Canonical Allele Identifier: CA377509631

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773915T>C (hg19) ; chr10:g.89014158T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014158T>C , CM000672.2:g.89014158T>C	GRCh38
NC_000010.10:g.90773915T>C , CM000672.1:g.90773915T>C	GRCh37
NC_000010.9:g.90763895T>C	NCBI36
NG_009089.2:g.28628T>C , LRG_134:g.28628T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1025T>C
ENST00000355740.8:c.*39T>C	ENSP00000347979.3:n.*39T>C
ENST00000357339.7:c.653T>C	ENSP00000349896.2:p.Val218Ala
ENST00000371857.8:n.2261T>C
ENST00000460510.6:c.-2T>C	ENSP00000512812.1:n.-2T>C
ENST00000466081.6:n.2365T>C
ENST00000477270.6:c.761T>C	ENSP00000512813.1:p.Val254Ala
ENST00000479522.6:c.*145T>C	ENSP00000424113.1:n.*145T>C
ENST00000484444.6:c.*157T>C	ENSP00000420975.1:n.*157T>C
ENST00000488877.6:c.607T>C	ENSP00000425159.1:n.607T>C
ENST00000492756.7:c.*145T>C	ENSP00000422453.1:n.*145T>C
ENST00000494799.6:c.-2T>C	ENSP00000512834.1:n.-2T>C
ENST00000562983.3:c.-2T>C	ENSP00000512845.1:n.-2T>C
ENST00000612663.6:c.*118T>C	ENSP00000477997.3:n.*118T>C
ENST00000640140.2:n.861T>C
ENST00000640250.2:n.215T>C
ENST00000640681.2:n.820T>C
ENST00000696723.1:n.4349T>C
ENST00000696741.1:n.2354T>C
ENST00000696742.1:n.2081T>C
ENST00000696743.1:n.3484T>C
ENST00000696744.1:n.755T>C
ENST00000696767.1:n.1050T>C
ENST00000696768.1:c.*39T>C	ENSP00000512859.1:n.*39T>C
ENST00000696769.1:n.2405T>C
ENST00000696771.1:c.-2T>C	ENSP00000512860.1:n.-2T>C
ENST00000696772.1:n.2319T>C
ENST00000696773.1:n.2058T>C
ENST00000696774.1:n.5826T>C
ENST00000696776.1:c.809T>C	ENSP00000512861.1:p.Val270Ala
ENST00000696777.1:n.2124T>C
ENST00000696778.1:n.1152T>C
ENST00000696779.1:c.323T>C	ENSP00000512862.1:p.Val108Ala
ENST00000696780.1:c.746T>C	ENSP00000512863.1:p.Val249Ala
ENST00000696781.1:c.461T>C	ENSP00000512864.1:p.Val154Ala
ENST00000696782.1:c.*118T>C	ENSP00000512865.1:n.*118T>C
ENST00000696783.1:n.2584T>C
ENST00000696992.1:n.1833T>C
ENST00000696995.1:n.4245T>C
ENST00000696996.1:n.2158T>C
ENST00000696997.1:c.*346T>C	ENSP00000513028.1:n.*346T>C
ENST00000696998.1:n.1970T>C
ENST00000696999.1:c.-2T>C	ENSP00000513029.1:n.-2T>C
ENST00000697035.1:c.*49T>C	ENSP00000513059.1:n.*49T>C
ENST00000697036.1:c.*132T>C	ENSP00000513060.1:n.*132T>C
ENST00000697037.1:n.751T>C
ENST00000697093.1:n.2952T>C
ENST00000697094.1:n.3299T>C
ENST00000697095.1:c.*1917T>C	ENSP00000513104.1:n.*1917T>C
ENST00000697096.1:n.1849T>C
ENST00000697097.1:c.-2T>C	ENSP00000513105.1:n.-2T>C
ENST00000562983.2:n.902T>C
ENST00000690268.1:c.797T>C	ENSP00000509810.1:p.Val266Ala
ENST00000355740.7:c.*42T>C	ENSP00000347979.3:n.*42T>C
ENST00000612663.5:c.*118T>C	ENSP00000477997.3:n.*118T>C
ENST00000640140.1:n.888T>C
ENST00000640250.1:n.215T>C
ENST00000640681.1:n.837T>C
ENST00000652046.1:c.716T>C MANE Select	ENSP00000498466.1:p.Val239Ala
ENST00000313771.9:n.1025T>C
ENST00000352159.8:c.*33T>C	ENSP00000345601.4:n.*33T>C
ENST00000355279.2:c.691T>C	ENSP00000347426.2:n.691T>C
ENST00000355740.6:c.716T>C	ENSP00000347979.2:p.Val239Ala
ENST00000357339.6:c.653T>C	ENSP00000349896.2:p.Val218Ala
ENST00000479522.5:c.*145T>C	ENSP00000424113.1:n.*145T>C
ENST00000484444.5:c.*157T>C	ENSP00000420975.1:n.*157T>C
ENST00000488877.5:c.*157T>C	ENSP00000425159.1:n.*157T>C
ENST00000492756.5:c.544T>C	ENSP00000422453.1:n.544T>C
ENST00000494410.5:c.*74T>C	ENSP00000423755.1:n.*74T>C
ENST00000494799.5:n.623T>C
ENST00000612663.4:c.*63T>C	ENSP00000477997.2:n.*63T>C
ENST00000615406.4:c.716T>C	ENSP00000484575.1:p.Val239Ala
ENST00000626542.2:c.714T>C	ENSP00000485876.1:p.Ser238=
NM_000043.4:c.716T>C , LRG_134t1:c.716T>C	NP_000034.1:p.Val239Ala
NM_152871.2:c.653T>C	NP_690610.1:p.Val218Ala
NM_152872.2:c.*28T>C	NP_690611.1:n.*28T>C
NR_028033.2:n.890T>C
NR_028034.2:n.752T>C
NR_028035.2:n.815T>C
NR_028036.2:n.953T>C
XM_006717819.2:c.797T>C	XP_006717882.1:p.Val266Ala
XM_011539764.1:c.878T>C	XP_011538066.1:p.Val293Ala
XM_011539765.1:c.815T>C	XP_011538067.1:p.Val272Ala
XM_011539766.1:c.797T>C	XP_011538068.1:p.Val266Ala
XM_011539767.1:c.761T>C	XP_011538069.1:p.Val254Ala
XR_945732.1:n.784T>C
XR_945733.1:n.721T>C
NM_000043.5:c.716T>C	NP_000034.1:p.Val239Ala
NM_001320619.1:c.*39T>C	NP_001307548.1:n.*39T>C
NM_152871.3:c.653T>C	NP_690610.1:p.Val218Ala
NM_152872.3:c.*28T>C	NP_690611.1:n.*28T>C
NR_028033.3:n.862T>C
NR_028034.3:n.724T>C
NR_028035.3:n.787T>C
NR_028036.3:n.925T>C
NR_135313.1:n.842T>C
NR_135314.1:n.1025T>C
NR_135315.1:n.778T>C
XM_006717819.3:c.797T>C	XP_006717882.1:p.Val266Ala
XM_011539764.2:c.878T>C	XP_011538066.1:p.Val293Ala
XM_011539765.2:c.815T>C	XP_011538067.1:p.Val272Ala
XM_011539766.2:c.797T>C	XP_011538068.1:p.Val266Ala
XM_011539767.3:c.761T>C	XP_011538069.1:p.Val254Ala
XR_945732.3:n.784T>C
XR_945733.2:n.721T>C
NM_000043.6:c.716T>C MANE Select	NP_000034.1:p.Val239Ala
NM_001320619.2:c.*39T>C	NP_001307548.1:n.*39T>C
NM_152871.4:c.653T>C	NP_690610.1:p.Val218Ala
NM_152872.4:c.*28T>C	NP_690611.1:n.*28T>C
NR_028033.4:n.623T>C
NR_028034.4:n.485T>C
NR_028035.4:n.548T>C
NR_028036.4:n.686T>C
NR_135313.2:n.603T>C
NR_135314.2:n.882T>C
NR_135315.2:n.635T>C