Canonical Allele Identifier: CA2695212389

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014272del , CM000672.2:g.89014272del	GRCh38
NC_000010.10:g.90774029del , CM000672.1:g.90774029del	GRCh37
NC_000010.9:g.90764009del	NCBI36
NG_009089.2:g.28742del , LRG_134:g.28742del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1139del
ENST00000355740.8:c.*153del	ENSP00000347979.3:n.*153del
ENST00000357339.7:c.767del	ENSP00000349896.2:p.Leu256ArgfsTer18
ENST00000371857.8:n.2375del
ENST00000460510.6:c.113del	ENSP00000512812.1:p.Leu38ArgfsTer18
ENST00000466081.6:n.2479del
ENST00000477270.6:c.875del	ENSP00000512813.1:p.Leu292ArgfsTer18
ENST00000479522.6:c.*259del	ENSP00000424113.1:n.*259del
ENST00000484444.6:c.*271del	ENSP00000420975.1:n.*271del
ENST00000488877.6:c.721del	ENSP00000425159.1:n.721del
ENST00000492756.7:c.*259del	ENSP00000422453.1:n.*259del
ENST00000494799.6:c.113del	ENSP00000512834.1:p.Leu38ArgfsTer18
ENST00000562983.3:c.113del	ENSP00000512845.1:p.Leu38ArgfsTer18
ENST00000612663.6:c.*232del	ENSP00000477997.3:n.*232del
ENST00000640140.2:n.975del
ENST00000640250.2:n.329del
ENST00000640681.2:n.934del
ENST00000696723.1:n.4463del
ENST00000696741.1:n.2468del
ENST00000696742.1:n.2195del
ENST00000696743.1:n.3598del
ENST00000696744.1:n.869del
ENST00000696767.1:n.1164del
ENST00000696768.1:c.*153del	ENSP00000512859.1:n.*153del
ENST00000696769.1:n.2519del
ENST00000696771.1:c.113del	ENSP00000512860.1:p.Leu38ArgfsTer18
ENST00000696772.1:n.2433del
ENST00000696773.1:n.2172del
ENST00000696774.1:n.5940del
ENST00000696776.1:c.923del	ENSP00000512861.1:p.Leu308ArgfsTer18
ENST00000696777.1:n.2238del
ENST00000696778.1:n.1266del
ENST00000696779.1:c.437del	ENSP00000512862.1:p.Leu146ArgfsTer18
ENST00000696780.1:c.860del	ENSP00000512863.1:p.Leu287ArgfsTer18
ENST00000696781.1:c.575del	ENSP00000512864.1:p.Leu192ArgfsTer18
ENST00000696782.1:c.*232del	ENSP00000512865.1:n.*232del
ENST00000696783.1:n.2698del
ENST00000696992.1:n.1947del
ENST00000696995.1:n.4359del
ENST00000696996.1:n.2272del
ENST00000696997.1:c.*460del	ENSP00000513028.1:n.*460del
ENST00000696998.1:n.2084del
ENST00000696999.1:c.113del	ENSP00000513029.1:p.Leu38ArgfsTer18
ENST00000697035.1:c.*163del	ENSP00000513059.1:n.*163del
ENST00000697036.1:c.*246del	ENSP00000513060.1:n.*246del
ENST00000697037.1:n.865del
ENST00000697093.1:n.3066del
ENST00000697094.1:n.3413del
ENST00000697095.1:c.*2031del	ENSP00000513104.1:n.*2031del
ENST00000697096.1:n.1963del
ENST00000697097.1:c.113del	ENSP00000513105.1:p.Leu38ArgfsTer18
ENST00000562983.2:n.1016del
ENST00000690268.1:c.911del	ENSP00000509810.1:p.Leu304ArgfsTer18
ENST00000355740.7:c.*156del	ENSP00000347979.3:n.*156del
ENST00000612663.5:c.*232del	ENSP00000477997.3:n.*232del
ENST00000640140.1:n.1002del
ENST00000640250.1:n.329del
ENST00000640681.1:n.951del
ENST00000652046.1:c.830del MANE Select	ENSP00000498466.1:p.Leu277ArgfsTer18
ENST00000352159.8:c.*147del	ENSP00000345601.4:n.*147del
ENST00000355279.2:c.805del	ENSP00000347426.2:n.805del
ENST00000355740.6:c.830del	ENSP00000347979.2:p.Leu277ArgfsTer18
ENST00000357339.6:c.767del	ENSP00000349896.2:p.Leu256ArgfsTer18
ENST00000479522.5:c.*259del	ENSP00000424113.1:n.*259del
ENST00000484444.5:c.*271del	ENSP00000420975.1:n.*271del
ENST00000488877.5:c.*271del	ENSP00000425159.1:n.*271del
ENST00000492756.5:c.658del	ENSP00000422453.1:n.658del
ENST00000494410.5:c.*188del	ENSP00000423755.1:n.*188del
ENST00000612663.4:c.*177del	ENSP00000477997.2:n.*177del
NM_000043.4:c.830del , LRG_134t1:c.830del	NP_000034.1:p.Leu277ArgfsTer18
NM_152871.2:c.767del	NP_690610.1:p.Leu256ArgfsTer18
NM_152872.2:c.*142del	NP_690611.1:n.*142del
NR_028033.2:n.1004del
NR_028034.2:n.866del
NR_028035.2:n.929del
NR_028036.2:n.1067del
XM_006717819.2:c.911del	XP_006717882.1:p.Leu304ArgfsTer18
XM_011539764.1:c.992del	XP_011538066.1:p.Leu331ArgfsTer18
XM_011539765.1:c.929del	XP_011538067.1:p.Leu310ArgfsTer18
XM_011539766.1:c.911del	XP_011538068.1:p.Leu304ArgfsTer18
XM_011539767.1:c.875del	XP_011538069.1:p.Leu292ArgfsTer18
XR_945732.1:n.898del
XR_945733.1:n.835del
NM_000043.5:c.830del	NP_000034.1:p.Leu277ArgfsTer18
NM_001320619.1:c.*153del	NP_001307548.1:n.*153del
NM_152871.3:c.767del	NP_690610.1:p.Leu256ArgfsTer18
NM_152872.3:c.*142del	NP_690611.1:n.*142del
NR_028033.3:n.976del
NR_028034.3:n.838del
NR_028035.3:n.901del
NR_028036.3:n.1039del
NR_135313.1:n.956del
NR_135314.1:n.1139del
NR_135315.1:n.892del
XM_006717819.3:c.911del	XP_006717882.1:p.Leu304ArgfsTer18
XM_011539764.2:c.992del	XP_011538066.1:p.Leu331ArgfsTer18
XM_011539765.2:c.929del	XP_011538067.1:p.Leu310ArgfsTer18
XM_011539766.2:c.911del	XP_011538068.1:p.Leu304ArgfsTer18
XM_011539767.3:c.875del	XP_011538069.1:p.Leu292ArgfsTer18
XR_945732.3:n.898del
XR_945733.2:n.835del
NM_000043.6:c.830del MANE Select	NP_000034.1:p.Leu277ArgfsTer18
NM_001320619.2:c.*153del	NP_001307548.1:n.*153del
NM_152871.4:c.767del	NP_690610.1:p.Leu256ArgfsTer18
NM_152872.4:c.*142del	NP_690611.1:n.*142del
NR_028033.4:n.737del
NR_028034.4:n.599del
NR_028035.4:n.662del
NR_028036.4:n.800del
NR_135313.2:n.717del
NR_135314.2:n.996del
NR_135315.2:n.749del