Canonical Allele Identifier: CA377509994

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774065A>C (hg19) ; chr10:g.89014308A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014308A>C , CM000672.2:g.89014308A>C	GRCh38
NC_000010.10:g.90774065A>C , CM000672.1:g.90774065A>C	GRCh37
NC_000010.9:g.90764045A>C	NCBI36
NG_009089.2:g.28778A>C , LRG_134:g.28778A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1175A>C
ENST00000355740.8:c.*189A>C	ENSP00000347979.3:n.*189A>C
ENST00000357339.7:c.803A>C	ENSP00000349896.2:p.Glu268Ala
ENST00000371857.8:n.2411A>C
ENST00000460510.6:c.149A>C	ENSP00000512812.1:p.Glu50Ala
ENST00000466081.6:n.2515A>C
ENST00000477270.6:c.911A>C	ENSP00000512813.1:p.Glu304Ala
ENST00000479522.6:c.*295A>C	ENSP00000424113.1:n.*295A>C
ENST00000484444.6:c.*307A>C	ENSP00000420975.1:n.*307A>C
ENST00000488877.6:c.757A>C	ENSP00000425159.1:n.757A>C
ENST00000492756.7:c.*295A>C	ENSP00000422453.1:n.*295A>C
ENST00000494799.6:c.149A>C	ENSP00000512834.1:p.Glu50Ala
ENST00000562983.3:c.149A>C	ENSP00000512845.1:p.Glu50Ala
ENST00000612663.6:c.*268A>C	ENSP00000477997.3:n.*268A>C
ENST00000640140.2:n.1011A>C
ENST00000640250.2:n.365A>C
ENST00000640681.2:n.970A>C
ENST00000696723.1:n.4499A>C
ENST00000696741.1:n.2504A>C
ENST00000696742.1:n.2231A>C
ENST00000696743.1:n.3634A>C
ENST00000696744.1:n.905A>C
ENST00000696767.1:n.1200A>C
ENST00000696768.1:c.*189A>C	ENSP00000512859.1:n.*189A>C
ENST00000696769.1:n.2555A>C
ENST00000696771.1:c.149A>C	ENSP00000512860.1:p.Glu50Ala
ENST00000696772.1:n.2469A>C
ENST00000696773.1:n.2208A>C
ENST00000696774.1:n.5976A>C
ENST00000696776.1:c.959A>C	ENSP00000512861.1:p.Glu320Ala
ENST00000696777.1:n.2274A>C
ENST00000696778.1:n.1302A>C
ENST00000696779.1:c.473A>C	ENSP00000512862.1:p.Glu158Ala
ENST00000696780.1:c.896A>C	ENSP00000512863.1:p.Glu299Ala
ENST00000696781.1:c.611A>C	ENSP00000512864.1:p.Glu204Ala
ENST00000696782.1:c.*268A>C	ENSP00000512865.1:n.*268A>C
ENST00000696783.1:n.2734A>C
ENST00000696992.1:n.1983A>C
ENST00000696995.1:n.4395A>C
ENST00000696996.1:n.2308A>C
ENST00000696997.1:c.*496A>C	ENSP00000513028.1:n.*496A>C
ENST00000696998.1:n.2120A>C
ENST00000696999.1:c.149A>C	ENSP00000513029.1:p.Glu50Ala
ENST00000697036.1:c.*282A>C	ENSP00000513060.1:n.*282A>C
ENST00000697037.1:n.901A>C
ENST00000697093.1:n.3102A>C
ENST00000697094.1:n.3449A>C
ENST00000697095.1:c.*2067A>C	ENSP00000513104.1:n.*2067A>C
ENST00000697096.1:n.1999A>C
ENST00000697097.1:c.149A>C	ENSP00000513105.1:p.Glu50Ala
ENST00000562983.2:n.1052A>C
ENST00000690268.1:c.947A>C	ENSP00000509810.1:p.Glu316Ala
ENST00000355740.7:c.*192A>C	ENSP00000347979.3:n.*192A>C
ENST00000612663.5:c.*268A>C	ENSP00000477997.3:n.*268A>C
ENST00000640140.1:n.1038A>C
ENST00000640250.1:n.365A>C
ENST00000640681.1:n.987A>C
ENST00000652046.1:c.866A>C MANE Select	ENSP00000498466.1:p.Glu289Ala
ENST00000352159.8:c.*183A>C	ENSP00000345601.4:n.*183A>C
ENST00000355279.2:c.841A>C	ENSP00000347426.2:n.841A>C
ENST00000355740.6:c.866A>C	ENSP00000347979.2:p.Glu289Ala
ENST00000357339.6:c.803A>C	ENSP00000349896.2:p.Glu268Ala
ENST00000479522.5:c.*295A>C	ENSP00000424113.1:n.*295A>C
ENST00000484444.5:c.*307A>C	ENSP00000420975.1:n.*307A>C
ENST00000488877.5:c.*307A>C	ENSP00000425159.1:n.*307A>C
ENST00000492756.5:c.694A>C	ENSP00000422453.1:n.694A>C
ENST00000494410.5:c.*224A>C	ENSP00000423755.1:n.*224A>C
ENST00000612663.4:c.*213A>C	ENSP00000477997.2:n.*213A>C
NM_000043.4:c.866A>C , LRG_134t1:c.866A>C	NP_000034.1:p.Glu289Ala
NM_152871.2:c.803A>C	NP_690610.1:p.Glu268Ala
NM_152872.2:c.*178A>C	NP_690611.1:n.*178A>C
NR_028033.2:n.1040A>C
NR_028034.2:n.902A>C
NR_028035.2:n.965A>C
NR_028036.2:n.1103A>C
XM_006717819.2:c.947A>C	XP_006717882.1:p.Glu316Ala
XM_011539764.1:c.1028A>C	XP_011538066.1:p.Glu343Ala
XM_011539765.1:c.965A>C	XP_011538067.1:p.Glu322Ala
XM_011539766.1:c.947A>C	XP_011538068.1:p.Glu316Ala
XM_011539767.1:c.911A>C	XP_011538069.1:p.Glu304Ala
XR_945732.1:n.934A>C
XR_945733.1:n.871A>C
NM_000043.5:c.866A>C	NP_000034.1:p.Glu289Ala
NM_001320619.1:c.*189A>C	NP_001307548.1:n.*189A>C
NM_152871.3:c.803A>C	NP_690610.1:p.Glu268Ala
NM_152872.3:c.*178A>C	NP_690611.1:n.*178A>C
NR_028033.3:n.1012A>C
NR_028034.3:n.874A>C
NR_028035.3:n.937A>C
NR_028036.3:n.1075A>C
NR_135313.1:n.992A>C
NR_135314.1:n.1175A>C
NR_135315.1:n.928A>C
XM_006717819.3:c.947A>C	XP_006717882.1:p.Glu316Ala
XM_011539764.2:c.1028A>C	XP_011538066.1:p.Glu343Ala
XM_011539765.2:c.965A>C	XP_011538067.1:p.Glu322Ala
XM_011539766.2:c.947A>C	XP_011538068.1:p.Glu316Ala
XM_011539767.3:c.911A>C	XP_011538069.1:p.Glu304Ala
XR_945732.3:n.934A>C
XR_945733.2:n.871A>C
NM_000043.6:c.866A>C MANE Select	NP_000034.1:p.Glu289Ala
NM_001320619.2:c.*189A>C	NP_001307548.1:n.*189A>C
NM_152871.4:c.803A>C	NP_690610.1:p.Glu268Ala
NM_152872.4:c.*178A>C	NP_690611.1:n.*178A>C
NR_028033.4:n.773A>C
NR_028034.4:n.635A>C
NR_028035.4:n.698A>C
NR_028036.4:n.836A>C
NR_135313.2:n.753A>C
NR_135314.2:n.1032A>C
NR_135315.2:n.785A>C