Canonical Allele Identifier: CA377509553

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773887A>G (hg19) ; chr10:g.89014130A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014130A>G , CM000672.2:g.89014130A>G	GRCh38
NC_000010.10:g.90773887A>G , CM000672.1:g.90773887A>G	GRCh37
NC_000010.9:g.90763867A>G	NCBI36
NG_009089.2:g.28600A>G , LRG_134:g.28600A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.997A>G
ENST00000355740.8:c.*11A>G	ENSP00000347979.3:n.*11A>G
ENST00000357339.7:c.625A>G	ENSP00000349896.2:p.Ser209Gly
ENST00000371857.8:n.2233A>G
ENST00000460510.6:c.-30A>G	ENSP00000512812.1:n.-30A>G
ENST00000466081.6:n.2337A>G
ENST00000477270.6:c.733A>G	ENSP00000512813.1:p.Ser245Gly
ENST00000479522.6:c.*117A>G	ENSP00000424113.1:n.*117A>G
ENST00000484444.6:c.*129A>G	ENSP00000420975.1:n.*129A>G
ENST00000488877.6:c.579A>G	ENSP00000425159.1:n.579A>G
ENST00000492756.7:c.*117A>G	ENSP00000422453.1:n.*117A>G
ENST00000494799.6:c.-30A>G	ENSP00000512834.1:n.-30A>G
ENST00000562983.3:c.-30A>G	ENSP00000512845.1:n.-30A>G
ENST00000612663.6:c.*90A>G	ENSP00000477997.3:n.*90A>G
ENST00000640140.2:n.833A>G
ENST00000640250.2:n.187A>G
ENST00000640681.2:n.792A>G
ENST00000696723.1:n.4321A>G
ENST00000696741.1:n.2326A>G
ENST00000696742.1:n.2053A>G
ENST00000696743.1:n.3456A>G
ENST00000696744.1:n.727A>G
ENST00000696767.1:n.1022A>G
ENST00000696768.1:c.*11A>G	ENSP00000512859.1:n.*11A>G
ENST00000696769.1:n.2377A>G
ENST00000696771.1:c.-30A>G	ENSP00000512860.1:n.-30A>G
ENST00000696772.1:n.2291A>G
ENST00000696773.1:n.2030A>G
ENST00000696774.1:n.5798A>G
ENST00000696776.1:c.781A>G	ENSP00000512861.1:p.Ser261Gly
ENST00000696777.1:n.2096A>G
ENST00000696778.1:n.1124A>G
ENST00000696779.1:c.295A>G	ENSP00000512862.1:p.Ser99Gly
ENST00000696780.1:c.718A>G	ENSP00000512863.1:p.Ser240Gly
ENST00000696781.1:c.433A>G	ENSP00000512864.1:p.Ser145Gly
ENST00000696782.1:c.*90A>G	ENSP00000512865.1:n.*90A>G
ENST00000696783.1:n.2556A>G
ENST00000696992.1:n.1805A>G
ENST00000696995.1:n.4217A>G
ENST00000696996.1:n.2130A>G
ENST00000696997.1:c.*318A>G	ENSP00000513028.1:n.*318A>G
ENST00000696998.1:n.1942A>G
ENST00000696999.1:c.-30A>G	ENSP00000513029.1:n.-30A>G
ENST00000697035.1:c.*21A>G	ENSP00000513059.1:n.*21A>G
ENST00000697036.1:c.*104A>G	ENSP00000513060.1:n.*104A>G
ENST00000697037.1:n.723A>G
ENST00000697093.1:n.2924A>G
ENST00000697094.1:n.3271A>G
ENST00000697095.1:c.*1889A>G	ENSP00000513104.1:n.*1889A>G
ENST00000697096.1:n.1821A>G
ENST00000697097.1:c.-30A>G	ENSP00000513105.1:n.-30A>G
ENST00000562983.2:n.874A>G
ENST00000690268.1:c.769A>G	ENSP00000509810.1:p.Ser257Gly
ENST00000355740.7:c.*14A>G	ENSP00000347979.3:n.*14A>G
ENST00000612663.5:c.*90A>G	ENSP00000477997.3:n.*90A>G
ENST00000640140.1:n.860A>G
ENST00000640250.1:n.187A>G
ENST00000640681.1:n.809A>G
ENST00000652046.1:c.688A>G MANE Select	ENSP00000498466.1:p.Ser230Gly
ENST00000313771.9:n.997A>G
ENST00000352159.8:c.*5A>G	ENSP00000345601.4:n.*5A>G
ENST00000355279.2:c.663A>G	ENSP00000347426.2:p.Ter221Trp
ENST00000355740.6:c.688A>G	ENSP00000347979.2:p.Ser230Gly
ENST00000357339.6:c.625A>G	ENSP00000349896.2:p.Ser209Gly
ENST00000479522.5:c.*117A>G	ENSP00000424113.1:n.*117A>G
ENST00000484444.5:c.*129A>G	ENSP00000420975.1:n.*129A>G
ENST00000488877.5:c.*129A>G	ENSP00000425159.1:n.*129A>G
ENST00000492756.5:c.516A>G	ENSP00000422453.1:n.516A>G
ENST00000494410.5:c.*46A>G	ENSP00000423755.1:n.*46A>G
ENST00000494799.5:n.595A>G
ENST00000612663.4:c.*35A>G	ENSP00000477997.2:n.*35A>G
ENST00000615406.4:c.688A>G	ENSP00000484575.1:p.Ser230Gly
ENST00000626542.2:c.688A>G	ENSP00000485876.1:p.Ser230Gly
NM_000043.4:c.688A>G , LRG_134t1:c.688A>G	NP_000034.1:p.Ser230Gly
NM_152871.2:c.625A>G	NP_690610.1:p.Ser209Gly
NM_152872.2:c.663A>G	NP_690611.1:p.Ter221Trp
NR_028033.2:n.862A>G
NR_028034.2:n.724A>G
NR_028035.2:n.787A>G
NR_028036.2:n.925A>G
XM_006717819.2:c.769A>G	XP_006717882.1:p.Ser257Gly
XM_011539764.1:c.850A>G	XP_011538066.1:p.Ser284Gly
XM_011539765.1:c.787A>G	XP_011538067.1:p.Ser263Gly
XM_011539766.1:c.769A>G	XP_011538068.1:p.Ser257Gly
XM_011539767.1:c.733A>G	XP_011538069.1:p.Ser245Gly
XR_945732.1:n.756A>G
XR_945733.1:n.693A>G
NM_000043.5:c.688A>G	NP_000034.1:p.Ser230Gly
NM_001320619.1:c.*11A>G	NP_001307548.1:n.*11A>G
NM_152871.3:c.625A>G	NP_690610.1:p.Ser209Gly
NM_152872.3:c.663A>G	NP_690611.1:p.Ter221Trp
NR_028033.3:n.834A>G
NR_028034.3:n.696A>G
NR_028035.3:n.759A>G
NR_028036.3:n.897A>G
NR_135313.1:n.814A>G
NR_135314.1:n.997A>G
NR_135315.1:n.750A>G
XM_006717819.3:c.769A>G	XP_006717882.1:p.Ser257Gly
XM_011539764.2:c.850A>G	XP_011538066.1:p.Ser284Gly
XM_011539765.2:c.787A>G	XP_011538067.1:p.Ser263Gly
XM_011539766.2:c.769A>G	XP_011538068.1:p.Ser257Gly
XM_011539767.3:c.733A>G	XP_011538069.1:p.Ser245Gly
XR_945732.3:n.756A>G
XR_945733.2:n.693A>G
NM_000043.6:c.688A>G MANE Select	NP_000034.1:p.Ser230Gly
NM_001320619.2:c.*11A>G	NP_001307548.1:n.*11A>G
NM_152871.4:c.625A>G	NP_690610.1:p.Ser209Gly
NM_152872.4:c.663A>G	NP_690611.1:p.Ter221Trp
NR_028033.4:n.595A>G
NR_028034.4:n.457A>G
NR_028035.4:n.520A>G
NR_028036.4:n.658A>G
NR_135313.2:n.575A>G
NR_135314.2:n.854A>G
NR_135315.2:n.607A>G