Canonical Allele Identifier: CA470974925

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774093C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014336C>G , CM000672.2:g.89014336C>G	GRCh38
NC_000010.10:g.90774093C>G , CM000672.1:g.90774093C>G	GRCh37
NC_000010.9:g.90764073C>G	NCBI36
NG_009089.2:g.28806C>G , LRG_134:g.28806C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1203C>G
ENST00000355740.8:c.*217C>G	ENSP00000347979.3:n.*217C>G
ENST00000357339.7:c.831C>G	ENSP00000349896.2:p.Leu277=
ENST00000371857.8:n.2439C>G
ENST00000460510.6:c.177C>G	ENSP00000512812.1:p.Leu59=
ENST00000466081.6:n.2543C>G
ENST00000477270.6:c.939C>G	ENSP00000512813.1:p.Leu313=
ENST00000479522.6:c.*323C>G	ENSP00000424113.1:n.*323C>G
ENST00000484444.6:c.*335C>G	ENSP00000420975.1:n.*335C>G
ENST00000488877.6:c.785C>G	ENSP00000425159.1:n.785C>G
ENST00000492756.7:c.*323C>G	ENSP00000422453.1:n.*323C>G
ENST00000494799.6:c.177C>G	ENSP00000512834.1:p.Leu59=
ENST00000562983.3:c.177C>G	ENSP00000512845.1:p.Leu59=
ENST00000612663.6:c.*296C>G	ENSP00000477997.3:n.*296C>G
ENST00000640140.2:n.1039C>G
ENST00000640250.2:n.393C>G
ENST00000640681.2:n.998C>G
ENST00000696723.1:n.4527C>G
ENST00000696741.1:n.2532C>G
ENST00000696742.1:n.2259C>G
ENST00000696743.1:n.3662C>G
ENST00000696744.1:n.933C>G
ENST00000696767.1:n.1228C>G
ENST00000696768.1:c.*217C>G	ENSP00000512859.1:n.*217C>G
ENST00000696769.1:n.2583C>G
ENST00000696771.1:c.177C>G	ENSP00000512860.1:p.Leu59=
ENST00000696772.1:n.2497C>G
ENST00000696773.1:n.2236C>G
ENST00000696774.1:n.6004C>G
ENST00000696776.1:c.987C>G	ENSP00000512861.1:p.Leu329=
ENST00000696777.1:n.2302C>G
ENST00000696778.1:n.1330C>G
ENST00000696779.1:c.501C>G	ENSP00000512862.1:p.Leu167=
ENST00000696780.1:c.924C>G	ENSP00000512863.1:p.Leu308=
ENST00000696781.1:c.639C>G	ENSP00000512864.1:p.Leu213=
ENST00000696782.1:c.*296C>G	ENSP00000512865.1:n.*296C>G
ENST00000696783.1:n.2762C>G
ENST00000696992.1:n.2011C>G
ENST00000696995.1:n.4423C>G
ENST00000696996.1:n.2336C>G
ENST00000696997.1:c.*524C>G	ENSP00000513028.1:n.*524C>G
ENST00000696998.1:n.2148C>G
ENST00000696999.1:c.177C>G	ENSP00000513029.1:p.Leu59=
ENST00000697036.1:c.*310C>G	ENSP00000513060.1:n.*310C>G
ENST00000697037.1:n.929C>G
ENST00000697093.1:n.3130C>G
ENST00000697094.1:n.3477C>G
ENST00000697095.1:c.*2095C>G	ENSP00000513104.1:n.*2095C>G
ENST00000697096.1:n.2027C>G
ENST00000697097.1:c.177C>G	ENSP00000513105.1:p.Leu59=
ENST00000562983.2:n.1080C>G
ENST00000690268.1:c.975C>G	ENSP00000509810.1:p.Leu325=
ENST00000355740.7:c.*220C>G	ENSP00000347979.3:n.*220C>G
ENST00000612663.5:c.*296C>G	ENSP00000477997.3:n.*296C>G
ENST00000640140.1:n.1066C>G
ENST00000640250.1:n.393C>G
ENST00000640681.1:n.1015C>G
ENST00000652046.1:c.894C>G MANE Select	ENSP00000498466.1:p.Leu298=
ENST00000352159.8:c.*211C>G	ENSP00000345601.4:n.*211C>G
ENST00000355279.2:c.869C>G	ENSP00000347426.2:n.869C>G
ENST00000355740.6:c.894C>G	ENSP00000347979.2:p.Leu298=
ENST00000357339.6:c.831C>G	ENSP00000349896.2:p.Leu277=
ENST00000479522.5:c.*323C>G	ENSP00000424113.1:n.*323C>G
ENST00000484444.5:c.*335C>G	ENSP00000420975.1:n.*335C>G
ENST00000488877.5:c.*335C>G	ENSP00000425159.1:n.*335C>G
ENST00000492756.5:c.722C>G	ENSP00000422453.1:n.722C>G
ENST00000494410.5:c.*252C>G	ENSP00000423755.1:n.*252C>G
ENST00000612663.4:c.*241C>G	ENSP00000477997.2:n.*241C>G
NM_000043.4:c.894C>G , LRG_134t1:c.894C>G	NP_000034.1:p.Leu298=
NM_152871.2:c.831C>G	NP_690610.1:p.Leu277=
NM_152872.2:c.*206C>G	NP_690611.1:n.*206C>G
NR_028033.2:n.1068C>G
NR_028034.2:n.930C>G
NR_028035.2:n.993C>G
NR_028036.2:n.1131C>G
XM_006717819.2:c.975C>G	XP_006717882.1:p.Leu325=
XM_011539764.1:c.1056C>G	XP_011538066.1:p.Leu352=
XM_011539765.1:c.993C>G	XP_011538067.1:p.Leu331=
XM_011539766.1:c.975C>G	XP_011538068.1:p.Leu325=
XM_011539767.1:c.939C>G	XP_011538069.1:p.Leu313=
XR_945732.1:n.962C>G
XR_945733.1:n.899C>G
NM_000043.5:c.894C>G	NP_000034.1:p.Leu298=
NM_001320619.1:c.*217C>G	NP_001307548.1:n.*217C>G
NM_152871.3:c.831C>G	NP_690610.1:p.Leu277=
NM_152872.3:c.*206C>G	NP_690611.1:n.*206C>G
NR_028033.3:n.1040C>G
NR_028034.3:n.902C>G
NR_028035.3:n.965C>G
NR_028036.3:n.1103C>G
NR_135313.1:n.1020C>G
NR_135314.1:n.1203C>G
NR_135315.1:n.956C>G
XM_006717819.3:c.975C>G	XP_006717882.1:p.Leu325=
XM_011539764.2:c.1056C>G	XP_011538066.1:p.Leu352=
XM_011539765.2:c.993C>G	XP_011538067.1:p.Leu331=
XM_011539766.2:c.975C>G	XP_011538068.1:p.Leu325=
XM_011539767.3:c.939C>G	XP_011538069.1:p.Leu313=
XR_945732.3:n.962C>G
XR_945733.2:n.899C>G
NM_000043.6:c.894C>G MANE Select	NP_000034.1:p.Leu298=
NM_001320619.2:c.*217C>G	NP_001307548.1:n.*217C>G
NM_152871.4:c.831C>G	NP_690610.1:p.Leu277=
NM_152872.4:c.*206C>G	NP_690611.1:n.*206C>G
NR_028033.4:n.801C>G
NR_028034.4:n.663C>G
NR_028035.4:n.726C>G
NR_028036.4:n.864C>G
NR_135313.2:n.781C>G
NR_135314.2:n.1060C>G
NR_135315.2:n.813C>G