Canonical Allele Identifier: CA377509828

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773993A>T (hg19) ; chr10:g.89014236A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014236A>T , CM000672.2:g.89014236A>T	GRCh38
NC_000010.10:g.90773993A>T , CM000672.1:g.90773993A>T	GRCh37
NC_000010.9:g.90763973A>T	NCBI36
NG_009089.2:g.28706A>T , LRG_134:g.28706A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1103A>T
ENST00000355740.8:c.*117A>T	ENSP00000347979.3:n.*117A>T
ENST00000357339.7:c.731A>T	ENSP00000349896.2:p.Asp244Val
ENST00000371857.8:n.2339A>T
ENST00000460510.6:c.77A>T	ENSP00000512812.1:p.Asp26Val
ENST00000466081.6:n.2443A>T
ENST00000477270.6:c.839A>T	ENSP00000512813.1:p.Asp280Val
ENST00000479522.6:c.*223A>T	ENSP00000424113.1:n.*223A>T
ENST00000484444.6:c.*235A>T	ENSP00000420975.1:n.*235A>T
ENST00000488877.6:c.685A>T	ENSP00000425159.1:n.685A>T
ENST00000492756.7:c.*223A>T	ENSP00000422453.1:n.*223A>T
ENST00000494799.6:c.77A>T	ENSP00000512834.1:p.Asp26Val
ENST00000562983.3:c.77A>T	ENSP00000512845.1:p.Asp26Val
ENST00000612663.6:c.*196A>T	ENSP00000477997.3:n.*196A>T
ENST00000640140.2:n.939A>T
ENST00000640250.2:n.293A>T
ENST00000640681.2:n.898A>T
ENST00000696723.1:n.4427A>T
ENST00000696741.1:n.2432A>T
ENST00000696742.1:n.2159A>T
ENST00000696743.1:n.3562A>T
ENST00000696744.1:n.833A>T
ENST00000696767.1:n.1128A>T
ENST00000696768.1:c.*117A>T	ENSP00000512859.1:n.*117A>T
ENST00000696769.1:n.2483A>T
ENST00000696771.1:c.77A>T	ENSP00000512860.1:p.Asp26Val
ENST00000696772.1:n.2397A>T
ENST00000696773.1:n.2136A>T
ENST00000696774.1:n.5904A>T
ENST00000696776.1:c.887A>T	ENSP00000512861.1:p.Asp296Val
ENST00000696777.1:n.2202A>T
ENST00000696778.1:n.1230A>T
ENST00000696779.1:c.401A>T	ENSP00000512862.1:p.Asp134Val
ENST00000696780.1:c.824A>T	ENSP00000512863.1:p.Asp275Val
ENST00000696781.1:c.539A>T	ENSP00000512864.1:p.Asp180Val
ENST00000696782.1:c.*196A>T	ENSP00000512865.1:n.*196A>T
ENST00000696783.1:n.2662A>T
ENST00000696992.1:n.1911A>T
ENST00000696995.1:n.4323A>T
ENST00000696996.1:n.2236A>T
ENST00000696997.1:c.*424A>T	ENSP00000513028.1:n.*424A>T
ENST00000696998.1:n.2048A>T
ENST00000696999.1:c.77A>T	ENSP00000513029.1:p.Asp26Val
ENST00000697035.1:c.*127A>T	ENSP00000513059.1:n.*127A>T
ENST00000697036.1:c.*210A>T	ENSP00000513060.1:n.*210A>T
ENST00000697037.1:n.829A>T
ENST00000697093.1:n.3030A>T
ENST00000697094.1:n.3377A>T
ENST00000697095.1:c.*1995A>T	ENSP00000513104.1:n.*1995A>T
ENST00000697096.1:n.1927A>T
ENST00000697097.1:c.77A>T	ENSP00000513105.1:p.Asp26Val
ENST00000562983.2:n.980A>T
ENST00000690268.1:c.875A>T	ENSP00000509810.1:p.Asp292Val
ENST00000355740.7:c.*120A>T	ENSP00000347979.3:n.*120A>T
ENST00000612663.5:c.*196A>T	ENSP00000477997.3:n.*196A>T
ENST00000640140.1:n.966A>T
ENST00000640250.1:n.293A>T
ENST00000640681.1:n.915A>T
ENST00000652046.1:c.794A>T MANE Select	ENSP00000498466.1:p.Asp265Val
ENST00000352159.8:c.*111A>T	ENSP00000345601.4:n.*111A>T
ENST00000355279.2:c.769A>T	ENSP00000347426.2:n.769A>T
ENST00000355740.6:c.794A>T	ENSP00000347979.2:p.Asp265Val
ENST00000357339.6:c.731A>T	ENSP00000349896.2:p.Asp244Val
ENST00000479522.5:c.*223A>T	ENSP00000424113.1:n.*223A>T
ENST00000484444.5:c.*235A>T	ENSP00000420975.1:n.*235A>T
ENST00000488877.5:c.*235A>T	ENSP00000425159.1:n.*235A>T
ENST00000492756.5:c.622A>T	ENSP00000422453.1:n.622A>T
ENST00000494410.5:c.*152A>T	ENSP00000423755.1:n.*152A>T
ENST00000612663.4:c.*141A>T	ENSP00000477997.2:n.*141A>T
NM_000043.4:c.794A>T , LRG_134t1:c.794A>T	NP_000034.1:p.Asp265Val
NM_152871.2:c.731A>T	NP_690610.1:p.Asp244Val
NM_152872.2:c.*106A>T	NP_690611.1:n.*106A>T
NR_028033.2:n.968A>T
NR_028034.2:n.830A>T
NR_028035.2:n.893A>T
NR_028036.2:n.1031A>T
XM_006717819.2:c.875A>T	XP_006717882.1:p.Asp292Val
XM_011539764.1:c.956A>T	XP_011538066.1:p.Asp319Val
XM_011539765.1:c.893A>T	XP_011538067.1:p.Asp298Val
XM_011539766.1:c.875A>T	XP_011538068.1:p.Asp292Val
XM_011539767.1:c.839A>T	XP_011538069.1:p.Asp280Val
XR_945732.1:n.862A>T
XR_945733.1:n.799A>T
NM_000043.5:c.794A>T	NP_000034.1:p.Asp265Val
NM_001320619.1:c.*117A>T	NP_001307548.1:n.*117A>T
NM_152871.3:c.731A>T	NP_690610.1:p.Asp244Val
NM_152872.3:c.*106A>T	NP_690611.1:n.*106A>T
NR_028033.3:n.940A>T
NR_028034.3:n.802A>T
NR_028035.3:n.865A>T
NR_028036.3:n.1003A>T
NR_135313.1:n.920A>T
NR_135314.1:n.1103A>T
NR_135315.1:n.856A>T
XM_006717819.3:c.875A>T	XP_006717882.1:p.Asp292Val
XM_011539764.2:c.956A>T	XP_011538066.1:p.Asp319Val
XM_011539765.2:c.893A>T	XP_011538067.1:p.Asp298Val
XM_011539766.2:c.875A>T	XP_011538068.1:p.Asp292Val
XM_011539767.3:c.839A>T	XP_011538069.1:p.Asp280Val
XR_945732.3:n.862A>T
XR_945733.2:n.799A>T
NM_000043.6:c.794A>T MANE Select	NP_000034.1:p.Asp265Val
NM_001320619.2:c.*117A>T	NP_001307548.1:n.*117A>T
NM_152871.4:c.731A>T	NP_690610.1:p.Asp244Val
NM_152872.4:c.*106A>T	NP_690611.1:n.*106A>T
NR_028033.4:n.701A>T
NR_028034.4:n.563A>T
NR_028035.4:n.626A>T
NR_028036.4:n.764A>T
NR_135313.2:n.681A>T
NR_135314.2:n.960A>T
NR_135315.2:n.713A>T