Canonical Allele Identifier: CA2574605506

Gene: FAS

Linked Data

• gnomAD v4: 10-89014550-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014554del , CM000672.2:g.89014554del	GRCh38
NC_000010.10:g.90774311del , CM000672.1:g.90774311del	GRCh37
NC_000010.9:g.90764291del	NCBI36
NG_009089.2:g.29024del , LRG_134:g.29024del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1421del
ENST00000355740.8:c.*435del	ENSP00000347979.3:n.*435del
ENST00000357339.7:c.*104del	ENSP00000349896.2:n.*104del
ENST00000371857.8:n.2657del
ENST00000460510.6:c.*104del	ENSP00000512812.1:n.*104del
ENST00000466081.6:n.2761del
ENST00000477270.6:c.*104del	ENSP00000512813.1:n.*104del
ENST00000479522.6:c.*541del	ENSP00000424113.1:n.*541del
ENST00000484444.6:c.*553del	ENSP00000420975.1:n.*553del
ENST00000488877.6:c.1003del	ENSP00000425159.1:n.1003del
ENST00000492756.7:c.*541del	ENSP00000422453.1:n.*541del
ENST00000494799.6:c.*104del	ENSP00000512834.1:n.*104del
ENST00000562983.3:c.*104del	ENSP00000512845.1:n.*104del
ENST00000612663.6:c.*514del	ENSP00000477997.3:n.*514del
ENST00000640140.2:n.1257del
ENST00000640250.2:n.611del
ENST00000640681.2:n.1216del
ENST00000696723.1:n.4745del
ENST00000696741.1:n.2750del
ENST00000696742.1:n.2477del
ENST00000696743.1:n.3880del
ENST00000696744.1:n.1151del
ENST00000696767.1:n.1446del
ENST00000696768.1:c.*435del	ENSP00000512859.1:n.*435del
ENST00000696769.1:n.2801del
ENST00000696771.1:c.*104del	ENSP00000512860.1:n.*104del
ENST00000696772.1:n.2715del
ENST00000696773.1:n.2454del
ENST00000696774.1:n.6222del
ENST00000696776.1:c.*104del	ENSP00000512861.1:n.*104del
ENST00000696777.1:n.2520del
ENST00000696778.1:n.1548del
ENST00000696779.1:c.*104del	ENSP00000512862.1:n.*104del
ENST00000696780.1:c.*104del	ENSP00000512863.1:n.*104del
ENST00000696781.1:c.*104del	ENSP00000512864.1:n.*104del
ENST00000696782.1:c.*514del	ENSP00000512865.1:n.*514del
ENST00000696783.1:n.2980del
ENST00000696992.1:n.2229del
ENST00000696995.1:n.4641del
ENST00000696996.1:n.2554del
ENST00000696997.1:c.*742del	ENSP00000513028.1:n.*742del
ENST00000696998.1:n.2366del
ENST00000696999.1:c.*104del	ENSP00000513029.1:n.*104del
ENST00000697036.1:c.*528del	ENSP00000513060.1:n.*528del
ENST00000697037.1:n.1147del
ENST00000697093.1:n.3348del
ENST00000697094.1:n.3695del
ENST00000697095.1:c.*2313del	ENSP00000513104.1:n.*2313del
ENST00000697096.1:n.2245del
ENST00000697097.1:c.*104del	ENSP00000513105.1:n.*104del
ENST00000562983.2:n.1298del
ENST00000690268.1:c.*104del	ENSP00000509810.1:n.*104del
ENST00000355740.7:c.*438del	ENSP00000347979.3:n.*438del
ENST00000640140.1:n.1284del
ENST00000640250.1:n.611del
ENST00000640681.1:n.1233del
ENST00000652046.1:c.*104del MANE Select	ENSP00000498466.1:n.*104del
ENST00000352159.8:c.*429del	ENSP00000345601.4:n.*429del
ENST00000355740.6:c.*104del	ENSP00000347979.2:n.*104del
ENST00000479522.5:c.*541del	ENSP00000424113.1:n.*541del
ENST00000484444.5:c.*553del	ENSP00000420975.1:n.*553del
ENST00000494410.5:c.*470del	ENSP00000423755.1:n.*470del
NM_000043.4:c.*104del , LRG_134t1:c.*104del	NP_000034.1:n.*104del
NM_152871.2:c.*104del	NP_690610.1:n.*104del
NM_152872.2:c.*424del	NP_690611.1:n.*424del
NR_028033.2:n.1286del
NR_028034.2:n.1148del
NR_028035.2:n.1211del
NR_028036.2:n.1349del
XM_006717819.2:c.*104del	XP_006717882.1:n.*104del
XM_011539764.1:c.*104del	XP_011538066.1:n.*104del
XM_011539765.1:c.*104del	XP_011538067.1:n.*104del
XM_011539766.1:c.*104del	XP_011538068.1:n.*104del
XM_011539767.1:c.*104del	XP_011538069.1:n.*104del
NM_000043.5:c.*104del	NP_000034.1:n.*104del
NM_001320619.1:c.*435del	NP_001307548.1:n.*435del
NM_152871.3:c.*104del	NP_690610.1:n.*104del
NM_152872.3:c.*424del	NP_690611.1:n.*424del
NR_028033.3:n.1258del
NR_028034.3:n.1120del
NR_028035.3:n.1183del
NR_028036.3:n.1321del
NR_135313.1:n.1238del
NR_135314.1:n.1421del
NR_135315.1:n.1174del
XM_006717819.3:c.*104del	XP_006717882.1:n.*104del
XM_011539764.2:c.*104del	XP_011538066.1:n.*104del
XM_011539765.2:c.*104del	XP_011538067.1:n.*104del
XM_011539766.2:c.*104del	XP_011538068.1:n.*104del
XM_011539767.3:c.*104del	XP_011538069.1:n.*104del
XR_945732.3:n.1180del
XR_945733.2:n.1117del
NM_000043.6:c.*104del MANE Select	NP_000034.1:n.*104del
NM_001320619.2:c.*435del	NP_001307548.1:n.*435del
NM_152871.4:c.*104del	NP_690610.1:n.*104del
NM_152872.4:c.*424del	NP_690611.1:n.*424del
NR_028033.4:n.1019del
NR_028034.4:n.881del
NR_028035.4:n.944del
NR_028036.4:n.1082del
NR_135313.2:n.999del
NR_135314.2:n.1278del
NR_135315.2:n.1031del