Canonical Allele Identifier: CA377509663

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773927G>T (hg19) ; chr10:g.89014170G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014170G>T , CM000672.2:g.89014170G>T	GRCh38
NC_000010.10:g.90773927G>T , CM000672.1:g.90773927G>T	GRCh37
NC_000010.9:g.90763907G>T	NCBI36
NG_009089.2:g.28640G>T , LRG_134:g.28640G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1037G>T
ENST00000355740.8:c.*51G>T	ENSP00000347979.3:n.*51G>T
ENST00000357339.7:c.665G>T	ENSP00000349896.2:p.Ser222Ile
ENST00000371857.8:n.2273G>T
ENST00000460510.6:c.11G>T	ENSP00000512812.1:p.Ser4Ile
ENST00000466081.6:n.2377G>T
ENST00000477270.6:c.773G>T	ENSP00000512813.1:p.Ser258Ile
ENST00000479522.6:c.*157G>T	ENSP00000424113.1:n.*157G>T
ENST00000484444.6:c.*169G>T	ENSP00000420975.1:n.*169G>T
ENST00000488877.6:c.619G>T	ENSP00000425159.1:n.619G>T
ENST00000492756.7:c.*157G>T	ENSP00000422453.1:n.*157G>T
ENST00000494799.6:c.11G>T	ENSP00000512834.1:p.Ser4Ile
ENST00000562983.3:c.11G>T	ENSP00000512845.1:p.Ser4Ile
ENST00000612663.6:c.*130G>T	ENSP00000477997.3:n.*130G>T
ENST00000640140.2:n.873G>T
ENST00000640250.2:n.227G>T
ENST00000640681.2:n.832G>T
ENST00000696723.1:n.4361G>T
ENST00000696741.1:n.2366G>T
ENST00000696742.1:n.2093G>T
ENST00000696743.1:n.3496G>T
ENST00000696744.1:n.767G>T
ENST00000696767.1:n.1062G>T
ENST00000696768.1:c.*51G>T	ENSP00000512859.1:n.*51G>T
ENST00000696769.1:n.2417G>T
ENST00000696771.1:c.11G>T	ENSP00000512860.1:p.Ser4Ile
ENST00000696772.1:n.2331G>T
ENST00000696773.1:n.2070G>T
ENST00000696774.1:n.5838G>T
ENST00000696776.1:c.821G>T	ENSP00000512861.1:p.Ser274Ile
ENST00000696777.1:n.2136G>T
ENST00000696778.1:n.1164G>T
ENST00000696779.1:c.335G>T	ENSP00000512862.1:p.Ser112Ile
ENST00000696780.1:c.758G>T	ENSP00000512863.1:p.Ser253Ile
ENST00000696781.1:c.473G>T	ENSP00000512864.1:p.Ser158Ile
ENST00000696782.1:c.*130G>T	ENSP00000512865.1:n.*130G>T
ENST00000696783.1:n.2596G>T
ENST00000696992.1:n.1845G>T
ENST00000696995.1:n.4257G>T
ENST00000696996.1:n.2170G>T
ENST00000696997.1:c.*358G>T	ENSP00000513028.1:n.*358G>T
ENST00000696998.1:n.1982G>T
ENST00000696999.1:c.11G>T	ENSP00000513029.1:p.Ser4Ile
ENST00000697035.1:c.*61G>T	ENSP00000513059.1:n.*61G>T
ENST00000697036.1:c.*144G>T	ENSP00000513060.1:n.*144G>T
ENST00000697037.1:n.763G>T
ENST00000697093.1:n.2964G>T
ENST00000697094.1:n.3311G>T
ENST00000697095.1:c.*1929G>T	ENSP00000513104.1:n.*1929G>T
ENST00000697096.1:n.1861G>T
ENST00000697097.1:c.11G>T	ENSP00000513105.1:p.Ser4Ile
ENST00000562983.2:n.914G>T
ENST00000690268.1:c.809G>T	ENSP00000509810.1:p.Ser270Ile
ENST00000355740.7:c.*54G>T	ENSP00000347979.3:n.*54G>T
ENST00000612663.5:c.*130G>T	ENSP00000477997.3:n.*130G>T
ENST00000640140.1:n.900G>T
ENST00000640250.1:n.227G>T
ENST00000640681.1:n.849G>T
ENST00000652046.1:c.728G>T MANE Select	ENSP00000498466.1:p.Ser243Ile
ENST00000313771.9:n.1037G>T
ENST00000352159.8:c.*45G>T	ENSP00000345601.4:n.*45G>T
ENST00000355279.2:c.703G>T	ENSP00000347426.2:n.703G>T
ENST00000355740.6:c.728G>T	ENSP00000347979.2:p.Ser243Ile
ENST00000357339.6:c.665G>T	ENSP00000349896.2:p.Ser222Ile
ENST00000479522.5:c.*157G>T	ENSP00000424113.1:n.*157G>T
ENST00000484444.5:c.*169G>T	ENSP00000420975.1:n.*169G>T
ENST00000488877.5:c.*169G>T	ENSP00000425159.1:n.*169G>T
ENST00000492756.5:c.556G>T	ENSP00000422453.1:n.556G>T
ENST00000494410.5:c.*86G>T	ENSP00000423755.1:n.*86G>T
ENST00000494799.5:n.635G>T
ENST00000612663.4:c.*75G>T	ENSP00000477997.2:n.*75G>T
ENST00000615406.4:c.728G>T	ENSP00000484575.1:p.Ser243Ile
ENST00000626542.2:c.726G>T	ENSP00000485876.1:p.Lys242Asn
NM_000043.4:c.728G>T , LRG_134t1:c.728G>T	NP_000034.1:p.Ser243Ile
NM_152871.2:c.665G>T	NP_690610.1:p.Ser222Ile
NM_152872.2:c.*40G>T	NP_690611.1:n.*40G>T
NR_028033.2:n.902G>T
NR_028034.2:n.764G>T
NR_028035.2:n.827G>T
NR_028036.2:n.965G>T
XM_006717819.2:c.809G>T	XP_006717882.1:p.Ser270Ile
XM_011539764.1:c.890G>T	XP_011538066.1:p.Ser297Ile
XM_011539765.1:c.827G>T	XP_011538067.1:p.Ser276Ile
XM_011539766.1:c.809G>T	XP_011538068.1:p.Ser270Ile
XM_011539767.1:c.773G>T	XP_011538069.1:p.Ser258Ile
XR_945732.1:n.796G>T
XR_945733.1:n.733G>T
NM_000043.5:c.728G>T	NP_000034.1:p.Ser243Ile
NM_001320619.1:c.*51G>T	NP_001307548.1:n.*51G>T
NM_152871.3:c.665G>T	NP_690610.1:p.Ser222Ile
NM_152872.3:c.*40G>T	NP_690611.1:n.*40G>T
NR_028033.3:n.874G>T
NR_028034.3:n.736G>T
NR_028035.3:n.799G>T
NR_028036.3:n.937G>T
NR_135313.1:n.854G>T
NR_135314.1:n.1037G>T
NR_135315.1:n.790G>T
XM_006717819.3:c.809G>T	XP_006717882.1:p.Ser270Ile
XM_011539764.2:c.890G>T	XP_011538066.1:p.Ser297Ile
XM_011539765.2:c.827G>T	XP_011538067.1:p.Ser276Ile
XM_011539766.2:c.809G>T	XP_011538068.1:p.Ser270Ile
XM_011539767.3:c.773G>T	XP_011538069.1:p.Ser258Ile
XR_945732.3:n.796G>T
XR_945733.2:n.733G>T
NM_000043.6:c.728G>T MANE Select	NP_000034.1:p.Ser243Ile
NM_001320619.2:c.*51G>T	NP_001307548.1:n.*51G>T
NM_152871.4:c.665G>T	NP_690610.1:p.Ser222Ile
NM_152872.4:c.*40G>T	NP_690611.1:n.*40G>T
NR_028033.4:n.635G>T
NR_028034.4:n.497G>T
NR_028035.4:n.560G>T
NR_028036.4:n.698G>T
NR_135313.2:n.615G>T
NR_135314.2:n.894G>T
NR_135315.2:n.647G>T