Canonical Allele Identifier: CA377509981

Gene: FAS

Linked Data

• gnomAD v4: 10-89014304-A-C
• MyVariant Identifiers: chr10:g.90774061A>C (hg19) ; chr10:g.89014304A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014304A>C , CM000672.2:g.89014304A>C	GRCh38
NC_000010.10:g.90774061A>C , CM000672.1:g.90774061A>C	GRCh37
NC_000010.9:g.90764041A>C	NCBI36
NG_009089.2:g.28774A>C , LRG_134:g.28774A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1171A>C
ENST00000355740.8:c.*185A>C	ENSP00000347979.3:n.*185A>C
ENST00000357339.7:c.799A>C	ENSP00000349896.2:p.Lys267Gln
ENST00000371857.8:n.2407A>C
ENST00000460510.6:c.145A>C	ENSP00000512812.1:p.Lys49Gln
ENST00000466081.6:n.2511A>C
ENST00000477270.6:c.907A>C	ENSP00000512813.1:p.Lys303Gln
ENST00000479522.6:c.*291A>C	ENSP00000424113.1:n.*291A>C
ENST00000484444.6:c.*303A>C	ENSP00000420975.1:n.*303A>C
ENST00000488877.6:c.753A>C	ENSP00000425159.1:n.753A>C
ENST00000492756.7:c.*291A>C	ENSP00000422453.1:n.*291A>C
ENST00000494799.6:c.145A>C	ENSP00000512834.1:p.Lys49Gln
ENST00000562983.3:c.145A>C	ENSP00000512845.1:p.Lys49Gln
ENST00000612663.6:c.*264A>C	ENSP00000477997.3:n.*264A>C
ENST00000640140.2:n.1007A>C
ENST00000640250.2:n.361A>C
ENST00000640681.2:n.966A>C
ENST00000696723.1:n.4495A>C
ENST00000696741.1:n.2500A>C
ENST00000696742.1:n.2227A>C
ENST00000696743.1:n.3630A>C
ENST00000696744.1:n.901A>C
ENST00000696767.1:n.1196A>C
ENST00000696768.1:c.*185A>C	ENSP00000512859.1:n.*185A>C
ENST00000696769.1:n.2551A>C
ENST00000696771.1:c.145A>C	ENSP00000512860.1:p.Lys49Gln
ENST00000696772.1:n.2465A>C
ENST00000696773.1:n.2204A>C
ENST00000696774.1:n.5972A>C
ENST00000696776.1:c.955A>C	ENSP00000512861.1:p.Lys319Gln
ENST00000696777.1:n.2270A>C
ENST00000696778.1:n.1298A>C
ENST00000696779.1:c.469A>C	ENSP00000512862.1:p.Lys157Gln
ENST00000696780.1:c.892A>C	ENSP00000512863.1:p.Lys298Gln
ENST00000696781.1:c.607A>C	ENSP00000512864.1:p.Lys203Gln
ENST00000696782.1:c.*264A>C	ENSP00000512865.1:n.*264A>C
ENST00000696783.1:n.2730A>C
ENST00000696992.1:n.1979A>C
ENST00000696995.1:n.4391A>C
ENST00000696996.1:n.2304A>C
ENST00000696997.1:c.*492A>C	ENSP00000513028.1:n.*492A>C
ENST00000696998.1:n.2116A>C
ENST00000696999.1:c.145A>C	ENSP00000513029.1:p.Lys49Gln
ENST00000697036.1:c.*278A>C	ENSP00000513060.1:n.*278A>C
ENST00000697037.1:n.897A>C
ENST00000697093.1:n.3098A>C
ENST00000697094.1:n.3445A>C
ENST00000697095.1:c.*2063A>C	ENSP00000513104.1:n.*2063A>C
ENST00000697096.1:n.1995A>C
ENST00000697097.1:c.145A>C	ENSP00000513105.1:p.Lys49Gln
ENST00000562983.2:n.1048A>C
ENST00000690268.1:c.943A>C	ENSP00000509810.1:p.Lys315Gln
ENST00000355740.7:c.*188A>C	ENSP00000347979.3:n.*188A>C
ENST00000612663.5:c.*264A>C	ENSP00000477997.3:n.*264A>C
ENST00000640140.1:n.1034A>C
ENST00000640250.1:n.361A>C
ENST00000640681.1:n.983A>C
ENST00000652046.1:c.862A>C MANE Select	ENSP00000498466.1:p.Lys288Gln
ENST00000352159.8:c.*179A>C	ENSP00000345601.4:n.*179A>C
ENST00000355279.2:c.837A>C	ENSP00000347426.2:n.837A>C
ENST00000355740.6:c.862A>C	ENSP00000347979.2:p.Lys288Gln
ENST00000357339.6:c.799A>C	ENSP00000349896.2:p.Lys267Gln
ENST00000479522.5:c.*291A>C	ENSP00000424113.1:n.*291A>C
ENST00000484444.5:c.*303A>C	ENSP00000420975.1:n.*303A>C
ENST00000488877.5:c.*303A>C	ENSP00000425159.1:n.*303A>C
ENST00000492756.5:c.690A>C	ENSP00000422453.1:n.690A>C
ENST00000494410.5:c.*220A>C	ENSP00000423755.1:n.*220A>C
ENST00000612663.4:c.*209A>C	ENSP00000477997.2:n.*209A>C
NM_000043.4:c.862A>C , LRG_134t1:c.862A>C	NP_000034.1:p.Lys288Gln
NM_152871.2:c.799A>C	NP_690610.1:p.Lys267Gln
NM_152872.2:c.*174A>C	NP_690611.1:n.*174A>C
NR_028033.2:n.1036A>C
NR_028034.2:n.898A>C
NR_028035.2:n.961A>C
NR_028036.2:n.1099A>C
XM_006717819.2:c.943A>C	XP_006717882.1:p.Lys315Gln
XM_011539764.1:c.1024A>C	XP_011538066.1:p.Lys342Gln
XM_011539765.1:c.961A>C	XP_011538067.1:p.Lys321Gln
XM_011539766.1:c.943A>C	XP_011538068.1:p.Lys315Gln
XM_011539767.1:c.907A>C	XP_011538069.1:p.Lys303Gln
XR_945732.1:n.930A>C
XR_945733.1:n.867A>C
NM_000043.5:c.862A>C	NP_000034.1:p.Lys288Gln
NM_001320619.1:c.*185A>C	NP_001307548.1:n.*185A>C
NM_152871.3:c.799A>C	NP_690610.1:p.Lys267Gln
NM_152872.3:c.*174A>C	NP_690611.1:n.*174A>C
NR_028033.3:n.1008A>C
NR_028034.3:n.870A>C
NR_028035.3:n.933A>C
NR_028036.3:n.1071A>C
NR_135313.1:n.988A>C
NR_135314.1:n.1171A>C
NR_135315.1:n.924A>C
XM_006717819.3:c.943A>C	XP_006717882.1:p.Lys315Gln
XM_011539764.2:c.1024A>C	XP_011538066.1:p.Lys342Gln
XM_011539765.2:c.961A>C	XP_011538067.1:p.Lys321Gln
XM_011539766.2:c.943A>C	XP_011538068.1:p.Lys315Gln
XM_011539767.3:c.907A>C	XP_011538069.1:p.Lys303Gln
XR_945732.3:n.930A>C
XR_945733.2:n.867A>C
NM_000043.6:c.862A>C MANE Select	NP_000034.1:p.Lys288Gln
NM_001320619.2:c.*185A>C	NP_001307548.1:n.*185A>C
NM_152871.4:c.799A>C	NP_690610.1:p.Lys267Gln
NM_152872.4:c.*174A>C	NP_690611.1:n.*174A>C
NR_028033.4:n.769A>C
NR_028034.4:n.631A>C
NR_028035.4:n.694A>C
NR_028036.4:n.832A>C
NR_135313.2:n.749A>C
NR_135314.2:n.1028A>C
NR_135315.2:n.781A>C