Canonical Allele Identifier: CA645542415
Gene: FAS HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014134_89014137dup , CM000672.2:g.89014134_89014137dup GRCh38
NC_000010.10:g.90773891_90773894dup , CM000672.1:g.90773891_90773894dup GRCh37
NC_000010.9:g.90763871_90763874dup NCBI36
NG_009089.2:g.28604_28607dup , LRG_134:g.28604_28607dup

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.1001_1004dup
ENST00000355740.8:c.*15_*18dup ENSP00000347979.3:n.*15_*18dup
ENST00000357339.7:c.629_632dup ENSP00000349896.2:p.Tyr211Ter
ENST00000371857.8:n.2237_2240dup
ENST00000460510.6:c.-26_-23dup ENSP00000512812.1:n.-26_-23dup
ENST00000466081.6:n.2341_2344dup
ENST00000477270.6:c.737_740dup ENSP00000512813.1:p.Tyr247Ter
ENST00000479522.6:c.*121_*124dup ENSP00000424113.1:n.*121_*124dup
ENST00000484444.6:c.*133_*136dup ENSP00000420975.1:n.*133_*136dup
ENST00000488877.6:c.583_586dup ENSP00000425159.1:n.583_586dup
ENST00000492756.7:c.*121_*124dup ENSP00000422453.1:n.*121_*124dup
ENST00000494799.6:c.-26_-23dup ENSP00000512834.1:n.-26_-23dup
ENST00000562983.3:c.-26_-23dup ENSP00000512845.1:n.-26_-23dup
ENST00000612663.6:c.*94_*97dup ENSP00000477997.3:n.*94_*97dup
ENST00000640140.2:n.837_840dup
ENST00000640250.2:n.191_194dup
ENST00000640681.2:n.796_799dup
ENST00000696723.1:n.4325_4328dup
ENST00000696741.1:n.2330_2333dup
ENST00000696742.1:n.2057_2060dup
ENST00000696743.1:n.3460_3463dup
ENST00000696744.1:n.731_734dup
ENST00000696767.1:n.1026_1029dup
ENST00000696768.1:c.*15_*18dup ENSP00000512859.1:n.*15_*18dup
ENST00000696769.1:n.2381_2384dup
ENST00000696771.1:c.-26_-23dup ENSP00000512860.1:n.-26_-23dup
ENST00000696772.1:n.2295_2298dup
ENST00000696773.1:n.2034_2037dup
ENST00000696774.1:n.5802_5805dup
ENST00000696776.1:c.785_788dup ENSP00000512861.1:p.Tyr263Ter
ENST00000696777.1:n.2100_2103dup
ENST00000696778.1:n.1128_1131dup
ENST00000696779.1:c.299_302dup ENSP00000512862.1:p.Tyr101Ter
ENST00000696780.1:c.722_725dup ENSP00000512863.1:p.Tyr242Ter
ENST00000696781.1:c.437_440dup ENSP00000512864.1:p.Tyr147Ter
ENST00000696782.1:c.*94_*97dup ENSP00000512865.1:n.*94_*97dup
ENST00000696783.1:n.2560_2563dup
ENST00000696992.1:n.1809_1812dup
ENST00000696995.1:n.4221_4224dup
ENST00000696996.1:n.2134_2137dup
ENST00000696997.1:c.*322_*325dup ENSP00000513028.1:n.*322_*325dup
ENST00000696998.1:n.1946_1949dup
ENST00000696999.1:c.-26_-23dup ENSP00000513029.1:n.-26_-23dup
ENST00000697035.1:c.*25_*28dup ENSP00000513059.1:n.*25_*28dup
ENST00000697036.1:c.*108_*111dup ENSP00000513060.1:n.*108_*111dup
ENST00000697037.1:n.727_730dup
ENST00000697093.1:n.2928_2931dup
ENST00000697094.1:n.3275_3278dup
ENST00000697095.1:c.*1893_*1896dup ENSP00000513104.1:n.*1893_*1896dup
ENST00000697096.1:n.1825_1828dup
ENST00000697097.1:c.-26_-23dup ENSP00000513105.1:n.-26_-23dup
ENST00000562983.2:n.878_881dup
ENST00000690268.1:c.773_776dup ENSP00000509810.1:p.Tyr259Ter
ENST00000355740.7:c.*18_*21dup ENSP00000347979.3:n.*18_*21dup
ENST00000612663.5:c.*94_*97dup ENSP00000477997.3:n.*94_*97dup
ENST00000640140.1:n.864_867dup
ENST00000640250.1:n.191_194dup
ENST00000640681.1:n.813_816dup
ENST00000652046.1:c.692_695dup MANE Select ENSP00000498466.1:p.Tyr232Ter
ENST00000313771.9:n.1001_1004dup
ENST00000352159.8:c.*9_*12dup ENSP00000345601.4:n.*9_*12dup
ENST00000355279.2:c.667_670dup ENSP00000347426.2:n.667_670dup
ENST00000355740.6:c.692_695dup ENSP00000347979.2:p.Tyr232Ter
ENST00000357339.6:c.629_632dup ENSP00000349896.2:p.Tyr211Ter
ENST00000479522.5:c.*121_*124dup ENSP00000424113.1:n.*121_*124dup
ENST00000484444.5:c.*133_*136dup ENSP00000420975.1:n.*133_*136dup
ENST00000488877.5:c.*133_*136dup ENSP00000425159.1:n.*133_*136dup
ENST00000492756.5:c.520_523dup ENSP00000422453.1:n.520_523dup
ENST00000494410.5:c.*50_*53dup ENSP00000423755.1:n.*50_*53dup
ENST00000494799.5:n.599_602dup
ENST00000612663.4:c.*39_*42dup ENSP00000477997.2:n.*39_*42dup
ENST00000615406.4:c.692_695dup ENSP00000484575.1:p.Tyr232Ter
ENST00000626542.2:c.692_695dup ENSP00000485876.1:p.Tyr232Ter
NM_000043.4:c.692_695dup , LRG_134t1:c.692_695dup NP_000034.1:p.Tyr232Ter
NM_152871.2:c.629_632dup NP_690610.1:p.Tyr211Ter
NM_152872.2:c.*4_*7dup NP_690611.1:n.*4_*7dup
NR_028033.2:n.866_869dup
NR_028034.2:n.728_731dup
NR_028035.2:n.791_794dup
NR_028036.2:n.929_932dup
XM_006717819.2:c.773_776dup XP_006717882.1:p.Tyr259Ter
XM_011539764.1:c.854_857dup XP_011538066.1:p.Tyr286Ter
XM_011539765.1:c.791_794dup XP_011538067.1:p.Tyr265Ter
XM_011539766.1:c.773_776dup XP_011538068.1:p.Tyr259Ter
XM_011539767.1:c.737_740dup XP_011538069.1:p.Tyr247Ter
XR_945732.1:n.760_763dup
XR_945733.1:n.697_700dup
NM_000043.5:c.692_695dup NP_000034.1:p.Tyr232Ter
NM_001320619.1:c.*15_*18dup NP_001307548.1:n.*15_*18dup
NM_152871.3:c.629_632dup NP_690610.1:p.Tyr211Ter
NM_152872.3:c.*4_*7dup NP_690611.1:n.*4_*7dup
NR_028033.3:n.838_841dup
NR_028034.3:n.700_703dup
NR_028035.3:n.763_766dup
NR_028036.3:n.901_904dup
NR_135313.1:n.818_821dup
NR_135314.1:n.1001_1004dup
NR_135315.1:n.754_757dup
XM_006717819.3:c.773_776dup XP_006717882.1:p.Tyr259Ter
XM_011539764.2:c.854_857dup XP_011538066.1:p.Tyr286Ter
XM_011539765.2:c.791_794dup XP_011538067.1:p.Tyr265Ter
XM_011539766.2:c.773_776dup XP_011538068.1:p.Tyr259Ter
XM_011539767.3:c.737_740dup XP_011538069.1:p.Tyr247Ter
XR_945732.3:n.760_763dup
XR_945733.2:n.697_700dup
NM_000043.6:c.692_695dup MANE Select NP_000034.1:p.Tyr232Ter
NM_001320619.2:c.*15_*18dup NP_001307548.1:n.*15_*18dup
NM_152871.4:c.629_632dup NP_690610.1:p.Tyr211Ter
NM_152872.4:c.*4_*7dup NP_690611.1:n.*4_*7dup
NR_028033.4:n.599_602dup
NR_028034.4:n.461_464dup
NR_028035.4:n.524_527dup
NR_028036.4:n.662_665dup
NR_135313.2:n.579_582dup
NR_135314.2:n.858_861dup
NR_135315.2:n.611_614dup