Canonical Allele Identifier: CA470974911

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773889T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014132T>C , CM000672.2:g.89014132T>C	GRCh38
NC_000010.10:g.90773889T>C , CM000672.1:g.90773889T>C	GRCh37
NC_000010.9:g.90763869T>C	NCBI36
NG_009089.2:g.28602T>C , LRG_134:g.28602T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.999T>C
ENST00000355740.8:c.*13T>C	ENSP00000347979.3:n.*13T>C
ENST00000357339.7:c.627T>C	ENSP00000349896.2:p.Ser209=
ENST00000371857.8:n.2235T>C
ENST00000460510.6:c.-28T>C	ENSP00000512812.1:n.-28T>C
ENST00000466081.6:n.2339T>C
ENST00000477270.6:c.735T>C	ENSP00000512813.1:p.Ser245=
ENST00000479522.6:c.*119T>C	ENSP00000424113.1:n.*119T>C
ENST00000484444.6:c.*131T>C	ENSP00000420975.1:n.*131T>C
ENST00000488877.6:c.581T>C	ENSP00000425159.1:n.581T>C
ENST00000492756.7:c.*119T>C	ENSP00000422453.1:n.*119T>C
ENST00000494799.6:c.-28T>C	ENSP00000512834.1:n.-28T>C
ENST00000562983.3:c.-28T>C	ENSP00000512845.1:n.-28T>C
ENST00000612663.6:c.*92T>C	ENSP00000477997.3:n.*92T>C
ENST00000640140.2:n.835T>C
ENST00000640250.2:n.189T>C
ENST00000640681.2:n.794T>C
ENST00000696723.1:n.4323T>C
ENST00000696741.1:n.2328T>C
ENST00000696742.1:n.2055T>C
ENST00000696743.1:n.3458T>C
ENST00000696744.1:n.729T>C
ENST00000696767.1:n.1024T>C
ENST00000696768.1:c.*13T>C	ENSP00000512859.1:n.*13T>C
ENST00000696769.1:n.2379T>C
ENST00000696771.1:c.-28T>C	ENSP00000512860.1:n.-28T>C
ENST00000696772.1:n.2293T>C
ENST00000696773.1:n.2032T>C
ENST00000696774.1:n.5800T>C
ENST00000696776.1:c.783T>C	ENSP00000512861.1:p.Ser261=
ENST00000696777.1:n.2098T>C
ENST00000696778.1:n.1126T>C
ENST00000696779.1:c.297T>C	ENSP00000512862.1:p.Ser99=
ENST00000696780.1:c.720T>C	ENSP00000512863.1:p.Ser240=
ENST00000696781.1:c.435T>C	ENSP00000512864.1:p.Ser145=
ENST00000696782.1:c.*92T>C	ENSP00000512865.1:n.*92T>C
ENST00000696783.1:n.2558T>C
ENST00000696992.1:n.1807T>C
ENST00000696995.1:n.4219T>C
ENST00000696996.1:n.2132T>C
ENST00000696997.1:c.*320T>C	ENSP00000513028.1:n.*320T>C
ENST00000696998.1:n.1944T>C
ENST00000696999.1:c.-28T>C	ENSP00000513029.1:n.-28T>C
ENST00000697035.1:c.*23T>C	ENSP00000513059.1:n.*23T>C
ENST00000697036.1:c.*106T>C	ENSP00000513060.1:n.*106T>C
ENST00000697037.1:n.725T>C
ENST00000697093.1:n.2926T>C
ENST00000697094.1:n.3273T>C
ENST00000697095.1:c.*1891T>C	ENSP00000513104.1:n.*1891T>C
ENST00000697096.1:n.1823T>C
ENST00000697097.1:c.-28T>C	ENSP00000513105.1:n.-28T>C
ENST00000562983.2:n.876T>C
ENST00000690268.1:c.771T>C	ENSP00000509810.1:p.Ser257=
ENST00000355740.7:c.*16T>C	ENSP00000347979.3:n.*16T>C
ENST00000612663.5:c.*92T>C	ENSP00000477997.3:n.*92T>C
ENST00000640140.1:n.862T>C
ENST00000640250.1:n.189T>C
ENST00000640681.1:n.811T>C
ENST00000652046.1:c.690T>C MANE Select	ENSP00000498466.1:p.Ser230=
ENST00000313771.9:n.999T>C
ENST00000352159.8:c.*7T>C	ENSP00000345601.4:n.*7T>C
ENST00000355279.2:c.665T>C	ENSP00000347426.2:n.665T>C
ENST00000355740.6:c.690T>C	ENSP00000347979.2:p.Ser230=
ENST00000357339.6:c.627T>C	ENSP00000349896.2:p.Ser209=
ENST00000479522.5:c.*119T>C	ENSP00000424113.1:n.*119T>C
ENST00000484444.5:c.*131T>C	ENSP00000420975.1:n.*131T>C
ENST00000488877.5:c.*131T>C	ENSP00000425159.1:n.*131T>C
ENST00000492756.5:c.518T>C	ENSP00000422453.1:n.518T>C
ENST00000494410.5:c.*48T>C	ENSP00000423755.1:n.*48T>C
ENST00000494799.5:n.597T>C
ENST00000612663.4:c.*37T>C	ENSP00000477997.2:n.*37T>C
ENST00000615406.4:c.690T>C	ENSP00000484575.1:p.Ser230=
ENST00000626542.2:c.690T>C	ENSP00000485876.1:p.Ser230=
NM_000043.4:c.690T>C , LRG_134t1:c.690T>C	NP_000034.1:p.Ser230=
NM_152871.2:c.627T>C	NP_690610.1:p.Ser209=
NM_152872.2:c.*2T>C	NP_690611.1:n.*2T>C
NR_028033.2:n.864T>C
NR_028034.2:n.726T>C
NR_028035.2:n.789T>C
NR_028036.2:n.927T>C
XM_006717819.2:c.771T>C	XP_006717882.1:p.Ser257=
XM_011539764.1:c.852T>C	XP_011538066.1:p.Ser284=
XM_011539765.1:c.789T>C	XP_011538067.1:p.Ser263=
XM_011539766.1:c.771T>C	XP_011538068.1:p.Ser257=
XM_011539767.1:c.735T>C	XP_011538069.1:p.Ser245=
XR_945732.1:n.758T>C
XR_945733.1:n.695T>C
NM_000043.5:c.690T>C	NP_000034.1:p.Ser230=
NM_001320619.1:c.*13T>C	NP_001307548.1:n.*13T>C
NM_152871.3:c.627T>C	NP_690610.1:p.Ser209=
NM_152872.3:c.*2T>C	NP_690611.1:n.*2T>C
NR_028033.3:n.836T>C
NR_028034.3:n.698T>C
NR_028035.3:n.761T>C
NR_028036.3:n.899T>C
NR_135313.1:n.816T>C
NR_135314.1:n.999T>C
NR_135315.1:n.752T>C
XM_006717819.3:c.771T>C	XP_006717882.1:p.Ser257=
XM_011539764.2:c.852T>C	XP_011538066.1:p.Ser284=
XM_011539765.2:c.789T>C	XP_011538067.1:p.Ser263=
XM_011539766.2:c.771T>C	XP_011538068.1:p.Ser257=
XM_011539767.3:c.735T>C	XP_011538069.1:p.Ser245=
XR_945732.3:n.758T>C
XR_945733.2:n.695T>C
NM_000043.6:c.690T>C MANE Select	NP_000034.1:p.Ser230=
NM_001320619.2:c.*13T>C	NP_001307548.1:n.*13T>C
NM_152871.4:c.627T>C	NP_690610.1:p.Ser209=
NM_152872.4:c.*2T>C	NP_690611.1:n.*2T>C
NR_028033.4:n.597T>C
NR_028034.4:n.459T>C
NR_028035.4:n.522T>C
NR_028036.4:n.660T>C
NR_135313.2:n.577T>C
NR_135314.2:n.856T>C
NR_135315.2:n.609T>C