Canonical Allele Identifier: CA377509969

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774055G>T (hg19) ; chr10:g.89014298G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014298G>T , CM000672.2:g.89014298G>T	GRCh38
NC_000010.10:g.90774055G>T , CM000672.1:g.90774055G>T	GRCh37
NC_000010.9:g.90764035G>T	NCBI36
NG_009089.2:g.28768G>T , LRG_134:g.28768G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1165G>T
ENST00000355740.8:c.*179G>T	ENSP00000347979.3:n.*179G>T
ENST00000357339.7:c.793G>T	ENSP00000349896.2:p.Gly265Ter
ENST00000371857.8:n.2401G>T
ENST00000460510.6:c.139G>T	ENSP00000512812.1:p.Gly47Ter
ENST00000466081.6:n.2505G>T
ENST00000477270.6:c.901G>T	ENSP00000512813.1:p.Gly301Ter
ENST00000479522.6:c.*285G>T	ENSP00000424113.1:n.*285G>T
ENST00000484444.6:c.*297G>T	ENSP00000420975.1:n.*297G>T
ENST00000488877.6:c.747G>T	ENSP00000425159.1:n.747G>T
ENST00000492756.7:c.*285G>T	ENSP00000422453.1:n.*285G>T
ENST00000494799.6:c.139G>T	ENSP00000512834.1:p.Gly47Ter
ENST00000562983.3:c.139G>T	ENSP00000512845.1:p.Gly47Ter
ENST00000612663.6:c.*258G>T	ENSP00000477997.3:n.*258G>T
ENST00000640140.2:n.1001G>T
ENST00000640250.2:n.355G>T
ENST00000640681.2:n.960G>T
ENST00000696723.1:n.4489G>T
ENST00000696741.1:n.2494G>T
ENST00000696742.1:n.2221G>T
ENST00000696743.1:n.3624G>T
ENST00000696744.1:n.895G>T
ENST00000696767.1:n.1190G>T
ENST00000696768.1:c.*179G>T	ENSP00000512859.1:n.*179G>T
ENST00000696769.1:n.2545G>T
ENST00000696771.1:c.139G>T	ENSP00000512860.1:p.Gly47Ter
ENST00000696772.1:n.2459G>T
ENST00000696773.1:n.2198G>T
ENST00000696774.1:n.5966G>T
ENST00000696776.1:c.949G>T	ENSP00000512861.1:p.Gly317Ter
ENST00000696777.1:n.2264G>T
ENST00000696778.1:n.1292G>T
ENST00000696779.1:c.463G>T	ENSP00000512862.1:p.Gly155Ter
ENST00000696780.1:c.886G>T	ENSP00000512863.1:p.Gly296Ter
ENST00000696781.1:c.601G>T	ENSP00000512864.1:p.Gly201Ter
ENST00000696782.1:c.*258G>T	ENSP00000512865.1:n.*258G>T
ENST00000696783.1:n.2724G>T
ENST00000696992.1:n.1973G>T
ENST00000696995.1:n.4385G>T
ENST00000696996.1:n.2298G>T
ENST00000696997.1:c.*486G>T	ENSP00000513028.1:n.*486G>T
ENST00000696998.1:n.2110G>T
ENST00000696999.1:c.139G>T	ENSP00000513029.1:p.Gly47Ter
ENST00000697035.1:c.*189G>T	ENSP00000513059.1:n.*189G>T
ENST00000697036.1:c.*272G>T	ENSP00000513060.1:n.*272G>T
ENST00000697037.1:n.891G>T
ENST00000697093.1:n.3092G>T
ENST00000697094.1:n.3439G>T
ENST00000697095.1:c.*2057G>T	ENSP00000513104.1:n.*2057G>T
ENST00000697096.1:n.1989G>T
ENST00000697097.1:c.139G>T	ENSP00000513105.1:p.Gly47Ter
ENST00000562983.2:n.1042G>T
ENST00000690268.1:c.937G>T	ENSP00000509810.1:p.Gly313Ter
ENST00000355740.7:c.*182G>T	ENSP00000347979.3:n.*182G>T
ENST00000612663.5:c.*258G>T	ENSP00000477997.3:n.*258G>T
ENST00000640140.1:n.1028G>T
ENST00000640250.1:n.355G>T
ENST00000640681.1:n.977G>T
ENST00000652046.1:c.856G>T MANE Select	ENSP00000498466.1:p.Gly286Ter
ENST00000352159.8:c.*173G>T	ENSP00000345601.4:n.*173G>T
ENST00000355279.2:c.831G>T	ENSP00000347426.2:n.831G>T
ENST00000355740.6:c.856G>T	ENSP00000347979.2:p.Gly286Ter
ENST00000357339.6:c.793G>T	ENSP00000349896.2:p.Gly265Ter
ENST00000479522.5:c.*285G>T	ENSP00000424113.1:n.*285G>T
ENST00000484444.5:c.*297G>T	ENSP00000420975.1:n.*297G>T
ENST00000488877.5:c.*297G>T	ENSP00000425159.1:n.*297G>T
ENST00000492756.5:c.684G>T	ENSP00000422453.1:n.684G>T
ENST00000494410.5:c.*214G>T	ENSP00000423755.1:n.*214G>T
ENST00000612663.4:c.*203G>T	ENSP00000477997.2:n.*203G>T
NM_000043.4:c.856G>T , LRG_134t1:c.856G>T	NP_000034.1:p.Gly286Ter
NM_152871.2:c.793G>T	NP_690610.1:p.Gly265Ter
NM_152872.2:c.*168G>T	NP_690611.1:n.*168G>T
NR_028033.2:n.1030G>T
NR_028034.2:n.892G>T
NR_028035.2:n.955G>T
NR_028036.2:n.1093G>T
XM_006717819.2:c.937G>T	XP_006717882.1:p.Gly313Ter
XM_011539764.1:c.1018G>T	XP_011538066.1:p.Gly340Ter
XM_011539765.1:c.955G>T	XP_011538067.1:p.Gly319Ter
XM_011539766.1:c.937G>T	XP_011538068.1:p.Gly313Ter
XM_011539767.1:c.901G>T	XP_011538069.1:p.Gly301Ter
XR_945732.1:n.924G>T
XR_945733.1:n.861G>T
NM_000043.5:c.856G>T	NP_000034.1:p.Gly286Ter
NM_001320619.1:c.*179G>T	NP_001307548.1:n.*179G>T
NM_152871.3:c.793G>T	NP_690610.1:p.Gly265Ter
NM_152872.3:c.*168G>T	NP_690611.1:n.*168G>T
NR_028033.3:n.1002G>T
NR_028034.3:n.864G>T
NR_028035.3:n.927G>T
NR_028036.3:n.1065G>T
NR_135313.1:n.982G>T
NR_135314.1:n.1165G>T
NR_135315.1:n.918G>T
XM_006717819.3:c.937G>T	XP_006717882.1:p.Gly313Ter
XM_011539764.2:c.1018G>T	XP_011538066.1:p.Gly340Ter
XM_011539765.2:c.955G>T	XP_011538067.1:p.Gly319Ter
XM_011539766.2:c.937G>T	XP_011538068.1:p.Gly313Ter
XM_011539767.3:c.901G>T	XP_011538069.1:p.Gly301Ter
XR_945732.3:n.924G>T
XR_945733.2:n.861G>T
NM_000043.6:c.856G>T MANE Select	NP_000034.1:p.Gly286Ter
NM_001320619.2:c.*179G>T	NP_001307548.1:n.*179G>T
NM_152871.4:c.793G>T	NP_690610.1:p.Gly265Ter
NM_152872.4:c.*168G>T	NP_690611.1:n.*168G>T
NR_028033.4:n.763G>T
NR_028034.4:n.625G>T
NR_028035.4:n.688G>T
NR_028036.4:n.826G>T
NR_135313.2:n.743G>T
NR_135314.2:n.1022G>T
NR_135315.2:n.775G>T