP00000512812.1:n.*108A>G
ENST00000466081.6:n.2765A>G
ENST00000477270.6:c.*108A>G	ENSP00000512813.1:n.*108A>G
ENST00000479522.6:c.*545A>G	ENSP00000424113.1:n.*545A>G
ENST00000484444.6:c.*557A>G	ENSP00000420975.1:n.*557A>G
ENST00000488877.6:c.1007A>G	ENSP00000425159.1:n.1007A>G
ENST00000492756.7:c.*545A>G	ENSP00000422453.1:n.*545A>G
ENST00000494799.6:c.*108A>G	ENSP00000512834.1:n.*108A>G
ENST00000562983.3:c.*108A>G	ENSP00000512845.1:n.*108A>G
ENST00000612663.6:c.*518A>G	ENSP00000477997.3:n.*518A>G
ENST00000640140.2:n.1261A>G
ENST00000640250.2:n.615A>G
ENST00000640681.2:n.1220A>G
ENST00000696723.1:n.4749A>G
ENST00000696741.1:n.2754A>G
ENST00000696742.1:n.2481A>G
ENST00000696743.1:n.3884A>G
ENST00000696744.1:n.1155A>G
ENST00000696767.1:n.1450A>G
ENST00000696768.1:c.*439A>G	ENSP00000512859.1:n.*439A>G
ENST00000696769.1:n.2805A>G
ENST00000696771.1:c.*108A>G	ENSP00000512860.1:n.*108A>G
ENST00000696772.1:n.2719A>G
ENST00000696773.1:n.2458A>G
ENST00000696774.1:n.6226A>G
ENST00000696776.1:c.*108A>G	ENSP00000512861.1:n.*108A>G
ENST00000696777.1:n.2524A>G
ENST00000696778.1:n.1552A>G
ENST00000696779.1:c.*108A>G	ENSP00000512862.1:n.*108A>G
ENST00000696780.1:c.*108A>G	ENSP00000512863.1:n.*108A>G
ENST00000696781.1:c.*108A>G	ENSP00000512864.1:n.*108A>G
ENST00000696782.1:c.*518A>G	ENSP00000512865.1:n.*518A>G
ENST00000696783.1:n.2984A>G
ENST00000696992.1:n.2233A>G
ENST00000696995.1:n.4645A>G
ENST00000696996.1:n.2558A>G
ENST00000696997.1:c.*746A>G	ENSP00000513028.1:n.*746A>G
ENST00000696998.1:n.2370A>G
ENST00000696999.1:c.*108A>G	ENSP00000513029.1:n.*108A>G
ENST00000697036.1:c.*532A>G	ENSP00000513060.1:n.*532A>G
ENST00000697037.1:n.1151A>G
ENST00000697093.1:n.3352A>G
ENST00000697094.1:n.3699A>G
ENST00000697095.1:c.*2317A>G	ENSP00000513104.1:n.*2317A>G
ENST00000697096.1:n.2249A>G
ENST00000697097.1:c.*108A>G	ENSP00000513105.1:n.*108A>G
ENST00000562983.2:n.1302A>G
ENST00000690268.1:c.*108A>G	ENSP00000509810.1:n.*108A>G
ENST00000355740.7:c.*442A>G	ENSP00000347979.3:n.*442A>G
ENST00000640140.1:n.1288A>G
ENST00000640250.1:n.615A>G
ENST00000640681.1:n.1237A>G
ENST00000652046.1:c.*108A>G MANE Select	ENSP00000498466.1:n.*108A>G
ENST00000352159.8:c.*433A>G	ENSP00000345601.4:n.*433A>G
ENST00000355740.6:c.*108A>G	ENSP00000347979.2:n.*108A>G
ENST00000479522.5:c.*545A>G	ENSP00000424113.1:n.*545A>G
ENST00000484444.5:c.*557A>G	ENSP00000420975.1:n.*557A>G
ENST00000494410.5:c.*474A>G	ENSP00000423755.1:n.*474A>G
NM_000043.4:c.*108A>G , LRG_134t1:c.*108A>G	NP_000034.1:n.*108A>G
NM_152871.2:c.*108A>G	NP_690610.1:n.*108A>G
NM_152872.2:c.*428A>G	NP_690611.1:n.*428A>G
NR_028033.2:n.1290A>G
NR_028034.2:n.1152A>G
NR_028035.2:n.1215A>G
NR_028036.2:n.1353A>G
XM_006717819.2:c.*108A>G	XP_006717882.1:n.*108A>G
XM_011539764.1:c.*108A>G	XP_011538066.1:n.*108A>G
XM_011539765.1:c.*108A>G	XP_011538067.1:n.*108A>G
XM_011539766.1:c.*108A>G	XP_011538068.1:n.*108A>G
XM_011539767.1:c.*108A>G	XP_011538069.1:n.*108A>G
NM_000043.5:c.*108A>G	NP_000034.1:n.*108A>G
NM_001320619.1:c.*439A>G	NP_001307548.1:n.*439A>G
NM_152871.3:c.*108A>G	NP_690610.1:n.*108A>G
NM_152872.3:c.*428A>G	NP_690611.1:n.*428A>G
NR_028033.3:n.1262A>G
NR_028034.3:n.1124A>G
NR_028035.3:n.1187A>G
NR_028036.3:n.1325A>G
NR_135313.1:n.1242A>G
NR_135314.1:n.1425A>G
NR_135315.1:n.1178A>G
XM_006717819.3:c.*108A>G	XP_006717882.1:n.*108A>G
XM_011539764.2:c.*108A>G	XP_011538066.1:n.*108A>G
XM_011539765.2:c.*108A>G	XP_011538067.1:n.*108A>G
XM_011539766.2:c.*108A>G	XP_011538068.1:n.*108A>G
XM_011539767.3:c.*108A>G	XP_011538069.1:n.*108A>G
XR_945732.3:n.1184A>G
XR_945733.2:n.1121A>G
NM_000043.6:c.*108A>G MANE Select	NP_000034.1:n.*108A>G
NM_001320619.2:c.*439A>G	NP_001307548.1:n.*439A>G
NM_152871.4:c.*108A>G	NP_690610.1:n.*108A>G
NM_152872.4:c.*428A>G	NP_690611.1:n.*428A>G
NR_028033.4:n.1023A>G
NR_028034.4:n.885A>G
NR_028035.4:n.948A>G
NR_028036.4:n.1086A>G
NR_135313.2:n.1003A>G
NR_135314.2:n.1282A>G
NR_135315.2:n.1035A>G