Canonical Allele Identifier: CA377509991

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774064G>T (hg19) ; chr10:g.89014307G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014307G>T , CM000672.2:g.89014307G>T	GRCh38
NC_000010.10:g.90774064G>T , CM000672.1:g.90774064G>T	GRCh37
NC_000010.9:g.90764044G>T	NCBI36
NG_009089.2:g.28777G>T , LRG_134:g.28777G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1174G>T
ENST00000355740.8:c.*188G>T	ENSP00000347979.3:n.*188G>T
ENST00000357339.7:c.802G>T	ENSP00000349896.2:p.Glu268Ter
ENST00000371857.8:n.2410G>T
ENST00000460510.6:c.148G>T	ENSP00000512812.1:p.Glu50Ter
ENST00000466081.6:n.2514G>T
ENST00000477270.6:c.910G>T	ENSP00000512813.1:p.Glu304Ter
ENST00000479522.6:c.*294G>T	ENSP00000424113.1:n.*294G>T
ENST00000484444.6:c.*306G>T	ENSP00000420975.1:n.*306G>T
ENST00000488877.6:c.756G>T	ENSP00000425159.1:n.756G>T
ENST00000492756.7:c.*294G>T	ENSP00000422453.1:n.*294G>T
ENST00000494799.6:c.148G>T	ENSP00000512834.1:p.Glu50Ter
ENST00000562983.3:c.148G>T	ENSP00000512845.1:p.Glu50Ter
ENST00000612663.6:c.*267G>T	ENSP00000477997.3:n.*267G>T
ENST00000640140.2:n.1010G>T
ENST00000640250.2:n.364G>T
ENST00000640681.2:n.969G>T
ENST00000696723.1:n.4498G>T
ENST00000696741.1:n.2503G>T
ENST00000696742.1:n.2230G>T
ENST00000696743.1:n.3633G>T
ENST00000696744.1:n.904G>T
ENST00000696767.1:n.1199G>T
ENST00000696768.1:c.*188G>T	ENSP00000512859.1:n.*188G>T
ENST00000696769.1:n.2554G>T
ENST00000696771.1:c.148G>T	ENSP00000512860.1:p.Glu50Ter
ENST00000696772.1:n.2468G>T
ENST00000696773.1:n.2207G>T
ENST00000696774.1:n.5975G>T
ENST00000696776.1:c.958G>T	ENSP00000512861.1:p.Glu320Ter
ENST00000696777.1:n.2273G>T
ENST00000696778.1:n.1301G>T
ENST00000696779.1:c.472G>T	ENSP00000512862.1:p.Glu158Ter
ENST00000696780.1:c.895G>T	ENSP00000512863.1:p.Glu299Ter
ENST00000696781.1:c.610G>T	ENSP00000512864.1:p.Glu204Ter
ENST00000696782.1:c.*267G>T	ENSP00000512865.1:n.*267G>T
ENST00000696783.1:n.2733G>T
ENST00000696992.1:n.1982G>T
ENST00000696995.1:n.4394G>T
ENST00000696996.1:n.2307G>T
ENST00000696997.1:c.*495G>T	ENSP00000513028.1:n.*495G>T
ENST00000696998.1:n.2119G>T
ENST00000696999.1:c.148G>T	ENSP00000513029.1:p.Glu50Ter
ENST00000697036.1:c.*281G>T	ENSP00000513060.1:n.*281G>T
ENST00000697037.1:n.900G>T
ENST00000697093.1:n.3101G>T
ENST00000697094.1:n.3448G>T
ENST00000697095.1:c.*2066G>T	ENSP00000513104.1:n.*2066G>T
ENST00000697096.1:n.1998G>T
ENST00000697097.1:c.148G>T	ENSP00000513105.1:p.Glu50Ter
ENST00000562983.2:n.1051G>T
ENST00000690268.1:c.946G>T	ENSP00000509810.1:p.Glu316Ter
ENST00000355740.7:c.*191G>T	ENSP00000347979.3:n.*191G>T
ENST00000612663.5:c.*267G>T	ENSP00000477997.3:n.*267G>T
ENST00000640140.1:n.1037G>T
ENST00000640250.1:n.364G>T
ENST00000640681.1:n.986G>T
ENST00000652046.1:c.865G>T MANE Select	ENSP00000498466.1:p.Glu289Ter
ENST00000352159.8:c.*182G>T	ENSP00000345601.4:n.*182G>T
ENST00000355279.2:c.840G>T	ENSP00000347426.2:n.840G>T
ENST00000355740.6:c.865G>T	ENSP00000347979.2:p.Glu289Ter
ENST00000357339.6:c.802G>T	ENSP00000349896.2:p.Glu268Ter
ENST00000479522.5:c.*294G>T	ENSP00000424113.1:n.*294G>T
ENST00000484444.5:c.*306G>T	ENSP00000420975.1:n.*306G>T
ENST00000488877.5:c.*306G>T	ENSP00000425159.1:n.*306G>T
ENST00000492756.5:c.693G>T	ENSP00000422453.1:n.693G>T
ENST00000494410.5:c.*223G>T	ENSP00000423755.1:n.*223G>T
ENST00000612663.4:c.*212G>T	ENSP00000477997.2:n.*212G>T
NM_000043.4:c.865G>T , LRG_134t1:c.865G>T	NP_000034.1:p.Glu289Ter
NM_152871.2:c.802G>T	NP_690610.1:p.Glu268Ter
NM_152872.2:c.*177G>T	NP_690611.1:n.*177G>T
NR_028033.2:n.1039G>T
NR_028034.2:n.901G>T
NR_028035.2:n.964G>T
NR_028036.2:n.1102G>T
XM_006717819.2:c.946G>T	XP_006717882.1:p.Glu316Ter
XM_011539764.1:c.1027G>T	XP_011538066.1:p.Glu343Ter
XM_011539765.1:c.964G>T	XP_011538067.1:p.Glu322Ter
XM_011539766.1:c.946G>T	XP_011538068.1:p.Glu316Ter
XM_011539767.1:c.910G>T	XP_011538069.1:p.Glu304Ter
XR_945732.1:n.933G>T
XR_945733.1:n.870G>T
NM_000043.5:c.865G>T	NP_000034.1:p.Glu289Ter
NM_001320619.1:c.*188G>T	NP_001307548.1:n.*188G>T
NM_152871.3:c.802G>T	NP_690610.1:p.Glu268Ter
NM_152872.3:c.*177G>T	NP_690611.1:n.*177G>T
NR_028033.3:n.1011G>T
NR_028034.3:n.873G>T
NR_028035.3:n.936G>T
NR_028036.3:n.1074G>T
NR_135313.1:n.991G>T
NR_135314.1:n.1174G>T
NR_135315.1:n.927G>T
XM_006717819.3:c.946G>T	XP_006717882.1:p.Glu316Ter
XM_011539764.2:c.1027G>T	XP_011538066.1:p.Glu343Ter
XM_011539765.2:c.964G>T	XP_011538067.1:p.Glu322Ter
XM_011539766.2:c.946G>T	XP_011538068.1:p.Glu316Ter
XM_011539767.3:c.910G>T	XP_011538069.1:p.Glu304Ter
XR_945732.3:n.933G>T
XR_945733.2:n.870G>T
NM_000043.6:c.865G>T MANE Select	NP_000034.1:p.Glu289Ter
NM_001320619.2:c.*188G>T	NP_001307548.1:n.*188G>T
NM_152871.4:c.802G>T	NP_690610.1:p.Glu268Ter
NM_152872.4:c.*177G>T	NP_690611.1:n.*177G>T
NR_028033.4:n.772G>T
NR_028034.4:n.634G>T
NR_028035.4:n.697G>T
NR_028036.4:n.835G>T
NR_135313.2:n.752G>T
NR_135314.2:n.1031G>T
NR_135315.2:n.784G>T