Canonical Allele Identifier: CA645542412

Gene: FAS

Linked Data

• COSMIC: COSM5703773

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014128del , CM000672.2:g.89014128del	GRCh38
NC_000010.10:g.90773885del , CM000672.1:g.90773885del	GRCh37
NC_000010.9:g.90763865del	NCBI36
NG_009089.2:g.28598del , LRG_134:g.28598del

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.995del
ENST00000355740.8:c.*9del	ENSP00000347979.3:n.*9del
ENST00000357339.7:c.623del	ENSP00000349896.2:p.Leu208Ter
ENST00000371857.8:n.2231del
ENST00000460510.6:c.-32del	ENSP00000512812.1:n.-32del
ENST00000466081.6:n.2335del
ENST00000477270.6:c.731del	ENSP00000512813.1:p.Leu244Ter
ENST00000479522.6:c.*115del	ENSP00000424113.1:n.*115del
ENST00000484444.6:c.*127del	ENSP00000420975.1:n.*127del
ENST00000488877.6:c.577del	ENSP00000425159.1:n.577del
ENST00000492756.7:c.*115del	ENSP00000422453.1:n.*115del
ENST00000494799.6:c.-32del	ENSP00000512834.1:n.-32del
ENST00000562983.3:c.-32del	ENSP00000512845.1:n.-32del
ENST00000612663.6:c.*88del	ENSP00000477997.3:n.*88del
ENST00000640140.2:n.831del
ENST00000640250.2:n.185del
ENST00000640681.2:n.790del
ENST00000696723.1:n.4319del
ENST00000696741.1:n.2324del
ENST00000696742.1:n.2051del
ENST00000696743.1:n.3454del
ENST00000696744.1:n.725del
ENST00000696767.1:n.1020del
ENST00000696768.1:c.*9del	ENSP00000512859.1:n.*9del
ENST00000696769.1:n.2375del
ENST00000696771.1:c.-32del	ENSP00000512860.1:n.-32del
ENST00000696772.1:n.2289del
ENST00000696773.1:n.2028del
ENST00000696774.1:n.5796del
ENST00000696776.1:c.779del	ENSP00000512861.1:p.Leu260Ter
ENST00000696777.1:n.2094del
ENST00000696778.1:n.1122del
ENST00000696779.1:c.293del	ENSP00000512862.1:p.Leu98Ter
ENST00000696780.1:c.716del	ENSP00000512863.1:p.Leu239Ter
ENST00000696781.1:c.431del	ENSP00000512864.1:p.Leu144Ter
ENST00000696782.1:c.*88del	ENSP00000512865.1:n.*88del
ENST00000696783.1:n.2554del
ENST00000696992.1:n.1803del
ENST00000696995.1:n.4215del
ENST00000696996.1:n.2128del
ENST00000696997.1:c.*316del	ENSP00000513028.1:n.*316del
ENST00000696998.1:n.1940del
ENST00000696999.1:c.-32del	ENSP00000513029.1:n.-32del
ENST00000697035.1:c.*19del	ENSP00000513059.1:n.*19del
ENST00000697036.1:c.*102del	ENSP00000513060.1:n.*102del
ENST00000697037.1:n.721del
ENST00000697093.1:n.2922del
ENST00000697094.1:n.3269del
ENST00000697095.1:c.*1887del	ENSP00000513104.1:n.*1887del
ENST00000697096.1:n.1819del
ENST00000697097.1:c.-32del	ENSP00000513105.1:n.-32del
ENST00000562983.2:n.872del
ENST00000690268.1:c.767del	ENSP00000509810.1:p.Leu256Ter
ENST00000355740.7:c.*12del	ENSP00000347979.3:n.*12del
ENST00000612663.5:c.*88del	ENSP00000477997.3:n.*88del
ENST00000640140.1:n.858del
ENST00000640250.1:n.185del
ENST00000640681.1:n.807del
ENST00000652046.1:c.686del MANE Select	ENSP00000498466.1:p.Leu229Ter
ENST00000313771.9:n.995del
ENST00000352159.8:c.*3del	ENSP00000345601.4:n.*3del
ENST00000355279.2:c.661del	ENSP00000347426.2:p.Ter221GluextTer2
ENST00000355740.6:c.686del	ENSP00000347979.2:p.Leu229Ter
ENST00000357339.6:c.623del	ENSP00000349896.2:p.Leu208Ter
ENST00000479522.5:c.*115del	ENSP00000424113.1:n.*115del
ENST00000484444.5:c.*127del	ENSP00000420975.1:n.*127del
ENST00000488877.5:c.*127del	ENSP00000425159.1:n.*127del
ENST00000492756.5:c.514del	ENSP00000422453.1:n.514del
ENST00000494410.5:c.*44del	ENSP00000423755.1:n.*44del
ENST00000494799.5:n.593del
ENST00000612663.4:c.*33del	ENSP00000477997.2:n.*33del
ENST00000615406.4:c.686del	ENSP00000484575.1:p.Leu229Ter
ENST00000626542.2:c.686del	ENSP00000485876.1:p.Leu229Ter
NM_000043.4:c.686del , LRG_134t1:c.686del	NP_000034.1:p.Leu229Ter
NM_152871.2:c.623del	NP_690610.1:p.Leu208Ter
NM_152872.2:c.661del	NP_690611.1:p.Ter221GluextTer2
NR_028033.2:n.860del
NR_028034.2:n.722del
NR_028035.2:n.785del
NR_028036.2:n.923del
XM_006717819.2:c.767del	XP_006717882.1:p.Leu256Ter
XM_011539764.1:c.848del	XP_011538066.1:p.Leu283Ter
XM_011539765.1:c.785del	XP_011538067.1:p.Leu262Ter
XM_011539766.1:c.767del	XP_011538068.1:p.Leu256Ter
XM_011539767.1:c.731del	XP_011538069.1:p.Leu244Ter
XR_945732.1:n.754del
XR_945733.1:n.691del
NM_000043.5:c.686del	NP_000034.1:p.Leu229Ter
NM_001320619.1:c.*9del	NP_001307548.1:n.*9del
NM_152871.3:c.623del	NP_690610.1:p.Leu208Ter
NM_152872.3:c.661del	NP_690611.1:p.Ter221GluextTer2
NR_028033.3:n.832del
NR_028034.3:n.694del
NR_028035.3:n.757del
NR_028036.3:n.895del
NR_135313.1:n.812del
NR_135314.1:n.995del
NR_135315.1:n.748del
XM_006717819.3:c.767del	XP_006717882.1:p.Leu256Ter
XM_011539764.2:c.848del	XP_011538066.1:p.Leu283Ter
XM_011539765.2:c.785del	XP_011538067.1:p.Leu262Ter
XM_011539766.2:c.767del	XP_011538068.1:p.Leu256Ter
XM_011539767.3:c.731del	XP_011538069.1:p.Leu244Ter
XR_945732.3:n.754del
XR_945733.2:n.691del
NM_000043.6:c.686del MANE Select	NP_000034.1:p.Leu229Ter
NM_001320619.2:c.*9del	NP_001307548.1:n.*9del
NM_152871.4:c.623del	NP_690610.1:p.Leu208Ter
NM_152872.4:c.661del	NP_690611.1:p.Ter221GluextTer2
NR_028033.4:n.593del
NR_028034.4:n.455del
NR_028035.4:n.518del
NR_028036.4:n.656del
NR_135313.2:n.573del
NR_135314.2:n.852del
NR_135315.2:n.605del