Canonical Allele Identifier: CA377510309

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774206A>C (hg19) ; chr10:g.89014449A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014449A>C , CM000672.2:g.89014449A>C	GRCh38
NC_000010.10:g.90774206A>C , CM000672.1:g.90774206A>C	GRCh37
NC_000010.9:g.90764186A>C	NCBI36
NG_009089.2:g.28919A>C , LRG_134:g.28919A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1316A>C
ENST00000355740.8:c.*330A>C	ENSP00000347979.3:n.*330A>C
ENST00000357339.7:c.944A>C	ENSP00000349896.2:p.Ter315Ser
ENST00000371857.8:n.2552A>C
ENST00000460510.6:c.290A>C	ENSP00000512812.1:p.Ter97Ser
ENST00000466081.6:n.2656A>C
ENST00000477270.6:c.1052A>C	ENSP00000512813.1:p.Ter351Ser
ENST00000479522.6:c.*436A>C	ENSP00000424113.1:n.*436A>C
ENST00000484444.6:c.*448A>C	ENSP00000420975.1:n.*448A>C
ENST00000488877.6:c.898A>C	ENSP00000425159.1:n.898A>C
ENST00000492756.7:c.*436A>C	ENSP00000422453.1:n.*436A>C
ENST00000494799.6:c.290A>C	ENSP00000512834.1:p.Ter97Ser
ENST00000562983.3:c.290A>C	ENSP00000512845.1:p.Ter97Ser
ENST00000612663.6:c.*409A>C	ENSP00000477997.3:n.*409A>C
ENST00000640140.2:n.1152A>C
ENST00000640250.2:n.506A>C
ENST00000640681.2:n.1111A>C
ENST00000696723.1:n.4640A>C
ENST00000696741.1:n.2645A>C
ENST00000696742.1:n.2372A>C
ENST00000696743.1:n.3775A>C
ENST00000696744.1:n.1046A>C
ENST00000696767.1:n.1341A>C
ENST00000696768.1:c.*330A>C	ENSP00000512859.1:n.*330A>C
ENST00000696769.1:n.2696A>C
ENST00000696771.1:c.290A>C	ENSP00000512860.1:p.Ter97Ser
ENST00000696772.1:n.2610A>C
ENST00000696773.1:n.2349A>C
ENST00000696774.1:n.6117A>C
ENST00000696776.1:c.1100A>C	ENSP00000512861.1:p.Ter367Ser
ENST00000696777.1:n.2415A>C
ENST00000696778.1:n.1443A>C
ENST00000696779.1:c.614A>C	ENSP00000512862.1:p.Ter205Ser
ENST00000696780.1:c.1037A>C	ENSP00000512863.1:p.Ter346Ser
ENST00000696781.1:c.752A>C	ENSP00000512864.1:p.Ter251Ser
ENST00000696782.1:c.*409A>C	ENSP00000512865.1:n.*409A>C
ENST00000696783.1:n.2875A>C
ENST00000696992.1:n.2124A>C
ENST00000696995.1:n.4536A>C
ENST00000696996.1:n.2449A>C
ENST00000696997.1:c.*637A>C	ENSP00000513028.1:n.*637A>C
ENST00000696998.1:n.2261A>C
ENST00000696999.1:c.290A>C	ENSP00000513029.1:p.Ter97Ser
ENST00000697036.1:c.*423A>C	ENSP00000513060.1:n.*423A>C
ENST00000697037.1:n.1042A>C
ENST00000697093.1:n.3243A>C
ENST00000697094.1:n.3590A>C
ENST00000697095.1:c.*2208A>C	ENSP00000513104.1:n.*2208A>C
ENST00000697096.1:n.2140A>C
ENST00000697097.1:c.290A>C	ENSP00000513105.1:p.Ter97Ser
ENST00000562983.2:n.1193A>C
ENST00000690268.1:c.1088A>C	ENSP00000509810.1:p.Ter363Ser
ENST00000355740.7:c.*333A>C	ENSP00000347979.3:n.*333A>C
ENST00000612663.5:c.*409A>C	ENSP00000477997.3:n.*409A>C
ENST00000640140.1:n.1179A>C
ENST00000640250.1:n.506A>C
ENST00000640681.1:n.1128A>C
ENST00000652046.1:c.1007A>C MANE Select	ENSP00000498466.1:p.Ter336Ser
ENST00000352159.8:c.*324A>C	ENSP00000345601.4:n.*324A>C
ENST00000355279.2:c.982A>C	ENSP00000347426.2:n.982A>C
ENST00000355740.6:c.1007A>C	ENSP00000347979.2:p.Ter336Ser
ENST00000357339.6:c.944A>C	ENSP00000349896.2:p.Ter315Ser
ENST00000479522.5:c.*436A>C	ENSP00000424113.1:n.*436A>C
ENST00000484444.5:c.*448A>C	ENSP00000420975.1:n.*448A>C
ENST00000488877.5:c.*448A>C	ENSP00000425159.1:n.*448A>C
ENST00000492756.5:c.835A>C	ENSP00000422453.1:n.835A>C
ENST00000494410.5:c.*365A>C	ENSP00000423755.1:n.*365A>C
ENST00000612663.4:c.*354A>C	ENSP00000477997.2:n.*354A>C
NM_000043.4:c.1007A>C , LRG_134t1:c.1007A>C	NP_000034.1:p.Ter336Ser
NM_152871.2:c.944A>C	NP_690610.1:p.Ter315Ser
NM_152872.2:c.*319A>C	NP_690611.1:n.*319A>C
NR_028033.2:n.1181A>C
NR_028034.2:n.1043A>C
NR_028035.2:n.1106A>C
NR_028036.2:n.1244A>C
XM_006717819.2:c.1088A>C	XP_006717882.1:p.Ter363Ser
XM_011539764.1:c.1169A>C	XP_011538066.1:p.Ter390Ser
XM_011539765.1:c.1106A>C	XP_011538067.1:p.Ter369Ser
XM_011539766.1:c.1088A>C	XP_011538068.1:p.Ter363Ser
XM_011539767.1:c.1052A>C	XP_011538069.1:p.Ter351Ser
XR_945733.1:n.1012A>C
NM_000043.5:c.1007A>C	NP_000034.1:p.Ter336Ser
NM_001320619.1:c.*330A>C	NP_001307548.1:n.*330A>C
NM_152871.3:c.944A>C	NP_690610.1:p.Ter315Ser
NM_152872.3:c.*319A>C	NP_690611.1:n.*319A>C
NR_028033.3:n.1153A>C
NR_028034.3:n.1015A>C
NR_028035.3:n.1078A>C
NR_028036.3:n.1216A>C
NR_135313.1:n.1133A>C
NR_135314.1:n.1316A>C
NR_135315.1:n.1069A>C
XM_006717819.3:c.1088A>C	XP_006717882.1:p.Ter363Ser
XM_011539764.2:c.1169A>C	XP_011538066.1:p.Ter390Ser
XM_011539765.2:c.1106A>C	XP_011538067.1:p.Ter369Ser
XM_011539766.2:c.1088A>C	XP_011538068.1:p.Ter363Ser
XM_011539767.3:c.1052A>C	XP_011538069.1:p.Ter351Ser
XR_945732.3:n.1075A>C
XR_945733.2:n.1012A>C
NM_000043.6:c.1007A>C MANE Select	NP_000034.1:p.Ter336Ser
NM_001320619.2:c.*330A>C	NP_001307548.1:n.*330A>C
NM_152871.4:c.944A>C	NP_690610.1:p.Ter315Ser
NM_152872.4:c.*319A>C	NP_690611.1:n.*319A>C
NR_028033.4:n.914A>C
NR_028034.4:n.776A>C
NR_028035.4:n.839A>C
NR_028036.4:n.977A>C
NR_135313.2:n.894A>C
NR_135314.2:n.1173A>C
NR_135315.2:n.926A>C