Canonical Allele Identifier: CA2695212388

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014254_89014256del , CM000672.2:g.89014254_89014256del	GRCh38
NC_000010.10:g.90774011_90774013del , CM000672.1:g.90774011_90774013del	GRCh37
NC_000010.9:g.90763991_90763993del	NCBI36
NG_009089.2:g.28724_28726del , LRG_134:g.28724_28726del

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1121_1123del
ENST00000355740.8:c.*135_*137del	ENSP00000347979.3:n.*135_*137del
ENST00000357339.7:c.749_751del	ENSP00000349896.2:p.Ala250del
ENST00000371857.8:n.2357_2359del
ENST00000460510.6:c.95_97del	ENSP00000512812.1:p.Ala32del
ENST00000466081.6:n.2461_2463del
ENST00000477270.6:c.857_859del	ENSP00000512813.1:p.Ala286del
ENST00000479522.6:c.*241_*243del	ENSP00000424113.1:n.*241_*243del
ENST00000484444.6:c.*253_*255del	ENSP00000420975.1:n.*253_*255del
ENST00000488877.6:c.703_705del	ENSP00000425159.1:n.703_705del
ENST00000492756.7:c.*241_*243del	ENSP00000422453.1:n.*241_*243del
ENST00000494799.6:c.95_97del	ENSP00000512834.1:p.Ala32del
ENST00000562983.3:c.95_97del	ENSP00000512845.1:p.Ala32del
ENST00000612663.6:c.*214_*216del	ENSP00000477997.3:n.*214_*216del
ENST00000640140.2:n.957_959del
ENST00000640250.2:n.311_313del
ENST00000640681.2:n.916_918del
ENST00000696723.1:n.4445_4447del
ENST00000696741.1:n.2450_2452del
ENST00000696742.1:n.2177_2179del
ENST00000696743.1:n.3580_3582del
ENST00000696744.1:n.851_853del
ENST00000696767.1:n.1146_1148del
ENST00000696768.1:c.*135_*137del	ENSP00000512859.1:n.*135_*137del
ENST00000696769.1:n.2501_2503del
ENST00000696771.1:c.95_97del	ENSP00000512860.1:p.Ala32del
ENST00000696772.1:n.2415_2417del
ENST00000696773.1:n.2154_2156del
ENST00000696774.1:n.5922_5924del
ENST00000696776.1:c.905_907del	ENSP00000512861.1:p.Ala302del
ENST00000696777.1:n.2220_2222del
ENST00000696778.1:n.1248_1250del
ENST00000696779.1:c.419_421del	ENSP00000512862.1:p.Ala140del
ENST00000696780.1:c.842_844del	ENSP00000512863.1:p.Ala281del
ENST00000696781.1:c.557_559del	ENSP00000512864.1:p.Ala186del
ENST00000696782.1:c.*214_*216del	ENSP00000512865.1:n.*214_*216del
ENST00000696783.1:n.2680_2682del
ENST00000696992.1:n.1929_1931del
ENST00000696995.1:n.4341_4343del
ENST00000696996.1:n.2254_2256del
ENST00000696997.1:c.*442_*444del	ENSP00000513028.1:n.*442_*444del
ENST00000696998.1:n.2066_2068del
ENST00000696999.1:c.95_97del	ENSP00000513029.1:p.Ala32del
ENST00000697035.1:c.*145_*147del	ENSP00000513059.1:n.*145_*147del
ENST00000697036.1:c.*228_*230del	ENSP00000513060.1:n.*228_*230del
ENST00000697037.1:n.847_849del
ENST00000697093.1:n.3048_3050del
ENST00000697094.1:n.3395_3397del
ENST00000697095.1:c.*2013_*2015del	ENSP00000513104.1:n.*2013_*2015del
ENST00000697096.1:n.1945_1947del
ENST00000697097.1:c.95_97del	ENSP00000513105.1:p.Ala32del
ENST00000562983.2:n.998_1000del
ENST00000690268.1:c.893_895del	ENSP00000509810.1:p.Ala298del
ENST00000355740.7:c.*138_*140del	ENSP00000347979.3:n.*138_*140del
ENST00000612663.5:c.*214_*216del	ENSP00000477997.3:n.*214_*216del
ENST00000640140.1:n.984_986del
ENST00000640250.1:n.311_313del
ENST00000640681.1:n.933_935del
ENST00000652046.1:c.812_814del MANE Select	ENSP00000498466.1:p.Ala271del
ENST00000352159.8:c.*129_*131del	ENSP00000345601.4:n.*129_*131del
ENST00000355279.2:c.787_789del	ENSP00000347426.2:n.787_789del
ENST00000355740.6:c.812_814del	ENSP00000347979.2:p.Ala271del
ENST00000357339.6:c.749_751del	ENSP00000349896.2:p.Ala250del
ENST00000479522.5:c.*241_*243del	ENSP00000424113.1:n.*241_*243del
ENST00000484444.5:c.*253_*255del	ENSP00000420975.1:n.*253_*255del
ENST00000488877.5:c.*253_*255del	ENSP00000425159.1:n.*253_*255del
ENST00000492756.5:c.640_642del	ENSP00000422453.1:n.640_642del
ENST00000494410.5:c.*170_*172del	ENSP00000423755.1:n.*170_*172del
ENST00000612663.4:c.*159_*161del	ENSP00000477997.2:n.*159_*161del
NM_000043.4:c.812_814del , LRG_134t1:c.812_814del	NP_000034.1:p.Ala271del
NM_152871.2:c.749_751del	NP_690610.1:p.Ala250del
NM_152872.2:c.*124_*126del	NP_690611.1:n.*124_*126del
NR_028033.2:n.986_988del
NR_028034.2:n.848_850del
NR_028035.2:n.911_913del
NR_028036.2:n.1049_1051del
XM_006717819.2:c.893_895del	XP_006717882.1:p.Ala298del
XM_011539764.1:c.974_976del	XP_011538066.1:p.Ala325del
XM_011539765.1:c.911_913del	XP_011538067.1:p.Ala304del
XM_011539766.1:c.893_895del	XP_011538068.1:p.Ala298del
XM_011539767.1:c.857_859del	XP_011538069.1:p.Ala286del
XR_945732.1:n.880_882del
XR_945733.1:n.817_819del
NM_000043.5:c.812_814del	NP_000034.1:p.Ala271del
NM_001320619.1:c.*135_*137del	NP_001307548.1:n.*135_*137del
NM_152871.3:c.749_751del	NP_690610.1:p.Ala250del
NM_152872.3:c.*124_*126del	NP_690611.1:n.*124_*126del
NR_028033.3:n.958_960del
NR_028034.3:n.820_822del
NR_028035.3:n.883_885del
NR_028036.3:n.1021_1023del
NR_135313.1:n.938_940del
NR_135314.1:n.1121_1123del
NR_135315.1:n.874_876del
XM_006717819.3:c.893_895del	XP_006717882.1:p.Ala298del
XM_011539764.2:c.974_976del	XP_011538066.1:p.Ala325del
XM_011539765.2:c.911_913del	XP_011538067.1:p.Ala304del
XM_011539766.2:c.893_895del	XP_011538068.1:p.Ala298del
XM_011539767.3:c.857_859del	XP_011538069.1:p.Ala286del
XR_945732.3:n.880_882del
XR_945733.2:n.817_819del
NM_000043.6:c.812_814del MANE Select	NP_000034.1:p.Ala271del
NM_001320619.2:c.*135_*137del	NP_001307548.1:n.*135_*137del
NM_152871.4:c.749_751del	NP_690610.1:p.Ala250del
NM_152872.4:c.*124_*126del	NP_690611.1:n.*124_*126del
NR_028033.4:n.719_721del
NR_028034.4:n.581_583del
NR_028035.4:n.644_646del
NR_028036.4:n.782_784del
NR_135313.2:n.699_701del
NR_135314.2:n.978_980del
NR_135315.2:n.731_733del