Canonical Allele Identifier: CA1926639400

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014361G= , CM000672.2:g.89014361G=	GRCh38
NC_000010.10:g.90774118G= , CM000672.1:g.90774118G=	GRCh37
NC_000010.9:g.90764098G=	NCBI36
NG_009089.2:g.28831G= , LRG_134:g.28831G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1228G=
ENST00000355740.8:c.*242G=	ENSP00000347979.3:n.*242G=
ENST00000357339.7:c.856G=	ENSP00000349896.2:p.Ala286=
ENST00000371857.8:n.2464G=
ENST00000460510.6:c.202G=	ENSP00000512812.1:p.Ala68=
ENST00000466081.6:n.2568G=
ENST00000477270.6:c.964G=	ENSP00000512813.1:p.Ala322=
ENST00000479522.6:c.*348G=	ENSP00000424113.1:n.*348G=
ENST00000484444.6:c.*360G=	ENSP00000420975.1:n.*360G=
ENST00000488877.6:c.810G=	ENSP00000425159.1:n.810G=
ENST00000492756.7:c.*348G=	ENSP00000422453.1:n.*348G=
ENST00000494799.6:c.202G=	ENSP00000512834.1:p.Ala68=
ENST00000562983.3:c.202G=	ENSP00000512845.1:p.Ala68=
ENST00000612663.6:c.*321G=	ENSP00000477997.3:n.*321G=
ENST00000640140.2:n.1064G=
ENST00000640250.2:n.418G=
ENST00000640681.2:n.1023G=
ENST00000696723.1:n.4552G=
ENST00000696741.1:n.2557G=
ENST00000696742.1:n.2284G=
ENST00000696743.1:n.3687G=
ENST00000696744.1:n.958G=
ENST00000696767.1:n.1253G=
ENST00000696768.1:c.*242G=	ENSP00000512859.1:n.*242G=
ENST00000696769.1:n.2608G=
ENST00000696771.1:c.202G=	ENSP00000512860.1:p.Ala68=
ENST00000696772.1:n.2522G=
ENST00000696773.1:n.2261G=
ENST00000696774.1:n.6029G=
ENST00000696776.1:c.1012G=	ENSP00000512861.1:p.Ala338=
ENST00000696777.1:n.2327G=
ENST00000696778.1:n.1355G=
ENST00000696779.1:c.526G=	ENSP00000512862.1:p.Ala176=
ENST00000696780.1:c.949G=	ENSP00000512863.1:p.Ala317=
ENST00000696781.1:c.664G=	ENSP00000512864.1:p.Ala222=
ENST00000696782.1:c.*321G=	ENSP00000512865.1:n.*321G=
ENST00000696783.1:n.2787G=
ENST00000696992.1:n.2036G=
ENST00000696995.1:n.4448G=
ENST00000696996.1:n.2361G=
ENST00000696997.1:c.*549G=	ENSP00000513028.1:n.*549G=
ENST00000696998.1:n.2173G=
ENST00000696999.1:c.202G=	ENSP00000513029.1:p.Ala68=
ENST00000697036.1:c.*335G=	ENSP00000513060.1:n.*335G=
ENST00000697037.1:n.954G=
ENST00000697093.1:n.3155G=
ENST00000697094.1:n.3502G=
ENST00000697095.1:c.*2120G=	ENSP00000513104.1:n.*2120G=
ENST00000697096.1:n.2052G=
ENST00000697097.1:c.202G=	ENSP00000513105.1:p.Ala68=
ENST00000562983.2:n.1105G=
ENST00000690268.1:c.1000G=	ENSP00000509810.1:p.Ala334=
ENST00000355740.7:c.*245G=	ENSP00000347979.3:n.*245G=
ENST00000612663.5:c.*321G=	ENSP00000477997.3:n.*321G=
ENST00000640140.1:n.1091G=
ENST00000640250.1:n.418G=
ENST00000640681.1:n.1040G=
ENST00000652046.1:c.919G= MANE Select	ENSP00000498466.1:p.Ala307=
ENST00000352159.8:c.*236G=	ENSP00000345601.4:n.*236G=
ENST00000355279.2:c.894G=	ENSP00000347426.2:n.894G=
ENST00000355740.6:c.919G=	ENSP00000347979.2:p.Ala307=
ENST00000357339.6:c.856G=	ENSP00000349896.2:p.Ala286=
ENST00000479522.5:c.*348G=	ENSP00000424113.1:n.*348G=
ENST00000484444.5:c.*360G=	ENSP00000420975.1:n.*360G=
ENST00000488877.5:c.*360G=	ENSP00000425159.1:n.*360G=
ENST00000492756.5:c.747G=	ENSP00000422453.1:n.747G=
ENST00000494410.5:c.*277G=	ENSP00000423755.1:n.*277G=
ENST00000612663.4:c.*266G=	ENSP00000477997.2:n.*266G=
NM_000043.4:c.919G= , LRG_134t1:c.919G=	NP_000034.1:p.Ala307=
NM_152871.2:c.856G=	NP_690610.1:p.Ala286=
NM_152872.2:c.*231G=	NP_690611.1:n.*231G=
NR_028033.2:n.1093G=
NR_028034.2:n.955G=
NR_028035.2:n.1018G=
NR_028036.2:n.1156G=
XM_006717819.2:c.1000G=	XP_006717882.1:p.Ala334=
XM_011539764.1:c.1081G=	XP_011538066.1:p.Ala361=
XM_011539765.1:c.1018G=	XP_011538067.1:p.Ala340=
XM_011539766.1:c.1000G=	XP_011538068.1:p.Ala334=
XM_011539767.1:c.964G=	XP_011538069.1:p.Ala322=
XR_945732.1:n.987G=
XR_945733.1:n.924G=
NM_000043.5:c.919G=	NP_000034.1:p.Ala307=
NM_001320619.1:c.*242G=	NP_001307548.1:n.*242G=
NM_152871.3:c.856G=	NP_690610.1:p.Ala286=
NM_152872.3:c.*231G=	NP_690611.1:n.*231G=
NR_028033.3:n.1065G=
NR_028034.3:n.927G=
NR_028035.3:n.990G=
NR_028036.3:n.1128G=
NR_135313.1:n.1045G=
NR_135314.1:n.1228G=
NR_135315.1:n.981G=
XM_006717819.3:c.1000G=	XP_006717882.1:p.Ala334=
XM_011539764.2:c.1081G=	XP_011538066.1:p.Ala361=
XM_011539765.2:c.1018G=	XP_011538067.1:p.Ala340=
XM_011539766.2:c.1000G=	XP_011538068.1:p.Ala334=
XM_011539767.3:c.964G=	XP_011538069.1:p.Ala322=
XR_945732.3:n.987G=
XR_945733.2:n.924G=
NM_000043.6:c.919G= MANE Select	NP_000034.1:p.Ala307=
NM_001320619.2:c.*242G=	NP_001307548.1:n.*242G=
NM_152871.4:c.856G=	NP_690610.1:p.Ala286=
NM_152872.4:c.*231G=	NP_690611.1:n.*231G=
NR_028033.4:n.826G=
NR_028034.4:n.688G=
NR_028035.4:n.751G=
NR_028036.4:n.889G=
NR_135313.2:n.806G=
NR_135314.2:n.1085G=
NR_135315.2:n.838G=