Canonical Allele Identifier: CA377509699

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773942T>A (hg19) ; chr10:g.89014185T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014185T>A , CM000672.2:g.89014185T>A	GRCh38
NC_000010.10:g.90773942T>A , CM000672.1:g.90773942T>A	GRCh37
NC_000010.9:g.90763922T>A	NCBI36
NG_009089.2:g.28655T>A , LRG_134:g.28655T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1052T>A
ENST00000355740.8:c.*66T>A	ENSP00000347979.3:n.*66T>A
ENST00000357339.7:c.680T>A	ENSP00000349896.2:p.Phe227Tyr
ENST00000371857.8:n.2288T>A
ENST00000460510.6:c.26T>A	ENSP00000512812.1:p.Phe9Tyr
ENST00000466081.6:n.2392T>A
ENST00000477270.6:c.788T>A	ENSP00000512813.1:p.Phe263Tyr
ENST00000479522.6:c.*172T>A	ENSP00000424113.1:n.*172T>A
ENST00000484444.6:c.*184T>A	ENSP00000420975.1:n.*184T>A
ENST00000488877.6:c.634T>A	ENSP00000425159.1:n.634T>A
ENST00000492756.7:c.*172T>A	ENSP00000422453.1:n.*172T>A
ENST00000494799.6:c.26T>A	ENSP00000512834.1:p.Phe9Tyr
ENST00000562983.3:c.26T>A	ENSP00000512845.1:p.Phe9Tyr
ENST00000612663.6:c.*145T>A	ENSP00000477997.3:n.*145T>A
ENST00000640140.2:n.888T>A
ENST00000640250.2:n.242T>A
ENST00000640681.2:n.847T>A
ENST00000696723.1:n.4376T>A
ENST00000696741.1:n.2381T>A
ENST00000696742.1:n.2108T>A
ENST00000696743.1:n.3511T>A
ENST00000696744.1:n.782T>A
ENST00000696767.1:n.1077T>A
ENST00000696768.1:c.*66T>A	ENSP00000512859.1:n.*66T>A
ENST00000696769.1:n.2432T>A
ENST00000696771.1:c.26T>A	ENSP00000512860.1:p.Phe9Tyr
ENST00000696772.1:n.2346T>A
ENST00000696773.1:n.2085T>A
ENST00000696774.1:n.5853T>A
ENST00000696776.1:c.836T>A	ENSP00000512861.1:p.Phe279Tyr
ENST00000696777.1:n.2151T>A
ENST00000696778.1:n.1179T>A
ENST00000696779.1:c.350T>A	ENSP00000512862.1:p.Phe117Tyr
ENST00000696780.1:c.773T>A	ENSP00000512863.1:p.Phe258Tyr
ENST00000696781.1:c.488T>A	ENSP00000512864.1:p.Phe163Tyr
ENST00000696782.1:c.*145T>A	ENSP00000512865.1:n.*145T>A
ENST00000696783.1:n.2611T>A
ENST00000696992.1:n.1860T>A
ENST00000696995.1:n.4272T>A
ENST00000696996.1:n.2185T>A
ENST00000696997.1:c.*373T>A	ENSP00000513028.1:n.*373T>A
ENST00000696998.1:n.1997T>A
ENST00000696999.1:c.26T>A	ENSP00000513029.1:p.Phe9Tyr
ENST00000697035.1:c.*76T>A	ENSP00000513059.1:n.*76T>A
ENST00000697036.1:c.*159T>A	ENSP00000513060.1:n.*159T>A
ENST00000697037.1:n.778T>A
ENST00000697093.1:n.2979T>A
ENST00000697094.1:n.3326T>A
ENST00000697095.1:c.*1944T>A	ENSP00000513104.1:n.*1944T>A
ENST00000697096.1:n.1876T>A
ENST00000697097.1:c.26T>A	ENSP00000513105.1:p.Phe9Tyr
ENST00000562983.2:n.929T>A
ENST00000690268.1:c.824T>A	ENSP00000509810.1:p.Phe275Tyr
ENST00000355740.7:c.*69T>A	ENSP00000347979.3:n.*69T>A
ENST00000612663.5:c.*145T>A	ENSP00000477997.3:n.*145T>A
ENST00000640140.1:n.915T>A
ENST00000640250.1:n.242T>A
ENST00000640681.1:n.864T>A
ENST00000652046.1:c.743T>A MANE Select	ENSP00000498466.1:p.Phe248Tyr
ENST00000352159.8:c.*60T>A	ENSP00000345601.4:n.*60T>A
ENST00000355279.2:c.718T>A	ENSP00000347426.2:n.718T>A
ENST00000355740.6:c.743T>A	ENSP00000347979.2:p.Phe248Tyr
ENST00000357339.6:c.680T>A	ENSP00000349896.2:p.Phe227Tyr
ENST00000479522.5:c.*172T>A	ENSP00000424113.1:n.*172T>A
ENST00000484444.5:c.*184T>A	ENSP00000420975.1:n.*184T>A
ENST00000488877.5:c.*184T>A	ENSP00000425159.1:n.*184T>A
ENST00000492756.5:c.571T>A	ENSP00000422453.1:n.571T>A
ENST00000494410.5:c.*101T>A	ENSP00000423755.1:n.*101T>A
ENST00000494799.5:n.650T>A
ENST00000612663.4:c.*90T>A	ENSP00000477997.2:n.*90T>A
ENST00000615406.4:c.743T>A	ENSP00000484575.1:p.Phe248Tyr
NM_000043.4:c.743T>A , LRG_134t1:c.743T>A	NP_000034.1:p.Phe248Tyr
NM_152871.2:c.680T>A	NP_690610.1:p.Phe227Tyr
NM_152872.2:c.*55T>A	NP_690611.1:n.*55T>A
NR_028033.2:n.917T>A
NR_028034.2:n.779T>A
NR_028035.2:n.842T>A
NR_028036.2:n.980T>A
XM_006717819.2:c.824T>A	XP_006717882.1:p.Phe275Tyr
XM_011539764.1:c.905T>A	XP_011538066.1:p.Phe302Tyr
XM_011539765.1:c.842T>A	XP_011538067.1:p.Phe281Tyr
XM_011539766.1:c.824T>A	XP_011538068.1:p.Phe275Tyr
XM_011539767.1:c.788T>A	XP_011538069.1:p.Phe263Tyr
XR_945732.1:n.811T>A
XR_945733.1:n.748T>A
NM_000043.5:c.743T>A	NP_000034.1:p.Phe248Tyr
NM_001320619.1:c.*66T>A	NP_001307548.1:n.*66T>A
NM_152871.3:c.680T>A	NP_690610.1:p.Phe227Tyr
NM_152872.3:c.*55T>A	NP_690611.1:n.*55T>A
NR_028033.3:n.889T>A
NR_028034.3:n.751T>A
NR_028035.3:n.814T>A
NR_028036.3:n.952T>A
NR_135313.1:n.869T>A
NR_135314.1:n.1052T>A
NR_135315.1:n.805T>A
XM_006717819.3:c.824T>A	XP_006717882.1:p.Phe275Tyr
XM_011539764.2:c.905T>A	XP_011538066.1:p.Phe302Tyr
XM_011539765.2:c.842T>A	XP_011538067.1:p.Phe281Tyr
XM_011539766.2:c.824T>A	XP_011538068.1:p.Phe275Tyr
XM_011539767.3:c.788T>A	XP_011538069.1:p.Phe263Tyr
XR_945732.3:n.811T>A
XR_945733.2:n.748T>A
NM_000043.6:c.743T>A MANE Select	NP_000034.1:p.Phe248Tyr
NM_001320619.2:c.*66T>A	NP_001307548.1:n.*66T>A
NM_152871.4:c.680T>A	NP_690610.1:p.Phe227Tyr
NM_152872.4:c.*55T>A	NP_690611.1:n.*55T>A
NR_028033.4:n.650T>A
NR_028034.4:n.512T>A
NR_028035.4:n.575T>A
NR_028036.4:n.713T>A
NR_135313.2:n.630T>A
NR_135314.2:n.909T>A
NR_135315.2:n.662T>A