Canonical Allele Identifier: CA377509926

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774038A>T (hg19) ; chr10:g.89014281A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014281A>T , CM000672.2:g.89014281A>T	GRCh38
NC_000010.10:g.90774038A>T , CM000672.1:g.90774038A>T	GRCh37
NC_000010.9:g.90764018A>T	NCBI36
NG_009089.2:g.28751A>T , LRG_134:g.28751A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1148A>T
ENST00000355740.8:c.*162A>T	ENSP00000347979.3:n.*162A>T
ENST00000357339.7:c.776A>T	ENSP00000349896.2:p.Asn259Ile
ENST00000371857.8:n.2384A>T
ENST00000460510.6:c.122A>T	ENSP00000512812.1:p.Asn41Ile
ENST00000466081.6:n.2488A>T
ENST00000477270.6:c.884A>T	ENSP00000512813.1:p.Asn295Ile
ENST00000479522.6:c.*268A>T	ENSP00000424113.1:n.*268A>T
ENST00000484444.6:c.*280A>T	ENSP00000420975.1:n.*280A>T
ENST00000488877.6:c.730A>T	ENSP00000425159.1:n.730A>T
ENST00000492756.7:c.*268A>T	ENSP00000422453.1:n.*268A>T
ENST00000494799.6:c.122A>T	ENSP00000512834.1:p.Asn41Ile
ENST00000562983.3:c.122A>T	ENSP00000512845.1:p.Asn41Ile
ENST00000612663.6:c.*241A>T	ENSP00000477997.3:n.*241A>T
ENST00000640140.2:n.984A>T
ENST00000640250.2:n.338A>T
ENST00000640681.2:n.943A>T
ENST00000696723.1:n.4472A>T
ENST00000696741.1:n.2477A>T
ENST00000696742.1:n.2204A>T
ENST00000696743.1:n.3607A>T
ENST00000696744.1:n.878A>T
ENST00000696767.1:n.1173A>T
ENST00000696768.1:c.*162A>T	ENSP00000512859.1:n.*162A>T
ENST00000696769.1:n.2528A>T
ENST00000696771.1:c.122A>T	ENSP00000512860.1:p.Asn41Ile
ENST00000696772.1:n.2442A>T
ENST00000696773.1:n.2181A>T
ENST00000696774.1:n.5949A>T
ENST00000696776.1:c.932A>T	ENSP00000512861.1:p.Asn311Ile
ENST00000696777.1:n.2247A>T
ENST00000696778.1:n.1275A>T
ENST00000696779.1:c.446A>T	ENSP00000512862.1:p.Asn149Ile
ENST00000696780.1:c.869A>T	ENSP00000512863.1:p.Asn290Ile
ENST00000696781.1:c.584A>T	ENSP00000512864.1:p.Asn195Ile
ENST00000696782.1:c.*241A>T	ENSP00000512865.1:n.*241A>T
ENST00000696783.1:n.2707A>T
ENST00000696992.1:n.1956A>T
ENST00000696995.1:n.4368A>T
ENST00000696996.1:n.2281A>T
ENST00000696997.1:c.*469A>T	ENSP00000513028.1:n.*469A>T
ENST00000696998.1:n.2093A>T
ENST00000696999.1:c.122A>T	ENSP00000513029.1:p.Asn41Ile
ENST00000697035.1:c.*172A>T	ENSP00000513059.1:n.*172A>T
ENST00000697036.1:c.*255A>T	ENSP00000513060.1:n.*255A>T
ENST00000697037.1:n.874A>T
ENST00000697093.1:n.3075A>T
ENST00000697094.1:n.3422A>T
ENST00000697095.1:c.*2040A>T	ENSP00000513104.1:n.*2040A>T
ENST00000697096.1:n.1972A>T
ENST00000697097.1:c.122A>T	ENSP00000513105.1:p.Asn41Ile
ENST00000562983.2:n.1025A>T
ENST00000690268.1:c.920A>T	ENSP00000509810.1:p.Asn307Ile
ENST00000355740.7:c.*165A>T	ENSP00000347979.3:n.*165A>T
ENST00000612663.5:c.*241A>T	ENSP00000477997.3:n.*241A>T
ENST00000640140.1:n.1011A>T
ENST00000640250.1:n.338A>T
ENST00000640681.1:n.960A>T
ENST00000652046.1:c.839A>T MANE Select	ENSP00000498466.1:p.Asn280Ile
ENST00000352159.8:c.*156A>T	ENSP00000345601.4:n.*156A>T
ENST00000355279.2:c.814A>T	ENSP00000347426.2:n.814A>T
ENST00000355740.6:c.839A>T	ENSP00000347979.2:p.Asn280Ile
ENST00000357339.6:c.776A>T	ENSP00000349896.2:p.Asn259Ile
ENST00000479522.5:c.*268A>T	ENSP00000424113.1:n.*268A>T
ENST00000484444.5:c.*280A>T	ENSP00000420975.1:n.*280A>T
ENST00000488877.5:c.*280A>T	ENSP00000425159.1:n.*280A>T
ENST00000492756.5:c.667A>T	ENSP00000422453.1:n.667A>T
ENST00000494410.5:c.*197A>T	ENSP00000423755.1:n.*197A>T
ENST00000612663.4:c.*186A>T	ENSP00000477997.2:n.*186A>T
NM_000043.4:c.839A>T , LRG_134t1:c.839A>T	NP_000034.1:p.Asn280Ile
NM_152871.2:c.776A>T	NP_690610.1:p.Asn259Ile
NM_152872.2:c.*151A>T	NP_690611.1:n.*151A>T
NR_028033.2:n.1013A>T
NR_028034.2:n.875A>T
NR_028035.2:n.938A>T
NR_028036.2:n.1076A>T
XM_006717819.2:c.920A>T	XP_006717882.1:p.Asn307Ile
XM_011539764.1:c.1001A>T	XP_011538066.1:p.Asn334Ile
XM_011539765.1:c.938A>T	XP_011538067.1:p.Asn313Ile
XM_011539766.1:c.920A>T	XP_011538068.1:p.Asn307Ile
XM_011539767.1:c.884A>T	XP_011538069.1:p.Asn295Ile
XR_945732.1:n.907A>T
XR_945733.1:n.844A>T
NM_000043.5:c.839A>T	NP_000034.1:p.Asn280Ile
NM_001320619.1:c.*162A>T	NP_001307548.1:n.*162A>T
NM_152871.3:c.776A>T	NP_690610.1:p.Asn259Ile
NM_152872.3:c.*151A>T	NP_690611.1:n.*151A>T
NR_028033.3:n.985A>T
NR_028034.3:n.847A>T
NR_028035.3:n.910A>T
NR_028036.3:n.1048A>T
NR_135313.1:n.965A>T
NR_135314.1:n.1148A>T
NR_135315.1:n.901A>T
XM_006717819.3:c.920A>T	XP_006717882.1:p.Asn307Ile
XM_011539764.2:c.1001A>T	XP_011538066.1:p.Asn334Ile
XM_011539765.2:c.938A>T	XP_011538067.1:p.Asn313Ile
XM_011539766.2:c.920A>T	XP_011538068.1:p.Asn307Ile
XM_011539767.3:c.884A>T	XP_011538069.1:p.Asn295Ile
XR_945732.3:n.907A>T
XR_945733.2:n.844A>T
NM_000043.6:c.839A>T MANE Select	NP_000034.1:p.Asn280Ile
NM_001320619.2:c.*162A>T	NP_001307548.1:n.*162A>T
NM_152871.4:c.776A>T	NP_690610.1:p.Asn259Ile
NM_152872.4:c.*151A>T	NP_690611.1:n.*151A>T
NR_028033.4:n.746A>T
NR_028034.4:n.608A>T
NR_028035.4:n.671A>T
NR_028036.4:n.809A>T
NR_135313.2:n.726A>T
NR_135314.2:n.1005A>T
NR_135315.2:n.758A>T