Canonical Allele Identifier: CA377509736

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773958T>A (hg19) ; chr10:g.89014201T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014201T>A , CM000672.2:g.89014201T>A	GRCh38
NC_000010.10:g.90773958T>A , CM000672.1:g.90773958T>A	GRCh37
NC_000010.9:g.90763938T>A	NCBI36
NG_009089.2:g.28671T>A , LRG_134:g.28671T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1068T>A
ENST00000355740.8:c.*82T>A	ENSP00000347979.3:n.*82T>A
ENST00000357339.7:c.696T>A	ENSP00000349896.2:p.Gly232=
ENST00000371857.8:n.2304T>A
ENST00000460510.6:c.42T>A	ENSP00000512812.1:p.Gly14=
ENST00000466081.6:n.2408T>A
ENST00000477270.6:c.804T>A	ENSP00000512813.1:p.Gly268=
ENST00000479522.6:c.*188T>A	ENSP00000424113.1:n.*188T>A
ENST00000484444.6:c.*200T>A	ENSP00000420975.1:n.*200T>A
ENST00000488877.6:c.650T>A	ENSP00000425159.1:n.650T>A
ENST00000492756.7:c.*188T>A	ENSP00000422453.1:n.*188T>A
ENST00000494799.6:c.42T>A	ENSP00000512834.1:p.Gly14=
ENST00000562983.3:c.42T>A	ENSP00000512845.1:p.Gly14=
ENST00000612663.6:c.*161T>A	ENSP00000477997.3:n.*161T>A
ENST00000640140.2:n.904T>A
ENST00000640250.2:n.258T>A
ENST00000640681.2:n.863T>A
ENST00000696723.1:n.4392T>A
ENST00000696741.1:n.2397T>A
ENST00000696742.1:n.2124T>A
ENST00000696743.1:n.3527T>A
ENST00000696744.1:n.798T>A
ENST00000696767.1:n.1093T>A
ENST00000696768.1:c.*82T>A	ENSP00000512859.1:n.*82T>A
ENST00000696769.1:n.2448T>A
ENST00000696771.1:c.42T>A	ENSP00000512860.1:p.Gly14=
ENST00000696772.1:n.2362T>A
ENST00000696773.1:n.2101T>A
ENST00000696774.1:n.5869T>A
ENST00000696776.1:c.852T>A	ENSP00000512861.1:p.Gly284=
ENST00000696777.1:n.2167T>A
ENST00000696778.1:n.1195T>A
ENST00000696779.1:c.366T>A	ENSP00000512862.1:p.Gly122=
ENST00000696780.1:c.789T>A	ENSP00000512863.1:p.Gly263=
ENST00000696781.1:c.504T>A	ENSP00000512864.1:p.Gly168=
ENST00000696782.1:c.*161T>A	ENSP00000512865.1:n.*161T>A
ENST00000696783.1:n.2627T>A
ENST00000696992.1:n.1876T>A
ENST00000696995.1:n.4288T>A
ENST00000696996.1:n.2201T>A
ENST00000696997.1:c.*389T>A	ENSP00000513028.1:n.*389T>A
ENST00000696998.1:n.2013T>A
ENST00000696999.1:c.42T>A	ENSP00000513029.1:p.Gly14=
ENST00000697035.1:c.*92T>A	ENSP00000513059.1:n.*92T>A
ENST00000697036.1:c.*175T>A	ENSP00000513060.1:n.*175T>A
ENST00000697037.1:n.794T>A
ENST00000697093.1:n.2995T>A
ENST00000697094.1:n.3342T>A
ENST00000697095.1:c.*1960T>A	ENSP00000513104.1:n.*1960T>A
ENST00000697096.1:n.1892T>A
ENST00000697097.1:c.42T>A	ENSP00000513105.1:p.Gly14=
ENST00000562983.2:n.945T>A
ENST00000690268.1:c.840T>A	ENSP00000509810.1:p.Gly280=
ENST00000355740.7:c.*85T>A	ENSP00000347979.3:n.*85T>A
ENST00000612663.5:c.*161T>A	ENSP00000477997.3:n.*161T>A
ENST00000640140.1:n.931T>A
ENST00000640250.1:n.258T>A
ENST00000640681.1:n.880T>A
ENST00000652046.1:c.759T>A MANE Select	ENSP00000498466.1:p.Gly253=
ENST00000352159.8:c.*76T>A	ENSP00000345601.4:n.*76T>A
ENST00000355279.2:c.734T>A	ENSP00000347426.2:n.734T>A
ENST00000355740.6:c.759T>A	ENSP00000347979.2:p.Gly253=
ENST00000357339.6:c.696T>A	ENSP00000349896.2:p.Gly232=
ENST00000479522.5:c.*188T>A	ENSP00000424113.1:n.*188T>A
ENST00000484444.5:c.*200T>A	ENSP00000420975.1:n.*200T>A
ENST00000488877.5:c.*200T>A	ENSP00000425159.1:n.*200T>A
ENST00000492756.5:c.587T>A	ENSP00000422453.1:n.587T>A
ENST00000494410.5:c.*117T>A	ENSP00000423755.1:n.*117T>A
ENST00000494799.5:n.666T>A
ENST00000612663.4:c.*106T>A	ENSP00000477997.2:n.*106T>A
ENST00000615406.4:c.757T>A	ENSP00000484575.1:p.Cys253Ser
NM_000043.4:c.759T>A , LRG_134t1:c.759T>A	NP_000034.1:p.Gly253=
NM_152871.2:c.696T>A	NP_690610.1:p.Gly232=
NM_152872.2:c.*71T>A	NP_690611.1:n.*71T>A
NR_028033.2:n.933T>A
NR_028034.2:n.795T>A
NR_028035.2:n.858T>A
NR_028036.2:n.996T>A
XM_006717819.2:c.840T>A	XP_006717882.1:p.Gly280=
XM_011539764.1:c.921T>A	XP_011538066.1:p.Gly307=
XM_011539765.1:c.858T>A	XP_011538067.1:p.Gly286=
XM_011539766.1:c.840T>A	XP_011538068.1:p.Gly280=
XM_011539767.1:c.804T>A	XP_011538069.1:p.Gly268=
XR_945732.1:n.827T>A
XR_945733.1:n.764T>A
NM_000043.5:c.759T>A	NP_000034.1:p.Gly253=
NM_001320619.1:c.*82T>A	NP_001307548.1:n.*82T>A
NM_152871.3:c.696T>A	NP_690610.1:p.Gly232=
NM_152872.3:c.*71T>A	NP_690611.1:n.*71T>A
NR_028033.3:n.905T>A
NR_028034.3:n.767T>A
NR_028035.3:n.830T>A
NR_028036.3:n.968T>A
NR_135313.1:n.885T>A
NR_135314.1:n.1068T>A
NR_135315.1:n.821T>A
XM_006717819.3:c.840T>A	XP_006717882.1:p.Gly280=
XM_011539764.2:c.921T>A	XP_011538066.1:p.Gly307=
XM_011539765.2:c.858T>A	XP_011538067.1:p.Gly286=
XM_011539766.2:c.840T>A	XP_011538068.1:p.Gly280=
XM_011539767.3:c.804T>A	XP_011538069.1:p.Gly268=
XR_945732.3:n.827T>A
XR_945733.2:n.764T>A
NM_000043.6:c.759T>A MANE Select	NP_000034.1:p.Gly253=
NM_001320619.2:c.*82T>A	NP_001307548.1:n.*82T>A
NM_152871.4:c.696T>A	NP_690610.1:p.Gly232=
NM_152872.4:c.*71T>A	NP_690611.1:n.*71T>A
NR_028033.4:n.666T>A
NR_028034.4:n.528T>A
NR_028035.4:n.591T>A
NR_028036.4:n.729T>A
NR_135313.2:n.646T>A
NR_135314.2:n.925T>A
NR_135315.2:n.678T>A