Canonical Allele Identifier: CA377509550

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773885T>G (hg19) ; chr10:g.89014128T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014128T>G , CM000672.2:g.89014128T>G	GRCh38
NC_000010.10:g.90773885T>G , CM000672.1:g.90773885T>G	GRCh37
NC_000010.9:g.90763865T>G	NCBI36
NG_009089.2:g.28598T>G , LRG_134:g.28598T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.995T>G
ENST00000355740.8:c.*9T>G	ENSP00000347979.3:n.*9T>G
ENST00000357339.7:c.623T>G	ENSP00000349896.2:p.Leu208Trp
ENST00000371857.8:n.2231T>G
ENST00000460510.6:c.-32T>G	ENSP00000512812.1:n.-32T>G
ENST00000466081.6:n.2335T>G
ENST00000477270.6:c.731T>G	ENSP00000512813.1:p.Leu244Trp
ENST00000479522.6:c.*115T>G	ENSP00000424113.1:n.*115T>G
ENST00000484444.6:c.*127T>G	ENSP00000420975.1:n.*127T>G
ENST00000488877.6:c.577T>G	ENSP00000425159.1:n.577T>G
ENST00000492756.7:c.*115T>G	ENSP00000422453.1:n.*115T>G
ENST00000494799.6:c.-32T>G	ENSP00000512834.1:n.-32T>G
ENST00000562983.3:c.-32T>G	ENSP00000512845.1:n.-32T>G
ENST00000612663.6:c.*88T>G	ENSP00000477997.3:n.*88T>G
ENST00000640140.2:n.831T>G
ENST00000640250.2:n.185T>G
ENST00000640681.2:n.790T>G
ENST00000696723.1:n.4319T>G
ENST00000696741.1:n.2324T>G
ENST00000696742.1:n.2051T>G
ENST00000696743.1:n.3454T>G
ENST00000696744.1:n.725T>G
ENST00000696767.1:n.1020T>G
ENST00000696768.1:c.*9T>G	ENSP00000512859.1:n.*9T>G
ENST00000696769.1:n.2375T>G
ENST00000696771.1:c.-32T>G	ENSP00000512860.1:n.-32T>G
ENST00000696772.1:n.2289T>G
ENST00000696773.1:n.2028T>G
ENST00000696774.1:n.5796T>G
ENST00000696776.1:c.779T>G	ENSP00000512861.1:p.Leu260Trp
ENST00000696777.1:n.2094T>G
ENST00000696778.1:n.1122T>G
ENST00000696779.1:c.293T>G	ENSP00000512862.1:p.Leu98Trp
ENST00000696780.1:c.716T>G	ENSP00000512863.1:p.Leu239Trp
ENST00000696781.1:c.431T>G	ENSP00000512864.1:p.Leu144Trp
ENST00000696782.1:c.*88T>G	ENSP00000512865.1:n.*88T>G
ENST00000696783.1:n.2554T>G
ENST00000696992.1:n.1803T>G
ENST00000696995.1:n.4215T>G
ENST00000696996.1:n.2128T>G
ENST00000696997.1:c.*316T>G	ENSP00000513028.1:n.*316T>G
ENST00000696998.1:n.1940T>G
ENST00000696999.1:c.-32T>G	ENSP00000513029.1:n.-32T>G
ENST00000697035.1:c.*19T>G	ENSP00000513059.1:n.*19T>G
ENST00000697036.1:c.*102T>G	ENSP00000513060.1:n.*102T>G
ENST00000697037.1:n.721T>G
ENST00000697093.1:n.2922T>G
ENST00000697094.1:n.3269T>G
ENST00000697095.1:c.*1887T>G	ENSP00000513104.1:n.*1887T>G
ENST00000697096.1:n.1819T>G
ENST00000697097.1:c.-32T>G	ENSP00000513105.1:n.-32T>G
ENST00000562983.2:n.872T>G
ENST00000690268.1:c.767T>G	ENSP00000509810.1:p.Leu256Trp
ENST00000355740.7:c.*12T>G	ENSP00000347979.3:n.*12T>G
ENST00000612663.5:c.*88T>G	ENSP00000477997.3:n.*88T>G
ENST00000640140.1:n.858T>G
ENST00000640250.1:n.185T>G
ENST00000640681.1:n.807T>G
ENST00000652046.1:c.686T>G MANE Select	ENSP00000498466.1:p.Leu229Trp
ENST00000313771.9:n.995T>G
ENST00000352159.8:c.*3T>G	ENSP00000345601.4:n.*3T>G
ENST00000355279.2:c.661T>G	ENSP00000347426.2:p.Ter221Gly
ENST00000355740.6:c.686T>G	ENSP00000347979.2:p.Leu229Trp
ENST00000357339.6:c.623T>G	ENSP00000349896.2:p.Leu208Trp
ENST00000479522.5:c.*115T>G	ENSP00000424113.1:n.*115T>G
ENST00000484444.5:c.*127T>G	ENSP00000420975.1:n.*127T>G
ENST00000488877.5:c.*127T>G	ENSP00000425159.1:n.*127T>G
ENST00000492756.5:c.514T>G	ENSP00000422453.1:n.514T>G
ENST00000494410.5:c.*44T>G	ENSP00000423755.1:n.*44T>G
ENST00000494799.5:n.593T>G
ENST00000612663.4:c.*33T>G	ENSP00000477997.2:n.*33T>G
ENST00000615406.4:c.686T>G	ENSP00000484575.1:p.Leu229Trp
ENST00000626542.2:c.686T>G	ENSP00000485876.1:p.Leu229Trp
NM_000043.4:c.686T>G , LRG_134t1:c.686T>G	NP_000034.1:p.Leu229Trp
NM_152871.2:c.623T>G	NP_690610.1:p.Leu208Trp
NM_152872.2:c.661T>G	NP_690611.1:p.Ter221Gly
NR_028033.2:n.860T>G
NR_028034.2:n.722T>G
NR_028035.2:n.785T>G
NR_028036.2:n.923T>G
XM_006717819.2:c.767T>G	XP_006717882.1:p.Leu256Trp
XM_011539764.1:c.848T>G	XP_011538066.1:p.Leu283Trp
XM_011539765.1:c.785T>G	XP_011538067.1:p.Leu262Trp
XM_011539766.1:c.767T>G	XP_011538068.1:p.Leu256Trp
XM_011539767.1:c.731T>G	XP_011538069.1:p.Leu244Trp
XR_945732.1:n.754T>G
XR_945733.1:n.691T>G
NM_000043.5:c.686T>G	NP_000034.1:p.Leu229Trp
NM_001320619.1:c.*9T>G	NP_001307548.1:n.*9T>G
NM_152871.3:c.623T>G	NP_690610.1:p.Leu208Trp
NM_152872.3:c.661T>G	NP_690611.1:p.Ter221Gly
NR_028033.3:n.832T>G
NR_028034.3:n.694T>G
NR_028035.3:n.757T>G
NR_028036.3:n.895T>G
NR_135313.1:n.812T>G
NR_135314.1:n.995T>G
NR_135315.1:n.748T>G
XM_006717819.3:c.767T>G	XP_006717882.1:p.Leu256Trp
XM_011539764.2:c.848T>G	XP_011538066.1:p.Leu283Trp
XM_011539765.2:c.785T>G	XP_011538067.1:p.Leu262Trp
XM_011539766.2:c.767T>G	XP_011538068.1:p.Leu256Trp
XM_011539767.3:c.731T>G	XP_011538069.1:p.Leu244Trp
XR_945732.3:n.754T>G
XR_945733.2:n.691T>G
NM_000043.6:c.686T>G MANE Select	NP_000034.1:p.Leu229Trp
NM_001320619.2:c.*9T>G	NP_001307548.1:n.*9T>G
NM_152871.4:c.623T>G	NP_690610.1:p.Leu208Trp
NM_152872.4:c.661T>G	NP_690611.1:p.Ter221Gly
NR_028033.4:n.593T>G
NR_028034.4:n.455T>G
NR_028035.4:n.518T>G
NR_028036.4:n.656T>G
NR_135313.2:n.573T>G
NR_135314.2:n.852T>G
NR_135315.2:n.605T>G