Canonical Allele Identifier: CA377510099

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774112A>T (hg19) ; chr10:g.89014355A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014355A>T , CM000672.2:g.89014355A>T	GRCh38
NC_000010.10:g.90774112A>T , CM000672.1:g.90774112A>T	GRCh37
NC_000010.9:g.90764092A>T	NCBI36
NG_009089.2:g.28825A>T , LRG_134:g.28825A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1222A>T
ENST00000355740.8:c.*236A>T	ENSP00000347979.3:n.*236A>T
ENST00000357339.7:c.850A>T	ENSP00000349896.2:p.Thr284Ser
ENST00000371857.8:n.2458A>T
ENST00000460510.6:c.196A>T	ENSP00000512812.1:p.Thr66Ser
ENST00000466081.6:n.2562A>T
ENST00000477270.6:c.958A>T	ENSP00000512813.1:p.Thr320Ser
ENST00000479522.6:c.*342A>T	ENSP00000424113.1:n.*342A>T
ENST00000484444.6:c.*354A>T	ENSP00000420975.1:n.*354A>T
ENST00000488877.6:c.804A>T	ENSP00000425159.1:n.804A>T
ENST00000492756.7:c.*342A>T	ENSP00000422453.1:n.*342A>T
ENST00000494799.6:c.196A>T	ENSP00000512834.1:p.Thr66Ser
ENST00000562983.3:c.196A>T	ENSP00000512845.1:p.Thr66Ser
ENST00000612663.6:c.*315A>T	ENSP00000477997.3:n.*315A>T
ENST00000640140.2:n.1058A>T
ENST00000640250.2:n.412A>T
ENST00000640681.2:n.1017A>T
ENST00000696723.1:n.4546A>T
ENST00000696741.1:n.2551A>T
ENST00000696742.1:n.2278A>T
ENST00000696743.1:n.3681A>T
ENST00000696744.1:n.952A>T
ENST00000696767.1:n.1247A>T
ENST00000696768.1:c.*236A>T	ENSP00000512859.1:n.*236A>T
ENST00000696769.1:n.2602A>T
ENST00000696771.1:c.196A>T	ENSP00000512860.1:p.Thr66Ser
ENST00000696772.1:n.2516A>T
ENST00000696773.1:n.2255A>T
ENST00000696774.1:n.6023A>T
ENST00000696776.1:c.1006A>T	ENSP00000512861.1:p.Thr336Ser
ENST00000696777.1:n.2321A>T
ENST00000696778.1:n.1349A>T
ENST00000696779.1:c.520A>T	ENSP00000512862.1:p.Thr174Ser
ENST00000696780.1:c.943A>T	ENSP00000512863.1:p.Thr315Ser
ENST00000696781.1:c.658A>T	ENSP00000512864.1:p.Thr220Ser
ENST00000696782.1:c.*315A>T	ENSP00000512865.1:n.*315A>T
ENST00000696783.1:n.2781A>T
ENST00000696992.1:n.2030A>T
ENST00000696995.1:n.4442A>T
ENST00000696996.1:n.2355A>T
ENST00000696997.1:c.*543A>T	ENSP00000513028.1:n.*543A>T
ENST00000696998.1:n.2167A>T
ENST00000696999.1:c.196A>T	ENSP00000513029.1:p.Thr66Ser
ENST00000697036.1:c.*329A>T	ENSP00000513060.1:n.*329A>T
ENST00000697037.1:n.948A>T
ENST00000697093.1:n.3149A>T
ENST00000697094.1:n.3496A>T
ENST00000697095.1:c.*2114A>T	ENSP00000513104.1:n.*2114A>T
ENST00000697096.1:n.2046A>T
ENST00000697097.1:c.196A>T	ENSP00000513105.1:p.Thr66Ser
ENST00000562983.2:n.1099A>T
ENST00000690268.1:c.994A>T	ENSP00000509810.1:p.Thr332Ser
ENST00000355740.7:c.*239A>T	ENSP00000347979.3:n.*239A>T
ENST00000612663.5:c.*315A>T	ENSP00000477997.3:n.*315A>T
ENST00000640140.1:n.1085A>T
ENST00000640250.1:n.412A>T
ENST00000640681.1:n.1034A>T
ENST00000652046.1:c.913A>T MANE Select	ENSP00000498466.1:p.Thr305Ser
ENST00000352159.8:c.*230A>T	ENSP00000345601.4:n.*230A>T
ENST00000355279.2:c.888A>T	ENSP00000347426.2:n.888A>T
ENST00000355740.6:c.913A>T	ENSP00000347979.2:p.Thr305Ser
ENST00000357339.6:c.850A>T	ENSP00000349896.2:p.Thr284Ser
ENST00000479522.5:c.*342A>T	ENSP00000424113.1:n.*342A>T
ENST00000484444.5:c.*354A>T	ENSP00000420975.1:n.*354A>T
ENST00000488877.5:c.*354A>T	ENSP00000425159.1:n.*354A>T
ENST00000492756.5:c.741A>T	ENSP00000422453.1:n.741A>T
ENST00000494410.5:c.*271A>T	ENSP00000423755.1:n.*271A>T
ENST00000612663.4:c.*260A>T	ENSP00000477997.2:n.*260A>T
NM_000043.4:c.913A>T , LRG_134t1:c.913A>T	NP_000034.1:p.Thr305Ser
NM_152871.2:c.850A>T	NP_690610.1:p.Thr284Ser
NM_152872.2:c.*225A>T	NP_690611.1:n.*225A>T
NR_028033.2:n.1087A>T
NR_028034.2:n.949A>T
NR_028035.2:n.1012A>T
NR_028036.2:n.1150A>T
XM_006717819.2:c.994A>T	XP_006717882.1:p.Thr332Ser
XM_011539764.1:c.1075A>T	XP_011538066.1:p.Thr359Ser
XM_011539765.1:c.1012A>T	XP_011538067.1:p.Thr338Ser
XM_011539766.1:c.994A>T	XP_011538068.1:p.Thr332Ser
XM_011539767.1:c.958A>T	XP_011538069.1:p.Thr320Ser
XR_945732.1:n.981A>T
XR_945733.1:n.918A>T
NM_000043.5:c.913A>T	NP_000034.1:p.Thr305Ser
NM_001320619.1:c.*236A>T	NP_001307548.1:n.*236A>T
NM_152871.3:c.850A>T	NP_690610.1:p.Thr284Ser
NM_152872.3:c.*225A>T	NP_690611.1:n.*225A>T
NR_028033.3:n.1059A>T
NR_028034.3:n.921A>T
NR_028035.3:n.984A>T
NR_028036.3:n.1122A>T
NR_135313.1:n.1039A>T
NR_135314.1:n.1222A>T
NR_135315.1:n.975A>T
XM_006717819.3:c.994A>T	XP_006717882.1:p.Thr332Ser
XM_011539764.2:c.1075A>T	XP_011538066.1:p.Thr359Ser
XM_011539765.2:c.1012A>T	XP_011538067.1:p.Thr338Ser
XM_011539766.2:c.994A>T	XP_011538068.1:p.Thr332Ser
XM_011539767.3:c.958A>T	XP_011538069.1:p.Thr320Ser
XR_945732.3:n.981A>T
XR_945733.2:n.918A>T
NM_000043.6:c.913A>T MANE Select	NP_000034.1:p.Thr305Ser
NM_001320619.2:c.*236A>T	NP_001307548.1:n.*236A>T
NM_152871.4:c.850A>T	NP_690610.1:p.Thr284Ser
NM_152872.4:c.*225A>T	NP_690611.1:n.*225A>T
NR_028033.4:n.820A>T
NR_028034.4:n.682A>T
NR_028035.4:n.745A>T
NR_028036.4:n.883A>T
NR_135313.2:n.800A>T
NR_135314.2:n.1079A>T
NR_135315.2:n.832A>T