Canonical Allele Identifier: CA377509686

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773935A>T (hg19) ; chr10:g.89014178A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014178A>T , CM000672.2:g.89014178A>T	GRCh38
NC_000010.10:g.90773935A>T , CM000672.1:g.90773935A>T	GRCh37
NC_000010.9:g.90763915A>T	NCBI36
NG_009089.2:g.28648A>T , LRG_134:g.28648A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1045A>T
ENST00000355740.8:c.*59A>T	ENSP00000347979.3:n.*59A>T
ENST00000357339.7:c.673A>T	ENSP00000349896.2:p.Lys225Ter
ENST00000371857.8:n.2281A>T
ENST00000460510.6:c.19A>T	ENSP00000512812.1:p.Lys7Ter
ENST00000466081.6:n.2385A>T
ENST00000477270.6:c.781A>T	ENSP00000512813.1:p.Lys261Ter
ENST00000479522.6:c.*165A>T	ENSP00000424113.1:n.*165A>T
ENST00000484444.6:c.*177A>T	ENSP00000420975.1:n.*177A>T
ENST00000488877.6:c.627A>T	ENSP00000425159.1:n.627A>T
ENST00000492756.7:c.*165A>T	ENSP00000422453.1:n.*165A>T
ENST00000494799.6:c.19A>T	ENSP00000512834.1:p.Lys7Ter
ENST00000562983.3:c.19A>T	ENSP00000512845.1:p.Lys7Ter
ENST00000612663.6:c.*138A>T	ENSP00000477997.3:n.*138A>T
ENST00000640140.2:n.881A>T
ENST00000640250.2:n.235A>T
ENST00000640681.2:n.840A>T
ENST00000696723.1:n.4369A>T
ENST00000696741.1:n.2374A>T
ENST00000696742.1:n.2101A>T
ENST00000696743.1:n.3504A>T
ENST00000696744.1:n.775A>T
ENST00000696767.1:n.1070A>T
ENST00000696768.1:c.*59A>T	ENSP00000512859.1:n.*59A>T
ENST00000696769.1:n.2425A>T
ENST00000696771.1:c.19A>T	ENSP00000512860.1:p.Lys7Ter
ENST00000696772.1:n.2339A>T
ENST00000696773.1:n.2078A>T
ENST00000696774.1:n.5846A>T
ENST00000696776.1:c.829A>T	ENSP00000512861.1:p.Lys277Ter
ENST00000696777.1:n.2144A>T
ENST00000696778.1:n.1172A>T
ENST00000696779.1:c.343A>T	ENSP00000512862.1:p.Lys115Ter
ENST00000696780.1:c.766A>T	ENSP00000512863.1:p.Lys256Ter
ENST00000696781.1:c.481A>T	ENSP00000512864.1:p.Lys161Ter
ENST00000696782.1:c.*138A>T	ENSP00000512865.1:n.*138A>T
ENST00000696783.1:n.2604A>T
ENST00000696992.1:n.1853A>T
ENST00000696995.1:n.4265A>T
ENST00000696996.1:n.2178A>T
ENST00000696997.1:c.*366A>T	ENSP00000513028.1:n.*366A>T
ENST00000696998.1:n.1990A>T
ENST00000696999.1:c.19A>T	ENSP00000513029.1:p.Lys7Ter
ENST00000697035.1:c.*69A>T	ENSP00000513059.1:n.*69A>T
ENST00000697036.1:c.*152A>T	ENSP00000513060.1:n.*152A>T
ENST00000697037.1:n.771A>T
ENST00000697093.1:n.2972A>T
ENST00000697094.1:n.3319A>T
ENST00000697095.1:c.*1937A>T	ENSP00000513104.1:n.*1937A>T
ENST00000697096.1:n.1869A>T
ENST00000697097.1:c.19A>T	ENSP00000513105.1:p.Lys7Ter
ENST00000562983.2:n.922A>T
ENST00000690268.1:c.817A>T	ENSP00000509810.1:p.Lys273Ter
ENST00000355740.7:c.*62A>T	ENSP00000347979.3:n.*62A>T
ENST00000612663.5:c.*138A>T	ENSP00000477997.3:n.*138A>T
ENST00000640140.1:n.908A>T
ENST00000640250.1:n.235A>T
ENST00000640681.1:n.857A>T
ENST00000652046.1:c.736A>T MANE Select	ENSP00000498466.1:p.Lys246Ter
ENST00000352159.8:c.*53A>T	ENSP00000345601.4:n.*53A>T
ENST00000355279.2:c.711A>T	ENSP00000347426.2:n.711A>T
ENST00000355740.6:c.736A>T	ENSP00000347979.2:p.Lys246Ter
ENST00000357339.6:c.673A>T	ENSP00000349896.2:p.Lys225Ter
ENST00000479522.5:c.*165A>T	ENSP00000424113.1:n.*165A>T
ENST00000484444.5:c.*177A>T	ENSP00000420975.1:n.*177A>T
ENST00000488877.5:c.*177A>T	ENSP00000425159.1:n.*177A>T
ENST00000492756.5:c.564A>T	ENSP00000422453.1:n.564A>T
ENST00000494410.5:c.*94A>T	ENSP00000423755.1:n.*94A>T
ENST00000494799.5:n.643A>T
ENST00000612663.4:c.*83A>T	ENSP00000477997.2:n.*83A>T
ENST00000615406.4:c.736A>T	ENSP00000484575.1:p.Lys246Ter
ENST00000626542.2:c.734A>T	ENSP00000485876.1:p.Ter245Leu
NM_000043.4:c.736A>T , LRG_134t1:c.736A>T	NP_000034.1:p.Lys246Ter
NM_152871.2:c.673A>T	NP_690610.1:p.Lys225Ter
NM_152872.2:c.*48A>T	NP_690611.1:n.*48A>T
NR_028033.2:n.910A>T
NR_028034.2:n.772A>T
NR_028035.2:n.835A>T
NR_028036.2:n.973A>T
XM_006717819.2:c.817A>T	XP_006717882.1:p.Lys273Ter
XM_011539764.1:c.898A>T	XP_011538066.1:p.Lys300Ter
XM_011539765.1:c.835A>T	XP_011538067.1:p.Lys279Ter
XM_011539766.1:c.817A>T	XP_011538068.1:p.Lys273Ter
XM_011539767.1:c.781A>T	XP_011538069.1:p.Lys261Ter
XR_945732.1:n.804A>T
XR_945733.1:n.741A>T
NM_000043.5:c.736A>T	NP_000034.1:p.Lys246Ter
NM_001320619.1:c.*59A>T	NP_001307548.1:n.*59A>T
NM_152871.3:c.673A>T	NP_690610.1:p.Lys225Ter
NM_152872.3:c.*48A>T	NP_690611.1:n.*48A>T
NR_028033.3:n.882A>T
NR_028034.3:n.744A>T
NR_028035.3:n.807A>T
NR_028036.3:n.945A>T
NR_135313.1:n.862A>T
NR_135314.1:n.1045A>T
NR_135315.1:n.798A>T
XM_006717819.3:c.817A>T	XP_006717882.1:p.Lys273Ter
XM_011539764.2:c.898A>T	XP_011538066.1:p.Lys300Ter
XM_011539765.2:c.835A>T	XP_011538067.1:p.Lys279Ter
XM_011539766.2:c.817A>T	XP_011538068.1:p.Lys273Ter
XM_011539767.3:c.781A>T	XP_011538069.1:p.Lys261Ter
XR_945732.3:n.804A>T
XR_945733.2:n.741A>T
NM_000043.6:c.736A>T MANE Select	NP_000034.1:p.Lys246Ter
NM_001320619.2:c.*59A>T	NP_001307548.1:n.*59A>T
NM_152871.4:c.673A>T	NP_690610.1:p.Lys225Ter
NM_152872.4:c.*48A>T	NP_690611.1:n.*48A>T
NR_028033.4:n.643A>T
NR_028034.4:n.505A>T
NR_028035.4:n.568A>T
NR_028036.4:n.706A>T
NR_135313.2:n.623A>T
NR_135314.2:n.902A>T
NR_135315.2:n.655A>T