Canonical Allele Identifier: CA377509940

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774043C>T (hg19) ; chr10:g.89014286C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014286C>T , CM000672.2:g.89014286C>T	GRCh38
NC_000010.10:g.90774043C>T , CM000672.1:g.90774043C>T	GRCh37
NC_000010.9:g.90764023C>T	NCBI36
NG_009089.2:g.28756C>T , LRG_134:g.28756C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1153C>T
ENST00000355740.8:c.*167C>T	ENSP00000347979.3:n.*167C>T
ENST00000357339.7:c.781C>T	ENSP00000349896.2:p.His261Tyr
ENST00000371857.8:n.2389C>T
ENST00000460510.6:c.127C>T	ENSP00000512812.1:p.His43Tyr
ENST00000466081.6:n.2493C>T
ENST00000477270.6:c.889C>T	ENSP00000512813.1:p.His297Tyr
ENST00000479522.6:c.*273C>T	ENSP00000424113.1:n.*273C>T
ENST00000484444.6:c.*285C>T	ENSP00000420975.1:n.*285C>T
ENST00000488877.6:c.735C>T	ENSP00000425159.1:n.735C>T
ENST00000492756.7:c.*273C>T	ENSP00000422453.1:n.*273C>T
ENST00000494799.6:c.127C>T	ENSP00000512834.1:p.His43Tyr
ENST00000562983.3:c.127C>T	ENSP00000512845.1:p.His43Tyr
ENST00000612663.6:c.*246C>T	ENSP00000477997.3:n.*246C>T
ENST00000640140.2:n.989C>T
ENST00000640250.2:n.343C>T
ENST00000640681.2:n.948C>T
ENST00000696723.1:n.4477C>T
ENST00000696741.1:n.2482C>T
ENST00000696742.1:n.2209C>T
ENST00000696743.1:n.3612C>T
ENST00000696744.1:n.883C>T
ENST00000696767.1:n.1178C>T
ENST00000696768.1:c.*167C>T	ENSP00000512859.1:n.*167C>T
ENST00000696769.1:n.2533C>T
ENST00000696771.1:c.127C>T	ENSP00000512860.1:p.His43Tyr
ENST00000696772.1:n.2447C>T
ENST00000696773.1:n.2186C>T
ENST00000696774.1:n.5954C>T
ENST00000696776.1:c.937C>T	ENSP00000512861.1:p.His313Tyr
ENST00000696777.1:n.2252C>T
ENST00000696778.1:n.1280C>T
ENST00000696779.1:c.451C>T	ENSP00000512862.1:p.His151Tyr
ENST00000696780.1:c.874C>T	ENSP00000512863.1:p.His292Tyr
ENST00000696781.1:c.589C>T	ENSP00000512864.1:p.His197Tyr
ENST00000696782.1:c.*246C>T	ENSP00000512865.1:n.*246C>T
ENST00000696783.1:n.2712C>T
ENST00000696992.1:n.1961C>T
ENST00000696995.1:n.4373C>T
ENST00000696996.1:n.2286C>T
ENST00000696997.1:c.*474C>T	ENSP00000513028.1:n.*474C>T
ENST00000696998.1:n.2098C>T
ENST00000696999.1:c.127C>T	ENSP00000513029.1:p.His43Tyr
ENST00000697035.1:c.*177C>T	ENSP00000513059.1:n.*177C>T
ENST00000697036.1:c.*260C>T	ENSP00000513060.1:n.*260C>T
ENST00000697037.1:n.879C>T
ENST00000697093.1:n.3080C>T
ENST00000697094.1:n.3427C>T
ENST00000697095.1:c.*2045C>T	ENSP00000513104.1:n.*2045C>T
ENST00000697096.1:n.1977C>T
ENST00000697097.1:c.127C>T	ENSP00000513105.1:p.His43Tyr
ENST00000562983.2:n.1030C>T
ENST00000690268.1:c.925C>T	ENSP00000509810.1:p.His309Tyr
ENST00000355740.7:c.*170C>T	ENSP00000347979.3:n.*170C>T
ENST00000612663.5:c.*246C>T	ENSP00000477997.3:n.*246C>T
ENST00000640140.1:n.1016C>T
ENST00000640250.1:n.343C>T
ENST00000640681.1:n.965C>T
ENST00000652046.1:c.844C>T MANE Select	ENSP00000498466.1:p.His282Tyr
ENST00000352159.8:c.*161C>T	ENSP00000345601.4:n.*161C>T
ENST00000355279.2:c.819C>T	ENSP00000347426.2:n.819C>T
ENST00000355740.6:c.844C>T	ENSP00000347979.2:p.His282Tyr
ENST00000357339.6:c.781C>T	ENSP00000349896.2:p.His261Tyr
ENST00000479522.5:c.*273C>T	ENSP00000424113.1:n.*273C>T
ENST00000484444.5:c.*285C>T	ENSP00000420975.1:n.*285C>T
ENST00000488877.5:c.*285C>T	ENSP00000425159.1:n.*285C>T
ENST00000492756.5:c.672C>T	ENSP00000422453.1:n.672C>T
ENST00000494410.5:c.*202C>T	ENSP00000423755.1:n.*202C>T
ENST00000612663.4:c.*191C>T	ENSP00000477997.2:n.*191C>T
NM_000043.4:c.844C>T , LRG_134t1:c.844C>T	NP_000034.1:p.His282Tyr
NM_152871.2:c.781C>T	NP_690610.1:p.His261Tyr
NM_152872.2:c.*156C>T	NP_690611.1:n.*156C>T
NR_028033.2:n.1018C>T
NR_028034.2:n.880C>T
NR_028035.2:n.943C>T
NR_028036.2:n.1081C>T
XM_006717819.2:c.925C>T	XP_006717882.1:p.His309Tyr
XM_011539764.1:c.1006C>T	XP_011538066.1:p.His336Tyr
XM_011539765.1:c.943C>T	XP_011538067.1:p.His315Tyr
XM_011539766.1:c.925C>T	XP_011538068.1:p.His309Tyr
XM_011539767.1:c.889C>T	XP_011538069.1:p.His297Tyr
XR_945732.1:n.912C>T
XR_945733.1:n.849C>T
NM_000043.5:c.844C>T	NP_000034.1:p.His282Tyr
NM_001320619.1:c.*167C>T	NP_001307548.1:n.*167C>T
NM_152871.3:c.781C>T	NP_690610.1:p.His261Tyr
NM_152872.3:c.*156C>T	NP_690611.1:n.*156C>T
NR_028033.3:n.990C>T
NR_028034.3:n.852C>T
NR_028035.3:n.915C>T
NR_028036.3:n.1053C>T
NR_135313.1:n.970C>T
NR_135314.1:n.1153C>T
NR_135315.1:n.906C>T
XM_006717819.3:c.925C>T	XP_006717882.1:p.His309Tyr
XM_011539764.2:c.1006C>T	XP_011538066.1:p.His336Tyr
XM_011539765.2:c.943C>T	XP_011538067.1:p.His315Tyr
XM_011539766.2:c.925C>T	XP_011538068.1:p.His309Tyr
XM_011539767.3:c.889C>T	XP_011538069.1:p.His297Tyr
XR_945732.3:n.912C>T
XR_945733.2:n.849C>T
NM_000043.6:c.844C>T MANE Select	NP_000034.1:p.His282Tyr
NM_001320619.2:c.*167C>T	NP_001307548.1:n.*167C>T
NM_152871.4:c.781C>T	NP_690610.1:p.His261Tyr
NM_152872.4:c.*156C>T	NP_690611.1:n.*156C>T
NR_028033.4:n.751C>T
NR_028034.4:n.613C>T
NR_028035.4:n.676C>T
NR_028036.4:n.814C>T
NR_135313.2:n.731C>T
NR_135314.2:n.1010C>T
NR_135315.2:n.763C>T