Canonical Allele Identifier: CA2610079709

Gene: FAS

Linked Data

• gnomAD v4: 10-89014563-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014563T>A , CM000672.2:g.89014563T>A	GRCh38
NC_000010.10:g.90774320T>A , CM000672.1:g.90774320T>A	GRCh37
NC_000010.9:g.90764300T>A	NCBI36
NG_009089.2:g.29033T>A , LRG_134:g.29033T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1430T>A
ENST00000355740.8:c.*444T>A	ENSP00000347979.3:n.*444T>A
ENST00000357339.7:c.*113T>A	ENSP00000349896.2:n.*113T>A
ENST00000371857.8:n.2666T>A
ENST00000460510.6:c.*113T>A	ENSP00000512812.1:n.*113T>A
ENST00000466081.6:n.2770T>A
ENST00000477270.6:c.*113T>A	ENSP00000512813.1:n.*113T>A
ENST00000479522.6:c.*550T>A	ENSP00000424113.1:n.*550T>A
ENST00000484444.6:c.*562T>A	ENSP00000420975.1:n.*562T>A
ENST00000488877.6:c.1012T>A	ENSP00000425159.1:n.1012T>A
ENST00000492756.7:c.*550T>A	ENSP00000422453.1:n.*550T>A
ENST00000494799.6:c.*113T>A	ENSP00000512834.1:n.*113T>A
ENST00000562983.3:c.*113T>A	ENSP00000512845.1:n.*113T>A
ENST00000612663.6:c.*523T>A	ENSP00000477997.3:n.*523T>A
ENST00000640140.2:n.1266T>A
ENST00000640250.2:n.620T>A
ENST00000640681.2:n.1225T>A
ENST00000696723.1:n.4754T>A
ENST00000696741.1:n.2759T>A
ENST00000696742.1:n.2486T>A
ENST00000696743.1:n.3889T>A
ENST00000696744.1:n.1160T>A
ENST00000696767.1:n.1455T>A
ENST00000696768.1:c.*444T>A	ENSP00000512859.1:n.*444T>A
ENST00000696769.1:n.2810T>A
ENST00000696771.1:c.*113T>A	ENSP00000512860.1:n.*113T>A
ENST00000696772.1:n.2724T>A
ENST00000696773.1:n.2463T>A
ENST00000696774.1:n.6231T>A
ENST00000696776.1:c.*113T>A	ENSP00000512861.1:n.*113T>A
ENST00000696777.1:n.2529T>A
ENST00000696778.1:n.1557T>A
ENST00000696779.1:c.*113T>A	ENSP00000512862.1:n.*113T>A
ENST00000696780.1:c.*113T>A	ENSP00000512863.1:n.*113T>A
ENST00000696781.1:c.*113T>A	ENSP00000512864.1:n.*113T>A
ENST00000696782.1:c.*523T>A	ENSP00000512865.1:n.*523T>A
ENST00000696783.1:n.2989T>A
ENST00000696992.1:n.2238T>A
ENST00000696995.1:n.4650T>A
ENST00000696996.1:n.2563T>A
ENST00000696997.1:c.*751T>A	ENSP00000513028.1:n.*751T>A
ENST00000696998.1:n.2375T>A
ENST00000696999.1:c.*113T>A	ENSP00000513029.1:n.*113T>A
ENST00000697036.1:c.*537T>A	ENSP00000513060.1:n.*537T>A
ENST00000697037.1:n.1156T>A
ENST00000697093.1:n.3357T>A
ENST00000697094.1:n.3704T>A
ENST00000697095.1:c.*2322T>A	ENSP00000513104.1:n.*2322T>A
ENST00000697096.1:n.2254T>A
ENST00000697097.1:c.*113T>A	ENSP00000513105.1:n.*113T>A
ENST00000562983.2:n.1307T>A
ENST00000690268.1:c.*113T>A	ENSP00000509810.1:n.*113T>A
ENST00000355740.7:c.*447T>A	ENSP00000347979.3:n.*447T>A
ENST00000640140.1:n.1293T>A
ENST00000640250.1:n.620T>A
ENST00000640681.1:n.1242T>A
ENST00000652046.1:c.*113T>A MANE Select	ENSP00000498466.1:n.*113T>A
ENST00000352159.8:c.*438T>A	ENSP00000345601.4:n.*438T>A
ENST00000355740.6:c.*113T>A	ENSP00000347979.2:n.*113T>A
ENST00000479522.5:c.*550T>A	ENSP00000424113.1:n.*550T>A
ENST00000484444.5:c.*562T>A	ENSP00000420975.1:n.*562T>A
ENST00000494410.5:c.*479T>A	ENSP00000423755.1:n.*479T>A
NM_000043.4:c.*113T>A , LRG_134t1:c.*113T>A	NP_000034.1:n.*113T>A
NM_152871.2:c.*113T>A	NP_690610.1:n.*113T>A
NM_152872.2:c.*433T>A	NP_690611.1:n.*433T>A
NR_028033.2:n.1295T>A
NR_028034.2:n.1157T>A
NR_028035.2:n.1220T>A
NR_028036.2:n.1358T>A
XM_006717819.2:c.*113T>A	XP_006717882.1:n.*113T>A
XM_011539764.1:c.*113T>A	XP_011538066.1:n.*113T>A
XM_011539765.1:c.*113T>A	XP_011538067.1:n.*113T>A
XM_011539766.1:c.*113T>A	XP_011538068.1:n.*113T>A
XM_011539767.1:c.*113T>A	XP_011538069.1:n.*113T>A
NM_000043.5:c.*113T>A	NP_000034.1:n.*113T>A
NM_001320619.1:c.*444T>A	NP_001307548.1:n.*444T>A
NM_152871.3:c.*113T>A	NP_690610.1:n.*113T>A
NM_152872.3:c.*433T>A	NP_690611.1:n.*433T>A
NR_028033.3:n.1267T>A
NR_028034.3:n.1129T>A
NR_028035.3:n.1192T>A
NR_028036.3:n.1330T>A
NR_135313.1:n.1247T>A
NR_135314.1:n.1430T>A
NR_135315.1:n.1183T>A
XM_006717819.3:c.*113T>A	XP_006717882.1:n.*113T>A
XM_011539764.2:c.*113T>A	XP_011538066.1:n.*113T>A
XM_011539765.2:c.*113T>A	XP_011538067.1:n.*113T>A
XM_011539766.2:c.*113T>A	XP_011538068.1:n.*113T>A
XM_011539767.3:c.*113T>A	XP_011538069.1:n.*113T>A
XR_945732.3:n.1189T>A
XR_945733.2:n.1126T>A
NM_000043.6:c.*113T>A MANE Select	NP_000034.1:n.*113T>A
NM_001320619.2:c.*444T>A	NP_001307548.1:n.*444T>A
NM_152871.4:c.*113T>A	NP_690610.1:n.*113T>A
NM_152872.4:c.*433T>A	NP_690611.1:n.*433T>A
NR_028033.4:n.1028T>A
NR_028034.4:n.890T>A
NR_028035.4:n.953T>A
NR_028036.4:n.1091T>A
NR_135313.2:n.1008T>A
NR_135314.2:n.1287T>A
NR_135315.2:n.1040T>A