Canonical Allele Identifier: CA377509944

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774045T>A (hg19) ; chr10:g.89014288T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014288T>A , CM000672.2:g.89014288T>A	GRCh38
NC_000010.10:g.90774045T>A , CM000672.1:g.90774045T>A	GRCh37
NC_000010.9:g.90764025T>A	NCBI36
NG_009089.2:g.28758T>A , LRG_134:g.28758T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1155T>A
ENST00000355740.8:c.*169T>A	ENSP00000347979.3:n.*169T>A
ENST00000357339.7:c.783T>A	ENSP00000349896.2:p.His261Gln
ENST00000371857.8:n.2391T>A
ENST00000460510.6:c.129T>A	ENSP00000512812.1:p.His43Gln
ENST00000466081.6:n.2495T>A
ENST00000477270.6:c.891T>A	ENSP00000512813.1:p.His297Gln
ENST00000479522.6:c.*275T>A	ENSP00000424113.1:n.*275T>A
ENST00000484444.6:c.*287T>A	ENSP00000420975.1:n.*287T>A
ENST00000488877.6:c.737T>A	ENSP00000425159.1:n.737T>A
ENST00000492756.7:c.*275T>A	ENSP00000422453.1:n.*275T>A
ENST00000494799.6:c.129T>A	ENSP00000512834.1:p.His43Gln
ENST00000562983.3:c.129T>A	ENSP00000512845.1:p.His43Gln
ENST00000612663.6:c.*248T>A	ENSP00000477997.3:n.*248T>A
ENST00000640140.2:n.991T>A
ENST00000640250.2:n.345T>A
ENST00000640681.2:n.950T>A
ENST00000696723.1:n.4479T>A
ENST00000696741.1:n.2484T>A
ENST00000696742.1:n.2211T>A
ENST00000696743.1:n.3614T>A
ENST00000696744.1:n.885T>A
ENST00000696767.1:n.1180T>A
ENST00000696768.1:c.*169T>A	ENSP00000512859.1:n.*169T>A
ENST00000696769.1:n.2535T>A
ENST00000696771.1:c.129T>A	ENSP00000512860.1:p.His43Gln
ENST00000696772.1:n.2449T>A
ENST00000696773.1:n.2188T>A
ENST00000696774.1:n.5956T>A
ENST00000696776.1:c.939T>A	ENSP00000512861.1:p.His313Gln
ENST00000696777.1:n.2254T>A
ENST00000696778.1:n.1282T>A
ENST00000696779.1:c.453T>A	ENSP00000512862.1:p.His151Gln
ENST00000696780.1:c.876T>A	ENSP00000512863.1:p.His292Gln
ENST00000696781.1:c.591T>A	ENSP00000512864.1:p.His197Gln
ENST00000696782.1:c.*248T>A	ENSP00000512865.1:n.*248T>A
ENST00000696783.1:n.2714T>A
ENST00000696992.1:n.1963T>A
ENST00000696995.1:n.4375T>A
ENST00000696996.1:n.2288T>A
ENST00000696997.1:c.*476T>A	ENSP00000513028.1:n.*476T>A
ENST00000696998.1:n.2100T>A
ENST00000696999.1:c.129T>A	ENSP00000513029.1:p.His43Gln
ENST00000697035.1:c.*179T>A	ENSP00000513059.1:n.*179T>A
ENST00000697036.1:c.*262T>A	ENSP00000513060.1:n.*262T>A
ENST00000697037.1:n.881T>A
ENST00000697093.1:n.3082T>A
ENST00000697094.1:n.3429T>A
ENST00000697095.1:c.*2047T>A	ENSP00000513104.1:n.*2047T>A
ENST00000697096.1:n.1979T>A
ENST00000697097.1:c.129T>A	ENSP00000513105.1:p.His43Gln
ENST00000562983.2:n.1032T>A
ENST00000690268.1:c.927T>A	ENSP00000509810.1:p.His309Gln
ENST00000355740.7:c.*172T>A	ENSP00000347979.3:n.*172T>A
ENST00000612663.5:c.*248T>A	ENSP00000477997.3:n.*248T>A
ENST00000640140.1:n.1018T>A
ENST00000640250.1:n.345T>A
ENST00000640681.1:n.967T>A
ENST00000652046.1:c.846T>A MANE Select	ENSP00000498466.1:p.His282Gln
ENST00000352159.8:c.*163T>A	ENSP00000345601.4:n.*163T>A
ENST00000355279.2:c.821T>A	ENSP00000347426.2:n.821T>A
ENST00000355740.6:c.846T>A	ENSP00000347979.2:p.His282Gln
ENST00000357339.6:c.783T>A	ENSP00000349896.2:p.His261Gln
ENST00000479522.5:c.*275T>A	ENSP00000424113.1:n.*275T>A
ENST00000484444.5:c.*287T>A	ENSP00000420975.1:n.*287T>A
ENST00000488877.5:c.*287T>A	ENSP00000425159.1:n.*287T>A
ENST00000492756.5:c.674T>A	ENSP00000422453.1:n.674T>A
ENST00000494410.5:c.*204T>A	ENSP00000423755.1:n.*204T>A
ENST00000612663.4:c.*193T>A	ENSP00000477997.2:n.*193T>A
NM_000043.4:c.846T>A , LRG_134t1:c.846T>A	NP_000034.1:p.His282Gln
NM_152871.2:c.783T>A	NP_690610.1:p.His261Gln
NM_152872.2:c.*158T>A	NP_690611.1:n.*158T>A
NR_028033.2:n.1020T>A
NR_028034.2:n.882T>A
NR_028035.2:n.945T>A
NR_028036.2:n.1083T>A
XM_006717819.2:c.927T>A	XP_006717882.1:p.His309Gln
XM_011539764.1:c.1008T>A	XP_011538066.1:p.His336Gln
XM_011539765.1:c.945T>A	XP_011538067.1:p.His315Gln
XM_011539766.1:c.927T>A	XP_011538068.1:p.His309Gln
XM_011539767.1:c.891T>A	XP_011538069.1:p.His297Gln
XR_945732.1:n.914T>A
XR_945733.1:n.851T>A
NM_000043.5:c.846T>A	NP_000034.1:p.His282Gln
NM_001320619.1:c.*169T>A	NP_001307548.1:n.*169T>A
NM_152871.3:c.783T>A	NP_690610.1:p.His261Gln
NM_152872.3:c.*158T>A	NP_690611.1:n.*158T>A
NR_028033.3:n.992T>A
NR_028034.3:n.854T>A
NR_028035.3:n.917T>A
NR_028036.3:n.1055T>A
NR_135313.1:n.972T>A
NR_135314.1:n.1155T>A
NR_135315.1:n.908T>A
XM_006717819.3:c.927T>A	XP_006717882.1:p.His309Gln
XM_011539764.2:c.1008T>A	XP_011538066.1:p.His336Gln
XM_011539765.2:c.945T>A	XP_011538067.1:p.His315Gln
XM_011539766.2:c.927T>A	XP_011538068.1:p.His309Gln
XM_011539767.3:c.891T>A	XP_011538069.1:p.His297Gln
XR_945732.3:n.914T>A
XR_945733.2:n.851T>A
NM_000043.6:c.846T>A MANE Select	NP_000034.1:p.His282Gln
NM_001320619.2:c.*169T>A	NP_001307548.1:n.*169T>A
NM_152871.4:c.783T>A	NP_690610.1:p.His261Gln
NM_152872.4:c.*158T>A	NP_690611.1:n.*158T>A
NR_028033.4:n.753T>A
NR_028034.4:n.615T>A
NR_028035.4:n.678T>A
NR_028036.4:n.816T>A
NR_135313.2:n.733T>A
NR_135314.2:n.1012T>A
NR_135315.2:n.765T>A