Canonical Allele Identifier: CA377509842

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773999T>C (hg19) ; chr10:g.89014242T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014242T>C , CM000672.2:g.89014242T>C	GRCh38
NC_000010.10:g.90773999T>C , CM000672.1:g.90773999T>C	GRCh37
NC_000010.9:g.90763979T>C	NCBI36
NG_009089.2:g.28712T>C , LRG_134:g.28712T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1109T>C
ENST00000355740.8:c.*123T>C	ENSP00000347979.3:n.*123T>C
ENST00000357339.7:c.737T>C	ENSP00000349896.2:p.Val246Ala
ENST00000371857.8:n.2345T>C
ENST00000460510.6:c.83T>C	ENSP00000512812.1:p.Val28Ala
ENST00000466081.6:n.2449T>C
ENST00000477270.6:c.845T>C	ENSP00000512813.1:p.Val282Ala
ENST00000479522.6:c.*229T>C	ENSP00000424113.1:n.*229T>C
ENST00000484444.6:c.*241T>C	ENSP00000420975.1:n.*241T>C
ENST00000488877.6:c.691T>C	ENSP00000425159.1:n.691T>C
ENST00000492756.7:c.*229T>C	ENSP00000422453.1:n.*229T>C
ENST00000494799.6:c.83T>C	ENSP00000512834.1:p.Val28Ala
ENST00000562983.3:c.83T>C	ENSP00000512845.1:p.Val28Ala
ENST00000612663.6:c.*202T>C	ENSP00000477997.3:n.*202T>C
ENST00000640140.2:n.945T>C
ENST00000640250.2:n.299T>C
ENST00000640681.2:n.904T>C
ENST00000696723.1:n.4433T>C
ENST00000696741.1:n.2438T>C
ENST00000696742.1:n.2165T>C
ENST00000696743.1:n.3568T>C
ENST00000696744.1:n.839T>C
ENST00000696767.1:n.1134T>C
ENST00000696768.1:c.*123T>C	ENSP00000512859.1:n.*123T>C
ENST00000696769.1:n.2489T>C
ENST00000696771.1:c.83T>C	ENSP00000512860.1:p.Val28Ala
ENST00000696772.1:n.2403T>C
ENST00000696773.1:n.2142T>C
ENST00000696774.1:n.5910T>C
ENST00000696776.1:c.893T>C	ENSP00000512861.1:p.Val298Ala
ENST00000696777.1:n.2208T>C
ENST00000696778.1:n.1236T>C
ENST00000696779.1:c.407T>C	ENSP00000512862.1:p.Val136Ala
ENST00000696780.1:c.830T>C	ENSP00000512863.1:p.Val277Ala
ENST00000696781.1:c.545T>C	ENSP00000512864.1:p.Val182Ala
ENST00000696782.1:c.*202T>C	ENSP00000512865.1:n.*202T>C
ENST00000696783.1:n.2668T>C
ENST00000696992.1:n.1917T>C
ENST00000696995.1:n.4329T>C
ENST00000696996.1:n.2242T>C
ENST00000696997.1:c.*430T>C	ENSP00000513028.1:n.*430T>C
ENST00000696998.1:n.2054T>C
ENST00000696999.1:c.83T>C	ENSP00000513029.1:p.Val28Ala
ENST00000697035.1:c.*133T>C	ENSP00000513059.1:n.*133T>C
ENST00000697036.1:c.*216T>C	ENSP00000513060.1:n.*216T>C
ENST00000697037.1:n.835T>C
ENST00000697093.1:n.3036T>C
ENST00000697094.1:n.3383T>C
ENST00000697095.1:c.*2001T>C	ENSP00000513104.1:n.*2001T>C
ENST00000697096.1:n.1933T>C
ENST00000697097.1:c.83T>C	ENSP00000513105.1:p.Val28Ala
ENST00000562983.2:n.986T>C
ENST00000690268.1:c.881T>C	ENSP00000509810.1:p.Val294Ala
ENST00000355740.7:c.*126T>C	ENSP00000347979.3:n.*126T>C
ENST00000612663.5:c.*202T>C	ENSP00000477997.3:n.*202T>C
ENST00000640140.1:n.972T>C
ENST00000640250.1:n.299T>C
ENST00000640681.1:n.921T>C
ENST00000652046.1:c.800T>C MANE Select	ENSP00000498466.1:p.Val267Ala
ENST00000352159.8:c.*117T>C	ENSP00000345601.4:n.*117T>C
ENST00000355279.2:c.775T>C	ENSP00000347426.2:n.775T>C
ENST00000355740.6:c.800T>C	ENSP00000347979.2:p.Val267Ala
ENST00000357339.6:c.737T>C	ENSP00000349896.2:p.Val246Ala
ENST00000479522.5:c.*229T>C	ENSP00000424113.1:n.*229T>C
ENST00000484444.5:c.*241T>C	ENSP00000420975.1:n.*241T>C
ENST00000488877.5:c.*241T>C	ENSP00000425159.1:n.*241T>C
ENST00000492756.5:c.628T>C	ENSP00000422453.1:n.628T>C
ENST00000494410.5:c.*158T>C	ENSP00000423755.1:n.*158T>C
ENST00000612663.4:c.*147T>C	ENSP00000477997.2:n.*147T>C
NM_000043.4:c.800T>C , LRG_134t1:c.800T>C	NP_000034.1:p.Val267Ala
NM_152871.2:c.737T>C	NP_690610.1:p.Val246Ala
NM_152872.2:c.*112T>C	NP_690611.1:n.*112T>C
NR_028033.2:n.974T>C
NR_028034.2:n.836T>C
NR_028035.2:n.899T>C
NR_028036.2:n.1037T>C
XM_006717819.2:c.881T>C	XP_006717882.1:p.Val294Ala
XM_011539764.1:c.962T>C	XP_011538066.1:p.Val321Ala
XM_011539765.1:c.899T>C	XP_011538067.1:p.Val300Ala
XM_011539766.1:c.881T>C	XP_011538068.1:p.Val294Ala
XM_011539767.1:c.845T>C	XP_011538069.1:p.Val282Ala
XR_945732.1:n.868T>C
XR_945733.1:n.805T>C
NM_000043.5:c.800T>C	NP_000034.1:p.Val267Ala
NM_001320619.1:c.*123T>C	NP_001307548.1:n.*123T>C
NM_152871.3:c.737T>C	NP_690610.1:p.Val246Ala
NM_152872.3:c.*112T>C	NP_690611.1:n.*112T>C
NR_028033.3:n.946T>C
NR_028034.3:n.808T>C
NR_028035.3:n.871T>C
NR_028036.3:n.1009T>C
NR_135313.1:n.926T>C
NR_135314.1:n.1109T>C
NR_135315.1:n.862T>C
XM_006717819.3:c.881T>C	XP_006717882.1:p.Val294Ala
XM_011539764.2:c.962T>C	XP_011538066.1:p.Val321Ala
XM_011539765.2:c.899T>C	XP_011538067.1:p.Val300Ala
XM_011539766.2:c.881T>C	XP_011538068.1:p.Val294Ala
XM_011539767.3:c.845T>C	XP_011538069.1:p.Val282Ala
XR_945732.3:n.868T>C
XR_945733.2:n.805T>C
NM_000043.6:c.800T>C MANE Select	NP_000034.1:p.Val267Ala
NM_001320619.2:c.*123T>C	NP_001307548.1:n.*123T>C
NM_152871.4:c.737T>C	NP_690610.1:p.Val246Ala
NM_152872.4:c.*112T>C	NP_690611.1:n.*112T>C
NR_028033.4:n.707T>C
NR_028034.4:n.569T>C
NR_028035.4:n.632T>C
NR_028036.4:n.770T>C
NR_135313.2:n.687T>C
NR_135314.2:n.966T>C
NR_135315.2:n.719T>C