Canonical Allele Identifier: CA916080420

Gene: FAS

Linked Data

• ClinVar Variation Id: 848671
• ClinVar RCV Id: RCV001052481
• dbSNP Id: rs1848666809

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014146_89014148del , CM000672.2:g.89014146_89014148del	GRCh38
NC_000010.10:g.90773903_90773905del , CM000672.1:g.90773903_90773905del	GRCh37
NC_000010.9:g.90763883_90763885del	NCBI36
NG_009089.2:g.28616_28618del , LRG_134:g.28616_28618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1013_1015del
ENST00000355740.8:c.*27_*29del	ENSP00000347979.3:n.*27_*29del
ENST00000357339.7:c.641_643del	ENSP00000349896.2:p.Thr214del
ENST00000371857.8:n.2249_2251del
ENST00000460510.6:c.-14_-12del	ENSP00000512812.1:n.-14_-12del
ENST00000466081.6:n.2353_2355del
ENST00000477270.6:c.749_751del	ENSP00000512813.1:p.Thr250del
ENST00000479522.6:c.*133_*135del	ENSP00000424113.1:n.*133_*135del
ENST00000484444.6:c.*145_*147del	ENSP00000420975.1:n.*145_*147del
ENST00000488877.6:c.595_597del	ENSP00000425159.1:n.595_597del
ENST00000492756.7:c.*133_*135del	ENSP00000422453.1:n.*133_*135del
ENST00000494799.6:c.-14_-12del	ENSP00000512834.1:n.-14_-12del
ENST00000562983.3:c.-14_-12del	ENSP00000512845.1:n.-14_-12del
ENST00000612663.6:c.*106_*108del	ENSP00000477997.3:n.*106_*108del
ENST00000640140.2:n.849_851del
ENST00000640250.2:n.203_205del
ENST00000640681.2:n.808_810del
ENST00000696723.1:n.4337_4339del
ENST00000696741.1:n.2342_2344del
ENST00000696742.1:n.2069_2071del
ENST00000696743.1:n.3472_3474del
ENST00000696744.1:n.743_745del
ENST00000696767.1:n.1038_1040del
ENST00000696768.1:c.*27_*29del	ENSP00000512859.1:n.*27_*29del
ENST00000696769.1:n.2393_2395del
ENST00000696771.1:c.-14_-12del	ENSP00000512860.1:n.-14_-12del
ENST00000696772.1:n.2307_2309del
ENST00000696773.1:n.2046_2048del
ENST00000696774.1:n.5814_5816del
ENST00000696776.1:c.797_799del	ENSP00000512861.1:p.Thr266del
ENST00000696777.1:n.2112_2114del
ENST00000696778.1:n.1140_1142del
ENST00000696779.1:c.311_313del	ENSP00000512862.1:p.Thr104del
ENST00000696780.1:c.734_736del	ENSP00000512863.1:p.Thr245del
ENST00000696781.1:c.449_451del	ENSP00000512864.1:p.Thr150del
ENST00000696782.1:c.*106_*108del	ENSP00000512865.1:n.*106_*108del
ENST00000696783.1:n.2572_2574del
ENST00000696992.1:n.1821_1823del
ENST00000696995.1:n.4233_4235del
ENST00000696996.1:n.2146_2148del
ENST00000696997.1:c.*334_*336del	ENSP00000513028.1:n.*334_*336del
ENST00000696998.1:n.1958_1960del
ENST00000696999.1:c.-14_-12del	ENSP00000513029.1:n.-14_-12del
ENST00000697035.1:c.*37_*39del	ENSP00000513059.1:n.*37_*39del
ENST00000697036.1:c.*120_*122del	ENSP00000513060.1:n.*120_*122del
ENST00000697037.1:n.739_741del
ENST00000697093.1:n.2940_2942del
ENST00000697094.1:n.3287_3289del
ENST00000697095.1:c.*1905_*1907del	ENSP00000513104.1:n.*1905_*1907del
ENST00000697096.1:n.1837_1839del
ENST00000697097.1:c.-14_-12del	ENSP00000513105.1:n.-14_-12del
ENST00000562983.2:n.890_892del
ENST00000690268.1:c.785_787del	ENSP00000509810.1:p.Thr262del
ENST00000355740.7:c.*30_*32del	ENSP00000347979.3:n.*30_*32del
ENST00000612663.5:c.*106_*108del	ENSP00000477997.3:n.*106_*108del
ENST00000640140.1:n.876_878del
ENST00000640250.1:n.203_205del
ENST00000640681.1:n.825_827del
ENST00000652046.1:c.704_706del MANE Select	ENSP00000498466.1:p.Thr235del
ENST00000313771.9:n.1013_1015del
ENST00000352159.8:c.*21_*23del	ENSP00000345601.4:n.*21_*23del
ENST00000355279.2:c.679_681del	ENSP00000347426.2:n.679_681del
ENST00000355740.6:c.704_706del	ENSP00000347979.2:p.Thr235del
ENST00000357339.6:c.641_643del	ENSP00000349896.2:p.Thr214del
ENST00000479522.5:c.*133_*135del	ENSP00000424113.1:n.*133_*135del
ENST00000484444.5:c.*145_*147del	ENSP00000420975.1:n.*145_*147del
ENST00000488877.5:c.*145_*147del	ENSP00000425159.1:n.*145_*147del
ENST00000492756.5:c.532_534del	ENSP00000422453.1:n.532_534del
ENST00000494410.5:c.*62_*64del	ENSP00000423755.1:n.*62_*64del
ENST00000494799.5:n.611_613del
ENST00000612663.4:c.*51_*53del	ENSP00000477997.2:n.*51_*53del
ENST00000615406.4:c.704_706del	ENSP00000484575.1:p.Thr235del
ENST00000626542.2:c.702_704del	ENSP00000485876.1:p.Tyr235del
NM_000043.4:c.704_706del , LRG_134t1:c.704_706del	NP_000034.1:p.Thr235del
NM_152871.2:c.641_643del	NP_690610.1:p.Thr214del
NM_152872.2:c.*16_*18del	NP_690611.1:n.*16_*18del
NR_028033.2:n.878_880del
NR_028034.2:n.740_742del
NR_028035.2:n.803_805del
NR_028036.2:n.941_943del
XM_006717819.2:c.785_787del	XP_006717882.1:p.Thr262del
XM_011539764.1:c.866_868del	XP_011538066.1:p.Thr289del
XM_011539765.1:c.803_805del	XP_011538067.1:p.Thr268del
XM_011539766.1:c.785_787del	XP_011538068.1:p.Thr262del
XM_011539767.1:c.749_751del	XP_011538069.1:p.Thr250del
XR_945732.1:n.772_774del
XR_945733.1:n.709_711del
NM_000043.5:c.704_706del	NP_000034.1:p.Thr235del
NM_001320619.1:c.*27_*29del	NP_001307548.1:n.*27_*29del
NM_152871.3:c.641_643del	NP_690610.1:p.Thr214del
NM_152872.3:c.*16_*18del	NP_690611.1:n.*16_*18del
NR_028033.3:n.850_852del
NR_028034.3:n.712_714del
NR_028035.3:n.775_777del
NR_028036.3:n.913_915del
NR_135313.1:n.830_832del
NR_135314.1:n.1013_1015del
NR_135315.1:n.766_768del
XM_006717819.3:c.785_787del	XP_006717882.1:p.Thr262del
XM_011539764.2:c.866_868del	XP_011538066.1:p.Thr289del
XM_011539765.2:c.803_805del	XP_011538067.1:p.Thr268del
XM_011539766.2:c.785_787del	XP_011538068.1:p.Thr262del
XM_011539767.3:c.749_751del	XP_011538069.1:p.Thr250del
XR_945732.3:n.772_774del
XR_945733.2:n.709_711del
NM_000043.6:c.704_706del MANE Select	NP_000034.1:p.Thr235del
NM_001320619.2:c.*27_*29del	NP_001307548.1:n.*27_*29del
NM_152871.4:c.641_643del	NP_690610.1:p.Thr214del
NM_152872.4:c.*16_*18del	NP_690611.1:n.*16_*18del
NR_028033.4:n.611_613del
NR_028034.4:n.473_475del
NR_028035.4:n.536_538del
NR_028036.4:n.674_676del
NR_135313.2:n.591_593del
NR_135314.2:n.870_872del
NR_135315.2:n.623_625del