Canonical Allele Identifier: CA377509763

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773967A>T (hg19) ; chr10:g.89014210A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014210A>T , CM000672.2:g.89014210A>T	GRCh38
NC_000010.10:g.90773967A>T , CM000672.1:g.90773967A>T	GRCh37
NC_000010.9:g.90763947A>T	NCBI36
NG_009089.2:g.28680A>T , LRG_134:g.28680A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1077A>T
ENST00000355740.8:c.*91A>T	ENSP00000347979.3:n.*91A>T
ENST00000357339.7:c.705A>T	ENSP00000349896.2:p.Glu235Asp
ENST00000371857.8:n.2313A>T
ENST00000460510.6:c.51A>T	ENSP00000512812.1:p.Glu17Asp
ENST00000466081.6:n.2417A>T
ENST00000477270.6:c.813A>T	ENSP00000512813.1:p.Glu271Asp
ENST00000479522.6:c.*197A>T	ENSP00000424113.1:n.*197A>T
ENST00000484444.6:c.*209A>T	ENSP00000420975.1:n.*209A>T
ENST00000488877.6:c.659A>T	ENSP00000425159.1:n.659A>T
ENST00000492756.7:c.*197A>T	ENSP00000422453.1:n.*197A>T
ENST00000494799.6:c.51A>T	ENSP00000512834.1:p.Glu17Asp
ENST00000562983.3:c.51A>T	ENSP00000512845.1:p.Glu17Asp
ENST00000612663.6:c.*170A>T	ENSP00000477997.3:n.*170A>T
ENST00000640140.2:n.913A>T
ENST00000640250.2:n.267A>T
ENST00000640681.2:n.872A>T
ENST00000696723.1:n.4401A>T
ENST00000696741.1:n.2406A>T
ENST00000696742.1:n.2133A>T
ENST00000696743.1:n.3536A>T
ENST00000696744.1:n.807A>T
ENST00000696767.1:n.1102A>T
ENST00000696768.1:c.*91A>T	ENSP00000512859.1:n.*91A>T
ENST00000696769.1:n.2457A>T
ENST00000696771.1:c.51A>T	ENSP00000512860.1:p.Glu17Asp
ENST00000696772.1:n.2371A>T
ENST00000696773.1:n.2110A>T
ENST00000696774.1:n.5878A>T
ENST00000696776.1:c.861A>T	ENSP00000512861.1:p.Glu287Asp
ENST00000696777.1:n.2176A>T
ENST00000696778.1:n.1204A>T
ENST00000696779.1:c.375A>T	ENSP00000512862.1:p.Glu125Asp
ENST00000696780.1:c.798A>T	ENSP00000512863.1:p.Glu266Asp
ENST00000696781.1:c.513A>T	ENSP00000512864.1:p.Glu171Asp
ENST00000696782.1:c.*170A>T	ENSP00000512865.1:n.*170A>T
ENST00000696783.1:n.2636A>T
ENST00000696992.1:n.1885A>T
ENST00000696995.1:n.4297A>T
ENST00000696996.1:n.2210A>T
ENST00000696997.1:c.*398A>T	ENSP00000513028.1:n.*398A>T
ENST00000696998.1:n.2022A>T
ENST00000696999.1:c.51A>T	ENSP00000513029.1:p.Glu17Asp
ENST00000697035.1:c.*101A>T	ENSP00000513059.1:n.*101A>T
ENST00000697036.1:c.*184A>T	ENSP00000513060.1:n.*184A>T
ENST00000697037.1:n.803A>T
ENST00000697093.1:n.3004A>T
ENST00000697094.1:n.3351A>T
ENST00000697095.1:c.*1969A>T	ENSP00000513104.1:n.*1969A>T
ENST00000697096.1:n.1901A>T
ENST00000697097.1:c.51A>T	ENSP00000513105.1:p.Glu17Asp
ENST00000562983.2:n.954A>T
ENST00000690268.1:c.849A>T	ENSP00000509810.1:p.Glu283Asp
ENST00000355740.7:c.*94A>T	ENSP00000347979.3:n.*94A>T
ENST00000612663.5:c.*170A>T	ENSP00000477997.3:n.*170A>T
ENST00000640140.1:n.940A>T
ENST00000640250.1:n.267A>T
ENST00000640681.1:n.889A>T
ENST00000652046.1:c.768A>T MANE Select	ENSP00000498466.1:p.Glu256Asp
ENST00000352159.8:c.*85A>T	ENSP00000345601.4:n.*85A>T
ENST00000355279.2:c.743A>T	ENSP00000347426.2:n.743A>T
ENST00000355740.6:c.768A>T	ENSP00000347979.2:p.Glu256Asp
ENST00000357339.6:c.705A>T	ENSP00000349896.2:p.Glu235Asp
ENST00000479522.5:c.*197A>T	ENSP00000424113.1:n.*197A>T
ENST00000484444.5:c.*209A>T	ENSP00000420975.1:n.*209A>T
ENST00000488877.5:c.*209A>T	ENSP00000425159.1:n.*209A>T
ENST00000492756.5:c.596A>T	ENSP00000422453.1:n.596A>T
ENST00000494410.5:c.*126A>T	ENSP00000423755.1:n.*126A>T
ENST00000494799.5:n.675A>T
ENST00000612663.4:c.*115A>T	ENSP00000477997.2:n.*115A>T
NM_000043.4:c.768A>T , LRG_134t1:c.768A>T	NP_000034.1:p.Glu256Asp
NM_152871.2:c.705A>T	NP_690610.1:p.Glu235Asp
NM_152872.2:c.*80A>T	NP_690611.1:n.*80A>T
NR_028033.2:n.942A>T
NR_028034.2:n.804A>T
NR_028035.2:n.867A>T
NR_028036.2:n.1005A>T
XM_006717819.2:c.849A>T	XP_006717882.1:p.Glu283Asp
XM_011539764.1:c.930A>T	XP_011538066.1:p.Glu310Asp
XM_011539765.1:c.867A>T	XP_011538067.1:p.Glu289Asp
XM_011539766.1:c.849A>T	XP_011538068.1:p.Glu283Asp
XM_011539767.1:c.813A>T	XP_011538069.1:p.Glu271Asp
XR_945732.1:n.836A>T
XR_945733.1:n.773A>T
NM_000043.5:c.768A>T	NP_000034.1:p.Glu256Asp
NM_001320619.1:c.*91A>T	NP_001307548.1:n.*91A>T
NM_152871.3:c.705A>T	NP_690610.1:p.Glu235Asp
NM_152872.3:c.*80A>T	NP_690611.1:n.*80A>T
NR_028033.3:n.914A>T
NR_028034.3:n.776A>T
NR_028035.3:n.839A>T
NR_028036.3:n.977A>T
NR_135313.1:n.894A>T
NR_135314.1:n.1077A>T
NR_135315.1:n.830A>T
XM_006717819.3:c.849A>T	XP_006717882.1:p.Glu283Asp
XM_011539764.2:c.930A>T	XP_011538066.1:p.Glu310Asp
XM_011539765.2:c.867A>T	XP_011538067.1:p.Glu289Asp
XM_011539766.2:c.849A>T	XP_011538068.1:p.Glu283Asp
XM_011539767.3:c.813A>T	XP_011538069.1:p.Glu271Asp
XR_945732.3:n.836A>T
XR_945733.2:n.773A>T
NM_000043.6:c.768A>T MANE Select	NP_000034.1:p.Glu256Asp
NM_001320619.2:c.*91A>T	NP_001307548.1:n.*91A>T
NM_152871.4:c.705A>T	NP_690610.1:p.Glu235Asp
NM_152872.4:c.*80A>T	NP_690611.1:n.*80A>T
NR_028033.4:n.675A>T
NR_028034.4:n.537A>T
NR_028035.4:n.600A>T
NR_028036.4:n.738A>T
NR_135313.2:n.655A>T
NR_135314.2:n.934A>T
NR_135315.2:n.687A>T