Canonical Allele Identifier: CA2610079636

Gene: FAS

Linked Data

• gnomAD v4: 10-89014469-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014469C>A , CM000672.2:g.89014469C>A	GRCh38
NC_000010.10:g.90774226C>A , CM000672.1:g.90774226C>A	GRCh37
NC_000010.9:g.90764206C>A	NCBI36
NG_009089.2:g.28939C>A , LRG_134:g.28939C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1336C>A
ENST00000355740.8:c.*350C>A	ENSP00000347979.3:n.*350C>A
ENST00000357339.7:c.*19C>A	ENSP00000349896.2:n.*19C>A
ENST00000371857.8:n.2572C>A
ENST00000460510.6:c.*19C>A	ENSP00000512812.1:n.*19C>A
ENST00000466081.6:n.2676C>A
ENST00000477270.6:c.*19C>A	ENSP00000512813.1:n.*19C>A
ENST00000479522.6:c.*456C>A	ENSP00000424113.1:n.*456C>A
ENST00000484444.6:c.*468C>A	ENSP00000420975.1:n.*468C>A
ENST00000488877.6:c.918C>A	ENSP00000425159.1:n.918C>A
ENST00000492756.7:c.*456C>A	ENSP00000422453.1:n.*456C>A
ENST00000494799.6:c.*19C>A	ENSP00000512834.1:n.*19C>A
ENST00000562983.3:c.*19C>A	ENSP00000512845.1:n.*19C>A
ENST00000612663.6:c.*429C>A	ENSP00000477997.3:n.*429C>A
ENST00000640140.2:n.1172C>A
ENST00000640250.2:n.526C>A
ENST00000640681.2:n.1131C>A
ENST00000696723.1:n.4660C>A
ENST00000696741.1:n.2665C>A
ENST00000696742.1:n.2392C>A
ENST00000696743.1:n.3795C>A
ENST00000696744.1:n.1066C>A
ENST00000696767.1:n.1361C>A
ENST00000696768.1:c.*350C>A	ENSP00000512859.1:n.*350C>A
ENST00000696769.1:n.2716C>A
ENST00000696771.1:c.*19C>A	ENSP00000512860.1:n.*19C>A
ENST00000696772.1:n.2630C>A
ENST00000696773.1:n.2369C>A
ENST00000696774.1:n.6137C>A
ENST00000696776.1:c.*19C>A	ENSP00000512861.1:n.*19C>A
ENST00000696777.1:n.2435C>A
ENST00000696778.1:n.1463C>A
ENST00000696779.1:c.*19C>A	ENSP00000512862.1:n.*19C>A
ENST00000696780.1:c.*19C>A	ENSP00000512863.1:n.*19C>A
ENST00000696781.1:c.*19C>A	ENSP00000512864.1:n.*19C>A
ENST00000696782.1:c.*429C>A	ENSP00000512865.1:n.*429C>A
ENST00000696783.1:n.2895C>A
ENST00000696992.1:n.2144C>A
ENST00000696995.1:n.4556C>A
ENST00000696996.1:n.2469C>A
ENST00000696997.1:c.*657C>A	ENSP00000513028.1:n.*657C>A
ENST00000696998.1:n.2281C>A
ENST00000696999.1:c.*19C>A	ENSP00000513029.1:n.*19C>A
ENST00000697036.1:c.*443C>A	ENSP00000513060.1:n.*443C>A
ENST00000697037.1:n.1062C>A
ENST00000697093.1:n.3263C>A
ENST00000697094.1:n.3610C>A
ENST00000697095.1:c.*2228C>A	ENSP00000513104.1:n.*2228C>A
ENST00000697096.1:n.2160C>A
ENST00000697097.1:c.*19C>A	ENSP00000513105.1:n.*19C>A
ENST00000562983.2:n.1213C>A
ENST00000690268.1:c.*19C>A	ENSP00000509810.1:n.*19C>A
ENST00000355740.7:c.*353C>A	ENSP00000347979.3:n.*353C>A
ENST00000612663.5:c.*429C>A	ENSP00000477997.3:n.*429C>A
ENST00000640140.1:n.1199C>A
ENST00000640250.1:n.526C>A
ENST00000640681.1:n.1148C>A
ENST00000652046.1:c.*19C>A MANE Select	ENSP00000498466.1:n.*19C>A
ENST00000352159.8:c.*344C>A	ENSP00000345601.4:n.*344C>A
ENST00000355740.6:c.*19C>A	ENSP00000347979.2:n.*19C>A
ENST00000479522.5:c.*456C>A	ENSP00000424113.1:n.*456C>A
ENST00000484444.5:c.*468C>A	ENSP00000420975.1:n.*468C>A
ENST00000494410.5:c.*385C>A	ENSP00000423755.1:n.*385C>A
NM_000043.4:c.*19C>A , LRG_134t1:c.*19C>A	NP_000034.1:n.*19C>A
NM_152871.2:c.*19C>A	NP_690610.1:n.*19C>A
NM_152872.2:c.*339C>A	NP_690611.1:n.*339C>A
NR_028033.2:n.1201C>A
NR_028034.2:n.1063C>A
NR_028035.2:n.1126C>A
NR_028036.2:n.1264C>A
XM_006717819.2:c.*19C>A	XP_006717882.1:n.*19C>A
XM_011539764.1:c.*19C>A	XP_011538066.1:n.*19C>A
XM_011539765.1:c.*19C>A	XP_011538067.1:n.*19C>A
XM_011539766.1:c.*19C>A	XP_011538068.1:n.*19C>A
XM_011539767.1:c.*19C>A	XP_011538069.1:n.*19C>A
XR_945733.1:n.1032C>A
NM_000043.5:c.*19C>A	NP_000034.1:n.*19C>A
NM_001320619.1:c.*350C>A	NP_001307548.1:n.*350C>A
NM_152871.3:c.*19C>A	NP_690610.1:n.*19C>A
NM_152872.3:c.*339C>A	NP_690611.1:n.*339C>A
NR_028033.3:n.1173C>A
NR_028034.3:n.1035C>A
NR_028035.3:n.1098C>A
NR_028036.3:n.1236C>A
NR_135313.1:n.1153C>A
NR_135314.1:n.1336C>A
NR_135315.1:n.1089C>A
XM_006717819.3:c.*19C>A	XP_006717882.1:n.*19C>A
XM_011539764.2:c.*19C>A	XP_011538066.1:n.*19C>A
XM_011539765.2:c.*19C>A	XP_011538067.1:n.*19C>A
XM_011539766.2:c.*19C>A	XP_011538068.1:n.*19C>A
XM_011539767.3:c.*19C>A	XP_011538069.1:n.*19C>A
XR_945732.3:n.1095C>A
XR_945733.2:n.1032C>A
NM_000043.6:c.*19C>A MANE Select	NP_000034.1:n.*19C>A
NM_001320619.2:c.*350C>A	NP_001307548.1:n.*350C>A
NM_152871.4:c.*19C>A	NP_690610.1:n.*19C>A
NM_152872.4:c.*339C>A	NP_690611.1:n.*339C>A
NR_028033.4:n.934C>A
NR_028034.4:n.796C>A
NR_028035.4:n.859C>A
NR_028036.4:n.997C>A
NR_135313.2:n.914C>A
NR_135314.2:n.1193C>A
NR_135315.2:n.946C>A