Canonical Allele Identifier: CA377510088

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774107T>A (hg19) ; chr10:g.89014350T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014350T>A , CM000672.2:g.89014350T>A	GRCh38
NC_000010.10:g.90774107T>A , CM000672.1:g.90774107T>A	GRCh37
NC_000010.9:g.90764087T>A	NCBI36
NG_009089.2:g.28820T>A , LRG_134:g.28820T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1217T>A
ENST00000355740.8:c.*231T>A	ENSP00000347979.3:n.*231T>A
ENST00000357339.7:c.845T>A	ENSP00000349896.2:p.Leu282His
ENST00000371857.8:n.2453T>A
ENST00000460510.6:c.191T>A	ENSP00000512812.1:p.Leu64His
ENST00000466081.6:n.2557T>A
ENST00000477270.6:c.953T>A	ENSP00000512813.1:p.Leu318His
ENST00000479522.6:c.*337T>A	ENSP00000424113.1:n.*337T>A
ENST00000484444.6:c.*349T>A	ENSP00000420975.1:n.*349T>A
ENST00000488877.6:c.799T>A	ENSP00000425159.1:n.799T>A
ENST00000492756.7:c.*337T>A	ENSP00000422453.1:n.*337T>A
ENST00000494799.6:c.191T>A	ENSP00000512834.1:p.Leu64His
ENST00000562983.3:c.191T>A	ENSP00000512845.1:p.Leu64His
ENST00000612663.6:c.*310T>A	ENSP00000477997.3:n.*310T>A
ENST00000640140.2:n.1053T>A
ENST00000640250.2:n.407T>A
ENST00000640681.2:n.1012T>A
ENST00000696723.1:n.4541T>A
ENST00000696741.1:n.2546T>A
ENST00000696742.1:n.2273T>A
ENST00000696743.1:n.3676T>A
ENST00000696744.1:n.947T>A
ENST00000696767.1:n.1242T>A
ENST00000696768.1:c.*231T>A	ENSP00000512859.1:n.*231T>A
ENST00000696769.1:n.2597T>A
ENST00000696771.1:c.191T>A	ENSP00000512860.1:p.Leu64His
ENST00000696772.1:n.2511T>A
ENST00000696773.1:n.2250T>A
ENST00000696774.1:n.6018T>A
ENST00000696776.1:c.1001T>A	ENSP00000512861.1:p.Leu334His
ENST00000696777.1:n.2316T>A
ENST00000696778.1:n.1344T>A
ENST00000696779.1:c.515T>A	ENSP00000512862.1:p.Leu172His
ENST00000696780.1:c.938T>A	ENSP00000512863.1:p.Leu313His
ENST00000696781.1:c.653T>A	ENSP00000512864.1:p.Leu218His
ENST00000696782.1:c.*310T>A	ENSP00000512865.1:n.*310T>A
ENST00000696783.1:n.2776T>A
ENST00000696992.1:n.2025T>A
ENST00000696995.1:n.4437T>A
ENST00000696996.1:n.2350T>A
ENST00000696997.1:c.*538T>A	ENSP00000513028.1:n.*538T>A
ENST00000696998.1:n.2162T>A
ENST00000696999.1:c.191T>A	ENSP00000513029.1:p.Leu64His
ENST00000697036.1:c.*324T>A	ENSP00000513060.1:n.*324T>A
ENST00000697037.1:n.943T>A
ENST00000697093.1:n.3144T>A
ENST00000697094.1:n.3491T>A
ENST00000697095.1:c.*2109T>A	ENSP00000513104.1:n.*2109T>A
ENST00000697096.1:n.2041T>A
ENST00000697097.1:c.191T>A	ENSP00000513105.1:p.Leu64His
ENST00000562983.2:n.1094T>A
ENST00000690268.1:c.989T>A	ENSP00000509810.1:p.Leu330His
ENST00000355740.7:c.*234T>A	ENSP00000347979.3:n.*234T>A
ENST00000612663.5:c.*310T>A	ENSP00000477997.3:n.*310T>A
ENST00000640140.1:n.1080T>A
ENST00000640250.1:n.407T>A
ENST00000640681.1:n.1029T>A
ENST00000652046.1:c.908T>A MANE Select	ENSP00000498466.1:p.Leu303His
ENST00000352159.8:c.*225T>A	ENSP00000345601.4:n.*225T>A
ENST00000355279.2:c.883T>A	ENSP00000347426.2:n.883T>A
ENST00000355740.6:c.908T>A	ENSP00000347979.2:p.Leu303His
ENST00000357339.6:c.845T>A	ENSP00000349896.2:p.Leu282His
ENST00000479522.5:c.*337T>A	ENSP00000424113.1:n.*337T>A
ENST00000484444.5:c.*349T>A	ENSP00000420975.1:n.*349T>A
ENST00000488877.5:c.*349T>A	ENSP00000425159.1:n.*349T>A
ENST00000492756.5:c.736T>A	ENSP00000422453.1:n.736T>A
ENST00000494410.5:c.*266T>A	ENSP00000423755.1:n.*266T>A
ENST00000612663.4:c.*255T>A	ENSP00000477997.2:n.*255T>A
NM_000043.4:c.908T>A , LRG_134t1:c.908T>A	NP_000034.1:p.Leu303His
NM_152871.2:c.845T>A	NP_690610.1:p.Leu282His
NM_152872.2:c.*220T>A	NP_690611.1:n.*220T>A
NR_028033.2:n.1082T>A
NR_028034.2:n.944T>A
NR_028035.2:n.1007T>A
NR_028036.2:n.1145T>A
XM_006717819.2:c.989T>A	XP_006717882.1:p.Leu330His
XM_011539764.1:c.1070T>A	XP_011538066.1:p.Leu357His
XM_011539765.1:c.1007T>A	XP_011538067.1:p.Leu336His
XM_011539766.1:c.989T>A	XP_011538068.1:p.Leu330His
XM_011539767.1:c.953T>A	XP_011538069.1:p.Leu318His
XR_945732.1:n.976T>A
XR_945733.1:n.913T>A
NM_000043.5:c.908T>A	NP_000034.1:p.Leu303His
NM_001320619.1:c.*231T>A	NP_001307548.1:n.*231T>A
NM_152871.3:c.845T>A	NP_690610.1:p.Leu282His
NM_152872.3:c.*220T>A	NP_690611.1:n.*220T>A
NR_028033.3:n.1054T>A
NR_028034.3:n.916T>A
NR_028035.3:n.979T>A
NR_028036.3:n.1117T>A
NR_135313.1:n.1034T>A
NR_135314.1:n.1217T>A
NR_135315.1:n.970T>A
XM_006717819.3:c.989T>A	XP_006717882.1:p.Leu330His
XM_011539764.2:c.1070T>A	XP_011538066.1:p.Leu357His
XM_011539765.2:c.1007T>A	XP_011538067.1:p.Leu336His
XM_011539766.2:c.989T>A	XP_011538068.1:p.Leu330His
XM_011539767.3:c.953T>A	XP_011538069.1:p.Leu318His
XR_945732.3:n.976T>A
XR_945733.2:n.913T>A
NM_000043.6:c.908T>A MANE Select	NP_000034.1:p.Leu303His
NM_001320619.2:c.*231T>A	NP_001307548.1:n.*231T>A
NM_152871.4:c.845T>A	NP_690610.1:p.Leu282His
NM_152872.4:c.*220T>A	NP_690611.1:n.*220T>A
NR_028033.4:n.815T>A
NR_028034.4:n.677T>A
NR_028035.4:n.740T>A
NR_028036.4:n.878T>A
NR_135313.2:n.795T>A
NR_135314.2:n.1074T>A
NR_135315.2:n.827T>A