Canonical Allele Identifier: CA377509797

Gene: FAS

Linked Data

• dbSNP Id: rs2119446013
• MyVariant Identifiers: chr10:g.90773981A>T (hg19) ; chr10:g.89014224A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014224A>T , CM000672.2:g.89014224A>T	GRCh38
NC_000010.10:g.90773981A>T , CM000672.1:g.90773981A>T	GRCh37
NC_000010.9:g.90763961A>T	NCBI36
NG_009089.2:g.28694A>T , LRG_134:g.28694A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1091A>T
ENST00000355740.8:c.*105A>T	ENSP00000347979.3:n.*105A>T
ENST00000357339.7:c.719A>T	ENSP00000349896.2:p.Glu240Val
ENST00000371857.8:n.2327A>T
ENST00000460510.6:c.65A>T	ENSP00000512812.1:p.Glu22Val
ENST00000466081.6:n.2431A>T
ENST00000477270.6:c.827A>T	ENSP00000512813.1:p.Glu276Val
ENST00000479522.6:c.*211A>T	ENSP00000424113.1:n.*211A>T
ENST00000484444.6:c.*223A>T	ENSP00000420975.1:n.*223A>T
ENST00000488877.6:c.673A>T	ENSP00000425159.1:n.673A>T
ENST00000492756.7:c.*211A>T	ENSP00000422453.1:n.*211A>T
ENST00000494799.6:c.65A>T	ENSP00000512834.1:p.Glu22Val
ENST00000562983.3:c.65A>T	ENSP00000512845.1:p.Glu22Val
ENST00000612663.6:c.*184A>T	ENSP00000477997.3:n.*184A>T
ENST00000640140.2:n.927A>T
ENST00000640250.2:n.281A>T
ENST00000640681.2:n.886A>T
ENST00000696723.1:n.4415A>T
ENST00000696741.1:n.2420A>T
ENST00000696742.1:n.2147A>T
ENST00000696743.1:n.3550A>T
ENST00000696744.1:n.821A>T
ENST00000696767.1:n.1116A>T
ENST00000696768.1:c.*105A>T	ENSP00000512859.1:n.*105A>T
ENST00000696769.1:n.2471A>T
ENST00000696771.1:c.65A>T	ENSP00000512860.1:p.Glu22Val
ENST00000696772.1:n.2385A>T
ENST00000696773.1:n.2124A>T
ENST00000696774.1:n.5892A>T
ENST00000696776.1:c.875A>T	ENSP00000512861.1:p.Glu292Val
ENST00000696777.1:n.2190A>T
ENST00000696778.1:n.1218A>T
ENST00000696779.1:c.389A>T	ENSP00000512862.1:p.Glu130Val
ENST00000696780.1:c.812A>T	ENSP00000512863.1:p.Glu271Val
ENST00000696781.1:c.527A>T	ENSP00000512864.1:p.Glu176Val
ENST00000696782.1:c.*184A>T	ENSP00000512865.1:n.*184A>T
ENST00000696783.1:n.2650A>T
ENST00000696992.1:n.1899A>T
ENST00000696995.1:n.4311A>T
ENST00000696996.1:n.2224A>T
ENST00000696997.1:c.*412A>T	ENSP00000513028.1:n.*412A>T
ENST00000696998.1:n.2036A>T
ENST00000696999.1:c.65A>T	ENSP00000513029.1:p.Glu22Val
ENST00000697035.1:c.*115A>T	ENSP00000513059.1:n.*115A>T
ENST00000697036.1:c.*198A>T	ENSP00000513060.1:n.*198A>T
ENST00000697037.1:n.817A>T
ENST00000697093.1:n.3018A>T
ENST00000697094.1:n.3365A>T
ENST00000697095.1:c.*1983A>T	ENSP00000513104.1:n.*1983A>T
ENST00000697096.1:n.1915A>T
ENST00000697097.1:c.65A>T	ENSP00000513105.1:p.Glu22Val
ENST00000562983.2:n.968A>T
ENST00000690268.1:c.863A>T	ENSP00000509810.1:p.Glu288Val
ENST00000355740.7:c.*108A>T	ENSP00000347979.3:n.*108A>T
ENST00000612663.5:c.*184A>T	ENSP00000477997.3:n.*184A>T
ENST00000640140.1:n.954A>T
ENST00000640250.1:n.281A>T
ENST00000640681.1:n.903A>T
ENST00000652046.1:c.782A>T MANE Select	ENSP00000498466.1:p.Glu261Val
ENST00000352159.8:c.*99A>T	ENSP00000345601.4:n.*99A>T
ENST00000355279.2:c.757A>T	ENSP00000347426.2:n.757A>T
ENST00000355740.6:c.782A>T	ENSP00000347979.2:p.Glu261Val
ENST00000357339.6:c.719A>T	ENSP00000349896.2:p.Glu240Val
ENST00000479522.5:c.*211A>T	ENSP00000424113.1:n.*211A>T
ENST00000484444.5:c.*223A>T	ENSP00000420975.1:n.*223A>T
ENST00000488877.5:c.*223A>T	ENSP00000425159.1:n.*223A>T
ENST00000492756.5:c.610A>T	ENSP00000422453.1:n.610A>T
ENST00000494410.5:c.*140A>T	ENSP00000423755.1:n.*140A>T
ENST00000612663.4:c.*129A>T	ENSP00000477997.2:n.*129A>T
NM_000043.4:c.782A>T , LRG_134t1:c.782A>T	NP_000034.1:p.Glu261Val
NM_152871.2:c.719A>T	NP_690610.1:p.Glu240Val
NM_152872.2:c.*94A>T	NP_690611.1:n.*94A>T
NR_028033.2:n.956A>T
NR_028034.2:n.818A>T
NR_028035.2:n.881A>T
NR_028036.2:n.1019A>T
XM_006717819.2:c.863A>T	XP_006717882.1:p.Glu288Val
XM_011539764.1:c.944A>T	XP_011538066.1:p.Glu315Val
XM_011539765.1:c.881A>T	XP_011538067.1:p.Glu294Val
XM_011539766.1:c.863A>T	XP_011538068.1:p.Glu288Val
XM_011539767.1:c.827A>T	XP_011538069.1:p.Glu276Val
XR_945732.1:n.850A>T
XR_945733.1:n.787A>T
NM_000043.5:c.782A>T	NP_000034.1:p.Glu261Val
NM_001320619.1:c.*105A>T	NP_001307548.1:n.*105A>T
NM_152871.3:c.719A>T	NP_690610.1:p.Glu240Val
NM_152872.3:c.*94A>T	NP_690611.1:n.*94A>T
NR_028033.3:n.928A>T
NR_028034.3:n.790A>T
NR_028035.3:n.853A>T
NR_028036.3:n.991A>T
NR_135313.1:n.908A>T
NR_135314.1:n.1091A>T
NR_135315.1:n.844A>T
XM_006717819.3:c.863A>T	XP_006717882.1:p.Glu288Val
XM_011539764.2:c.944A>T	XP_011538066.1:p.Glu315Val
XM_011539765.2:c.881A>T	XP_011538067.1:p.Glu294Val
XM_011539766.2:c.863A>T	XP_011538068.1:p.Glu288Val
XM_011539767.3:c.827A>T	XP_011538069.1:p.Glu276Val
XR_945732.3:n.850A>T
XR_945733.2:n.787A>T
NM_000043.6:c.782A>T MANE Select	NP_000034.1:p.Glu261Val
NM_001320619.2:c.*105A>T	NP_001307548.1:n.*105A>T
NM_152871.4:c.719A>T	NP_690610.1:p.Glu240Val
NM_152872.4:c.*94A>T	NP_690611.1:n.*94A>T
NR_028033.4:n.689A>T
NR_028034.4:n.551A>T
NR_028035.4:n.614A>T
NR_028036.4:n.752A>T
NR_135313.2:n.669A>T
NR_135314.2:n.948A>T
NR_135315.2:n.701A>T