Canonical Allele Identifier: CA669680029

Gene: FAS

Linked Data

• dbSNP Id: rs1359225405
• MyVariant Identifiers: chr10:g.90774303G>A (hg19) ; chr10:g.89014546G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014546G>A , CM000672.2:g.89014546G>A	GRCh38
NC_000010.10:g.90774303G>A , CM000672.1:g.90774303G>A	GRCh37
NC_000010.9:g.90764283G>A	NCBI36
NG_009089.2:g.29016G>A , LRG_134:g.29016G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1413G>A
ENST00000355740.8:c.*427G>A	ENSP00000347979.3:n.*427G>A
ENST00000357339.7:c.*96G>A	ENSP00000349896.2:n.*96G>A
ENST00000371857.8:n.2649G>A
ENST00000460510.6:c.*96G>A	ENSP00000512812.1:n.*96G>A
ENST00000466081.6:n.2753G>A
ENST00000477270.6:c.*96G>A	ENSP00000512813.1:n.*96G>A
ENST00000479522.6:c.*533G>A	ENSP00000424113.1:n.*533G>A
ENST00000484444.6:c.*545G>A	ENSP00000420975.1:n.*545G>A
ENST00000488877.6:c.995G>A	ENSP00000425159.1:n.995G>A
ENST00000492756.7:c.*533G>A	ENSP00000422453.1:n.*533G>A
ENST00000494799.6:c.*96G>A	ENSP00000512834.1:n.*96G>A
ENST00000562983.3:c.*96G>A	ENSP00000512845.1:n.*96G>A
ENST00000612663.6:c.*506G>A	ENSP00000477997.3:n.*506G>A
ENST00000640140.2:n.1249G>A
ENST00000640250.2:n.603G>A
ENST00000640681.2:n.1208G>A
ENST00000696723.1:n.4737G>A
ENST00000696741.1:n.2742G>A
ENST00000696742.1:n.2469G>A
ENST00000696743.1:n.3872G>A
ENST00000696744.1:n.1143G>A
ENST00000696767.1:n.1438G>A
ENST00000696768.1:c.*427G>A	ENSP00000512859.1:n.*427G>A
ENST00000696769.1:n.2793G>A
ENST00000696771.1:c.*96G>A	ENSP00000512860.1:n.*96G>A
ENST00000696772.1:n.2707G>A
ENST00000696773.1:n.2446G>A
ENST00000696774.1:n.6214G>A
ENST00000696776.1:c.*96G>A	ENSP00000512861.1:n.*96G>A
ENST00000696777.1:n.2512G>A
ENST00000696778.1:n.1540G>A
ENST00000696779.1:c.*96G>A	ENSP00000512862.1:n.*96G>A
ENST00000696780.1:c.*96G>A	ENSP00000512863.1:n.*96G>A
ENST00000696781.1:c.*96G>A	ENSP00000512864.1:n.*96G>A
ENST00000696782.1:c.*506G>A	ENSP00000512865.1:n.*506G>A
ENST00000696783.1:n.2972G>A
ENST00000696992.1:n.2221G>A
ENST00000696995.1:n.4633G>A
ENST00000696996.1:n.2546G>A
ENST00000696997.1:c.*734G>A	ENSP00000513028.1:n.*734G>A
ENST00000696998.1:n.2358G>A
ENST00000696999.1:c.*96G>A	ENSP00000513029.1:n.*96G>A
ENST00000697036.1:c.*520G>A	ENSP00000513060.1:n.*520G>A
ENST00000697037.1:n.1139G>A
ENST00000697093.1:n.3340G>A
ENST00000697094.1:n.3687G>A
ENST00000697095.1:c.*2305G>A	ENSP00000513104.1:n.*2305G>A
ENST00000697096.1:n.2237G>A
ENST00000697097.1:c.*96G>A	ENSP00000513105.1:n.*96G>A
ENST00000562983.2:n.1290G>A
ENST00000690268.1:c.*96G>A	ENSP00000509810.1:n.*96G>A
ENST00000355740.7:c.*430G>A	ENSP00000347979.3:n.*430G>A
ENST00000640140.1:n.1276G>A
ENST00000640250.1:n.603G>A
ENST00000640681.1:n.1225G>A
ENST00000652046.1:c.*96G>A MANE Select	ENSP00000498466.1:n.*96G>A
ENST00000352159.8:c.*421G>A	ENSP00000345601.4:n.*421G>A
ENST00000355740.6:c.*96G>A	ENSP00000347979.2:n.*96G>A
ENST00000479522.5:c.*533G>A	ENSP00000424113.1:n.*533G>A
ENST00000484444.5:c.*545G>A	ENSP00000420975.1:n.*545G>A
ENST00000494410.5:c.*462G>A	ENSP00000423755.1:n.*462G>A
NM_000043.4:c.*96G>A , LRG_134t1:c.*96G>A	NP_000034.1:n.*96G>A
NM_152871.2:c.*96G>A	NP_690610.1:n.*96G>A
NM_152872.2:c.*416G>A	NP_690611.1:n.*416G>A
NR_028033.2:n.1278G>A
NR_028034.2:n.1140G>A
NR_028035.2:n.1203G>A
NR_028036.2:n.1341G>A
XM_006717819.2:c.*96G>A	XP_006717882.1:n.*96G>A
XM_011539764.1:c.*96G>A	XP_011538066.1:n.*96G>A
XM_011539765.1:c.*96G>A	XP_011538067.1:n.*96G>A
XM_011539766.1:c.*96G>A	XP_011538068.1:n.*96G>A
XM_011539767.1:c.*96G>A	XP_011538069.1:n.*96G>A
NM_000043.5:c.*96G>A	NP_000034.1:n.*96G>A
NM_001320619.1:c.*427G>A	NP_001307548.1:n.*427G>A
NM_152871.3:c.*96G>A	NP_690610.1:n.*96G>A
NM_152872.3:c.*416G>A	NP_690611.1:n.*416G>A
NR_028033.3:n.1250G>A
NR_028034.3:n.1112G>A
NR_028035.3:n.1175G>A
NR_028036.3:n.1313G>A
NR_135313.1:n.1230G>A
NR_135314.1:n.1413G>A
NR_135315.1:n.1166G>A
XM_006717819.3:c.*96G>A	XP_006717882.1:n.*96G>A
XM_011539764.2:c.*96G>A	XP_011538066.1:n.*96G>A
XM_011539765.2:c.*96G>A	XP_011538067.1:n.*96G>A
XM_011539766.2:c.*96G>A	XP_011538068.1:n.*96G>A
XM_011539767.3:c.*96G>A	XP_011538069.1:n.*96G>A
XR_945732.3:n.1172G>A
XR_945733.2:n.1109G>A
NM_000043.6:c.*96G>A MANE Select	NP_000034.1:n.*96G>A
NM_001320619.2:c.*427G>A	NP_001307548.1:n.*427G>A
NM_152871.4:c.*96G>A	NP_690610.1:n.*96G>A
NM_152872.4:c.*416G>A	NP_690611.1:n.*416G>A
NR_028033.4:n.1011G>A
NR_028034.4:n.873G>A
NR_028035.4:n.936G>A
NR_028036.4:n.1074G>A
NR_135313.2:n.991G>A
NR_135314.2:n.1270G>A
NR_135315.2:n.1023G>A