Canonical Allele Identifier: CA470974915

Gene: FAS

Linked Data

• ClinVar Variation Id: 1602227
• ClinVar RCV Id: RCV002129928
• dbSNP Id: rs1413117342
• gnomAD v2: 10-90774078-A-G
• gnomAD v4: 10-89014321-A-G
• MyVariant Identifiers: chr10:g.90774078A>G (hg19) ; chr10:g.89014321A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014321A>G , CM000672.2:g.89014321A>G	GRCh38
NC_000010.10:g.90774078A>G , CM000672.1:g.90774078A>G	GRCh37
NC_000010.9:g.90764058A>G	NCBI36
NG_009089.2:g.28791A>G , LRG_134:g.28791A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1188A>G
ENST00000355740.8:c.*202A>G	ENSP00000347979.3:n.*202A>G
ENST00000357339.7:c.816A>G	ENSP00000349896.2:p.Thr272=
ENST00000371857.8:n.2424A>G
ENST00000460510.6:c.162A>G	ENSP00000512812.1:p.Thr54=
ENST00000466081.6:n.2528A>G
ENST00000477270.6:c.924A>G	ENSP00000512813.1:p.Thr308=
ENST00000479522.6:c.*308A>G	ENSP00000424113.1:n.*308A>G
ENST00000484444.6:c.*320A>G	ENSP00000420975.1:n.*320A>G
ENST00000488877.6:c.770A>G	ENSP00000425159.1:n.770A>G
ENST00000492756.7:c.*308A>G	ENSP00000422453.1:n.*308A>G
ENST00000494799.6:c.162A>G	ENSP00000512834.1:p.Thr54=
ENST00000562983.3:c.162A>G	ENSP00000512845.1:p.Thr54=
ENST00000612663.6:c.*281A>G	ENSP00000477997.3:n.*281A>G
ENST00000640140.2:n.1024A>G
ENST00000640250.2:n.378A>G
ENST00000640681.2:n.983A>G
ENST00000696723.1:n.4512A>G
ENST00000696741.1:n.2517A>G
ENST00000696742.1:n.2244A>G
ENST00000696743.1:n.3647A>G
ENST00000696744.1:n.918A>G
ENST00000696767.1:n.1213A>G
ENST00000696768.1:c.*202A>G	ENSP00000512859.1:n.*202A>G
ENST00000696769.1:n.2568A>G
ENST00000696771.1:c.162A>G	ENSP00000512860.1:p.Thr54=
ENST00000696772.1:n.2482A>G
ENST00000696773.1:n.2221A>G
ENST00000696774.1:n.5989A>G
ENST00000696776.1:c.972A>G	ENSP00000512861.1:p.Thr324=
ENST00000696777.1:n.2287A>G
ENST00000696778.1:n.1315A>G
ENST00000696779.1:c.486A>G	ENSP00000512862.1:p.Thr162=
ENST00000696780.1:c.909A>G	ENSP00000512863.1:p.Thr303=
ENST00000696781.1:c.624A>G	ENSP00000512864.1:p.Thr208=
ENST00000696782.1:c.*281A>G	ENSP00000512865.1:n.*281A>G
ENST00000696783.1:n.2747A>G
ENST00000696992.1:n.1996A>G
ENST00000696995.1:n.4408A>G
ENST00000696996.1:n.2321A>G
ENST00000696997.1:c.*509A>G	ENSP00000513028.1:n.*509A>G
ENST00000696998.1:n.2133A>G
ENST00000696999.1:c.162A>G	ENSP00000513029.1:p.Thr54=
ENST00000697036.1:c.*295A>G	ENSP00000513060.1:n.*295A>G
ENST00000697037.1:n.914A>G
ENST00000697093.1:n.3115A>G
ENST00000697094.1:n.3462A>G
ENST00000697095.1:c.*2080A>G	ENSP00000513104.1:n.*2080A>G
ENST00000697096.1:n.2012A>G
ENST00000697097.1:c.162A>G	ENSP00000513105.1:p.Thr54=
ENST00000562983.2:n.1065A>G
ENST00000690268.1:c.960A>G	ENSP00000509810.1:p.Thr320=
ENST00000355740.7:c.*205A>G	ENSP00000347979.3:n.*205A>G
ENST00000612663.5:c.*281A>G	ENSP00000477997.3:n.*281A>G
ENST00000640140.1:n.1051A>G
ENST00000640250.1:n.378A>G
ENST00000640681.1:n.1000A>G
ENST00000652046.1:c.879A>G MANE Select	ENSP00000498466.1:p.Thr293=
ENST00000352159.8:c.*196A>G	ENSP00000345601.4:n.*196A>G
ENST00000355279.2:c.854A>G	ENSP00000347426.2:n.854A>G
ENST00000355740.6:c.879A>G	ENSP00000347979.2:p.Thr293=
ENST00000357339.6:c.816A>G	ENSP00000349896.2:p.Thr272=
ENST00000479522.5:c.*308A>G	ENSP00000424113.1:n.*308A>G
ENST00000484444.5:c.*320A>G	ENSP00000420975.1:n.*320A>G
ENST00000488877.5:c.*320A>G	ENSP00000425159.1:n.*320A>G
ENST00000492756.5:c.707A>G	ENSP00000422453.1:n.707A>G
ENST00000494410.5:c.*237A>G	ENSP00000423755.1:n.*237A>G
ENST00000612663.4:c.*226A>G	ENSP00000477997.2:n.*226A>G
NM_000043.4:c.879A>G , LRG_134t1:c.879A>G	NP_000034.1:p.Thr293=
NM_152871.2:c.816A>G	NP_690610.1:p.Thr272=
NM_152872.2:c.*191A>G	NP_690611.1:n.*191A>G
NR_028033.2:n.1053A>G
NR_028034.2:n.915A>G
NR_028035.2:n.978A>G
NR_028036.2:n.1116A>G
XM_006717819.2:c.960A>G	XP_006717882.1:p.Thr320=
XM_011539764.1:c.1041A>G	XP_011538066.1:p.Thr347=
XM_011539765.1:c.978A>G	XP_011538067.1:p.Thr326=
XM_011539766.1:c.960A>G	XP_011538068.1:p.Thr320=
XM_011539767.1:c.924A>G	XP_011538069.1:p.Thr308=
XR_945732.1:n.947A>G
XR_945733.1:n.884A>G
NM_000043.5:c.879A>G	NP_000034.1:p.Thr293=
NM_001320619.1:c.*202A>G	NP_001307548.1:n.*202A>G
NM_152871.3:c.816A>G	NP_690610.1:p.Thr272=
NM_152872.3:c.*191A>G	NP_690611.1:n.*191A>G
NR_028033.3:n.1025A>G
NR_028034.3:n.887A>G
NR_028035.3:n.950A>G
NR_028036.3:n.1088A>G
NR_135313.1:n.1005A>G
NR_135314.1:n.1188A>G
NR_135315.1:n.941A>G
XM_006717819.3:c.960A>G	XP_006717882.1:p.Thr320=
XM_011539764.2:c.1041A>G	XP_011538066.1:p.Thr347=
XM_011539765.2:c.978A>G	XP_011538067.1:p.Thr326=
XM_011539766.2:c.960A>G	XP_011538068.1:p.Thr320=
XM_011539767.3:c.924A>G	XP_011538069.1:p.Thr308=
XR_945732.3:n.947A>G
XR_945733.2:n.884A>G
NM_000043.6:c.879A>G MANE Select	NP_000034.1:p.Thr293=
NM_001320619.2:c.*202A>G	NP_001307548.1:n.*202A>G
NM_152871.4:c.816A>G	NP_690610.1:p.Thr272=
NM_152872.4:c.*191A>G	NP_690611.1:n.*191A>G
NR_028033.4:n.786A>G
NR_028034.4:n.648A>G
NR_028035.4:n.711A>G
NR_028036.4:n.849A>G
NR_135313.2:n.766A>G
NR_135314.2:n.1045A>G
NR_135315.2:n.798A>G