Canonical Allele Identifier: CA377509850

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774003A>C (hg19) ; chr10:g.89014246A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014246A>C , CM000672.2:g.89014246A>C	GRCh38
NC_000010.10:g.90774003A>C , CM000672.1:g.90774003A>C	GRCh37
NC_000010.9:g.90763983A>C	NCBI36
NG_009089.2:g.28716A>C , LRG_134:g.28716A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1113A>C
ENST00000355740.8:c.*127A>C	ENSP00000347979.3:n.*127A>C
ENST00000357339.7:c.741A>C	ENSP00000349896.2:p.Gln247His
ENST00000371857.8:n.2349A>C
ENST00000460510.6:c.87A>C	ENSP00000512812.1:p.Gln29His
ENST00000466081.6:n.2453A>C
ENST00000477270.6:c.849A>C	ENSP00000512813.1:p.Gln283His
ENST00000479522.6:c.*233A>C	ENSP00000424113.1:n.*233A>C
ENST00000484444.6:c.*245A>C	ENSP00000420975.1:n.*245A>C
ENST00000488877.6:c.695A>C	ENSP00000425159.1:n.695A>C
ENST00000492756.7:c.*233A>C	ENSP00000422453.1:n.*233A>C
ENST00000494799.6:c.87A>C	ENSP00000512834.1:p.Gln29His
ENST00000562983.3:c.87A>C	ENSP00000512845.1:p.Gln29His
ENST00000612663.6:c.*206A>C	ENSP00000477997.3:n.*206A>C
ENST00000640140.2:n.949A>C
ENST00000640250.2:n.303A>C
ENST00000640681.2:n.908A>C
ENST00000696723.1:n.4437A>C
ENST00000696741.1:n.2442A>C
ENST00000696742.1:n.2169A>C
ENST00000696743.1:n.3572A>C
ENST00000696744.1:n.843A>C
ENST00000696767.1:n.1138A>C
ENST00000696768.1:c.*127A>C	ENSP00000512859.1:n.*127A>C
ENST00000696769.1:n.2493A>C
ENST00000696771.1:c.87A>C	ENSP00000512860.1:p.Gln29His
ENST00000696772.1:n.2407A>C
ENST00000696773.1:n.2146A>C
ENST00000696774.1:n.5914A>C
ENST00000696776.1:c.897A>C	ENSP00000512861.1:p.Gln299His
ENST00000696777.1:n.2212A>C
ENST00000696778.1:n.1240A>C
ENST00000696779.1:c.411A>C	ENSP00000512862.1:p.Gln137His
ENST00000696780.1:c.834A>C	ENSP00000512863.1:p.Gln278His
ENST00000696781.1:c.549A>C	ENSP00000512864.1:p.Gln183His
ENST00000696782.1:c.*206A>C	ENSP00000512865.1:n.*206A>C
ENST00000696783.1:n.2672A>C
ENST00000696992.1:n.1921A>C
ENST00000696995.1:n.4333A>C
ENST00000696996.1:n.2246A>C
ENST00000696997.1:c.*434A>C	ENSP00000513028.1:n.*434A>C
ENST00000696998.1:n.2058A>C
ENST00000696999.1:c.87A>C	ENSP00000513029.1:p.Gln29His
ENST00000697035.1:c.*137A>C	ENSP00000513059.1:n.*137A>C
ENST00000697036.1:c.*220A>C	ENSP00000513060.1:n.*220A>C
ENST00000697037.1:n.839A>C
ENST00000697093.1:n.3040A>C
ENST00000697094.1:n.3387A>C
ENST00000697095.1:c.*2005A>C	ENSP00000513104.1:n.*2005A>C
ENST00000697096.1:n.1937A>C
ENST00000697097.1:c.87A>C	ENSP00000513105.1:p.Gln29His
ENST00000562983.2:n.990A>C
ENST00000690268.1:c.885A>C	ENSP00000509810.1:p.Gln295His
ENST00000355740.7:c.*130A>C	ENSP00000347979.3:n.*130A>C
ENST00000612663.5:c.*206A>C	ENSP00000477997.3:n.*206A>C
ENST00000640140.1:n.976A>C
ENST00000640250.1:n.303A>C
ENST00000640681.1:n.925A>C
ENST00000652046.1:c.804A>C MANE Select	ENSP00000498466.1:p.Gln268His
ENST00000352159.8:c.*121A>C	ENSP00000345601.4:n.*121A>C
ENST00000355279.2:c.779A>C	ENSP00000347426.2:n.779A>C
ENST00000355740.6:c.804A>C	ENSP00000347979.2:p.Gln268His
ENST00000357339.6:c.741A>C	ENSP00000349896.2:p.Gln247His
ENST00000479522.5:c.*233A>C	ENSP00000424113.1:n.*233A>C
ENST00000484444.5:c.*245A>C	ENSP00000420975.1:n.*245A>C
ENST00000488877.5:c.*245A>C	ENSP00000425159.1:n.*245A>C
ENST00000492756.5:c.632A>C	ENSP00000422453.1:n.632A>C
ENST00000494410.5:c.*162A>C	ENSP00000423755.1:n.*162A>C
ENST00000612663.4:c.*151A>C	ENSP00000477997.2:n.*151A>C
NM_000043.4:c.804A>C , LRG_134t1:c.804A>C	NP_000034.1:p.Gln268His
NM_152871.2:c.741A>C	NP_690610.1:p.Gln247His
NM_152872.2:c.*116A>C	NP_690611.1:n.*116A>C
NR_028033.2:n.978A>C
NR_028034.2:n.840A>C
NR_028035.2:n.903A>C
NR_028036.2:n.1041A>C
XM_006717819.2:c.885A>C	XP_006717882.1:p.Gln295His
XM_011539764.1:c.966A>C	XP_011538066.1:p.Gln322His
XM_011539765.1:c.903A>C	XP_011538067.1:p.Gln301His
XM_011539766.1:c.885A>C	XP_011538068.1:p.Gln295His
XM_011539767.1:c.849A>C	XP_011538069.1:p.Gln283His
XR_945732.1:n.872A>C
XR_945733.1:n.809A>C
NM_000043.5:c.804A>C	NP_000034.1:p.Gln268His
NM_001320619.1:c.*127A>C	NP_001307548.1:n.*127A>C
NM_152871.3:c.741A>C	NP_690610.1:p.Gln247His
NM_152872.3:c.*116A>C	NP_690611.1:n.*116A>C
NR_028033.3:n.950A>C
NR_028034.3:n.812A>C
NR_028035.3:n.875A>C
NR_028036.3:n.1013A>C
NR_135313.1:n.930A>C
NR_135314.1:n.1113A>C
NR_135315.1:n.866A>C
XM_006717819.3:c.885A>C	XP_006717882.1:p.Gln295His
XM_011539764.2:c.966A>C	XP_011538066.1:p.Gln322His
XM_011539765.2:c.903A>C	XP_011538067.1:p.Gln301His
XM_011539766.2:c.885A>C	XP_011538068.1:p.Gln295His
XM_011539767.3:c.849A>C	XP_011538069.1:p.Gln283His
XR_945732.3:n.872A>C
XR_945733.2:n.809A>C
NM_000043.6:c.804A>C MANE Select	NP_000034.1:p.Gln268His
NM_001320619.2:c.*127A>C	NP_001307548.1:n.*127A>C
NM_152871.4:c.741A>C	NP_690610.1:p.Gln247His
NM_152872.4:c.*116A>C	NP_690611.1:n.*116A>C
NR_028033.4:n.711A>C
NR_028034.4:n.573A>C
NR_028035.4:n.636A>C
NR_028036.4:n.774A>C
NR_135313.2:n.691A>C
NR_135314.2:n.970A>C
NR_135315.2:n.723A>C