Canonical Allele Identifier: CA377509857

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774006C>A (hg19) ; chr10:g.89014249C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014249C>A , CM000672.2:g.89014249C>A	GRCh38
NC_000010.10:g.90774006C>A , CM000672.1:g.90774006C>A	GRCh37
NC_000010.9:g.90763986C>A	NCBI36
NG_009089.2:g.28719C>A , LRG_134:g.28719C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1116C>A
ENST00000355740.8:c.*130C>A	ENSP00000347979.3:n.*130C>A
ENST00000357339.7:c.744C>A	ENSP00000349896.2:p.Asp248Glu
ENST00000371857.8:n.2352C>A
ENST00000460510.6:c.90C>A	ENSP00000512812.1:p.Asp30Glu
ENST00000466081.6:n.2456C>A
ENST00000477270.6:c.852C>A	ENSP00000512813.1:p.Asp284Glu
ENST00000479522.6:c.*236C>A	ENSP00000424113.1:n.*236C>A
ENST00000484444.6:c.*248C>A	ENSP00000420975.1:n.*248C>A
ENST00000488877.6:c.698C>A	ENSP00000425159.1:n.698C>A
ENST00000492756.7:c.*236C>A	ENSP00000422453.1:n.*236C>A
ENST00000494799.6:c.90C>A	ENSP00000512834.1:p.Asp30Glu
ENST00000562983.3:c.90C>A	ENSP00000512845.1:p.Asp30Glu
ENST00000612663.6:c.*209C>A	ENSP00000477997.3:n.*209C>A
ENST00000640140.2:n.952C>A
ENST00000640250.2:n.306C>A
ENST00000640681.2:n.911C>A
ENST00000696723.1:n.4440C>A
ENST00000696741.1:n.2445C>A
ENST00000696742.1:n.2172C>A
ENST00000696743.1:n.3575C>A
ENST00000696744.1:n.846C>A
ENST00000696767.1:n.1141C>A
ENST00000696768.1:c.*130C>A	ENSP00000512859.1:n.*130C>A
ENST00000696769.1:n.2496C>A
ENST00000696771.1:c.90C>A	ENSP00000512860.1:p.Asp30Glu
ENST00000696772.1:n.2410C>A
ENST00000696773.1:n.2149C>A
ENST00000696774.1:n.5917C>A
ENST00000696776.1:c.900C>A	ENSP00000512861.1:p.Asp300Glu
ENST00000696777.1:n.2215C>A
ENST00000696778.1:n.1243C>A
ENST00000696779.1:c.414C>A	ENSP00000512862.1:p.Asp138Glu
ENST00000696780.1:c.837C>A	ENSP00000512863.1:p.Asp279Glu
ENST00000696781.1:c.552C>A	ENSP00000512864.1:p.Asp184Glu
ENST00000696782.1:c.*209C>A	ENSP00000512865.1:n.*209C>A
ENST00000696783.1:n.2675C>A
ENST00000696992.1:n.1924C>A
ENST00000696995.1:n.4336C>A
ENST00000696996.1:n.2249C>A
ENST00000696997.1:c.*437C>A	ENSP00000513028.1:n.*437C>A
ENST00000696998.1:n.2061C>A
ENST00000696999.1:c.90C>A	ENSP00000513029.1:p.Asp30Glu
ENST00000697035.1:c.*140C>A	ENSP00000513059.1:n.*140C>A
ENST00000697036.1:c.*223C>A	ENSP00000513060.1:n.*223C>A
ENST00000697037.1:n.842C>A
ENST00000697093.1:n.3043C>A
ENST00000697094.1:n.3390C>A
ENST00000697095.1:c.*2008C>A	ENSP00000513104.1:n.*2008C>A
ENST00000697096.1:n.1940C>A
ENST00000697097.1:c.90C>A	ENSP00000513105.1:p.Asp30Glu
ENST00000562983.2:n.993C>A
ENST00000690268.1:c.888C>A	ENSP00000509810.1:p.Asp296Glu
ENST00000355740.7:c.*133C>A	ENSP00000347979.3:n.*133C>A
ENST00000612663.5:c.*209C>A	ENSP00000477997.3:n.*209C>A
ENST00000640140.1:n.979C>A
ENST00000640250.1:n.306C>A
ENST00000640681.1:n.928C>A
ENST00000652046.1:c.807C>A MANE Select	ENSP00000498466.1:p.Asp269Glu
ENST00000352159.8:c.*124C>A	ENSP00000345601.4:n.*124C>A
ENST00000355279.2:c.782C>A	ENSP00000347426.2:n.782C>A
ENST00000355740.6:c.807C>A	ENSP00000347979.2:p.Asp269Glu
ENST00000357339.6:c.744C>A	ENSP00000349896.2:p.Asp248Glu
ENST00000479522.5:c.*236C>A	ENSP00000424113.1:n.*236C>A
ENST00000484444.5:c.*248C>A	ENSP00000420975.1:n.*248C>A
ENST00000488877.5:c.*248C>A	ENSP00000425159.1:n.*248C>A
ENST00000492756.5:c.635C>A	ENSP00000422453.1:n.635C>A
ENST00000494410.5:c.*165C>A	ENSP00000423755.1:n.*165C>A
ENST00000612663.4:c.*154C>A	ENSP00000477997.2:n.*154C>A
NM_000043.4:c.807C>A , LRG_134t1:c.807C>A	NP_000034.1:p.Asp269Glu
NM_152871.2:c.744C>A	NP_690610.1:p.Asp248Glu
NM_152872.2:c.*119C>A	NP_690611.1:n.*119C>A
NR_028033.2:n.981C>A
NR_028034.2:n.843C>A
NR_028035.2:n.906C>A
NR_028036.2:n.1044C>A
XM_006717819.2:c.888C>A	XP_006717882.1:p.Asp296Glu
XM_011539764.1:c.969C>A	XP_011538066.1:p.Asp323Glu
XM_011539765.1:c.906C>A	XP_011538067.1:p.Asp302Glu
XM_011539766.1:c.888C>A	XP_011538068.1:p.Asp296Glu
XM_011539767.1:c.852C>A	XP_011538069.1:p.Asp284Glu
XR_945732.1:n.875C>A
XR_945733.1:n.812C>A
NM_000043.5:c.807C>A	NP_000034.1:p.Asp269Glu
NM_001320619.1:c.*130C>A	NP_001307548.1:n.*130C>A
NM_152871.3:c.744C>A	NP_690610.1:p.Asp248Glu
NM_152872.3:c.*119C>A	NP_690611.1:n.*119C>A
NR_028033.3:n.953C>A
NR_028034.3:n.815C>A
NR_028035.3:n.878C>A
NR_028036.3:n.1016C>A
NR_135313.1:n.933C>A
NR_135314.1:n.1116C>A
NR_135315.1:n.869C>A
XM_006717819.3:c.888C>A	XP_006717882.1:p.Asp296Glu
XM_011539764.2:c.969C>A	XP_011538066.1:p.Asp323Glu
XM_011539765.2:c.906C>A	XP_011538067.1:p.Asp302Glu
XM_011539766.2:c.888C>A	XP_011538068.1:p.Asp296Glu
XM_011539767.3:c.852C>A	XP_011538069.1:p.Asp284Glu
XR_945732.3:n.875C>A
XR_945733.2:n.812C>A
NM_000043.6:c.807C>A MANE Select	NP_000034.1:p.Asp269Glu
NM_001320619.2:c.*130C>A	NP_001307548.1:n.*130C>A
NM_152871.4:c.744C>A	NP_690610.1:p.Asp248Glu
NM_152872.4:c.*119C>A	NP_690611.1:n.*119C>A
NR_028033.4:n.714C>A
NR_028034.4:n.576C>A
NR_028035.4:n.639C>A
NR_028036.4:n.777C>A
NR_135313.2:n.694C>A
NR_135314.2:n.973C>A
NR_135315.2:n.726C>A