Canonical Allele Identifier: CA470975019

Gene: FAS

Linked Data

• dbSNP Id: rs1375193873
• gnomAD v2: 10-90774027-A-G
• gnomAD v4: 10-89014270-A-G
• MyVariant Identifiers: chr10:g.90774027A>G (hg19) ; chr10:g.89014270A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014270A>G , CM000672.2:g.89014270A>G	GRCh38
NC_000010.10:g.90774027A>G , CM000672.1:g.90774027A>G	GRCh37
NC_000010.9:g.90764007A>G	NCBI36
NG_009089.2:g.28740A>G , LRG_134:g.28740A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1137A>G
ENST00000355740.8:c.*151A>G	ENSP00000347979.3:n.*151A>G
ENST00000357339.7:c.765A>G	ENSP00000349896.2:p.Gln255=
ENST00000371857.8:n.2373A>G
ENST00000460510.6:c.111A>G	ENSP00000512812.1:p.Gln37=
ENST00000466081.6:n.2477A>G
ENST00000477270.6:c.873A>G	ENSP00000512813.1:p.Gln291=
ENST00000479522.6:c.*257A>G	ENSP00000424113.1:n.*257A>G
ENST00000484444.6:c.*269A>G	ENSP00000420975.1:n.*269A>G
ENST00000488877.6:c.719A>G	ENSP00000425159.1:n.719A>G
ENST00000492756.7:c.*257A>G	ENSP00000422453.1:n.*257A>G
ENST00000494799.6:c.111A>G	ENSP00000512834.1:p.Gln37=
ENST00000562983.3:c.111A>G	ENSP00000512845.1:p.Gln37=
ENST00000612663.6:c.*230A>G	ENSP00000477997.3:n.*230A>G
ENST00000640140.2:n.973A>G
ENST00000640250.2:n.327A>G
ENST00000640681.2:n.932A>G
ENST00000696723.1:n.4461A>G
ENST00000696741.1:n.2466A>G
ENST00000696742.1:n.2193A>G
ENST00000696743.1:n.3596A>G
ENST00000696744.1:n.867A>G
ENST00000696767.1:n.1162A>G
ENST00000696768.1:c.*151A>G	ENSP00000512859.1:n.*151A>G
ENST00000696769.1:n.2517A>G
ENST00000696771.1:c.111A>G	ENSP00000512860.1:p.Gln37=
ENST00000696772.1:n.2431A>G
ENST00000696773.1:n.2170A>G
ENST00000696774.1:n.5938A>G
ENST00000696776.1:c.921A>G	ENSP00000512861.1:p.Gln307=
ENST00000696777.1:n.2236A>G
ENST00000696778.1:n.1264A>G
ENST00000696779.1:c.435A>G	ENSP00000512862.1:p.Gln145=
ENST00000696780.1:c.858A>G	ENSP00000512863.1:p.Gln286=
ENST00000696781.1:c.573A>G	ENSP00000512864.1:p.Gln191=
ENST00000696782.1:c.*230A>G	ENSP00000512865.1:n.*230A>G
ENST00000696783.1:n.2696A>G
ENST00000696992.1:n.1945A>G
ENST00000696995.1:n.4357A>G
ENST00000696996.1:n.2270A>G
ENST00000696997.1:c.*458A>G	ENSP00000513028.1:n.*458A>G
ENST00000696998.1:n.2082A>G
ENST00000696999.1:c.111A>G	ENSP00000513029.1:p.Gln37=
ENST00000697035.1:c.*161A>G	ENSP00000513059.1:n.*161A>G
ENST00000697036.1:c.*244A>G	ENSP00000513060.1:n.*244A>G
ENST00000697037.1:n.863A>G
ENST00000697093.1:n.3064A>G
ENST00000697094.1:n.3411A>G
ENST00000697095.1:c.*2029A>G	ENSP00000513104.1:n.*2029A>G
ENST00000697096.1:n.1961A>G
ENST00000697097.1:c.111A>G	ENSP00000513105.1:p.Gln37=
ENST00000562983.2:n.1014A>G
ENST00000690268.1:c.909A>G	ENSP00000509810.1:p.Gln303=
ENST00000355740.7:c.*154A>G	ENSP00000347979.3:n.*154A>G
ENST00000612663.5:c.*230A>G	ENSP00000477997.3:n.*230A>G
ENST00000640140.1:n.1000A>G
ENST00000640250.1:n.327A>G
ENST00000640681.1:n.949A>G
ENST00000652046.1:c.828A>G MANE Select	ENSP00000498466.1:p.Gln276=
ENST00000352159.8:c.*145A>G	ENSP00000345601.4:n.*145A>G
ENST00000355279.2:c.803A>G	ENSP00000347426.2:n.803A>G
ENST00000355740.6:c.828A>G	ENSP00000347979.2:p.Gln276=
ENST00000357339.6:c.765A>G	ENSP00000349896.2:p.Gln255=
ENST00000479522.5:c.*257A>G	ENSP00000424113.1:n.*257A>G
ENST00000484444.5:c.*269A>G	ENSP00000420975.1:n.*269A>G
ENST00000488877.5:c.*269A>G	ENSP00000425159.1:n.*269A>G
ENST00000492756.5:c.656A>G	ENSP00000422453.1:n.656A>G
ENST00000494410.5:c.*186A>G	ENSP00000423755.1:n.*186A>G
ENST00000612663.4:c.*175A>G	ENSP00000477997.2:n.*175A>G
NM_000043.4:c.828A>G , LRG_134t1:c.828A>G	NP_000034.1:p.Gln276=
NM_152871.2:c.765A>G	NP_690610.1:p.Gln255=
NM_152872.2:c.*140A>G	NP_690611.1:n.*140A>G
NR_028033.2:n.1002A>G
NR_028034.2:n.864A>G
NR_028035.2:n.927A>G
NR_028036.2:n.1065A>G
XM_006717819.2:c.909A>G	XP_006717882.1:p.Gln303=
XM_011539764.1:c.990A>G	XP_011538066.1:p.Gln330=
XM_011539765.1:c.927A>G	XP_011538067.1:p.Gln309=
XM_011539766.1:c.909A>G	XP_011538068.1:p.Gln303=
XM_011539767.1:c.873A>G	XP_011538069.1:p.Gln291=
XR_945732.1:n.896A>G
XR_945733.1:n.833A>G
NM_000043.5:c.828A>G	NP_000034.1:p.Gln276=
NM_001320619.1:c.*151A>G	NP_001307548.1:n.*151A>G
NM_152871.3:c.765A>G	NP_690610.1:p.Gln255=
NM_152872.3:c.*140A>G	NP_690611.1:n.*140A>G
NR_028033.3:n.974A>G
NR_028034.3:n.836A>G
NR_028035.3:n.899A>G
NR_028036.3:n.1037A>G
NR_135313.1:n.954A>G
NR_135314.1:n.1137A>G
NR_135315.1:n.890A>G
XM_006717819.3:c.909A>G	XP_006717882.1:p.Gln303=
XM_011539764.2:c.990A>G	XP_011538066.1:p.Gln330=
XM_011539765.2:c.927A>G	XP_011538067.1:p.Gln309=
XM_011539766.2:c.909A>G	XP_011538068.1:p.Gln303=
XM_011539767.3:c.873A>G	XP_011538069.1:p.Gln291=
XR_945732.3:n.896A>G
XR_945733.2:n.833A>G
NM_000043.6:c.828A>G MANE Select	NP_000034.1:p.Gln276=
NM_001320619.2:c.*151A>G	NP_001307548.1:n.*151A>G
NM_152871.4:c.765A>G	NP_690610.1:p.Gln255=
NM_152872.4:c.*140A>G	NP_690611.1:n.*140A>G
NR_028033.4:n.735A>G
NR_028034.4:n.597A>G
NR_028035.4:n.660A>G
NR_028036.4:n.798A>G
NR_135313.2:n.715A>G
NR_135314.2:n.994A>G
NR_135315.2:n.747A>G