Canonical Allele Identifier: CA377509863

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774008C>G (hg19) ; chr10:g.89014251C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014251C>G , CM000672.2:g.89014251C>G	GRCh38
NC_000010.10:g.90774008C>G , CM000672.1:g.90774008C>G	GRCh37
NC_000010.9:g.90763988C>G	NCBI36
NG_009089.2:g.28721C>G , LRG_134:g.28721C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1118C>G
ENST00000355740.8:c.*132C>G	ENSP00000347979.3:n.*132C>G
ENST00000357339.7:c.746C>G	ENSP00000349896.2:p.Thr249Arg
ENST00000371857.8:n.2354C>G
ENST00000460510.6:c.92C>G	ENSP00000512812.1:p.Thr31Arg
ENST00000466081.6:n.2458C>G
ENST00000477270.6:c.854C>G	ENSP00000512813.1:p.Thr285Arg
ENST00000479522.6:c.*238C>G	ENSP00000424113.1:n.*238C>G
ENST00000484444.6:c.*250C>G	ENSP00000420975.1:n.*250C>G
ENST00000488877.6:c.700C>G	ENSP00000425159.1:n.700C>G
ENST00000492756.7:c.*238C>G	ENSP00000422453.1:n.*238C>G
ENST00000494799.6:c.92C>G	ENSP00000512834.1:p.Thr31Arg
ENST00000562983.3:c.92C>G	ENSP00000512845.1:p.Thr31Arg
ENST00000612663.6:c.*211C>G	ENSP00000477997.3:n.*211C>G
ENST00000640140.2:n.954C>G
ENST00000640250.2:n.308C>G
ENST00000640681.2:n.913C>G
ENST00000696723.1:n.4442C>G
ENST00000696741.1:n.2447C>G
ENST00000696742.1:n.2174C>G
ENST00000696743.1:n.3577C>G
ENST00000696744.1:n.848C>G
ENST00000696767.1:n.1143C>G
ENST00000696768.1:c.*132C>G	ENSP00000512859.1:n.*132C>G
ENST00000696769.1:n.2498C>G
ENST00000696771.1:c.92C>G	ENSP00000512860.1:p.Thr31Arg
ENST00000696772.1:n.2412C>G
ENST00000696773.1:n.2151C>G
ENST00000696774.1:n.5919C>G
ENST00000696776.1:c.902C>G	ENSP00000512861.1:p.Thr301Arg
ENST00000696777.1:n.2217C>G
ENST00000696778.1:n.1245C>G
ENST00000696779.1:c.416C>G	ENSP00000512862.1:p.Thr139Arg
ENST00000696780.1:c.839C>G	ENSP00000512863.1:p.Thr280Arg
ENST00000696781.1:c.554C>G	ENSP00000512864.1:p.Thr185Arg
ENST00000696782.1:c.*211C>G	ENSP00000512865.1:n.*211C>G
ENST00000696783.1:n.2677C>G
ENST00000696992.1:n.1926C>G
ENST00000696995.1:n.4338C>G
ENST00000696996.1:n.2251C>G
ENST00000696997.1:c.*439C>G	ENSP00000513028.1:n.*439C>G
ENST00000696998.1:n.2063C>G
ENST00000696999.1:c.92C>G	ENSP00000513029.1:p.Thr31Arg
ENST00000697035.1:c.*142C>G	ENSP00000513059.1:n.*142C>G
ENST00000697036.1:c.*225C>G	ENSP00000513060.1:n.*225C>G
ENST00000697037.1:n.844C>G
ENST00000697093.1:n.3045C>G
ENST00000697094.1:n.3392C>G
ENST00000697095.1:c.*2010C>G	ENSP00000513104.1:n.*2010C>G
ENST00000697096.1:n.1942C>G
ENST00000697097.1:c.92C>G	ENSP00000513105.1:p.Thr31Arg
ENST00000562983.2:n.995C>G
ENST00000690268.1:c.890C>G	ENSP00000509810.1:p.Thr297Arg
ENST00000355740.7:c.*135C>G	ENSP00000347979.3:n.*135C>G
ENST00000612663.5:c.*211C>G	ENSP00000477997.3:n.*211C>G
ENST00000640140.1:n.981C>G
ENST00000640250.1:n.308C>G
ENST00000640681.1:n.930C>G
ENST00000652046.1:c.809C>G MANE Select	ENSP00000498466.1:p.Thr270Arg
ENST00000352159.8:c.*126C>G	ENSP00000345601.4:n.*126C>G
ENST00000355279.2:c.784C>G	ENSP00000347426.2:n.784C>G
ENST00000355740.6:c.809C>G	ENSP00000347979.2:p.Thr270Arg
ENST00000357339.6:c.746C>G	ENSP00000349896.2:p.Thr249Arg
ENST00000479522.5:c.*238C>G	ENSP00000424113.1:n.*238C>G
ENST00000484444.5:c.*250C>G	ENSP00000420975.1:n.*250C>G
ENST00000488877.5:c.*250C>G	ENSP00000425159.1:n.*250C>G
ENST00000492756.5:c.637C>G	ENSP00000422453.1:n.637C>G
ENST00000494410.5:c.*167C>G	ENSP00000423755.1:n.*167C>G
ENST00000612663.4:c.*156C>G	ENSP00000477997.2:n.*156C>G
NM_000043.4:c.809C>G , LRG_134t1:c.809C>G	NP_000034.1:p.Thr270Arg
NM_152871.2:c.746C>G	NP_690610.1:p.Thr249Arg
NM_152872.2:c.*121C>G	NP_690611.1:n.*121C>G
NR_028033.2:n.983C>G
NR_028034.2:n.845C>G
NR_028035.2:n.908C>G
NR_028036.2:n.1046C>G
XM_006717819.2:c.890C>G	XP_006717882.1:p.Thr297Arg
XM_011539764.1:c.971C>G	XP_011538066.1:p.Thr324Arg
XM_011539765.1:c.908C>G	XP_011538067.1:p.Thr303Arg
XM_011539766.1:c.890C>G	XP_011538068.1:p.Thr297Arg
XM_011539767.1:c.854C>G	XP_011538069.1:p.Thr285Arg
XR_945732.1:n.877C>G
XR_945733.1:n.814C>G
NM_000043.5:c.809C>G	NP_000034.1:p.Thr270Arg
NM_001320619.1:c.*132C>G	NP_001307548.1:n.*132C>G
NM_152871.3:c.746C>G	NP_690610.1:p.Thr249Arg
NM_152872.3:c.*121C>G	NP_690611.1:n.*121C>G
NR_028033.3:n.955C>G
NR_028034.3:n.817C>G
NR_028035.3:n.880C>G
NR_028036.3:n.1018C>G
NR_135313.1:n.935C>G
NR_135314.1:n.1118C>G
NR_135315.1:n.871C>G
XM_006717819.3:c.890C>G	XP_006717882.1:p.Thr297Arg
XM_011539764.2:c.971C>G	XP_011538066.1:p.Thr324Arg
XM_011539765.2:c.908C>G	XP_011538067.1:p.Thr303Arg
XM_011539766.2:c.890C>G	XP_011538068.1:p.Thr297Arg
XM_011539767.3:c.854C>G	XP_011538069.1:p.Thr285Arg
XR_945732.3:n.877C>G
XR_945733.2:n.814C>G
NM_000043.6:c.809C>G MANE Select	NP_000034.1:p.Thr270Arg
NM_001320619.2:c.*132C>G	NP_001307548.1:n.*132C>G
NM_152871.4:c.746C>G	NP_690610.1:p.Thr249Arg
NM_152872.4:c.*121C>G	NP_690611.1:n.*121C>G
NR_028033.4:n.716C>G
NR_028034.4:n.578C>G
NR_028035.4:n.641C>G
NR_028036.4:n.779C>G
NR_135313.2:n.696C>G
NR_135314.2:n.975C>G
NR_135315.2:n.728C>G