Canonical Allele Identifier: CA377510060

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774095A>T (hg19) ; chr10:g.89014338A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014338A>T , CM000672.2:g.89014338A>T	GRCh38
NC_000010.10:g.90774095A>T , CM000672.1:g.90774095A>T	GRCh37
NC_000010.9:g.90764075A>T	NCBI36
NG_009089.2:g.28808A>T , LRG_134:g.28808A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1205A>T
ENST00000355740.8:c.*219A>T	ENSP00000347979.3:n.*219A>T
ENST00000357339.7:c.833A>T	ENSP00000349896.2:p.Lys278Ile
ENST00000371857.8:n.2441A>T
ENST00000460510.6:c.179A>T	ENSP00000512812.1:p.Lys60Ile
ENST00000466081.6:n.2545A>T
ENST00000477270.6:c.941A>T	ENSP00000512813.1:p.Lys314Ile
ENST00000479522.6:c.*325A>T	ENSP00000424113.1:n.*325A>T
ENST00000484444.6:c.*337A>T	ENSP00000420975.1:n.*337A>T
ENST00000488877.6:c.787A>T	ENSP00000425159.1:n.787A>T
ENST00000492756.7:c.*325A>T	ENSP00000422453.1:n.*325A>T
ENST00000494799.6:c.179A>T	ENSP00000512834.1:p.Lys60Ile
ENST00000562983.3:c.179A>T	ENSP00000512845.1:p.Lys60Ile
ENST00000612663.6:c.*298A>T	ENSP00000477997.3:n.*298A>T
ENST00000640140.2:n.1041A>T
ENST00000640250.2:n.395A>T
ENST00000640681.2:n.1000A>T
ENST00000696723.1:n.4529A>T
ENST00000696741.1:n.2534A>T
ENST00000696742.1:n.2261A>T
ENST00000696743.1:n.3664A>T
ENST00000696744.1:n.935A>T
ENST00000696767.1:n.1230A>T
ENST00000696768.1:c.*219A>T	ENSP00000512859.1:n.*219A>T
ENST00000696769.1:n.2585A>T
ENST00000696771.1:c.179A>T	ENSP00000512860.1:p.Lys60Ile
ENST00000696772.1:n.2499A>T
ENST00000696773.1:n.2238A>T
ENST00000696774.1:n.6006A>T
ENST00000696776.1:c.989A>T	ENSP00000512861.1:p.Lys330Ile
ENST00000696777.1:n.2304A>T
ENST00000696778.1:n.1332A>T
ENST00000696779.1:c.503A>T	ENSP00000512862.1:p.Lys168Ile
ENST00000696780.1:c.926A>T	ENSP00000512863.1:p.Lys309Ile
ENST00000696781.1:c.641A>T	ENSP00000512864.1:p.Lys214Ile
ENST00000696782.1:c.*298A>T	ENSP00000512865.1:n.*298A>T
ENST00000696783.1:n.2764A>T
ENST00000696992.1:n.2013A>T
ENST00000696995.1:n.4425A>T
ENST00000696996.1:n.2338A>T
ENST00000696997.1:c.*526A>T	ENSP00000513028.1:n.*526A>T
ENST00000696998.1:n.2150A>T
ENST00000696999.1:c.179A>T	ENSP00000513029.1:p.Lys60Ile
ENST00000697036.1:c.*312A>T	ENSP00000513060.1:n.*312A>T
ENST00000697037.1:n.931A>T
ENST00000697093.1:n.3132A>T
ENST00000697094.1:n.3479A>T
ENST00000697095.1:c.*2097A>T	ENSP00000513104.1:n.*2097A>T
ENST00000697096.1:n.2029A>T
ENST00000697097.1:c.179A>T	ENSP00000513105.1:p.Lys60Ile
ENST00000562983.2:n.1082A>T
ENST00000690268.1:c.977A>T	ENSP00000509810.1:p.Lys326Ile
ENST00000355740.7:c.*222A>T	ENSP00000347979.3:n.*222A>T
ENST00000612663.5:c.*298A>T	ENSP00000477997.3:n.*298A>T
ENST00000640140.1:n.1068A>T
ENST00000640250.1:n.395A>T
ENST00000640681.1:n.1017A>T
ENST00000652046.1:c.896A>T MANE Select	ENSP00000498466.1:p.Lys299Ile
ENST00000352159.8:c.*213A>T	ENSP00000345601.4:n.*213A>T
ENST00000355279.2:c.871A>T	ENSP00000347426.2:n.871A>T
ENST00000355740.6:c.896A>T	ENSP00000347979.2:p.Lys299Ile
ENST00000357339.6:c.833A>T	ENSP00000349896.2:p.Lys278Ile
ENST00000479522.5:c.*325A>T	ENSP00000424113.1:n.*325A>T
ENST00000484444.5:c.*337A>T	ENSP00000420975.1:n.*337A>T
ENST00000488877.5:c.*337A>T	ENSP00000425159.1:n.*337A>T
ENST00000492756.5:c.724A>T	ENSP00000422453.1:n.724A>T
ENST00000494410.5:c.*254A>T	ENSP00000423755.1:n.*254A>T
ENST00000612663.4:c.*243A>T	ENSP00000477997.2:n.*243A>T
NM_000043.4:c.896A>T , LRG_134t1:c.896A>T	NP_000034.1:p.Lys299Ile
NM_152871.2:c.833A>T	NP_690610.1:p.Lys278Ile
NM_152872.2:c.*208A>T	NP_690611.1:n.*208A>T
NR_028033.2:n.1070A>T
NR_028034.2:n.932A>T
NR_028035.2:n.995A>T
NR_028036.2:n.1133A>T
XM_006717819.2:c.977A>T	XP_006717882.1:p.Lys326Ile
XM_011539764.1:c.1058A>T	XP_011538066.1:p.Lys353Ile
XM_011539765.1:c.995A>T	XP_011538067.1:p.Lys332Ile
XM_011539766.1:c.977A>T	XP_011538068.1:p.Lys326Ile
XM_011539767.1:c.941A>T	XP_011538069.1:p.Lys314Ile
XR_945732.1:n.964A>T
XR_945733.1:n.901A>T
NM_000043.5:c.896A>T	NP_000034.1:p.Lys299Ile
NM_001320619.1:c.*219A>T	NP_001307548.1:n.*219A>T
NM_152871.3:c.833A>T	NP_690610.1:p.Lys278Ile
NM_152872.3:c.*208A>T	NP_690611.1:n.*208A>T
NR_028033.3:n.1042A>T
NR_028034.3:n.904A>T
NR_028035.3:n.967A>T
NR_028036.3:n.1105A>T
NR_135313.1:n.1022A>T
NR_135314.1:n.1205A>T
NR_135315.1:n.958A>T
XM_006717819.3:c.977A>T	XP_006717882.1:p.Lys326Ile
XM_011539764.2:c.1058A>T	XP_011538066.1:p.Lys353Ile
XM_011539765.2:c.995A>T	XP_011538067.1:p.Lys332Ile
XM_011539766.2:c.977A>T	XP_011538068.1:p.Lys326Ile
XM_011539767.3:c.941A>T	XP_011538069.1:p.Lys314Ile
XR_945732.3:n.964A>T
XR_945733.2:n.901A>T
NM_000043.6:c.896A>T MANE Select	NP_000034.1:p.Lys299Ile
NM_001320619.2:c.*219A>T	NP_001307548.1:n.*219A>T
NM_152871.4:c.833A>T	NP_690610.1:p.Lys278Ile
NM_152872.4:c.*208A>T	NP_690611.1:n.*208A>T
NR_028033.4:n.803A>T
NR_028034.4:n.665A>T
NR_028035.4:n.728A>T
NR_028036.4:n.866A>T
NR_135313.2:n.783A>T
NR_135314.2:n.1062A>T
NR_135315.2:n.815A>T