Canonical Allele Identifier: CA15638308
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1250840
ClinVar RCV Id: RCV001655193
dbSNP Id: rs1571019
gnomAD v2: 10-90773303-A-G
gnomAD v3: 10-89013546-A-G
gnomAD v4: 10-89013546-A-G
MyVariant Identifiers: chr10:g.90773303A>G (hg19) chr10:g.89013546A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89013546A>G , CM000672.2:g.89013546A>G GRCh38
NC_000010.10:g.90773303A>G , CM000672.1:g.90773303A>G GRCh37
NC_000010.9:g.90763283A>G NCBI36
NG_009089.2:g.28016A>G , LRG_134:g.28016A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.985+179A>G
ENST00000355740.8:c.593+179A>G ENSP00000347979.3:n.593+179A>G
ENST00000357339.7:c.613+179A>G ENSP00000349896.2:n.613+179A>G
ENST00000371857.8:n.2221+179A>G
ENST00000460510.6:c.-42+179A>G ENSP00000512812.1:n.-42+179A>G
ENST00000466081.6:n.2325+179A>G
ENST00000477270.6:c.721+179A>G ENSP00000512813.1:n.721+179A>G
ENST00000479522.6:c.*105+179A>G ENSP00000424113.1:n.*105+179A>G
ENST00000484444.6:c.*117+179A>G ENSP00000420975.1:n.*117+179A>G
ENST00000488877.6:c.567+179A>G ENSP00000425159.1:n.567+179A>G
ENST00000492756.7:c.*105+179A>G ENSP00000422453.1:n.*105+179A>G
ENST00000494799.6:c.-42+179A>G ENSP00000512834.1:n.-42+179A>G
ENST00000562983.3:c.-42+179A>G ENSP00000512845.1:n.-42+179A>G
ENST00000612663.6:c.*78+179A>G ENSP00000477997.3:n.*78+179A>G
ENST00000640140.2:n.821+179A>G
ENST00000640250.2:n.175+179A>G
ENST00000640681.2:n.780+179A>G
ENST00000696723.1:n.4309+179A>G
ENST00000696741.1:n.2314+179A>G
ENST00000696742.1:n.2041+179A>G
ENST00000696743.1:n.3444+179A>G
ENST00000696744.1:n.715+179A>G
ENST00000696767.1:n.1010+179A>G
ENST00000696768.1:c.530+179A>G ENSP00000512859.1:n.530+179A>G
ENST00000696769.1:n.2365+179A>G
ENST00000696771.1:c.-42+179A>G ENSP00000512860.1:n.-42+179A>G
ENST00000696772.1:n.2279+179A>G
ENST00000696773.1:n.2018+179A>G
ENST00000696774.1:n.5214A>G
ENST00000696776.1:c.769+179A>G ENSP00000512861.1:n.769+179A>G
ENST00000696777.1:n.2084+179A>G
ENST00000696778.1:n.1112+179A>G
ENST00000696779.1:c.283+179A>G ENSP00000512862.1:n.283+179A>G
ENST00000696780.1:c.706+179A>G ENSP00000512863.1:n.706+179A>G
ENST00000696781.1:c.421+179A>G ENSP00000512864.1:n.421+179A>G
ENST00000696782.1:c.*78+179A>G ENSP00000512865.1:n.*78+179A>G
ENST00000696783.1:n.2544+179A>G
ENST00000696992.1:n.1793+179A>G
ENST00000696995.1:n.3633A>G
ENST00000696996.1:n.2118+179A>G
ENST00000696997.1:c.*306+179A>G ENSP00000513028.1:n.*306+179A>G
ENST00000696998.1:n.1930+179A>G
ENST00000696999.1:c.-42+179A>G ENSP00000513029.1:n.-42+179A>G
ENST00000697035.1:c.*9+179A>G ENSP00000513059.1:n.*9+179A>G
ENST00000697036.1:c.*93-573A>G ENSP00000513060.1:n.*93-573A>G
ENST00000697037.1:n.711+179A>G
ENST00000697093.1:n.2340A>G
ENST00000697094.1:n.3259+179A>G
ENST00000697095.1:c.*1877+179A>G ENSP00000513104.1:n.*1877+179A>G
ENST00000697096.1:n.1809+179A>G
ENST00000697097.1:c.-42+179A>G ENSP00000513105.1:n.-42+179A>G
ENST00000562983.2:n.862+179A>G
ENST00000690268.1:c.757+179A>G ENSP00000509810.1:n.757+179A>G
ENST00000355740.7:c.*2+179A>G ENSP00000347979.3:n.*2+179A>G
ENST00000612663.5:c.*78+179A>G ENSP00000477997.3:n.*78+179A>G
ENST00000640140.1:n.848+179A>G
ENST00000640250.1:n.175+179A>G
ENST00000640681.1:n.797+179A>G
ENST00000652046.1:c.676+179A>G MANE Select ENSP00000498466.1:n.676+179A>G
ENST00000313771.9:n.985+179A>G
ENST00000352159.8:c.676+179A>G ENSP00000345601.4:n.676+179A>G
ENST00000355279.2:c.652-573A>G ENSP00000347426.2:n.652-573A>G
ENST00000355740.6:c.676+179A>G ENSP00000347979.2:n.676+179A>G
ENST00000357339.6:c.613+179A>G ENSP00000349896.2:n.613+179A>G
ENST00000479522.5:c.*105+179A>G ENSP00000424113.1:n.*105+179A>G
ENST00000484444.5:c.*117+179A>G ENSP00000420975.1:n.*117+179A>G
ENST00000488877.5:c.*117+179A>G ENSP00000425159.1:n.*117+179A>G
ENST00000492756.5:c.504+179A>G ENSP00000422453.1:n.504+179A>G
ENST00000494410.5:c.*34+179A>G ENSP00000423755.1:n.*34+179A>G
ENST00000494799.5:n.583+179A>G
ENST00000612663.4:c.*23+179A>G ENSP00000477997.2:n.*23+179A>G
ENST00000615406.4:c.676+179A>G ENSP00000484575.1:n.676+179A>G
ENST00000626542.2:c.676+179A>G ENSP00000485876.1:n.676+179A>G
NM_000043.4:c.676+179A>G , LRG_134t1:c.676+179A>G NP_000034.1:n.676+179A>G
NM_152871.2:c.613+179A>G NP_690610.1:n.613+179A>G
NM_152872.2:c.652-573A>G NP_690611.1:n.652-573A>G
NR_028033.2:n.850+179A>G
NR_028034.2:n.712+179A>G
NR_028035.2:n.775+179A>G
NR_028036.2:n.913+179A>G
XM_006717819.2:c.757+179A>G XP_006717882.1:n.757+179A>G
XM_011539764.1:c.838+179A>G XP_011538066.1:n.838+179A>G
XM_011539765.1:c.775+179A>G XP_011538067.1:n.775+179A>G
XM_011539766.1:c.757+179A>G XP_011538068.1:n.757+179A>G
XM_011539767.1:c.721+179A>G XP_011538069.1:n.721+179A>G
XR_945732.1:n.744+179A>G
XR_945733.1:n.681+179A>G
NM_000043.5:c.676+179A>G NP_000034.1:n.676+179A>G
NM_001320619.1:c.593+179A>G NP_001307548.1:n.593+179A>G
NM_152871.3:c.613+179A>G NP_690610.1:n.613+179A>G
NM_152872.3:c.652-573A>G NP_690611.1:n.652-573A>G
NR_028033.3:n.822+179A>G
NR_028034.3:n.684+179A>G
NR_028035.3:n.747+179A>G
NR_028036.3:n.885+179A>G
NR_135313.1:n.802+179A>G
NR_135314.1:n.985+179A>G
NR_135315.1:n.738+179A>G
XM_006717819.3:c.757+179A>G XP_006717882.1:n.757+179A>G
XM_011539764.2:c.838+179A>G XP_011538066.1:n.838+179A>G
XM_011539765.2:c.775+179A>G XP_011538067.1:n.775+179A>G
XM_011539766.2:c.757+179A>G XP_011538068.1:n.757+179A>G
XM_011539767.3:c.721+179A>G XP_011538069.1:n.721+179A>G
XR_945732.3:n.744+179A>G
XR_945733.2:n.681+179A>G
NM_000043.6:c.676+179A>G MANE Select NP_000034.1:n.676+179A>G
NM_001320619.2:c.593+179A>G NP_001307548.1:n.593+179A>G
NM_152871.4:c.613+179A>G NP_690610.1:n.613+179A>G
NM_152872.4:c.652-573A>G NP_690611.1:n.652-573A>G
NR_028033.4:n.583+179A>G
NR_028034.4:n.445+179A>G
NR_028035.4:n.508+179A>G
NR_028036.4:n.646+179A>G
NR_135313.2:n.563+179A>G
NR_135314.2:n.842+179A>G
NR_135315.2:n.595+179A>G
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