Canonical Allele Identifier: CA377509895

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774022G>T (hg19) ; chr10:g.89014265G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014265G>T , CM000672.2:g.89014265G>T	GRCh38
NC_000010.10:g.90774022G>T , CM000672.1:g.90774022G>T	GRCh37
NC_000010.9:g.90764002G>T	NCBI36
NG_009089.2:g.28735G>T , LRG_134:g.28735G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1132G>T
ENST00000355740.8:c.*146G>T	ENSP00000347979.3:n.*146G>T
ENST00000357339.7:c.760G>T	ENSP00000349896.2:p.Val254Phe
ENST00000371857.8:n.2368G>T
ENST00000460510.6:c.106G>T	ENSP00000512812.1:p.Val36Phe
ENST00000466081.6:n.2472G>T
ENST00000477270.6:c.868G>T	ENSP00000512813.1:p.Val290Phe
ENST00000479522.6:c.*252G>T	ENSP00000424113.1:n.*252G>T
ENST00000484444.6:c.*264G>T	ENSP00000420975.1:n.*264G>T
ENST00000488877.6:c.714G>T	ENSP00000425159.1:n.714G>T
ENST00000492756.7:c.*252G>T	ENSP00000422453.1:n.*252G>T
ENST00000494799.6:c.106G>T	ENSP00000512834.1:p.Val36Phe
ENST00000562983.3:c.106G>T	ENSP00000512845.1:p.Val36Phe
ENST00000612663.6:c.*225G>T	ENSP00000477997.3:n.*225G>T
ENST00000640140.2:n.968G>T
ENST00000640250.2:n.322G>T
ENST00000640681.2:n.927G>T
ENST00000696723.1:n.4456G>T
ENST00000696741.1:n.2461G>T
ENST00000696742.1:n.2188G>T
ENST00000696743.1:n.3591G>T
ENST00000696744.1:n.862G>T
ENST00000696767.1:n.1157G>T
ENST00000696768.1:c.*146G>T	ENSP00000512859.1:n.*146G>T
ENST00000696769.1:n.2512G>T
ENST00000696771.1:c.106G>T	ENSP00000512860.1:p.Val36Phe
ENST00000696772.1:n.2426G>T
ENST00000696773.1:n.2165G>T
ENST00000696774.1:n.5933G>T
ENST00000696776.1:c.916G>T	ENSP00000512861.1:p.Val306Phe
ENST00000696777.1:n.2231G>T
ENST00000696778.1:n.1259G>T
ENST00000696779.1:c.430G>T	ENSP00000512862.1:p.Val144Phe
ENST00000696780.1:c.853G>T	ENSP00000512863.1:p.Val285Phe
ENST00000696781.1:c.568G>T	ENSP00000512864.1:p.Val190Phe
ENST00000696782.1:c.*225G>T	ENSP00000512865.1:n.*225G>T
ENST00000696783.1:n.2691G>T
ENST00000696992.1:n.1940G>T
ENST00000696995.1:n.4352G>T
ENST00000696996.1:n.2265G>T
ENST00000696997.1:c.*453G>T	ENSP00000513028.1:n.*453G>T
ENST00000696998.1:n.2077G>T
ENST00000696999.1:c.106G>T	ENSP00000513029.1:p.Val36Phe
ENST00000697035.1:c.*156G>T	ENSP00000513059.1:n.*156G>T
ENST00000697036.1:c.*239G>T	ENSP00000513060.1:n.*239G>T
ENST00000697037.1:n.858G>T
ENST00000697093.1:n.3059G>T
ENST00000697094.1:n.3406G>T
ENST00000697095.1:c.*2024G>T	ENSP00000513104.1:n.*2024G>T
ENST00000697096.1:n.1956G>T
ENST00000697097.1:c.106G>T	ENSP00000513105.1:p.Val36Phe
ENST00000562983.2:n.1009G>T
ENST00000690268.1:c.904G>T	ENSP00000509810.1:p.Val302Phe
ENST00000355740.7:c.*149G>T	ENSP00000347979.3:n.*149G>T
ENST00000612663.5:c.*225G>T	ENSP00000477997.3:n.*225G>T
ENST00000640140.1:n.995G>T
ENST00000640250.1:n.322G>T
ENST00000640681.1:n.944G>T
ENST00000652046.1:c.823G>T MANE Select	ENSP00000498466.1:p.Val275Phe
ENST00000352159.8:c.*140G>T	ENSP00000345601.4:n.*140G>T
ENST00000355279.2:c.798G>T	ENSP00000347426.2:n.798G>T
ENST00000355740.6:c.823G>T	ENSP00000347979.2:p.Val275Phe
ENST00000357339.6:c.760G>T	ENSP00000349896.2:p.Val254Phe
ENST00000479522.5:c.*252G>T	ENSP00000424113.1:n.*252G>T
ENST00000484444.5:c.*264G>T	ENSP00000420975.1:n.*264G>T
ENST00000488877.5:c.*264G>T	ENSP00000425159.1:n.*264G>T
ENST00000492756.5:c.651G>T	ENSP00000422453.1:n.651G>T
ENST00000494410.5:c.*181G>T	ENSP00000423755.1:n.*181G>T
ENST00000612663.4:c.*170G>T	ENSP00000477997.2:n.*170G>T
NM_000043.4:c.823G>T , LRG_134t1:c.823G>T	NP_000034.1:p.Val275Phe
NM_152871.2:c.760G>T	NP_690610.1:p.Val254Phe
NM_152872.2:c.*135G>T	NP_690611.1:n.*135G>T
NR_028033.2:n.997G>T
NR_028034.2:n.859G>T
NR_028035.2:n.922G>T
NR_028036.2:n.1060G>T
XM_006717819.2:c.904G>T	XP_006717882.1:p.Val302Phe
XM_011539764.1:c.985G>T	XP_011538066.1:p.Val329Phe
XM_011539765.1:c.922G>T	XP_011538067.1:p.Val308Phe
XM_011539766.1:c.904G>T	XP_011538068.1:p.Val302Phe
XM_011539767.1:c.868G>T	XP_011538069.1:p.Val290Phe
XR_945732.1:n.891G>T
XR_945733.1:n.828G>T
NM_000043.5:c.823G>T	NP_000034.1:p.Val275Phe
NM_001320619.1:c.*146G>T	NP_001307548.1:n.*146G>T
NM_152871.3:c.760G>T	NP_690610.1:p.Val254Phe
NM_152872.3:c.*135G>T	NP_690611.1:n.*135G>T
NR_028033.3:n.969G>T
NR_028034.3:n.831G>T
NR_028035.3:n.894G>T
NR_028036.3:n.1032G>T
NR_135313.1:n.949G>T
NR_135314.1:n.1132G>T
NR_135315.1:n.885G>T
XM_006717819.3:c.904G>T	XP_006717882.1:p.Val302Phe
XM_011539764.2:c.985G>T	XP_011538066.1:p.Val329Phe
XM_011539765.2:c.922G>T	XP_011538067.1:p.Val308Phe
XM_011539766.2:c.904G>T	XP_011538068.1:p.Val302Phe
XM_011539767.3:c.868G>T	XP_011538069.1:p.Val290Phe
XR_945732.3:n.891G>T
XR_945733.2:n.828G>T
NM_000043.6:c.823G>T MANE Select	NP_000034.1:p.Val275Phe
NM_001320619.2:c.*146G>T	NP_001307548.1:n.*146G>T
NM_152871.4:c.760G>T	NP_690610.1:p.Val254Phe
NM_152872.4:c.*135G>T	NP_690611.1:n.*135G>T
NR_028033.4:n.730G>T
NR_028034.4:n.592G>T
NR_028035.4:n.655G>T
NR_028036.4:n.793G>T
NR_135313.2:n.710G>T
NR_135314.2:n.989G>T
NR_135315.2:n.742G>T