Canonical Allele Identifier: CA377509978

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774059A>C (hg19) ; chr10:g.89014302A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014302A>C , CM000672.2:g.89014302A>C	GRCh38
NC_000010.10:g.90774059A>C , CM000672.1:g.90774059A>C	GRCh37
NC_000010.9:g.90764039A>C	NCBI36
NG_009089.2:g.28772A>C , LRG_134:g.28772A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1169A>C
ENST00000355740.8:c.*183A>C	ENSP00000347979.3:n.*183A>C
ENST00000357339.7:c.797A>C	ENSP00000349896.2:p.Lys266Thr
ENST00000371857.8:n.2405A>C
ENST00000460510.6:c.143A>C	ENSP00000512812.1:p.Lys48Thr
ENST00000466081.6:n.2509A>C
ENST00000477270.6:c.905A>C	ENSP00000512813.1:p.Lys302Thr
ENST00000479522.6:c.*289A>C	ENSP00000424113.1:n.*289A>C
ENST00000484444.6:c.*301A>C	ENSP00000420975.1:n.*301A>C
ENST00000488877.6:c.751A>C	ENSP00000425159.1:n.751A>C
ENST00000492756.7:c.*289A>C	ENSP00000422453.1:n.*289A>C
ENST00000494799.6:c.143A>C	ENSP00000512834.1:p.Lys48Thr
ENST00000562983.3:c.143A>C	ENSP00000512845.1:p.Lys48Thr
ENST00000612663.6:c.*262A>C	ENSP00000477997.3:n.*262A>C
ENST00000640140.2:n.1005A>C
ENST00000640250.2:n.359A>C
ENST00000640681.2:n.964A>C
ENST00000696723.1:n.4493A>C
ENST00000696741.1:n.2498A>C
ENST00000696742.1:n.2225A>C
ENST00000696743.1:n.3628A>C
ENST00000696744.1:n.899A>C
ENST00000696767.1:n.1194A>C
ENST00000696768.1:c.*183A>C	ENSP00000512859.1:n.*183A>C
ENST00000696769.1:n.2549A>C
ENST00000696771.1:c.143A>C	ENSP00000512860.1:p.Lys48Thr
ENST00000696772.1:n.2463A>C
ENST00000696773.1:n.2202A>C
ENST00000696774.1:n.5970A>C
ENST00000696776.1:c.953A>C	ENSP00000512861.1:p.Lys318Thr
ENST00000696777.1:n.2268A>C
ENST00000696778.1:n.1296A>C
ENST00000696779.1:c.467A>C	ENSP00000512862.1:p.Lys156Thr
ENST00000696780.1:c.890A>C	ENSP00000512863.1:p.Lys297Thr
ENST00000696781.1:c.605A>C	ENSP00000512864.1:p.Lys202Thr
ENST00000696782.1:c.*262A>C	ENSP00000512865.1:n.*262A>C
ENST00000696783.1:n.2728A>C
ENST00000696992.1:n.1977A>C
ENST00000696995.1:n.4389A>C
ENST00000696996.1:n.2302A>C
ENST00000696997.1:c.*490A>C	ENSP00000513028.1:n.*490A>C
ENST00000696998.1:n.2114A>C
ENST00000696999.1:c.143A>C	ENSP00000513029.1:p.Lys48Thr
ENST00000697035.1:c.*193A>C	ENSP00000513059.1:n.*193A>C
ENST00000697036.1:c.*276A>C	ENSP00000513060.1:n.*276A>C
ENST00000697037.1:n.895A>C
ENST00000697093.1:n.3096A>C
ENST00000697094.1:n.3443A>C
ENST00000697095.1:c.*2061A>C	ENSP00000513104.1:n.*2061A>C
ENST00000697096.1:n.1993A>C
ENST00000697097.1:c.143A>C	ENSP00000513105.1:p.Lys48Thr
ENST00000562983.2:n.1046A>C
ENST00000690268.1:c.941A>C	ENSP00000509810.1:p.Lys314Thr
ENST00000355740.7:c.*186A>C	ENSP00000347979.3:n.*186A>C
ENST00000612663.5:c.*262A>C	ENSP00000477997.3:n.*262A>C
ENST00000640140.1:n.1032A>C
ENST00000640250.1:n.359A>C
ENST00000640681.1:n.981A>C
ENST00000652046.1:c.860A>C MANE Select	ENSP00000498466.1:p.Lys287Thr
ENST00000352159.8:c.*177A>C	ENSP00000345601.4:n.*177A>C
ENST00000355279.2:c.835A>C	ENSP00000347426.2:n.835A>C
ENST00000355740.6:c.860A>C	ENSP00000347979.2:p.Lys287Thr
ENST00000357339.6:c.797A>C	ENSP00000349896.2:p.Lys266Thr
ENST00000479522.5:c.*289A>C	ENSP00000424113.1:n.*289A>C
ENST00000484444.5:c.*301A>C	ENSP00000420975.1:n.*301A>C
ENST00000488877.5:c.*301A>C	ENSP00000425159.1:n.*301A>C
ENST00000492756.5:c.688A>C	ENSP00000422453.1:n.688A>C
ENST00000494410.5:c.*218A>C	ENSP00000423755.1:n.*218A>C
ENST00000612663.4:c.*207A>C	ENSP00000477997.2:n.*207A>C
NM_000043.4:c.860A>C , LRG_134t1:c.860A>C	NP_000034.1:p.Lys287Thr
NM_152871.2:c.797A>C	NP_690610.1:p.Lys266Thr
NM_152872.2:c.*172A>C	NP_690611.1:n.*172A>C
NR_028033.2:n.1034A>C
NR_028034.2:n.896A>C
NR_028035.2:n.959A>C
NR_028036.2:n.1097A>C
XM_006717819.2:c.941A>C	XP_006717882.1:p.Lys314Thr
XM_011539764.1:c.1022A>C	XP_011538066.1:p.Lys341Thr
XM_011539765.1:c.959A>C	XP_011538067.1:p.Lys320Thr
XM_011539766.1:c.941A>C	XP_011538068.1:p.Lys314Thr
XM_011539767.1:c.905A>C	XP_011538069.1:p.Lys302Thr
XR_945732.1:n.928A>C
XR_945733.1:n.865A>C
NM_000043.5:c.860A>C	NP_000034.1:p.Lys287Thr
NM_001320619.1:c.*183A>C	NP_001307548.1:n.*183A>C
NM_152871.3:c.797A>C	NP_690610.1:p.Lys266Thr
NM_152872.3:c.*172A>C	NP_690611.1:n.*172A>C
NR_028033.3:n.1006A>C
NR_028034.3:n.868A>C
NR_028035.3:n.931A>C
NR_028036.3:n.1069A>C
NR_135313.1:n.986A>C
NR_135314.1:n.1169A>C
NR_135315.1:n.922A>C
XM_006717819.3:c.941A>C	XP_006717882.1:p.Lys314Thr
XM_011539764.2:c.1022A>C	XP_011538066.1:p.Lys341Thr
XM_011539765.2:c.959A>C	XP_011538067.1:p.Lys320Thr
XM_011539766.2:c.941A>C	XP_011538068.1:p.Lys314Thr
XM_011539767.3:c.905A>C	XP_011538069.1:p.Lys302Thr
XR_945732.3:n.928A>C
XR_945733.2:n.865A>C
NM_000043.6:c.860A>C MANE Select	NP_000034.1:p.Lys287Thr
NM_001320619.2:c.*183A>C	NP_001307548.1:n.*183A>C
NM_152871.4:c.797A>C	NP_690610.1:p.Lys266Thr
NM_152872.4:c.*172A>C	NP_690611.1:n.*172A>C
NR_028033.4:n.767A>C
NR_028034.4:n.629A>C
NR_028035.4:n.692A>C
NR_028036.4:n.830A>C
NR_135313.2:n.747A>C
NR_135314.2:n.1026A>C
NR_135315.2:n.779A>C