Canonical Allele Identifier: CA594943250

Gene: FAS

Linked Data

• dbSNP Id: rs1269597670
• gnomAD v2: 10-90774316-T-G
• gnomAD v4: 10-89014559-T-G
• MyVariant Identifiers: chr10:g.90774316T>G (hg19) ; chr10:g.89014559T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014559T>G , CM000672.2:g.89014559T>G	GRCh38
NC_000010.10:g.90774316T>G , CM000672.1:g.90774316T>G	GRCh37
NC_000010.9:g.90764296T>G	NCBI36
NG_009089.2:g.29029T>G , LRG_134:g.29029T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1426T>G
ENST00000355740.8:c.*440T>G	ENSP00000347979.3:n.*440T>G
ENST00000357339.7:c.*109T>G	ENSP00000349896.2:n.*109T>G
ENST00000371857.8:n.2662T>G
ENST00000460510.6:c.*109T>G	ENSP00000512812.1:n.*109T>G
ENST00000466081.6:n.2766T>G
ENST00000477270.6:c.*109T>G	ENSP00000512813.1:n.*109T>G
ENST00000479522.6:c.*546T>G	ENSP00000424113.1:n.*546T>G
ENST00000484444.6:c.*558T>G	ENSP00000420975.1:n.*558T>G
ENST00000488877.6:c.1008T>G	ENSP00000425159.1:n.1008T>G
ENST00000492756.7:c.*546T>G	ENSP00000422453.1:n.*546T>G
ENST00000494799.6:c.*109T>G	ENSP00000512834.1:n.*109T>G
ENST00000562983.3:c.*109T>G	ENSP00000512845.1:n.*109T>G
ENST00000612663.6:c.*519T>G	ENSP00000477997.3:n.*519T>G
ENST00000640140.2:n.1262T>G
ENST00000640250.2:n.616T>G
ENST00000640681.2:n.1221T>G
ENST00000696723.1:n.4750T>G
ENST00000696741.1:n.2755T>G
ENST00000696742.1:n.2482T>G
ENST00000696743.1:n.3885T>G
ENST00000696744.1:n.1156T>G
ENST00000696767.1:n.1451T>G
ENST00000696768.1:c.*440T>G	ENSP00000512859.1:n.*440T>G
ENST00000696769.1:n.2806T>G
ENST00000696771.1:c.*109T>G	ENSP00000512860.1:n.*109T>G
ENST00000696772.1:n.2720T>G
ENST00000696773.1:n.2459T>G
ENST00000696774.1:n.6227T>G
ENST00000696776.1:c.*109T>G	ENSP00000512861.1:n.*109T>G
ENST00000696777.1:n.2525T>G
ENST00000696778.1:n.1553T>G
ENST00000696779.1:c.*109T>G	ENSP00000512862.1:n.*109T>G
ENST00000696780.1:c.*109T>G	ENSP00000512863.1:n.*109T>G
ENST00000696781.1:c.*109T>G	ENSP00000512864.1:n.*109T>G
ENST00000696782.1:c.*519T>G	ENSP00000512865.1:n.*519T>G
ENST00000696783.1:n.2985T>G
ENST00000696992.1:n.2234T>G
ENST00000696995.1:n.4646T>G
ENST00000696996.1:n.2559T>G
ENST00000696997.1:c.*747T>G	ENSP00000513028.1:n.*747T>G
ENST00000696998.1:n.2371T>G
ENST00000696999.1:c.*109T>G	ENSP00000513029.1:n.*109T>G
ENST00000697036.1:c.*533T>G	ENSP00000513060.1:n.*533T>G
ENST00000697037.1:n.1152T>G
ENST00000697093.1:n.3353T>G
ENST00000697094.1:n.3700T>G
ENST00000697095.1:c.*2318T>G	ENSP00000513104.1:n.*2318T>G
ENST00000697096.1:n.2250T>G
ENST00000697097.1:c.*109T>G	ENSP00000513105.1:n.*109T>G
ENST00000562983.2:n.1303T>G
ENST00000690268.1:c.*109T>G	ENSP00000509810.1:n.*109T>G
ENST00000355740.7:c.*443T>G	ENSP00000347979.3:n.*443T>G
ENST00000640140.1:n.1289T>G
ENST00000640250.1:n.616T>G
ENST00000640681.1:n.1238T>G
ENST00000652046.1:c.*109T>G MANE Select	ENSP00000498466.1:n.*109T>G
ENST00000352159.8:c.*434T>G	ENSP00000345601.4:n.*434T>G
ENST00000355740.6:c.*109T>G	ENSP00000347979.2:n.*109T>G
ENST00000479522.5:c.*546T>G	ENSP00000424113.1:n.*546T>G
ENST00000484444.5:c.*558T>G	ENSP00000420975.1:n.*558T>G
ENST00000494410.5:c.*475T>G	ENSP00000423755.1:n.*475T>G
NM_000043.4:c.*109T>G , LRG_134t1:c.*109T>G	NP_000034.1:n.*109T>G
NM_152871.2:c.*109T>G	NP_690610.1:n.*109T>G
NM_152872.2:c.*429T>G	NP_690611.1:n.*429T>G
NR_028033.2:n.1291T>G
NR_028034.2:n.1153T>G
NR_028035.2:n.1216T>G
NR_028036.2:n.1354T>G
XM_006717819.2:c.*109T>G	XP_006717882.1:n.*109T>G
XM_011539764.1:c.*109T>G	XP_011538066.1:n.*109T>G
XM_011539765.1:c.*109T>G	XP_011538067.1:n.*109T>G
XM_011539766.1:c.*109T>G	XP_011538068.1:n.*109T>G
XM_011539767.1:c.*109T>G	XP_011538069.1:n.*109T>G
NM_000043.5:c.*109T>G	NP_000034.1:n.*109T>G
NM_001320619.1:c.*440T>G	NP_001307548.1:n.*440T>G
NM_152871.3:c.*109T>G	NP_690610.1:n.*109T>G
NM_152872.3:c.*429T>G	NP_690611.1:n.*429T>G
NR_028033.3:n.1263T>G
NR_028034.3:n.1125T>G
NR_028035.3:n.1188T>G
NR_028036.3:n.1326T>G
NR_135313.1:n.1243T>G
NR_135314.1:n.1426T>G
NR_135315.1:n.1179T>G
XM_006717819.3:c.*109T>G	XP_006717882.1:n.*109T>G
XM_011539764.2:c.*109T>G	XP_011538066.1:n.*109T>G
XM_011539765.2:c.*109T>G	XP_011538067.1:n.*109T>G
XM_011539766.2:c.*109T>G	XP_011538068.1:n.*109T>G
XM_011539767.3:c.*109T>G	XP_011538069.1:n.*109T>G
XR_945732.3:n.1185T>G
XR_945733.2:n.1122T>G
NM_000043.6:c.*109T>G MANE Select	NP_000034.1:n.*109T>G
NM_001320619.2:c.*440T>G	NP_001307548.1:n.*440T>G
NM_152871.4:c.*109T>G	NP_690610.1:n.*109T>G
NM_152872.4:c.*429T>G	NP_690611.1:n.*429T>G
NR_028033.4:n.1024T>G
NR_028034.4:n.886T>G
NR_028035.4:n.949T>G
NR_028036.4:n.1087T>G
NR_135313.2:n.1004T>G
NR_135314.2:n.1283T>G
NR_135315.2:n.1036T>G