Canonical Allele Identifier: CA470975008

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774012A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014255A>T , CM000672.2:g.89014255A>T	GRCh38
NC_000010.10:g.90774012A>T , CM000672.1:g.90774012A>T	GRCh37
NC_000010.9:g.90763992A>T	NCBI36
NG_009089.2:g.28725A>T , LRG_134:g.28725A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1122A>T
ENST00000355740.8:c.*136A>T	ENSP00000347979.3:n.*136A>T
ENST00000357339.7:c.750A>T	ENSP00000349896.2:p.Ala250=
ENST00000371857.8:n.2358A>T
ENST00000460510.6:c.96A>T	ENSP00000512812.1:p.Ala32=
ENST00000466081.6:n.2462A>T
ENST00000477270.6:c.858A>T	ENSP00000512813.1:p.Ala286=
ENST00000479522.6:c.*242A>T	ENSP00000424113.1:n.*242A>T
ENST00000484444.6:c.*254A>T	ENSP00000420975.1:n.*254A>T
ENST00000488877.6:c.704A>T	ENSP00000425159.1:n.704A>T
ENST00000492756.7:c.*242A>T	ENSP00000422453.1:n.*242A>T
ENST00000494799.6:c.96A>T	ENSP00000512834.1:p.Ala32=
ENST00000562983.3:c.96A>T	ENSP00000512845.1:p.Ala32=
ENST00000612663.6:c.*215A>T	ENSP00000477997.3:n.*215A>T
ENST00000640140.2:n.958A>T
ENST00000640250.2:n.312A>T
ENST00000640681.2:n.917A>T
ENST00000696723.1:n.4446A>T
ENST00000696741.1:n.2451A>T
ENST00000696742.1:n.2178A>T
ENST00000696743.1:n.3581A>T
ENST00000696744.1:n.852A>T
ENST00000696767.1:n.1147A>T
ENST00000696768.1:c.*136A>T	ENSP00000512859.1:n.*136A>T
ENST00000696769.1:n.2502A>T
ENST00000696771.1:c.96A>T	ENSP00000512860.1:p.Ala32=
ENST00000696772.1:n.2416A>T
ENST00000696773.1:n.2155A>T
ENST00000696774.1:n.5923A>T
ENST00000696776.1:c.906A>T	ENSP00000512861.1:p.Ala302=
ENST00000696777.1:n.2221A>T
ENST00000696778.1:n.1249A>T
ENST00000696779.1:c.420A>T	ENSP00000512862.1:p.Ala140=
ENST00000696780.1:c.843A>T	ENSP00000512863.1:p.Ala281=
ENST00000696781.1:c.558A>T	ENSP00000512864.1:p.Ala186=
ENST00000696782.1:c.*215A>T	ENSP00000512865.1:n.*215A>T
ENST00000696783.1:n.2681A>T
ENST00000696992.1:n.1930A>T
ENST00000696995.1:n.4342A>T
ENST00000696996.1:n.2255A>T
ENST00000696997.1:c.*443A>T	ENSP00000513028.1:n.*443A>T
ENST00000696998.1:n.2067A>T
ENST00000696999.1:c.96A>T	ENSP00000513029.1:p.Ala32=
ENST00000697035.1:c.*146A>T	ENSP00000513059.1:n.*146A>T
ENST00000697036.1:c.*229A>T	ENSP00000513060.1:n.*229A>T
ENST00000697037.1:n.848A>T
ENST00000697093.1:n.3049A>T
ENST00000697094.1:n.3396A>T
ENST00000697095.1:c.*2014A>T	ENSP00000513104.1:n.*2014A>T
ENST00000697096.1:n.1946A>T
ENST00000697097.1:c.96A>T	ENSP00000513105.1:p.Ala32=
ENST00000562983.2:n.999A>T
ENST00000690268.1:c.894A>T	ENSP00000509810.1:p.Ala298=
ENST00000355740.7:c.*139A>T	ENSP00000347979.3:n.*139A>T
ENST00000612663.5:c.*215A>T	ENSP00000477997.3:n.*215A>T
ENST00000640140.1:n.985A>T
ENST00000640250.1:n.312A>T
ENST00000640681.1:n.934A>T
ENST00000652046.1:c.813A>T MANE Select	ENSP00000498466.1:p.Ala271=
ENST00000352159.8:c.*130A>T	ENSP00000345601.4:n.*130A>T
ENST00000355279.2:c.788A>T	ENSP00000347426.2:n.788A>T
ENST00000355740.6:c.813A>T	ENSP00000347979.2:p.Ala271=
ENST00000357339.6:c.750A>T	ENSP00000349896.2:p.Ala250=
ENST00000479522.5:c.*242A>T	ENSP00000424113.1:n.*242A>T
ENST00000484444.5:c.*254A>T	ENSP00000420975.1:n.*254A>T
ENST00000488877.5:c.*254A>T	ENSP00000425159.1:n.*254A>T
ENST00000492756.5:c.641A>T	ENSP00000422453.1:n.641A>T
ENST00000494410.5:c.*171A>T	ENSP00000423755.1:n.*171A>T
ENST00000612663.4:c.*160A>T	ENSP00000477997.2:n.*160A>T
NM_000043.4:c.813A>T , LRG_134t1:c.813A>T	NP_000034.1:p.Ala271=
NM_152871.2:c.750A>T	NP_690610.1:p.Ala250=
NM_152872.2:c.*125A>T	NP_690611.1:n.*125A>T
NR_028033.2:n.987A>T
NR_028034.2:n.849A>T
NR_028035.2:n.912A>T
NR_028036.2:n.1050A>T
XM_006717819.2:c.894A>T	XP_006717882.1:p.Ala298=
XM_011539764.1:c.975A>T	XP_011538066.1:p.Ala325=
XM_011539765.1:c.912A>T	XP_011538067.1:p.Ala304=
XM_011539766.1:c.894A>T	XP_011538068.1:p.Ala298=
XM_011539767.1:c.858A>T	XP_011538069.1:p.Ala286=
XR_945732.1:n.881A>T
XR_945733.1:n.818A>T
NM_000043.5:c.813A>T	NP_000034.1:p.Ala271=
NM_001320619.1:c.*136A>T	NP_001307548.1:n.*136A>T
NM_152871.3:c.750A>T	NP_690610.1:p.Ala250=
NM_152872.3:c.*125A>T	NP_690611.1:n.*125A>T
NR_028033.3:n.959A>T
NR_028034.3:n.821A>T
NR_028035.3:n.884A>T
NR_028036.3:n.1022A>T
NR_135313.1:n.939A>T
NR_135314.1:n.1122A>T
NR_135315.1:n.875A>T
XM_006717819.3:c.894A>T	XP_006717882.1:p.Ala298=
XM_011539764.2:c.975A>T	XP_011538066.1:p.Ala325=
XM_011539765.2:c.912A>T	XP_011538067.1:p.Ala304=
XM_011539766.2:c.894A>T	XP_011538068.1:p.Ala298=
XM_011539767.3:c.858A>T	XP_011538069.1:p.Ala286=
XR_945732.3:n.881A>T
XR_945733.2:n.818A>T
NM_000043.6:c.813A>T MANE Select	NP_000034.1:p.Ala271=
NM_001320619.2:c.*136A>T	NP_001307548.1:n.*136A>T
NM_152871.4:c.750A>T	NP_690610.1:p.Ala250=
NM_152872.4:c.*125A>T	NP_690611.1:n.*125A>T
NR_028033.4:n.720A>T
NR_028034.4:n.582A>T
NR_028035.4:n.645A>T
NR_028036.4:n.783A>T
NR_135313.2:n.700A>T
NR_135314.2:n.979A>T
NR_135315.2:n.732A>T