Canonical Allele Identifier: CA2610079759

Gene: FAS

Linked Data

• gnomAD v4: 10-89014622-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014622G>T , CM000672.2:g.89014622G>T	GRCh38
NC_000010.10:g.90774379G>T , CM000672.1:g.90774379G>T	GRCh37
NC_000010.9:g.90764359G>T	NCBI36
NG_009089.2:g.29092G>T , LRG_134:g.29092G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1489G>T
ENST00000355740.8:c.*503G>T	ENSP00000347979.3:n.*503G>T
ENST00000357339.7:c.*172G>T	ENSP00000349896.2:n.*172G>T
ENST00000371857.8:n.2725G>T
ENST00000460510.6:c.*172G>T	ENSP00000512812.1:n.*172G>T
ENST00000466081.6:n.2829G>T
ENST00000477270.6:c.*172G>T	ENSP00000512813.1:n.*172G>T
ENST00000488877.6:c.1071G>T	ENSP00000425159.1:n.1071G>T
ENST00000492756.7:c.*609G>T	ENSP00000422453.1:n.*609G>T
ENST00000494799.6:c.*172G>T	ENSP00000512834.1:n.*172G>T
ENST00000562983.3:c.*172G>T	ENSP00000512845.1:n.*172G>T
ENST00000612663.6:c.*582G>T	ENSP00000477997.3:n.*582G>T
ENST00000640140.2:n.1325G>T
ENST00000640250.2:n.679G>T
ENST00000640681.2:n.1284G>T
ENST00000696723.1:n.4813G>T
ENST00000696741.1:n.2818G>T
ENST00000696742.1:n.2545G>T
ENST00000696743.1:n.3948G>T
ENST00000696744.1:n.1219G>T
ENST00000696767.1:n.1514G>T
ENST00000696768.1:c.*503G>T	ENSP00000512859.1:n.*503G>T
ENST00000696771.1:c.*172G>T	ENSP00000512860.1:n.*172G>T
ENST00000696772.1:n.2783G>T
ENST00000696773.1:n.2522G>T
ENST00000696774.1:n.6290G>T
ENST00000696776.1:c.*172G>T	ENSP00000512861.1:n.*172G>T
ENST00000696777.1:n.2588G>T
ENST00000696778.1:n.1616G>T
ENST00000696779.1:c.*172G>T	ENSP00000512862.1:n.*172G>T
ENST00000696780.1:c.*172G>T	ENSP00000512863.1:n.*172G>T
ENST00000696781.1:c.*172G>T	ENSP00000512864.1:n.*172G>T
ENST00000696782.1:c.*582G>T	ENSP00000512865.1:n.*582G>T
ENST00000696783.1:n.3048G>T
ENST00000696992.1:n.2297G>T
ENST00000696995.1:n.4709G>T
ENST00000696996.1:n.2622G>T
ENST00000696997.1:c.*810G>T	ENSP00000513028.1:n.*810G>T
ENST00000696998.1:n.2434G>T
ENST00000696999.1:c.*172G>T	ENSP00000513029.1:n.*172G>T
ENST00000697036.1:c.*596G>T	ENSP00000513060.1:n.*596G>T
ENST00000697037.1:n.1215G>T
ENST00000697093.1:n.3416G>T
ENST00000697094.1:n.3763G>T
ENST00000697095.1:c.*2381G>T	ENSP00000513104.1:n.*2381G>T
ENST00000697096.1:n.2313G>T
ENST00000697097.1:c.*172G>T	ENSP00000513105.1:n.*172G>T
ENST00000562983.2:n.1366G>T
ENST00000690268.1:c.*172G>T	ENSP00000509810.1:n.*172G>T
ENST00000355740.7:c.*506G>T	ENSP00000347979.3:n.*506G>T
ENST00000640140.1:n.1352G>T
ENST00000640250.1:n.679G>T
ENST00000640681.1:n.1301G>T
ENST00000652046.1:c.*172G>T MANE Select	ENSP00000498466.1:n.*172G>T
ENST00000352159.8:c.*497G>T	ENSP00000345601.4:n.*497G>T
ENST00000355740.6:c.*172G>T	ENSP00000347979.2:n.*172G>T
NM_000043.4:c.*172G>T , LRG_134t1:c.*172G>T	NP_000034.1:n.*172G>T
NM_152871.2:c.*172G>T	NP_690610.1:n.*172G>T
NM_152872.2:c.*492G>T	NP_690611.1:n.*492G>T
NR_028033.2:n.1354G>T
NR_028034.2:n.1216G>T
NR_028035.2:n.1279G>T
NR_028036.2:n.1417G>T
XM_006717819.2:c.*172G>T	XP_006717882.1:n.*172G>T
XM_011539764.1:c.*172G>T	XP_011538066.1:n.*172G>T
XM_011539765.1:c.*172G>T	XP_011538067.1:n.*172G>T
XM_011539766.1:c.*172G>T	XP_011538068.1:n.*172G>T
XM_011539767.1:c.*172G>T	XP_011538069.1:n.*172G>T
NM_000043.5:c.*172G>T	NP_000034.1:n.*172G>T
NM_001320619.1:c.*503G>T	NP_001307548.1:n.*503G>T
NM_152871.3:c.*172G>T	NP_690610.1:n.*172G>T
NM_152872.3:c.*492G>T	NP_690611.1:n.*492G>T
NR_028033.3:n.1326G>T
NR_028034.3:n.1188G>T
NR_028035.3:n.1251G>T
NR_028036.3:n.1389G>T
NR_135313.1:n.1306G>T
NR_135314.1:n.1489G>T
NR_135315.1:n.1242G>T
XM_006717819.3:c.*172G>T	XP_006717882.1:n.*172G>T
XM_011539764.2:c.*172G>T	XP_011538066.1:n.*172G>T
XM_011539765.2:c.*172G>T	XP_011538067.1:n.*172G>T
XM_011539766.2:c.*172G>T	XP_011538068.1:n.*172G>T
XM_011539767.3:c.*172G>T	XP_011538069.1:n.*172G>T
XR_945732.3:n.1248G>T
XR_945733.2:n.1185G>T
NM_000043.6:c.*172G>T MANE Select	NP_000034.1:n.*172G>T
NM_001320619.2:c.*503G>T	NP_001307548.1:n.*503G>T
NM_152871.4:c.*172G>T	NP_690610.1:n.*172G>T
NM_152872.4:c.*492G>T	NP_690611.1:n.*492G>T
NR_028033.4:n.1087G>T
NR_028034.4:n.949G>T
NR_028035.4:n.1012G>T
NR_028036.4:n.1150G>T
NR_135313.2:n.1067G>T
NR_135314.2:n.1346G>T
NR_135315.2:n.1099G>T