Canonical Allele Identifier: CA470974957
Gene: FAS HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.90773946T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89014189T>G , CM000672.2:g.89014189T>G GRCh38
NC_000010.10:g.90773946T>G , CM000672.1:g.90773946T>G GRCh37
NC_000010.9:g.90763926T>G NCBI36
NG_009089.2:g.28659T>G , LRG_134:g.28659T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000313771.10:n.1056T>G
ENST00000355740.8:c.*70T>G ENSP00000347979.3:n.*70T>G
ENST00000357339.7:c.684T>G ENSP00000349896.2:p.Val228=
ENST00000371857.8:n.2292T>G
ENST00000460510.6:c.30T>G ENSP00000512812.1:p.Val10=
ENST00000466081.6:n.2396T>G
ENST00000477270.6:c.792T>G ENSP00000512813.1:p.Val264=
ENST00000479522.6:c.*176T>G ENSP00000424113.1:n.*176T>G
ENST00000484444.6:c.*188T>G ENSP00000420975.1:n.*188T>G
ENST00000488877.6:c.638T>G ENSP00000425159.1:n.638T>G
ENST00000492756.7:c.*176T>G ENSP00000422453.1:n.*176T>G
ENST00000494799.6:c.30T>G ENSP00000512834.1:p.Val10=
ENST00000562983.3:c.30T>G ENSP00000512845.1:p.Val10=
ENST00000612663.6:c.*149T>G ENSP00000477997.3:n.*149T>G
ENST00000640140.2:n.892T>G
ENST00000640250.2:n.246T>G
ENST00000640681.2:n.851T>G
ENST00000696723.1:n.4380T>G
ENST00000696741.1:n.2385T>G
ENST00000696742.1:n.2112T>G
ENST00000696743.1:n.3515T>G
ENST00000696744.1:n.786T>G
ENST00000696767.1:n.1081T>G
ENST00000696768.1:c.*70T>G ENSP00000512859.1:n.*70T>G
ENST00000696769.1:n.2436T>G
ENST00000696771.1:c.30T>G ENSP00000512860.1:p.Val10=
ENST00000696772.1:n.2350T>G
ENST00000696773.1:n.2089T>G
ENST00000696774.1:n.5857T>G
ENST00000696776.1:c.840T>G ENSP00000512861.1:p.Val280=
ENST00000696777.1:n.2155T>G
ENST00000696778.1:n.1183T>G
ENST00000696779.1:c.354T>G ENSP00000512862.1:p.Val118=
ENST00000696780.1:c.777T>G ENSP00000512863.1:p.Val259=
ENST00000696781.1:c.492T>G ENSP00000512864.1:p.Val164=
ENST00000696782.1:c.*149T>G ENSP00000512865.1:n.*149T>G
ENST00000696783.1:n.2615T>G
ENST00000696992.1:n.1864T>G
ENST00000696995.1:n.4276T>G
ENST00000696996.1:n.2189T>G
ENST00000696997.1:c.*377T>G ENSP00000513028.1:n.*377T>G
ENST00000696998.1:n.2001T>G
ENST00000696999.1:c.30T>G ENSP00000513029.1:p.Val10=
ENST00000697035.1:c.*80T>G ENSP00000513059.1:n.*80T>G
ENST00000697036.1:c.*163T>G ENSP00000513060.1:n.*163T>G
ENST00000697037.1:n.782T>G
ENST00000697093.1:n.2983T>G
ENST00000697094.1:n.3330T>G
ENST00000697095.1:c.*1948T>G ENSP00000513104.1:n.*1948T>G
ENST00000697096.1:n.1880T>G
ENST00000697097.1:c.30T>G ENSP00000513105.1:p.Val10=
ENST00000562983.2:n.933T>G
ENST00000690268.1:c.828T>G ENSP00000509810.1:p.Val276=
ENST00000355740.7:c.*73T>G ENSP00000347979.3:n.*73T>G
ENST00000612663.5:c.*149T>G ENSP00000477997.3:n.*149T>G
ENST00000640140.1:n.919T>G
ENST00000640250.1:n.246T>G
ENST00000640681.1:n.868T>G
ENST00000652046.1:c.747T>G MANE Select ENSP00000498466.1:p.Val249=
ENST00000352159.8:c.*64T>G ENSP00000345601.4:n.*64T>G
ENST00000355279.2:c.722T>G ENSP00000347426.2:n.722T>G
ENST00000355740.6:c.747T>G ENSP00000347979.2:p.Val249=
ENST00000357339.6:c.684T>G ENSP00000349896.2:p.Val228=
ENST00000479522.5:c.*176T>G ENSP00000424113.1:n.*176T>G
ENST00000484444.5:c.*188T>G ENSP00000420975.1:n.*188T>G
ENST00000488877.5:c.*188T>G ENSP00000425159.1:n.*188T>G
ENST00000492756.5:c.575T>G ENSP00000422453.1:n.575T>G
ENST00000494410.5:c.*105T>G ENSP00000423755.1:n.*105T>G
ENST00000494799.5:n.654T>G
ENST00000612663.4:c.*94T>G ENSP00000477997.2:n.*94T>G
ENST00000615406.4:c.747T>G ENSP00000484575.1:p.Val249=
NM_000043.4:c.747T>G , LRG_134t1:c.747T>G NP_000034.1:p.Val249=
NM_152871.2:c.684T>G NP_690610.1:p.Val228=
NM_152872.2:c.*59T>G NP_690611.1:n.*59T>G
NR_028033.2:n.921T>G
NR_028034.2:n.783T>G
NR_028035.2:n.846T>G
NR_028036.2:n.984T>G
XM_006717819.2:c.828T>G XP_006717882.1:p.Val276=
XM_011539764.1:c.909T>G XP_011538066.1:p.Val303=
XM_011539765.1:c.846T>G XP_011538067.1:p.Val282=
XM_011539766.1:c.828T>G XP_011538068.1:p.Val276=
XM_011539767.1:c.792T>G XP_011538069.1:p.Val264=
XR_945732.1:n.815T>G
XR_945733.1:n.752T>G
NM_000043.5:c.747T>G NP_000034.1:p.Val249=
NM_001320619.1:c.*70T>G NP_001307548.1:n.*70T>G
NM_152871.3:c.684T>G NP_690610.1:p.Val228=
NM_152872.3:c.*59T>G NP_690611.1:n.*59T>G
NR_028033.3:n.893T>G
NR_028034.3:n.755T>G
NR_028035.3:n.818T>G
NR_028036.3:n.956T>G
NR_135313.1:n.873T>G
NR_135314.1:n.1056T>G
NR_135315.1:n.809T>G
XM_006717819.3:c.828T>G XP_006717882.1:p.Val276=
XM_011539764.2:c.909T>G XP_011538066.1:p.Val303=
XM_011539765.2:c.846T>G XP_011538067.1:p.Val282=
XM_011539766.2:c.828T>G XP_011538068.1:p.Val276=
XM_011539767.3:c.792T>G XP_011538069.1:p.Val264=
XR_945732.3:n.815T>G
XR_945733.2:n.752T>G
NM_000043.6:c.747T>G MANE Select NP_000034.1:p.Val249=
NM_001320619.2:c.*70T>G NP_001307548.1:n.*70T>G
NM_152871.4:c.684T>G NP_690610.1:p.Val228=
NM_152872.4:c.*59T>G NP_690611.1:n.*59T>G
NR_028033.4:n.654T>G
NR_028034.4:n.516T>G
NR_028035.4:n.579T>G
NR_028036.4:n.717T>G
NR_135313.2:n.634T>G
NR_135314.2:n.913T>G
NR_135315.2:n.666T>G