Canonical Allele Identifier: CA2610079637

Gene: FAS

Linked Data

• gnomAD v4: 10-89014471-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014471G>T , CM000672.2:g.89014471G>T	GRCh38
NC_000010.10:g.90774228G>T , CM000672.1:g.90774228G>T	GRCh37
NC_000010.9:g.90764208G>T	NCBI36
NG_009089.2:g.28941G>T , LRG_134:g.28941G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1338G>T
ENST00000355740.8:c.*352G>T	ENSP00000347979.3:n.*352G>T
ENST00000357339.7:c.*21G>T	ENSP00000349896.2:n.*21G>T
ENST00000371857.8:n.2574G>T
ENST00000460510.6:c.*21G>T	ENSP00000512812.1:n.*21G>T
ENST00000466081.6:n.2678G>T
ENST00000477270.6:c.*21G>T	ENSP00000512813.1:n.*21G>T
ENST00000479522.6:c.*458G>T	ENSP00000424113.1:n.*458G>T
ENST00000484444.6:c.*470G>T	ENSP00000420975.1:n.*470G>T
ENST00000488877.6:c.920G>T	ENSP00000425159.1:n.920G>T
ENST00000492756.7:c.*458G>T	ENSP00000422453.1:n.*458G>T
ENST00000494799.6:c.*21G>T	ENSP00000512834.1:n.*21G>T
ENST00000562983.3:c.*21G>T	ENSP00000512845.1:n.*21G>T
ENST00000612663.6:c.*431G>T	ENSP00000477997.3:n.*431G>T
ENST00000640140.2:n.1174G>T
ENST00000640250.2:n.528G>T
ENST00000640681.2:n.1133G>T
ENST00000696723.1:n.4662G>T
ENST00000696741.1:n.2667G>T
ENST00000696742.1:n.2394G>T
ENST00000696743.1:n.3797G>T
ENST00000696744.1:n.1068G>T
ENST00000696767.1:n.1363G>T
ENST00000696768.1:c.*352G>T	ENSP00000512859.1:n.*352G>T
ENST00000696769.1:n.2718G>T
ENST00000696771.1:c.*21G>T	ENSP00000512860.1:n.*21G>T
ENST00000696772.1:n.2632G>T
ENST00000696773.1:n.2371G>T
ENST00000696774.1:n.6139G>T
ENST00000696776.1:c.*21G>T	ENSP00000512861.1:n.*21G>T
ENST00000696777.1:n.2437G>T
ENST00000696778.1:n.1465G>T
ENST00000696779.1:c.*21G>T	ENSP00000512862.1:n.*21G>T
ENST00000696780.1:c.*21G>T	ENSP00000512863.1:n.*21G>T
ENST00000696781.1:c.*21G>T	ENSP00000512864.1:n.*21G>T
ENST00000696782.1:c.*431G>T	ENSP00000512865.1:n.*431G>T
ENST00000696783.1:n.2897G>T
ENST00000696992.1:n.2146G>T
ENST00000696995.1:n.4558G>T
ENST00000696996.1:n.2471G>T
ENST00000696997.1:c.*659G>T	ENSP00000513028.1:n.*659G>T
ENST00000696998.1:n.2283G>T
ENST00000696999.1:c.*21G>T	ENSP00000513029.1:n.*21G>T
ENST00000697036.1:c.*445G>T	ENSP00000513060.1:n.*445G>T
ENST00000697037.1:n.1064G>T
ENST00000697093.1:n.3265G>T
ENST00000697094.1:n.3612G>T
ENST00000697095.1:c.*2230G>T	ENSP00000513104.1:n.*2230G>T
ENST00000697096.1:n.2162G>T
ENST00000697097.1:c.*21G>T	ENSP00000513105.1:n.*21G>T
ENST00000562983.2:n.1215G>T
ENST00000690268.1:c.*21G>T	ENSP00000509810.1:n.*21G>T
ENST00000355740.7:c.*355G>T	ENSP00000347979.3:n.*355G>T
ENST00000612663.5:c.*431G>T	ENSP00000477997.3:n.*431G>T
ENST00000640140.1:n.1201G>T
ENST00000640250.1:n.528G>T
ENST00000640681.1:n.1150G>T
ENST00000652046.1:c.*21G>T MANE Select	ENSP00000498466.1:n.*21G>T
ENST00000352159.8:c.*346G>T	ENSP00000345601.4:n.*346G>T
ENST00000355740.6:c.*21G>T	ENSP00000347979.2:n.*21G>T
ENST00000479522.5:c.*458G>T	ENSP00000424113.1:n.*458G>T
ENST00000484444.5:c.*470G>T	ENSP00000420975.1:n.*470G>T
ENST00000494410.5:c.*387G>T	ENSP00000423755.1:n.*387G>T
NM_000043.4:c.*21G>T , LRG_134t1:c.*21G>T	NP_000034.1:n.*21G>T
NM_152871.2:c.*21G>T	NP_690610.1:n.*21G>T
NM_152872.2:c.*341G>T	NP_690611.1:n.*341G>T
NR_028033.2:n.1203G>T
NR_028034.2:n.1065G>T
NR_028035.2:n.1128G>T
NR_028036.2:n.1266G>T
XM_006717819.2:c.*21G>T	XP_006717882.1:n.*21G>T
XM_011539764.1:c.*21G>T	XP_011538066.1:n.*21G>T
XM_011539765.1:c.*21G>T	XP_011538067.1:n.*21G>T
XM_011539766.1:c.*21G>T	XP_011538068.1:n.*21G>T
XM_011539767.1:c.*21G>T	XP_011538069.1:n.*21G>T
XR_945733.1:n.1034G>T
NM_000043.5:c.*21G>T	NP_000034.1:n.*21G>T
NM_001320619.1:c.*352G>T	NP_001307548.1:n.*352G>T
NM_152871.3:c.*21G>T	NP_690610.1:n.*21G>T
NM_152872.3:c.*341G>T	NP_690611.1:n.*341G>T
NR_028033.3:n.1175G>T
NR_028034.3:n.1037G>T
NR_028035.3:n.1100G>T
NR_028036.3:n.1238G>T
NR_135313.1:n.1155G>T
NR_135314.1:n.1338G>T
NR_135315.1:n.1091G>T
XM_006717819.3:c.*21G>T	XP_006717882.1:n.*21G>T
XM_011539764.2:c.*21G>T	XP_011538066.1:n.*21G>T
XM_011539765.2:c.*21G>T	XP_011538067.1:n.*21G>T
XM_011539766.2:c.*21G>T	XP_011538068.1:n.*21G>T
XM_011539767.3:c.*21G>T	XP_011538069.1:n.*21G>T
XR_945732.3:n.1097G>T
XR_945733.2:n.1034G>T
NM_000043.6:c.*21G>T MANE Select	NP_000034.1:n.*21G>T
NM_001320619.2:c.*352G>T	NP_001307548.1:n.*352G>T
NM_152871.4:c.*21G>T	NP_690610.1:n.*21G>T
NM_152872.4:c.*341G>T	NP_690611.1:n.*341G>T
NR_028033.4:n.936G>T
NR_028034.4:n.798G>T
NR_028035.4:n.861G>T
NR_028036.4:n.999G>T
NR_135313.2:n.916G>T
NR_135314.2:n.1195G>T
NR_135315.2:n.948G>T