Canonical Allele Identifier: CA377509874

Gene: FAS

Linked Data

• ClinVar Variation Id: 636699
• ClinVar RCV Id: RCV000788605
• dbSNP Id: rs1589491089
• MyVariant Identifiers: chr10:g.90774014A>C (hg19) ; chr10:g.89014257A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014257A>C , CM000672.2:g.89014257A>C	GRCh38
NC_000010.10:g.90774014A>C , CM000672.1:g.90774014A>C	GRCh37
NC_000010.9:g.90763994A>C	NCBI36
NG_009089.2:g.28727A>C , LRG_134:g.28727A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1124A>C
ENST00000355740.8:c.*138A>C	ENSP00000347979.3:n.*138A>C
ENST00000357339.7:c.752A>C	ENSP00000349896.2:p.Glu251Ala
ENST00000371857.8:n.2360A>C
ENST00000460510.6:c.98A>C	ENSP00000512812.1:p.Glu33Ala
ENST00000466081.6:n.2464A>C
ENST00000477270.6:c.860A>C	ENSP00000512813.1:p.Glu287Ala
ENST00000479522.6:c.*244A>C	ENSP00000424113.1:n.*244A>C
ENST00000484444.6:c.*256A>C	ENSP00000420975.1:n.*256A>C
ENST00000488877.6:c.706A>C	ENSP00000425159.1:n.706A>C
ENST00000492756.7:c.*244A>C	ENSP00000422453.1:n.*244A>C
ENST00000494799.6:c.98A>C	ENSP00000512834.1:p.Glu33Ala
ENST00000562983.3:c.98A>C	ENSP00000512845.1:p.Glu33Ala
ENST00000612663.6:c.*217A>C	ENSP00000477997.3:n.*217A>C
ENST00000640140.2:n.960A>C
ENST00000640250.2:n.314A>C
ENST00000640681.2:n.919A>C
ENST00000696723.1:n.4448A>C
ENST00000696741.1:n.2453A>C
ENST00000696742.1:n.2180A>C
ENST00000696743.1:n.3583A>C
ENST00000696744.1:n.854A>C
ENST00000696767.1:n.1149A>C
ENST00000696768.1:c.*138A>C	ENSP00000512859.1:n.*138A>C
ENST00000696769.1:n.2504A>C
ENST00000696771.1:c.98A>C	ENSP00000512860.1:p.Glu33Ala
ENST00000696772.1:n.2418A>C
ENST00000696773.1:n.2157A>C
ENST00000696774.1:n.5925A>C
ENST00000696776.1:c.908A>C	ENSP00000512861.1:p.Glu303Ala
ENST00000696777.1:n.2223A>C
ENST00000696778.1:n.1251A>C
ENST00000696779.1:c.422A>C	ENSP00000512862.1:p.Glu141Ala
ENST00000696780.1:c.845A>C	ENSP00000512863.1:p.Glu282Ala
ENST00000696781.1:c.560A>C	ENSP00000512864.1:p.Glu187Ala
ENST00000696782.1:c.*217A>C	ENSP00000512865.1:n.*217A>C
ENST00000696783.1:n.2683A>C
ENST00000696992.1:n.1932A>C
ENST00000696995.1:n.4344A>C
ENST00000696996.1:n.2257A>C
ENST00000696997.1:c.*445A>C	ENSP00000513028.1:n.*445A>C
ENST00000696998.1:n.2069A>C
ENST00000696999.1:c.98A>C	ENSP00000513029.1:p.Glu33Ala
ENST00000697035.1:c.*148A>C	ENSP00000513059.1:n.*148A>C
ENST00000697036.1:c.*231A>C	ENSP00000513060.1:n.*231A>C
ENST00000697037.1:n.850A>C
ENST00000697093.1:n.3051A>C
ENST00000697094.1:n.3398A>C
ENST00000697095.1:c.*2016A>C	ENSP00000513104.1:n.*2016A>C
ENST00000697096.1:n.1948A>C
ENST00000697097.1:c.98A>C	ENSP00000513105.1:p.Glu33Ala
ENST00000562983.2:n.1001A>C
ENST00000690268.1:c.896A>C	ENSP00000509810.1:p.Glu299Ala
ENST00000355740.7:c.*141A>C	ENSP00000347979.3:n.*141A>C
ENST00000612663.5:c.*217A>C	ENSP00000477997.3:n.*217A>C
ENST00000640140.1:n.987A>C
ENST00000640250.1:n.314A>C
ENST00000640681.1:n.936A>C
ENST00000652046.1:c.815A>C MANE Select	ENSP00000498466.1:p.Glu272Ala
ENST00000352159.8:c.*132A>C	ENSP00000345601.4:n.*132A>C
ENST00000355279.2:c.790A>C	ENSP00000347426.2:n.790A>C
ENST00000355740.6:c.815A>C	ENSP00000347979.2:p.Glu272Ala
ENST00000357339.6:c.752A>C	ENSP00000349896.2:p.Glu251Ala
ENST00000479522.5:c.*244A>C	ENSP00000424113.1:n.*244A>C
ENST00000484444.5:c.*256A>C	ENSP00000420975.1:n.*256A>C
ENST00000488877.5:c.*256A>C	ENSP00000425159.1:n.*256A>C
ENST00000492756.5:c.643A>C	ENSP00000422453.1:n.643A>C
ENST00000494410.5:c.*173A>C	ENSP00000423755.1:n.*173A>C
ENST00000612663.4:c.*162A>C	ENSP00000477997.2:n.*162A>C
NM_000043.4:c.815A>C , LRG_134t1:c.815A>C	NP_000034.1:p.Glu272Ala
NM_152871.2:c.752A>C	NP_690610.1:p.Glu251Ala
NM_152872.2:c.*127A>C	NP_690611.1:n.*127A>C
NR_028033.2:n.989A>C
NR_028034.2:n.851A>C
NR_028035.2:n.914A>C
NR_028036.2:n.1052A>C
XM_006717819.2:c.896A>C	XP_006717882.1:p.Glu299Ala
XM_011539764.1:c.977A>C	XP_011538066.1:p.Glu326Ala
XM_011539765.1:c.914A>C	XP_011538067.1:p.Glu305Ala
XM_011539766.1:c.896A>C	XP_011538068.1:p.Glu299Ala
XM_011539767.1:c.860A>C	XP_011538069.1:p.Glu287Ala
XR_945732.1:n.883A>C
XR_945733.1:n.820A>C
NM_000043.5:c.815A>C	NP_000034.1:p.Glu272Ala
NM_001320619.1:c.*138A>C	NP_001307548.1:n.*138A>C
NM_152871.3:c.752A>C	NP_690610.1:p.Glu251Ala
NM_152872.3:c.*127A>C	NP_690611.1:n.*127A>C
NR_028033.3:n.961A>C
NR_028034.3:n.823A>C
NR_028035.3:n.886A>C
NR_028036.3:n.1024A>C
NR_135313.1:n.941A>C
NR_135314.1:n.1124A>C
NR_135315.1:n.877A>C
XM_006717819.3:c.896A>C	XP_006717882.1:p.Glu299Ala
XM_011539764.2:c.977A>C	XP_011538066.1:p.Glu326Ala
XM_011539765.2:c.914A>C	XP_011538067.1:p.Glu305Ala
XM_011539766.2:c.896A>C	XP_011538068.1:p.Glu299Ala
XM_011539767.3:c.860A>C	XP_011538069.1:p.Glu287Ala
XR_945732.3:n.883A>C
XR_945733.2:n.820A>C
NM_000043.6:c.815A>C MANE Select	NP_000034.1:p.Glu272Ala
NM_001320619.2:c.*138A>C	NP_001307548.1:n.*138A>C
NM_152871.4:c.752A>C	NP_690610.1:p.Glu251Ala
NM_152872.4:c.*127A>C	NP_690611.1:n.*127A>C
NR_028033.4:n.722A>C
NR_028034.4:n.584A>C
NR_028035.4:n.647A>C
NR_028036.4:n.785A>C
NR_135313.2:n.702A>C
NR_135314.2:n.981A>C
NR_135315.2:n.734A>C