Canonical Allele Identifier: CA2610079696

Gene: FAS

Linked Data

• gnomAD v4: 10-89014550-ATTTTATCATTTATTAGCGCTGAAGAGCCAACATATTTGTAGAT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014556_89014598del , CM000672.2:g.89014556_89014598del	GRCh38
NC_000010.10:g.90774313_90774355del , CM000672.1:g.90774313_90774355del	GRCh37
NC_000010.9:g.90764293_90764335del	NCBI36
NG_009089.2:g.29026_29068del , LRG_134:g.29026_29068del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1423_1465del
ENST00000355740.8:c.*437_*479del	ENSP00000347979.3:n.*437_*479del
ENST00000357339.7:c.*106_*148del	ENSP00000349896.2:n.*106_*148del
ENST00000371857.8:n.2659_2701del
ENST00000460510.6:c.*106_*148del	ENSP00000512812.1:n.*106_*148del
ENST00000466081.6:n.2763_2805del
ENST00000477270.6:c.*106_*148del	ENSP00000512813.1:n.*106_*148del
ENST00000488877.6:c.1005_1047del	ENSP00000425159.1:n.1005_1047del
ENST00000492756.7:c.*543_*585del	ENSP00000422453.1:n.*543_*585del
ENST00000494799.6:c.*106_*148del	ENSP00000512834.1:n.*106_*148del
ENST00000562983.3:c.*106_*148del	ENSP00000512845.1:n.*106_*148del
ENST00000612663.6:c.*516_*558del	ENSP00000477997.3:n.*516_*558del
ENST00000640140.2:n.1259_1301del
ENST00000640250.2:n.613_655del
ENST00000640681.2:n.1218_1260del
ENST00000696723.1:n.4747_4789del
ENST00000696741.1:n.2752_2794del
ENST00000696742.1:n.2479_2521del
ENST00000696743.1:n.3882_3924del
ENST00000696744.1:n.1153_1195del
ENST00000696767.1:n.1448_1490del
ENST00000696768.1:c.*437_*479del	ENSP00000512859.1:n.*437_*479del
ENST00000696771.1:c.*106_*148del	ENSP00000512860.1:n.*106_*148del
ENST00000696772.1:n.2717_2759del
ENST00000696773.1:n.2456_2498del
ENST00000696774.1:n.6224_6266del
ENST00000696776.1:c.*106_*148del	ENSP00000512861.1:n.*106_*148del
ENST00000696777.1:n.2522_2564del
ENST00000696778.1:n.1550_1592del
ENST00000696779.1:c.*106_*148del	ENSP00000512862.1:n.*106_*148del
ENST00000696780.1:c.*106_*148del	ENSP00000512863.1:n.*106_*148del
ENST00000696781.1:c.*106_*148del	ENSP00000512864.1:n.*106_*148del
ENST00000696782.1:c.*516_*558del	ENSP00000512865.1:n.*516_*558del
ENST00000696783.1:n.2982_3024del
ENST00000696992.1:n.2231_2273del
ENST00000696995.1:n.4643_4685del
ENST00000696996.1:n.2556_2598del
ENST00000696997.1:c.*744_*786del	ENSP00000513028.1:n.*744_*786del
ENST00000696998.1:n.2368_2410del
ENST00000696999.1:c.*106_*148del	ENSP00000513029.1:n.*106_*148del
ENST00000697036.1:c.*530_*572del	ENSP00000513060.1:n.*530_*572del
ENST00000697037.1:n.1149_1191del
ENST00000697093.1:n.3350_3392del
ENST00000697094.1:n.3697_3739del
ENST00000697095.1:c.*2315_*2357del	ENSP00000513104.1:n.*2315_*2357del
ENST00000697096.1:n.2247_2289del
ENST00000697097.1:c.*106_*148del	ENSP00000513105.1:n.*106_*148del
ENST00000562983.2:n.1300_1342del
ENST00000690268.1:c.*106_*148del	ENSP00000509810.1:n.*106_*148del
ENST00000355740.7:c.*440_*482del	ENSP00000347979.3:n.*440_*482del
ENST00000640140.1:n.1286_1328del
ENST00000640250.1:n.613_655del
ENST00000640681.1:n.1235_1277del
ENST00000652046.1:c.*106_*148del MANE Select	ENSP00000498466.1:n.*106_*148del
ENST00000352159.8:c.*431_*473del	ENSP00000345601.4:n.*431_*473del
ENST00000355740.6:c.*106_*148del	ENSP00000347979.2:n.*106_*148del
ENST00000484444.5:c.*555_*597del	ENSP00000420975.1:n.*555_*597del
NM_000043.4:c.*106_*148del , LRG_134t1:c.*106_*148del	NP_000034.1:n.*106_*148del
NM_152871.2:c.*106_*148del	NP_690610.1:n.*106_*148del
NM_152872.2:c.*426_*468del	NP_690611.1:n.*426_*468del
NR_028033.2:n.1288_1330del
NR_028034.2:n.1150_1192del
NR_028035.2:n.1213_1255del
NR_028036.2:n.1351_1393del
XM_006717819.2:c.*106_*148del	XP_006717882.1:n.*106_*148del
XM_011539764.1:c.*106_*148del	XP_011538066.1:n.*106_*148del
XM_011539765.1:c.*106_*148del	XP_011538067.1:n.*106_*148del
XM_011539766.1:c.*106_*148del	XP_011538068.1:n.*106_*148del
XM_011539767.1:c.*106_*148del	XP_011538069.1:n.*106_*148del
NM_000043.5:c.*106_*148del	NP_000034.1:n.*106_*148del
NM_001320619.1:c.*437_*479del	NP_001307548.1:n.*437_*479del
NM_152871.3:c.*106_*148del	NP_690610.1:n.*106_*148del
NM_152872.3:c.*426_*468del	NP_690611.1:n.*426_*468del
NR_028033.3:n.1260_1302del
NR_028034.3:n.1122_1164del
NR_028035.3:n.1185_1227del
NR_028036.3:n.1323_1365del
NR_135313.1:n.1240_1282del
NR_135314.1:n.1423_1465del
NR_135315.1:n.1176_1218del
XM_006717819.3:c.*106_*148del	XP_006717882.1:n.*106_*148del
XM_011539764.2:c.*106_*148del	XP_011538066.1:n.*106_*148del
XM_011539765.2:c.*106_*148del	XP_011538067.1:n.*106_*148del
XM_011539766.2:c.*106_*148del	XP_011538068.1:n.*106_*148del
XM_011539767.3:c.*106_*148del	XP_011538069.1:n.*106_*148del
XR_945732.3:n.1182_1224del
XR_945733.2:n.1119_1161del
NM_000043.6:c.*106_*148del MANE Select	NP_000034.1:n.*106_*148del
NM_001320619.2:c.*437_*479del	NP_001307548.1:n.*437_*479del
NM_152871.4:c.*106_*148del	NP_690610.1:n.*106_*148del
NM_152872.4:c.*426_*468del	NP_690611.1:n.*426_*468del
NR_028033.4:n.1021_1063del
NR_028034.4:n.883_925del
NR_028035.4:n.946_988del
NR_028036.4:n.1084_1126del
NR_135313.2:n.1001_1043del
NR_135314.2:n.1280_1322del
NR_135315.2:n.1033_1075del