Canonical Allele Identifier: CA1926639443

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014472T= , CM000672.2:g.89014472T=	GRCh38
NC_000010.10:g.90774229T= , CM000672.1:g.90774229T=	GRCh37
NC_000010.9:g.90764209T=	NCBI36
NG_009089.2:g.28942T= , LRG_134:g.28942T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1339T=
ENST00000355740.8:c.*353T=	ENSP00000347979.3:n.*353T=
ENST00000357339.7:c.*22T=	ENSP00000349896.2:n.*22T=
ENST00000371857.8:n.2575T=
ENST00000460510.6:c.*22T=	ENSP00000512812.1:n.*22T=
ENST00000466081.6:n.2679T=
ENST00000477270.6:c.*22T=	ENSP00000512813.1:n.*22T=
ENST00000479522.6:c.*459T=	ENSP00000424113.1:n.*459T=
ENST00000484444.6:c.*471T=	ENSP00000420975.1:n.*471T=
ENST00000488877.6:c.921T=	ENSP00000425159.1:n.921T=
ENST00000492756.7:c.*459T=	ENSP00000422453.1:n.*459T=
ENST00000494799.6:c.*22T=	ENSP00000512834.1:n.*22T=
ENST00000562983.3:c.*22T=	ENSP00000512845.1:n.*22T=
ENST00000612663.6:c.*432T=	ENSP00000477997.3:n.*432T=
ENST00000640140.2:n.1175T=
ENST00000640250.2:n.529T=
ENST00000640681.2:n.1134T=
ENST00000696723.1:n.4663T=
ENST00000696741.1:n.2668T=
ENST00000696742.1:n.2395T=
ENST00000696743.1:n.3798T=
ENST00000696744.1:n.1069T=
ENST00000696767.1:n.1364T=
ENST00000696768.1:c.*353T=	ENSP00000512859.1:n.*353T=
ENST00000696769.1:n.2719T=
ENST00000696771.1:c.*22T=	ENSP00000512860.1:n.*22T=
ENST00000696772.1:n.2633T=
ENST00000696773.1:n.2372T=
ENST00000696774.1:n.6140T=
ENST00000696776.1:c.*22T=	ENSP00000512861.1:n.*22T=
ENST00000696777.1:n.2438T=
ENST00000696778.1:n.1466T=
ENST00000696779.1:c.*22T=	ENSP00000512862.1:n.*22T=
ENST00000696780.1:c.*22T=	ENSP00000512863.1:n.*22T=
ENST00000696781.1:c.*22T=	ENSP00000512864.1:n.*22T=
ENST00000696782.1:c.*432T=	ENSP00000512865.1:n.*432T=
ENST00000696783.1:n.2898T=
ENST00000696992.1:n.2147T=
ENST00000696995.1:n.4559T=
ENST00000696996.1:n.2472T=
ENST00000696997.1:c.*660T=	ENSP00000513028.1:n.*660T=
ENST00000696998.1:n.2284T=
ENST00000696999.1:c.*22T=	ENSP00000513029.1:n.*22T=
ENST00000697036.1:c.*446T=	ENSP00000513060.1:n.*446T=
ENST00000697037.1:n.1065T=
ENST00000697093.1:n.3266T=
ENST00000697094.1:n.3613T=
ENST00000697095.1:c.*2231T=	ENSP00000513104.1:n.*2231T=
ENST00000697096.1:n.2163T=
ENST00000697097.1:c.*22T=	ENSP00000513105.1:n.*22T=
ENST00000562983.2:n.1216T=
ENST00000690268.1:c.*22T=	ENSP00000509810.1:n.*22T=
ENST00000355740.7:c.*356T=	ENSP00000347979.3:n.*356T=
ENST00000612663.5:c.*432T=	ENSP00000477997.3:n.*432T=
ENST00000640140.1:n.1202T=
ENST00000640250.1:n.529T=
ENST00000640681.1:n.1151T=
ENST00000652046.1:c.*22T= MANE Select	ENSP00000498466.1:n.*22T=
ENST00000352159.8:c.*347T=	ENSP00000345601.4:n.*347T=
ENST00000355740.6:c.*22T=	ENSP00000347979.2:n.*22T=
ENST00000479522.5:c.*459T=	ENSP00000424113.1:n.*459T=
ENST00000484444.5:c.*471T=	ENSP00000420975.1:n.*471T=
ENST00000494410.5:c.*388T=	ENSP00000423755.1:n.*388T=
NM_000043.4:c.*22T= , LRG_134t1:c.*22T=	NP_000034.1:n.*22T=
NM_152871.2:c.*22T=	NP_690610.1:n.*22T=
NM_152872.2:c.*342T=	NP_690611.1:n.*342T=
NR_028033.2:n.1204T=
NR_028034.2:n.1066T=
NR_028035.2:n.1129T=
NR_028036.2:n.1267T=
XM_006717819.2:c.*22T=	XP_006717882.1:n.*22T=
XM_011539764.1:c.*22T=	XP_011538066.1:n.*22T=
XM_011539765.1:c.*22T=	XP_011538067.1:n.*22T=
XM_011539766.1:c.*22T=	XP_011538068.1:n.*22T=
XM_011539767.1:c.*22T=	XP_011538069.1:n.*22T=
XR_945733.1:n.1035T=
NM_000043.5:c.*22T=	NP_000034.1:n.*22T=
NM_001320619.1:c.*353T=	NP_001307548.1:n.*353T=
NM_152871.3:c.*22T=	NP_690610.1:n.*22T=
NM_152872.3:c.*342T=	NP_690611.1:n.*342T=
NR_028033.3:n.1176T=
NR_028034.3:n.1038T=
NR_028035.3:n.1101T=
NR_028036.3:n.1239T=
NR_135313.1:n.1156T=
NR_135314.1:n.1339T=
NR_135315.1:n.1092T=
XM_006717819.3:c.*22T=	XP_006717882.1:n.*22T=
XM_011539764.2:c.*22T=	XP_011538066.1:n.*22T=
XM_011539765.2:c.*22T=	XP_011538067.1:n.*22T=
XM_011539766.2:c.*22T=	XP_011538068.1:n.*22T=
XM_011539767.3:c.*22T=	XP_011538069.1:n.*22T=
XR_945732.3:n.1098T=
XR_945733.2:n.1035T=
NM_000043.6:c.*22T= MANE Select	NP_000034.1:n.*22T=
NM_001320619.2:c.*353T=	NP_001307548.1:n.*353T=
NM_152871.4:c.*22T=	NP_690610.1:n.*22T=
NM_152872.4:c.*342T=	NP_690611.1:n.*342T=
NR_028033.4:n.937T=
NR_028034.4:n.799T=
NR_028035.4:n.862T=
NR_028036.4:n.1000T=
NR_135313.2:n.917T=
NR_135314.2:n.1196T=
NR_135315.2:n.949T=