Canonical Allele Identifier: CA5593225

Gene: FAS

Linked Data

• dbSNP Id: rs772863534
• ExAC: 10:90774036 T / C
• gnomAD v2: 10-90774036-T-C
• gnomAD v4: 10-89014279-T-C
• MyVariant Identifiers: chr10:g.90774036T>C (hg19) ; chr10:g.89014279T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014279T>C , CM000672.2:g.89014279T>C	GRCh38
NC_000010.10:g.90774036T>C , CM000672.1:g.90774036T>C	GRCh37
NC_000010.9:g.90764016T>C	NCBI36
NG_009089.2:g.28749T>C , LRG_134:g.28749T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1146T>C
ENST00000355740.8:c.*160T>C	ENSP00000347979.3:n.*160T>C
ENST00000357339.7:c.774T>C	ENSP00000349896.2:p.Arg258=
ENST00000371857.8:n.2382T>C
ENST00000460510.6:c.120T>C	ENSP00000512812.1:p.Arg40=
ENST00000466081.6:n.2486T>C
ENST00000477270.6:c.882T>C	ENSP00000512813.1:p.Arg294=
ENST00000479522.6:c.*266T>C	ENSP00000424113.1:n.*266T>C
ENST00000484444.6:c.*278T>C	ENSP00000420975.1:n.*278T>C
ENST00000488877.6:c.728T>C	ENSP00000425159.1:n.728T>C
ENST00000492756.7:c.*266T>C	ENSP00000422453.1:n.*266T>C
ENST00000494799.6:c.120T>C	ENSP00000512834.1:p.Arg40=
ENST00000562983.3:c.120T>C	ENSP00000512845.1:p.Arg40=
ENST00000612663.6:c.*239T>C	ENSP00000477997.3:n.*239T>C
ENST00000640140.2:n.982T>C
ENST00000640250.2:n.336T>C
ENST00000640681.2:n.941T>C
ENST00000696723.1:n.4470T>C
ENST00000696741.1:n.2475T>C
ENST00000696742.1:n.2202T>C
ENST00000696743.1:n.3605T>C
ENST00000696744.1:n.876T>C
ENST00000696767.1:n.1171T>C
ENST00000696768.1:c.*160T>C	ENSP00000512859.1:n.*160T>C
ENST00000696769.1:n.2526T>C
ENST00000696771.1:c.120T>C	ENSP00000512860.1:p.Arg40=
ENST00000696772.1:n.2440T>C
ENST00000696773.1:n.2179T>C
ENST00000696774.1:n.5947T>C
ENST00000696776.1:c.930T>C	ENSP00000512861.1:p.Arg310=
ENST00000696777.1:n.2245T>C
ENST00000696778.1:n.1273T>C
ENST00000696779.1:c.444T>C	ENSP00000512862.1:p.Arg148=
ENST00000696780.1:c.867T>C	ENSP00000512863.1:p.Arg289=
ENST00000696781.1:c.582T>C	ENSP00000512864.1:p.Arg194=
ENST00000696782.1:c.*239T>C	ENSP00000512865.1:n.*239T>C
ENST00000696783.1:n.2705T>C
ENST00000696992.1:n.1954T>C
ENST00000696995.1:n.4366T>C
ENST00000696996.1:n.2279T>C
ENST00000696997.1:c.*467T>C	ENSP00000513028.1:n.*467T>C
ENST00000696998.1:n.2091T>C
ENST00000696999.1:c.120T>C	ENSP00000513029.1:p.Arg40=
ENST00000697035.1:c.*170T>C	ENSP00000513059.1:n.*170T>C
ENST00000697036.1:c.*253T>C	ENSP00000513060.1:n.*253T>C
ENST00000697037.1:n.872T>C
ENST00000697093.1:n.3073T>C
ENST00000697094.1:n.3420T>C
ENST00000697095.1:c.*2038T>C	ENSP00000513104.1:n.*2038T>C
ENST00000697096.1:n.1970T>C
ENST00000697097.1:c.120T>C	ENSP00000513105.1:p.Arg40=
ENST00000562983.2:n.1023T>C
ENST00000690268.1:c.918T>C	ENSP00000509810.1:p.Arg306=
ENST00000355740.7:c.*163T>C	ENSP00000347979.3:n.*163T>C
ENST00000612663.5:c.*239T>C	ENSP00000477997.3:n.*239T>C
ENST00000640140.1:n.1009T>C
ENST00000640250.1:n.336T>C
ENST00000640681.1:n.958T>C
ENST00000652046.1:c.837T>C MANE Select	ENSP00000498466.1:p.Arg279=
ENST00000352159.8:c.*154T>C	ENSP00000345601.4:n.*154T>C
ENST00000355279.2:c.812T>C	ENSP00000347426.2:n.812T>C
ENST00000355740.6:c.837T>C	ENSP00000347979.2:p.Arg279=
ENST00000357339.6:c.774T>C	ENSP00000349896.2:p.Arg258=
ENST00000479522.5:c.*266T>C	ENSP00000424113.1:n.*266T>C
ENST00000484444.5:c.*278T>C	ENSP00000420975.1:n.*278T>C
ENST00000488877.5:c.*278T>C	ENSP00000425159.1:n.*278T>C
ENST00000492756.5:c.665T>C	ENSP00000422453.1:n.665T>C
ENST00000494410.5:c.*195T>C	ENSP00000423755.1:n.*195T>C
ENST00000612663.4:c.*184T>C	ENSP00000477997.2:n.*184T>C
NM_000043.4:c.837T>C , LRG_134t1:c.837T>C	NP_000034.1:p.Arg279=
NM_152871.2:c.774T>C	NP_690610.1:p.Arg258=
NM_152872.2:c.*149T>C	NP_690611.1:n.*149T>C
NR_028033.2:n.1011T>C
NR_028034.2:n.873T>C
NR_028035.2:n.936T>C
NR_028036.2:n.1074T>C
XM_006717819.2:c.918T>C	XP_006717882.1:p.Arg306=
XM_011539764.1:c.999T>C	XP_011538066.1:p.Arg333=
XM_011539765.1:c.936T>C	XP_011538067.1:p.Arg312=
XM_011539766.1:c.918T>C	XP_011538068.1:p.Arg306=
XM_011539767.1:c.882T>C	XP_011538069.1:p.Arg294=
XR_945732.1:n.905T>C
XR_945733.1:n.842T>C
NM_000043.5:c.837T>C	NP_000034.1:p.Arg279=
NM_001320619.1:c.*160T>C	NP_001307548.1:n.*160T>C
NM_152871.3:c.774T>C	NP_690610.1:p.Arg258=
NM_152872.3:c.*149T>C	NP_690611.1:n.*149T>C
NR_028033.3:n.983T>C
NR_028034.3:n.845T>C
NR_028035.3:n.908T>C
NR_028036.3:n.1046T>C
NR_135313.1:n.963T>C
NR_135314.1:n.1146T>C
NR_135315.1:n.899T>C
XM_006717819.3:c.918T>C	XP_006717882.1:p.Arg306=
XM_011539764.2:c.999T>C	XP_011538066.1:p.Arg333=
XM_011539765.2:c.936T>C	XP_011538067.1:p.Arg312=
XM_011539766.2:c.918T>C	XP_011538068.1:p.Arg306=
XM_011539767.3:c.882T>C	XP_011538069.1:p.Arg294=
XR_945732.3:n.905T>C
XR_945733.2:n.842T>C
NM_000043.6:c.837T>C MANE Select	NP_000034.1:p.Arg279=
NM_001320619.2:c.*160T>C	NP_001307548.1:n.*160T>C
NM_152871.4:c.774T>C	NP_690610.1:p.Arg258=
NM_152872.4:c.*149T>C	NP_690611.1:n.*149T>C
NR_028033.4:n.744T>C
NR_028034.4:n.606T>C
NR_028035.4:n.669T>C
NR_028036.4:n.807T>C
NR_135313.2:n.724T>C
NR_135314.2:n.1003T>C
NR_135315.2:n.756T>C