Canonical Allele Identifier: CA2695212384

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014150_89014153del , CM000672.2:g.89014150_89014153del	GRCh38
NC_000010.10:g.90773907_90773910del , CM000672.1:g.90773907_90773910del	GRCh37
NC_000010.9:g.90763887_90763890del	NCBI36
NG_009089.2:g.28620_28623del , LRG_134:g.28620_28623del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1017_1020del
ENST00000355740.8:c.*31_*34del	ENSP00000347979.3:n.*31_*34del
ENST00000357339.7:c.645_648del	ENSP00000349896.2:p.Ile215MetfsTer4
ENST00000371857.8:n.2253_2256del
ENST00000460510.6:c.-10_-7del	ENSP00000512812.1:n.-10_-7del
ENST00000466081.6:n.2357_2360del
ENST00000477270.6:c.753_756del	ENSP00000512813.1:p.Ile251MetfsTer4
ENST00000479522.6:c.*137_*140del	ENSP00000424113.1:n.*137_*140del
ENST00000484444.6:c.*149_*152del	ENSP00000420975.1:n.*149_*152del
ENST00000488877.6:c.599_602del	ENSP00000425159.1:n.599_602del
ENST00000492756.7:c.*137_*140del	ENSP00000422453.1:n.*137_*140del
ENST00000494799.6:c.-10_-7del	ENSP00000512834.1:n.-10_-7del
ENST00000562983.3:c.-10_-7del	ENSP00000512845.1:n.-10_-7del
ENST00000612663.6:c.*110_*113del	ENSP00000477997.3:n.*110_*113del
ENST00000640140.2:n.853_856del
ENST00000640250.2:n.207_210del
ENST00000640681.2:n.812_815del
ENST00000696723.1:n.4341_4344del
ENST00000696741.1:n.2346_2349del
ENST00000696742.1:n.2073_2076del
ENST00000696743.1:n.3476_3479del
ENST00000696744.1:n.747_750del
ENST00000696767.1:n.1042_1045del
ENST00000696768.1:c.*31_*34del	ENSP00000512859.1:n.*31_*34del
ENST00000696769.1:n.2397_2400del
ENST00000696771.1:c.-10_-7del	ENSP00000512860.1:n.-10_-7del
ENST00000696772.1:n.2311_2314del
ENST00000696773.1:n.2050_2053del
ENST00000696774.1:n.5818_5821del
ENST00000696776.1:c.801_804del	ENSP00000512861.1:p.Ile267MetfsTer4
ENST00000696777.1:n.2116_2119del
ENST00000696778.1:n.1144_1147del
ENST00000696779.1:c.315_318del	ENSP00000512862.1:p.Ile105MetfsTer4
ENST00000696780.1:c.738_741del	ENSP00000512863.1:p.Ile246MetfsTer4
ENST00000696781.1:c.453_456del	ENSP00000512864.1:p.Ile151MetfsTer4
ENST00000696782.1:c.*110_*113del	ENSP00000512865.1:n.*110_*113del
ENST00000696783.1:n.2576_2579del
ENST00000696992.1:n.1825_1828del
ENST00000696995.1:n.4237_4240del
ENST00000696996.1:n.2150_2153del
ENST00000696997.1:c.*338_*341del	ENSP00000513028.1:n.*338_*341del
ENST00000696998.1:n.1962_1965del
ENST00000696999.1:c.-10_-7del	ENSP00000513029.1:n.-10_-7del
ENST00000697035.1:c.*41_*44del	ENSP00000513059.1:n.*41_*44del
ENST00000697036.1:c.*124_*127del	ENSP00000513060.1:n.*124_*127del
ENST00000697037.1:n.743_746del
ENST00000697093.1:n.2944_2947del
ENST00000697094.1:n.3291_3294del
ENST00000697095.1:c.*1909_*1912del	ENSP00000513104.1:n.*1909_*1912del
ENST00000697096.1:n.1841_1844del
ENST00000697097.1:c.-10_-7del	ENSP00000513105.1:n.-10_-7del
ENST00000562983.2:n.894_897del
ENST00000690268.1:c.789_792del	ENSP00000509810.1:p.Ile263MetfsTer4
ENST00000355740.7:c.*34_*37del	ENSP00000347979.3:n.*34_*37del
ENST00000612663.5:c.*110_*113del	ENSP00000477997.3:n.*110_*113del
ENST00000640140.1:n.880_883del
ENST00000640250.1:n.207_210del
ENST00000640681.1:n.829_832del
ENST00000652046.1:c.708_711del MANE Select	ENSP00000498466.1:p.Ile236MetfsTer4
ENST00000313771.9:n.1017_1020del
ENST00000352159.8:c.*25_*28del	ENSP00000345601.4:n.*25_*28del
ENST00000355279.2:c.683_686del	ENSP00000347426.2:n.683_686del
ENST00000355740.6:c.708_711del	ENSP00000347979.2:p.Ile236MetfsTer4
ENST00000357339.6:c.645_648del	ENSP00000349896.2:p.Ile215MetfsTer4
ENST00000479522.5:c.*137_*140del	ENSP00000424113.1:n.*137_*140del
ENST00000484444.5:c.*149_*152del	ENSP00000420975.1:n.*149_*152del
ENST00000488877.5:c.*149_*152del	ENSP00000425159.1:n.*149_*152del
ENST00000492756.5:c.536_539del	ENSP00000422453.1:n.536_539del
ENST00000494410.5:c.*66_*69del	ENSP00000423755.1:n.*66_*69del
ENST00000494799.5:n.615_618del
ENST00000612663.4:c.*55_*58del	ENSP00000477997.2:n.*55_*58del
ENST00000615406.4:c.708_711del	ENSP00000484575.1:p.Ile236MetfsTer4
ENST00000626542.2:c.706_709del	ENSP00000485876.1:p.Cys236GlyfsTer?
NM_000043.4:c.708_711del , LRG_134t1:c.708_711del	NP_000034.1:p.Ile236MetfsTer4
NM_152871.2:c.645_648del	NP_690610.1:p.Ile215MetfsTer4
NM_152872.2:c.*20_*23del	NP_690611.1:n.*20_*23del
NR_028033.2:n.882_885del
NR_028034.2:n.744_747del
NR_028035.2:n.807_810del
NR_028036.2:n.945_948del
XM_006717819.2:c.789_792del	XP_006717882.1:p.Ile263MetfsTer4
XM_011539764.1:c.870_873del	XP_011538066.1:p.Ile290MetfsTer4
XM_011539765.1:c.807_810del	XP_011538067.1:p.Ile269MetfsTer4
XM_011539766.1:c.789_792del	XP_011538068.1:p.Ile263MetfsTer4
XM_011539767.1:c.753_756del	XP_011538069.1:p.Ile251MetfsTer4
XR_945732.1:n.776_779del
XR_945733.1:n.713_716del
NM_000043.5:c.708_711del	NP_000034.1:p.Ile236MetfsTer4
NM_001320619.1:c.*31_*34del	NP_001307548.1:n.*31_*34del
NM_152871.3:c.645_648del	NP_690610.1:p.Ile215MetfsTer4
NM_152872.3:c.*20_*23del	NP_690611.1:n.*20_*23del
NR_028033.3:n.854_857del
NR_028034.3:n.716_719del
NR_028035.3:n.779_782del
NR_028036.3:n.917_920del
NR_135313.1:n.834_837del
NR_135314.1:n.1017_1020del
NR_135315.1:n.770_773del
XM_006717819.3:c.789_792del	XP_006717882.1:p.Ile263MetfsTer4
XM_011539764.2:c.870_873del	XP_011538066.1:p.Ile290MetfsTer4
XM_011539765.2:c.807_810del	XP_011538067.1:p.Ile269MetfsTer4
XM_011539766.2:c.789_792del	XP_011538068.1:p.Ile263MetfsTer4
XM_011539767.3:c.753_756del	XP_011538069.1:p.Ile251MetfsTer4
XR_945732.3:n.776_779del
XR_945733.2:n.713_716del
NM_000043.6:c.708_711del MANE Select	NP_000034.1:p.Ile236MetfsTer4
NM_001320619.2:c.*31_*34del	NP_001307548.1:n.*31_*34del
NM_152871.4:c.645_648del	NP_690610.1:p.Ile215MetfsTer4
NM_152872.4:c.*20_*23del	NP_690611.1:n.*20_*23del
NR_028033.4:n.615_618del
NR_028034.4:n.477_480del
NR_028035.4:n.540_543del
NR_028036.4:n.678_681del
NR_135313.2:n.595_598del
NR_135314.2:n.874_877del
NR_135315.2:n.627_630del