Canonical Allele Identifier: CA2610079437
Gene: FAS HGNC NCBI

Linked Data

gnomAD v4: 10-89013479-T-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.89013479T>C , CM000672.2:g.89013479T>C GRCh38
NC_000010.10:g.90773236T>C , CM000672.1:g.90773236T>C GRCh37
NC_000010.9:g.90763216T>C NCBI36
NG_009089.2:g.27949T>C , LRG_134:g.27949T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000313771.10:n.985+112T>C
ENST00000355740.8:c.593+112T>C ENSP00000347979.3:n.593+112T>C
ENST00000357339.7:c.613+112T>C ENSP00000349896.2:n.613+112T>C
ENST00000371857.8:n.2221+112T>C
ENST00000460510.6:c.-42+112T>C ENSP00000512812.1:n.-42+112T>C
ENST00000466081.6:n.2325+112T>C
ENST00000477270.6:c.721+112T>C ENSP00000512813.1:n.721+112T>C
ENST00000479522.6:c.*105+112T>C ENSP00000424113.1:n.*105+112T>C
ENST00000484444.6:c.*117+112T>C ENSP00000420975.1:n.*117+112T>C
ENST00000488877.6:c.567+112T>C ENSP00000425159.1:n.567+112T>C
ENST00000492756.7:c.*105+112T>C ENSP00000422453.1:n.*105+112T>C
ENST00000494799.6:c.-42+112T>C ENSP00000512834.1:n.-42+112T>C
ENST00000562983.3:c.-42+112T>C ENSP00000512845.1:n.-42+112T>C
ENST00000612663.6:c.*78+112T>C ENSP00000477997.3:n.*78+112T>C
ENST00000640140.2:n.821+112T>C
ENST00000640250.2:n.175+112T>C
ENST00000640681.2:n.780+112T>C
ENST00000696723.1:n.4309+112T>C
ENST00000696741.1:n.2314+112T>C
ENST00000696742.1:n.2041+112T>C
ENST00000696743.1:n.3444+112T>C
ENST00000696744.1:n.715+112T>C
ENST00000696767.1:n.1010+112T>C
ENST00000696768.1:c.530+112T>C ENSP00000512859.1:n.530+112T>C
ENST00000696769.1:n.2365+112T>C
ENST00000696771.1:c.-42+112T>C ENSP00000512860.1:n.-42+112T>C
ENST00000696772.1:n.2279+112T>C
ENST00000696773.1:n.2018+112T>C
ENST00000696774.1:n.5147T>C
ENST00000696776.1:c.769+112T>C ENSP00000512861.1:n.769+112T>C
ENST00000696777.1:n.2084+112T>C
ENST00000696778.1:n.1112+112T>C
ENST00000696779.1:c.283+112T>C ENSP00000512862.1:n.283+112T>C
ENST00000696780.1:c.706+112T>C ENSP00000512863.1:n.706+112T>C
ENST00000696781.1:c.421+112T>C ENSP00000512864.1:n.421+112T>C
ENST00000696782.1:c.*78+112T>C ENSP00000512865.1:n.*78+112T>C
ENST00000696783.1:n.2544+112T>C
ENST00000696992.1:n.1793+112T>C
ENST00000696995.1:n.3566T>C
ENST00000696996.1:n.2118+112T>C
ENST00000696997.1:c.*306+112T>C ENSP00000513028.1:n.*306+112T>C
ENST00000696998.1:n.1930+112T>C
ENST00000696999.1:c.-42+112T>C ENSP00000513029.1:n.-42+112T>C
ENST00000697035.1:c.*9+112T>C ENSP00000513059.1:n.*9+112T>C
ENST00000697036.1:c.*93-640T>C ENSP00000513060.1:n.*93-640T>C
ENST00000697037.1:n.711+112T>C
ENST00000697093.1:n.2273T>C
ENST00000697094.1:n.3259+112T>C
ENST00000697095.1:c.*1877+112T>C ENSP00000513104.1:n.*1877+112T>C
ENST00000697096.1:n.1809+112T>C
ENST00000697097.1:c.-42+112T>C ENSP00000513105.1:n.-42+112T>C
ENST00000562983.2:n.862+112T>C
ENST00000690268.1:c.757+112T>C ENSP00000509810.1:n.757+112T>C
ENST00000355740.7:c.*2+112T>C ENSP00000347979.3:n.*2+112T>C
ENST00000612663.5:c.*78+112T>C ENSP00000477997.3:n.*78+112T>C
ENST00000640140.1:n.848+112T>C
ENST00000640250.1:n.175+112T>C
ENST00000640681.1:n.797+112T>C
ENST00000652046.1:c.676+112T>C MANE Select ENSP00000498466.1:n.676+112T>C
ENST00000313771.9:n.985+112T>C
ENST00000352159.8:c.676+112T>C ENSP00000345601.4:n.676+112T>C
ENST00000355279.2:c.652-640T>C ENSP00000347426.2:n.652-640T>C
ENST00000355740.6:c.676+112T>C ENSP00000347979.2:n.676+112T>C
ENST00000357339.6:c.613+112T>C ENSP00000349896.2:n.613+112T>C
ENST00000479522.5:c.*105+112T>C ENSP00000424113.1:n.*105+112T>C
ENST00000484444.5:c.*117+112T>C ENSP00000420975.1:n.*117+112T>C
ENST00000488877.5:c.*117+112T>C ENSP00000425159.1:n.*117+112T>C
ENST00000492756.5:c.504+112T>C ENSP00000422453.1:n.504+112T>C
ENST00000494410.5:c.*34+112T>C ENSP00000423755.1:n.*34+112T>C
ENST00000494799.5:n.583+112T>C
ENST00000612663.4:c.*23+112T>C ENSP00000477997.2:n.*23+112T>C
ENST00000615406.4:c.676+112T>C ENSP00000484575.1:n.676+112T>C
ENST00000626542.2:c.676+112T>C ENSP00000485876.1:n.676+112T>C
NM_000043.4:c.676+112T>C , LRG_134t1:c.676+112T>C NP_000034.1:n.676+112T>C
NM_152871.2:c.613+112T>C NP_690610.1:n.613+112T>C
NM_152872.2:c.652-640T>C NP_690611.1:n.652-640T>C
NR_028033.2:n.850+112T>C
NR_028034.2:n.712+112T>C
NR_028035.2:n.775+112T>C
NR_028036.2:n.913+112T>C
XM_006717819.2:c.757+112T>C XP_006717882.1:n.757+112T>C
XM_011539764.1:c.838+112T>C XP_011538066.1:n.838+112T>C
XM_011539765.1:c.775+112T>C XP_011538067.1:n.775+112T>C
XM_011539766.1:c.757+112T>C XP_011538068.1:n.757+112T>C
XM_011539767.1:c.721+112T>C XP_011538069.1:n.721+112T>C
XR_945732.1:n.744+112T>C
XR_945733.1:n.681+112T>C
NM_000043.5:c.676+112T>C NP_000034.1:n.676+112T>C
NM_001320619.1:c.593+112T>C NP_001307548.1:n.593+112T>C
NM_152871.3:c.613+112T>C NP_690610.1:n.613+112T>C
NM_152872.3:c.652-640T>C NP_690611.1:n.652-640T>C
NR_028033.3:n.822+112T>C
NR_028034.3:n.684+112T>C
NR_028035.3:n.747+112T>C
NR_028036.3:n.885+112T>C
NR_135313.1:n.802+112T>C
NR_135314.1:n.985+112T>C
NR_135315.1:n.738+112T>C
XM_006717819.3:c.757+112T>C XP_006717882.1:n.757+112T>C
XM_011539764.2:c.838+112T>C XP_011538066.1:n.838+112T>C
XM_011539765.2:c.775+112T>C XP_011538067.1:n.775+112T>C
XM_011539766.2:c.757+112T>C XP_011538068.1:n.757+112T>C
XM_011539767.3:c.721+112T>C XP_011538069.1:n.721+112T>C
XR_945732.3:n.744+112T>C
XR_945733.2:n.681+112T>C
NM_000043.6:c.676+112T>C MANE Select NP_000034.1:n.676+112T>C
NM_001320619.2:c.593+112T>C NP_001307548.1:n.593+112T>C
NM_152871.4:c.613+112T>C NP_690610.1:n.613+112T>C
NM_152872.4:c.652-640T>C NP_690611.1:n.652-640T>C
NR_028033.4:n.583+112T>C
NR_028034.4:n.445+112T>C
NR_028035.4:n.508+112T>C
NR_028036.4:n.646+112T>C
NR_135313.2:n.563+112T>C
NR_135314.2:n.842+112T>C
NR_135315.2:n.595+112T>C
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