Canonical Allele Identifier: CA377509988

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774063A>T (hg19) ; chr10:g.89014306A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014306A>T , CM000672.2:g.89014306A>T	GRCh38
NC_000010.10:g.90774063A>T , CM000672.1:g.90774063A>T	GRCh37
NC_000010.9:g.90764043A>T	NCBI36
NG_009089.2:g.28776A>T , LRG_134:g.28776A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1173A>T
ENST00000355740.8:c.*187A>T	ENSP00000347979.3:n.*187A>T
ENST00000357339.7:c.801A>T	ENSP00000349896.2:p.Lys267Asn
ENST00000371857.8:n.2409A>T
ENST00000460510.6:c.147A>T	ENSP00000512812.1:p.Lys49Asn
ENST00000466081.6:n.2513A>T
ENST00000477270.6:c.909A>T	ENSP00000512813.1:p.Lys303Asn
ENST00000479522.6:c.*293A>T	ENSP00000424113.1:n.*293A>T
ENST00000484444.6:c.*305A>T	ENSP00000420975.1:n.*305A>T
ENST00000488877.6:c.755A>T	ENSP00000425159.1:n.755A>T
ENST00000492756.7:c.*293A>T	ENSP00000422453.1:n.*293A>T
ENST00000494799.6:c.147A>T	ENSP00000512834.1:p.Lys49Asn
ENST00000562983.3:c.147A>T	ENSP00000512845.1:p.Lys49Asn
ENST00000612663.6:c.*266A>T	ENSP00000477997.3:n.*266A>T
ENST00000640140.2:n.1009A>T
ENST00000640250.2:n.363A>T
ENST00000640681.2:n.968A>T
ENST00000696723.1:n.4497A>T
ENST00000696741.1:n.2502A>T
ENST00000696742.1:n.2229A>T
ENST00000696743.1:n.3632A>T
ENST00000696744.1:n.903A>T
ENST00000696767.1:n.1198A>T
ENST00000696768.1:c.*187A>T	ENSP00000512859.1:n.*187A>T
ENST00000696769.1:n.2553A>T
ENST00000696771.1:c.147A>T	ENSP00000512860.1:p.Lys49Asn
ENST00000696772.1:n.2467A>T
ENST00000696773.1:n.2206A>T
ENST00000696774.1:n.5974A>T
ENST00000696776.1:c.957A>T	ENSP00000512861.1:p.Lys319Asn
ENST00000696777.1:n.2272A>T
ENST00000696778.1:n.1300A>T
ENST00000696779.1:c.471A>T	ENSP00000512862.1:p.Lys157Asn
ENST00000696780.1:c.894A>T	ENSP00000512863.1:p.Lys298Asn
ENST00000696781.1:c.609A>T	ENSP00000512864.1:p.Lys203Asn
ENST00000696782.1:c.*266A>T	ENSP00000512865.1:n.*266A>T
ENST00000696783.1:n.2732A>T
ENST00000696992.1:n.1981A>T
ENST00000696995.1:n.4393A>T
ENST00000696996.1:n.2306A>T
ENST00000696997.1:c.*494A>T	ENSP00000513028.1:n.*494A>T
ENST00000696998.1:n.2118A>T
ENST00000696999.1:c.147A>T	ENSP00000513029.1:p.Lys49Asn
ENST00000697036.1:c.*280A>T	ENSP00000513060.1:n.*280A>T
ENST00000697037.1:n.899A>T
ENST00000697093.1:n.3100A>T
ENST00000697094.1:n.3447A>T
ENST00000697095.1:c.*2065A>T	ENSP00000513104.1:n.*2065A>T
ENST00000697096.1:n.1997A>T
ENST00000697097.1:c.147A>T	ENSP00000513105.1:p.Lys49Asn
ENST00000562983.2:n.1050A>T
ENST00000690268.1:c.945A>T	ENSP00000509810.1:p.Lys315Asn
ENST00000355740.7:c.*190A>T	ENSP00000347979.3:n.*190A>T
ENST00000612663.5:c.*266A>T	ENSP00000477997.3:n.*266A>T
ENST00000640140.1:n.1036A>T
ENST00000640250.1:n.363A>T
ENST00000640681.1:n.985A>T
ENST00000652046.1:c.864A>T MANE Select	ENSP00000498466.1:p.Lys288Asn
ENST00000352159.8:c.*181A>T	ENSP00000345601.4:n.*181A>T
ENST00000355279.2:c.839A>T	ENSP00000347426.2:n.839A>T
ENST00000355740.6:c.864A>T	ENSP00000347979.2:p.Lys288Asn
ENST00000357339.6:c.801A>T	ENSP00000349896.2:p.Lys267Asn
ENST00000479522.5:c.*293A>T	ENSP00000424113.1:n.*293A>T
ENST00000484444.5:c.*305A>T	ENSP00000420975.1:n.*305A>T
ENST00000488877.5:c.*305A>T	ENSP00000425159.1:n.*305A>T
ENST00000492756.5:c.692A>T	ENSP00000422453.1:n.692A>T
ENST00000494410.5:c.*222A>T	ENSP00000423755.1:n.*222A>T
ENST00000612663.4:c.*211A>T	ENSP00000477997.2:n.*211A>T
NM_000043.4:c.864A>T , LRG_134t1:c.864A>T	NP_000034.1:p.Lys288Asn
NM_152871.2:c.801A>T	NP_690610.1:p.Lys267Asn
NM_152872.2:c.*176A>T	NP_690611.1:n.*176A>T
NR_028033.2:n.1038A>T
NR_028034.2:n.900A>T
NR_028035.2:n.963A>T
NR_028036.2:n.1101A>T
XM_006717819.2:c.945A>T	XP_006717882.1:p.Lys315Asn
XM_011539764.1:c.1026A>T	XP_011538066.1:p.Lys342Asn
XM_011539765.1:c.963A>T	XP_011538067.1:p.Lys321Asn
XM_011539766.1:c.945A>T	XP_011538068.1:p.Lys315Asn
XM_011539767.1:c.909A>T	XP_011538069.1:p.Lys303Asn
XR_945732.1:n.932A>T
XR_945733.1:n.869A>T
NM_000043.5:c.864A>T	NP_000034.1:p.Lys288Asn
NM_001320619.1:c.*187A>T	NP_001307548.1:n.*187A>T
NM_152871.3:c.801A>T	NP_690610.1:p.Lys267Asn
NM_152872.3:c.*176A>T	NP_690611.1:n.*176A>T
NR_028033.3:n.1010A>T
NR_028034.3:n.872A>T
NR_028035.3:n.935A>T
NR_028036.3:n.1073A>T
NR_135313.1:n.990A>T
NR_135314.1:n.1173A>T
NR_135315.1:n.926A>T
XM_006717819.3:c.945A>T	XP_006717882.1:p.Lys315Asn
XM_011539764.2:c.1026A>T	XP_011538066.1:p.Lys342Asn
XM_011539765.2:c.963A>T	XP_011538067.1:p.Lys321Asn
XM_011539766.2:c.945A>T	XP_011538068.1:p.Lys315Asn
XM_011539767.3:c.909A>T	XP_011538069.1:p.Lys303Asn
XR_945732.3:n.932A>T
XR_945733.2:n.869A>T
NM_000043.6:c.864A>T MANE Select	NP_000034.1:p.Lys288Asn
NM_001320619.2:c.*187A>T	NP_001307548.1:n.*187A>T
NM_152871.4:c.801A>T	NP_690610.1:p.Lys267Asn
NM_152872.4:c.*176A>T	NP_690611.1:n.*176A>T
NR_028033.4:n.771A>T
NR_028034.4:n.633A>T
NR_028035.4:n.696A>T
NR_028036.4:n.834A>T
NR_135313.2:n.751A>T
NR_135314.2:n.1030A>T
NR_135315.2:n.783A>T