Canonical Allele Identifier: CA377510286

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774196A>T (hg19) ; chr10:g.89014439A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014439A>T , CM000672.2:g.89014439A>T	GRCh38
NC_000010.10:g.90774196A>T , CM000672.1:g.90774196A>T	GRCh37
NC_000010.9:g.90764176A>T	NCBI36
NG_009089.2:g.28909A>T , LRG_134:g.28909A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1306A>T
ENST00000355740.8:c.*320A>T	ENSP00000347979.3:n.*320A>T
ENST00000357339.7:c.934A>T	ENSP00000349896.2:p.Ser312Cys
ENST00000371857.8:n.2542A>T
ENST00000460510.6:c.280A>T	ENSP00000512812.1:p.Ser94Cys
ENST00000466081.6:n.2646A>T
ENST00000477270.6:c.1042A>T	ENSP00000512813.1:p.Ser348Cys
ENST00000479522.6:c.*426A>T	ENSP00000424113.1:n.*426A>T
ENST00000484444.6:c.*438A>T	ENSP00000420975.1:n.*438A>T
ENST00000488877.6:c.888A>T	ENSP00000425159.1:n.888A>T
ENST00000492756.7:c.*426A>T	ENSP00000422453.1:n.*426A>T
ENST00000494799.6:c.280A>T	ENSP00000512834.1:p.Ser94Cys
ENST00000562983.3:c.280A>T	ENSP00000512845.1:p.Ser94Cys
ENST00000612663.6:c.*399A>T	ENSP00000477997.3:n.*399A>T
ENST00000640140.2:n.1142A>T
ENST00000640250.2:n.496A>T
ENST00000640681.2:n.1101A>T
ENST00000696723.1:n.4630A>T
ENST00000696741.1:n.2635A>T
ENST00000696742.1:n.2362A>T
ENST00000696743.1:n.3765A>T
ENST00000696744.1:n.1036A>T
ENST00000696767.1:n.1331A>T
ENST00000696768.1:c.*320A>T	ENSP00000512859.1:n.*320A>T
ENST00000696769.1:n.2686A>T
ENST00000696771.1:c.280A>T	ENSP00000512860.1:p.Ser94Cys
ENST00000696772.1:n.2600A>T
ENST00000696773.1:n.2339A>T
ENST00000696774.1:n.6107A>T
ENST00000696776.1:c.1090A>T	ENSP00000512861.1:p.Ser364Cys
ENST00000696777.1:n.2405A>T
ENST00000696778.1:n.1433A>T
ENST00000696779.1:c.604A>T	ENSP00000512862.1:p.Ser202Cys
ENST00000696780.1:c.1027A>T	ENSP00000512863.1:p.Ser343Cys
ENST00000696781.1:c.742A>T	ENSP00000512864.1:p.Ser248Cys
ENST00000696782.1:c.*399A>T	ENSP00000512865.1:n.*399A>T
ENST00000696783.1:n.2865A>T
ENST00000696992.1:n.2114A>T
ENST00000696995.1:n.4526A>T
ENST00000696996.1:n.2439A>T
ENST00000696997.1:c.*627A>T	ENSP00000513028.1:n.*627A>T
ENST00000696998.1:n.2251A>T
ENST00000696999.1:c.280A>T	ENSP00000513029.1:p.Ser94Cys
ENST00000697036.1:c.*413A>T	ENSP00000513060.1:n.*413A>T
ENST00000697037.1:n.1032A>T
ENST00000697093.1:n.3233A>T
ENST00000697094.1:n.3580A>T
ENST00000697095.1:c.*2198A>T	ENSP00000513104.1:n.*2198A>T
ENST00000697096.1:n.2130A>T
ENST00000697097.1:c.280A>T	ENSP00000513105.1:p.Ser94Cys
ENST00000562983.2:n.1183A>T
ENST00000690268.1:c.1078A>T	ENSP00000509810.1:p.Ser360Cys
ENST00000355740.7:c.*323A>T	ENSP00000347979.3:n.*323A>T
ENST00000612663.5:c.*399A>T	ENSP00000477997.3:n.*399A>T
ENST00000640140.1:n.1169A>T
ENST00000640250.1:n.496A>T
ENST00000640681.1:n.1118A>T
ENST00000652046.1:c.997A>T MANE Select	ENSP00000498466.1:p.Ser333Cys
ENST00000352159.8:c.*314A>T	ENSP00000345601.4:n.*314A>T
ENST00000355279.2:c.972A>T	ENSP00000347426.2:n.972A>T
ENST00000355740.6:c.997A>T	ENSP00000347979.2:p.Ser333Cys
ENST00000357339.6:c.934A>T	ENSP00000349896.2:p.Ser312Cys
ENST00000479522.5:c.*426A>T	ENSP00000424113.1:n.*426A>T
ENST00000484444.5:c.*438A>T	ENSP00000420975.1:n.*438A>T
ENST00000488877.5:c.*438A>T	ENSP00000425159.1:n.*438A>T
ENST00000492756.5:c.825A>T	ENSP00000422453.1:n.825A>T
ENST00000494410.5:c.*355A>T	ENSP00000423755.1:n.*355A>T
ENST00000612663.4:c.*344A>T	ENSP00000477997.2:n.*344A>T
NM_000043.4:c.997A>T , LRG_134t1:c.997A>T	NP_000034.1:p.Ser333Cys
NM_152871.2:c.934A>T	NP_690610.1:p.Ser312Cys
NM_152872.2:c.*309A>T	NP_690611.1:n.*309A>T
NR_028033.2:n.1171A>T
NR_028034.2:n.1033A>T
NR_028035.2:n.1096A>T
NR_028036.2:n.1234A>T
XM_006717819.2:c.1078A>T	XP_006717882.1:p.Ser360Cys
XM_011539764.1:c.1159A>T	XP_011538066.1:p.Ser387Cys
XM_011539765.1:c.1096A>T	XP_011538067.1:p.Ser366Cys
XM_011539766.1:c.1078A>T	XP_011538068.1:p.Ser360Cys
XM_011539767.1:c.1042A>T	XP_011538069.1:p.Ser348Cys
XR_945733.1:n.1002A>T
NM_000043.5:c.997A>T	NP_000034.1:p.Ser333Cys
NM_001320619.1:c.*320A>T	NP_001307548.1:n.*320A>T
NM_152871.3:c.934A>T	NP_690610.1:p.Ser312Cys
NM_152872.3:c.*309A>T	NP_690611.1:n.*309A>T
NR_028033.3:n.1143A>T
NR_028034.3:n.1005A>T
NR_028035.3:n.1068A>T
NR_028036.3:n.1206A>T
NR_135313.1:n.1123A>T
NR_135314.1:n.1306A>T
NR_135315.1:n.1059A>T
XM_006717819.3:c.1078A>T	XP_006717882.1:p.Ser360Cys
XM_011539764.2:c.1159A>T	XP_011538066.1:p.Ser387Cys
XM_011539765.2:c.1096A>T	XP_011538067.1:p.Ser366Cys
XM_011539766.2:c.1078A>T	XP_011538068.1:p.Ser360Cys
XM_011539767.3:c.1042A>T	XP_011538069.1:p.Ser348Cys
XR_945732.3:n.1065A>T
XR_945733.2:n.1002A>T
NM_000043.6:c.997A>T MANE Select	NP_000034.1:p.Ser333Cys
NM_001320619.2:c.*320A>T	NP_001307548.1:n.*320A>T
NM_152871.4:c.934A>T	NP_690610.1:p.Ser312Cys
NM_152872.4:c.*309A>T	NP_690611.1:n.*309A>T
NR_028033.4:n.904A>T
NR_028034.4:n.766A>T
NR_028035.4:n.829A>T
NR_028036.4:n.967A>T
NR_135313.2:n.884A>T
NR_135314.2:n.1163A>T
NR_135315.2:n.916A>T