Canonical Allele Identifier: CA645542414

Gene: FAS

Linked Data

• COSMIC: COSM5703775

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014131_89014134dup , CM000672.2:g.89014131_89014134dup	GRCh38
NC_000010.10:g.90773888_90773891dup , CM000672.1:g.90773888_90773891dup	GRCh37
NC_000010.9:g.90763868_90763871dup	NCBI36
NG_009089.2:g.28601_28604dup , LRG_134:g.28601_28604dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.998_1001dup
ENST00000355740.8:c.*12_*15dup	ENSP00000347979.3:n.*12_*15dup
ENST00000357339.7:c.626_629dup	ENSP00000349896.2:p.Tyr211Ter
ENST00000371857.8:n.2234_2237dup
ENST00000460510.6:c.-29_-26dup	ENSP00000512812.1:n.-29_-26dup
ENST00000466081.6:n.2338_2341dup
ENST00000477270.6:c.734_737dup	ENSP00000512813.1:p.Tyr247Ter
ENST00000479522.6:c.*118_*121dup	ENSP00000424113.1:n.*118_*121dup
ENST00000484444.6:c.*130_*133dup	ENSP00000420975.1:n.*130_*133dup
ENST00000488877.6:c.580_583dup	ENSP00000425159.1:n.580_583dup
ENST00000492756.7:c.*118_*121dup	ENSP00000422453.1:n.*118_*121dup
ENST00000494799.6:c.-29_-26dup	ENSP00000512834.1:n.-29_-26dup
ENST00000562983.3:c.-29_-26dup	ENSP00000512845.1:n.-29_-26dup
ENST00000612663.6:c.*91_*94dup	ENSP00000477997.3:n.*91_*94dup
ENST00000640140.2:n.834_837dup
ENST00000640250.2:n.188_191dup
ENST00000640681.2:n.793_796dup
ENST00000696723.1:n.4322_4325dup
ENST00000696741.1:n.2327_2330dup
ENST00000696742.1:n.2054_2057dup
ENST00000696743.1:n.3457_3460dup
ENST00000696744.1:n.728_731dup
ENST00000696767.1:n.1023_1026dup
ENST00000696768.1:c.*12_*15dup	ENSP00000512859.1:n.*12_*15dup
ENST00000696769.1:n.2378_2381dup
ENST00000696771.1:c.-29_-26dup	ENSP00000512860.1:n.-29_-26dup
ENST00000696772.1:n.2292_2295dup
ENST00000696773.1:n.2031_2034dup
ENST00000696774.1:n.5799_5802dup
ENST00000696776.1:c.782_785dup	ENSP00000512861.1:p.Tyr263Ter
ENST00000696777.1:n.2097_2100dup
ENST00000696778.1:n.1125_1128dup
ENST00000696779.1:c.296_299dup	ENSP00000512862.1:p.Tyr101Ter
ENST00000696780.1:c.719_722dup	ENSP00000512863.1:p.Tyr242Ter
ENST00000696781.1:c.434_437dup	ENSP00000512864.1:p.Tyr147Ter
ENST00000696782.1:c.*91_*94dup	ENSP00000512865.1:n.*91_*94dup
ENST00000696783.1:n.2557_2560dup
ENST00000696992.1:n.1806_1809dup
ENST00000696995.1:n.4218_4221dup
ENST00000696996.1:n.2131_2134dup
ENST00000696997.1:c.*319_*322dup	ENSP00000513028.1:n.*319_*322dup
ENST00000696998.1:n.1943_1946dup
ENST00000696999.1:c.-29_-26dup	ENSP00000513029.1:n.-29_-26dup
ENST00000697035.1:c.*22_*25dup	ENSP00000513059.1:n.*22_*25dup
ENST00000697036.1:c.*105_*108dup	ENSP00000513060.1:n.*105_*108dup
ENST00000697037.1:n.724_727dup
ENST00000697093.1:n.2925_2928dup
ENST00000697094.1:n.3272_3275dup
ENST00000697095.1:c.*1890_*1893dup	ENSP00000513104.1:n.*1890_*1893dup
ENST00000697096.1:n.1822_1825dup
ENST00000697097.1:c.-29_-26dup	ENSP00000513105.1:n.-29_-26dup
ENST00000562983.2:n.875_878dup
ENST00000690268.1:c.770_773dup	ENSP00000509810.1:p.Tyr259Ter
ENST00000355740.7:c.*15_*18dup	ENSP00000347979.3:n.*15_*18dup
ENST00000612663.5:c.*91_*94dup	ENSP00000477997.3:n.*91_*94dup
ENST00000640140.1:n.861_864dup
ENST00000640250.1:n.188_191dup
ENST00000640681.1:n.810_813dup
ENST00000652046.1:c.689_692dup MANE Select	ENSP00000498466.1:p.Tyr232Ter
ENST00000313771.9:n.998_1001dup
ENST00000352159.8:c.*6_*9dup	ENSP00000345601.4:n.*6_*9dup
ENST00000355279.2:c.664_667dup	ENSP00000347426.2:n.664_667dup
ENST00000355740.6:c.689_692dup	ENSP00000347979.2:p.Tyr232Ter
ENST00000357339.6:c.626_629dup	ENSP00000349896.2:p.Tyr211Ter
ENST00000479522.5:c.*118_*121dup	ENSP00000424113.1:n.*118_*121dup
ENST00000484444.5:c.*130_*133dup	ENSP00000420975.1:n.*130_*133dup
ENST00000488877.5:c.*130_*133dup	ENSP00000425159.1:n.*130_*133dup
ENST00000492756.5:c.517_520dup	ENSP00000422453.1:n.517_520dup
ENST00000494410.5:c.*47_*50dup	ENSP00000423755.1:n.*47_*50dup
ENST00000494799.5:n.596_599dup
ENST00000612663.4:c.*36_*39dup	ENSP00000477997.2:n.*36_*39dup
ENST00000615406.4:c.689_692dup	ENSP00000484575.1:p.Tyr232Ter
ENST00000626542.2:c.689_692dup	ENSP00000485876.1:p.Tyr232Ter
NM_000043.4:c.689_692dup , LRG_134t1:c.689_692dup	NP_000034.1:p.Tyr232Ter
NM_152871.2:c.626_629dup	NP_690610.1:p.Tyr211Ter
NM_152872.2:c.*1_*4dup	NP_690611.1:n.*1_*4dup
NR_028033.2:n.863_866dup
NR_028034.2:n.725_728dup
NR_028035.2:n.788_791dup
NR_028036.2:n.926_929dup
XM_006717819.2:c.770_773dup	XP_006717882.1:p.Tyr259Ter
XM_011539764.1:c.851_854dup	XP_011538066.1:p.Tyr286Ter
XM_011539765.1:c.788_791dup	XP_011538067.1:p.Tyr265Ter
XM_011539766.1:c.770_773dup	XP_011538068.1:p.Tyr259Ter
XM_011539767.1:c.734_737dup	XP_011538069.1:p.Tyr247Ter
XR_945732.1:n.757_760dup
XR_945733.1:n.694_697dup
NM_000043.5:c.689_692dup	NP_000034.1:p.Tyr232Ter
NM_001320619.1:c.*12_*15dup	NP_001307548.1:n.*12_*15dup
NM_152871.3:c.626_629dup	NP_690610.1:p.Tyr211Ter
NM_152872.3:c.*1_*4dup	NP_690611.1:n.*1_*4dup
NR_028033.3:n.835_838dup
NR_028034.3:n.697_700dup
NR_028035.3:n.760_763dup
NR_028036.3:n.898_901dup
NR_135313.1:n.815_818dup
NR_135314.1:n.998_1001dup
NR_135315.1:n.751_754dup
XM_006717819.3:c.770_773dup	XP_006717882.1:p.Tyr259Ter
XM_011539764.2:c.851_854dup	XP_011538066.1:p.Tyr286Ter
XM_011539765.2:c.788_791dup	XP_011538067.1:p.Tyr265Ter
XM_011539766.2:c.770_773dup	XP_011538068.1:p.Tyr259Ter
XM_011539767.3:c.734_737dup	XP_011538069.1:p.Tyr247Ter
XR_945732.3:n.757_760dup
XR_945733.2:n.694_697dup
NM_000043.6:c.689_692dup MANE Select	NP_000034.1:p.Tyr232Ter
NM_001320619.2:c.*12_*15dup	NP_001307548.1:n.*12_*15dup
NM_152871.4:c.626_629dup	NP_690610.1:p.Tyr211Ter
NM_152872.4:c.*1_*4dup	NP_690611.1:n.*1_*4dup
NR_028033.4:n.596_599dup
NR_028034.4:n.458_461dup
NR_028035.4:n.521_524dup
NR_028036.4:n.659_662dup
NR_135313.2:n.576_579dup
NR_135314.2:n.855_858dup
NR_135315.2:n.608_611dup