Canonical Allele Identifier: CA377509606

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773907T>A (hg19) ; chr10:g.89014150T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014150T>A , CM000672.2:g.89014150T>A	GRCh38
NC_000010.10:g.90773907T>A , CM000672.1:g.90773907T>A	GRCh37
NC_000010.9:g.90763887T>A	NCBI36
NG_009089.2:g.28620T>A , LRG_134:g.28620T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1017T>A
ENST00000355740.8:c.*31T>A	ENSP00000347979.3:n.*31T>A
ENST00000357339.7:c.645T>A	ENSP00000349896.2:p.Ile215=
ENST00000371857.8:n.2253T>A
ENST00000460510.6:c.-10T>A	ENSP00000512812.1:n.-10T>A
ENST00000466081.6:n.2357T>A
ENST00000477270.6:c.753T>A	ENSP00000512813.1:p.Ile251=
ENST00000479522.6:c.*137T>A	ENSP00000424113.1:n.*137T>A
ENST00000484444.6:c.*149T>A	ENSP00000420975.1:n.*149T>A
ENST00000488877.6:c.599T>A	ENSP00000425159.1:n.599T>A
ENST00000492756.7:c.*137T>A	ENSP00000422453.1:n.*137T>A
ENST00000494799.6:c.-10T>A	ENSP00000512834.1:n.-10T>A
ENST00000562983.3:c.-10T>A	ENSP00000512845.1:n.-10T>A
ENST00000612663.6:c.*110T>A	ENSP00000477997.3:n.*110T>A
ENST00000640140.2:n.853T>A
ENST00000640250.2:n.207T>A
ENST00000640681.2:n.812T>A
ENST00000696723.1:n.4341T>A
ENST00000696741.1:n.2346T>A
ENST00000696742.1:n.2073T>A
ENST00000696743.1:n.3476T>A
ENST00000696744.1:n.747T>A
ENST00000696767.1:n.1042T>A
ENST00000696768.1:c.*31T>A	ENSP00000512859.1:n.*31T>A
ENST00000696769.1:n.2397T>A
ENST00000696771.1:c.-10T>A	ENSP00000512860.1:n.-10T>A
ENST00000696772.1:n.2311T>A
ENST00000696773.1:n.2050T>A
ENST00000696774.1:n.5818T>A
ENST00000696776.1:c.801T>A	ENSP00000512861.1:p.Ile267=
ENST00000696777.1:n.2116T>A
ENST00000696778.1:n.1144T>A
ENST00000696779.1:c.315T>A	ENSP00000512862.1:p.Ile105=
ENST00000696780.1:c.738T>A	ENSP00000512863.1:p.Ile246=
ENST00000696781.1:c.453T>A	ENSP00000512864.1:p.Ile151=
ENST00000696782.1:c.*110T>A	ENSP00000512865.1:n.*110T>A
ENST00000696783.1:n.2576T>A
ENST00000696992.1:n.1825T>A
ENST00000696995.1:n.4237T>A
ENST00000696996.1:n.2150T>A
ENST00000696997.1:c.*338T>A	ENSP00000513028.1:n.*338T>A
ENST00000696998.1:n.1962T>A
ENST00000696999.1:c.-10T>A	ENSP00000513029.1:n.-10T>A
ENST00000697035.1:c.*41T>A	ENSP00000513059.1:n.*41T>A
ENST00000697036.1:c.*124T>A	ENSP00000513060.1:n.*124T>A
ENST00000697037.1:n.743T>A
ENST00000697093.1:n.2944T>A
ENST00000697094.1:n.3291T>A
ENST00000697095.1:c.*1909T>A	ENSP00000513104.1:n.*1909T>A
ENST00000697096.1:n.1841T>A
ENST00000697097.1:c.-10T>A	ENSP00000513105.1:n.-10T>A
ENST00000562983.2:n.894T>A
ENST00000690268.1:c.789T>A	ENSP00000509810.1:p.Ile263=
ENST00000355740.7:c.*34T>A	ENSP00000347979.3:n.*34T>A
ENST00000612663.5:c.*110T>A	ENSP00000477997.3:n.*110T>A
ENST00000640140.1:n.880T>A
ENST00000640250.1:n.207T>A
ENST00000640681.1:n.829T>A
ENST00000652046.1:c.708T>A MANE Select	ENSP00000498466.1:p.Ile236=
ENST00000313771.9:n.1017T>A
ENST00000352159.8:c.*25T>A	ENSP00000345601.4:n.*25T>A
ENST00000355279.2:c.683T>A	ENSP00000347426.2:n.683T>A
ENST00000355740.6:c.708T>A	ENSP00000347979.2:p.Ile236=
ENST00000357339.6:c.645T>A	ENSP00000349896.2:p.Ile215=
ENST00000479522.5:c.*137T>A	ENSP00000424113.1:n.*137T>A
ENST00000484444.5:c.*149T>A	ENSP00000420975.1:n.*149T>A
ENST00000488877.5:c.*149T>A	ENSP00000425159.1:n.*149T>A
ENST00000492756.5:c.536T>A	ENSP00000422453.1:n.536T>A
ENST00000494410.5:c.*66T>A	ENSP00000423755.1:n.*66T>A
ENST00000494799.5:n.615T>A
ENST00000612663.4:c.*55T>A	ENSP00000477997.2:n.*55T>A
ENST00000615406.4:c.708T>A	ENSP00000484575.1:p.Ile236=
ENST00000626542.2:c.706T>A	ENSP00000485876.1:p.Cys236Ser
NM_000043.4:c.708T>A , LRG_134t1:c.708T>A	NP_000034.1:p.Ile236=
NM_152871.2:c.645T>A	NP_690610.1:p.Ile215=
NM_152872.2:c.*20T>A	NP_690611.1:n.*20T>A
NR_028033.2:n.882T>A
NR_028034.2:n.744T>A
NR_028035.2:n.807T>A
NR_028036.2:n.945T>A
XM_006717819.2:c.789T>A	XP_006717882.1:p.Ile263=
XM_011539764.1:c.870T>A	XP_011538066.1:p.Ile290=
XM_011539765.1:c.807T>A	XP_011538067.1:p.Ile269=
XM_011539766.1:c.789T>A	XP_011538068.1:p.Ile263=
XM_011539767.1:c.753T>A	XP_011538069.1:p.Ile251=
XR_945732.1:n.776T>A
XR_945733.1:n.713T>A
NM_000043.5:c.708T>A	NP_000034.1:p.Ile236=
NM_001320619.1:c.*31T>A	NP_001307548.1:n.*31T>A
NM_152871.3:c.645T>A	NP_690610.1:p.Ile215=
NM_152872.3:c.*20T>A	NP_690611.1:n.*20T>A
NR_028033.3:n.854T>A
NR_028034.3:n.716T>A
NR_028035.3:n.779T>A
NR_028036.3:n.917T>A
NR_135313.1:n.834T>A
NR_135314.1:n.1017T>A
NR_135315.1:n.770T>A
XM_006717819.3:c.789T>A	XP_006717882.1:p.Ile263=
XM_011539764.2:c.870T>A	XP_011538066.1:p.Ile290=
XM_011539765.2:c.807T>A	XP_011538067.1:p.Ile269=
XM_011539766.2:c.789T>A	XP_011538068.1:p.Ile263=
XM_011539767.3:c.753T>A	XP_011538069.1:p.Ile251=
XR_945732.3:n.776T>A
XR_945733.2:n.713T>A
NM_000043.6:c.708T>A MANE Select	NP_000034.1:p.Ile236=
NM_001320619.2:c.*31T>A	NP_001307548.1:n.*31T>A
NM_152871.4:c.645T>A	NP_690610.1:p.Ile215=
NM_152872.4:c.*20T>A	NP_690611.1:n.*20T>A
NR_028033.4:n.615T>A
NR_028034.4:n.477T>A
NR_028035.4:n.540T>A
NR_028036.4:n.678T>A
NR_135313.2:n.595T>A
NR_135314.2:n.874T>A
NR_135315.2:n.627T>A