Canonical Allele Identifier: CA1926639392

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014345C= , CM000672.2:g.89014345C=	GRCh38
NC_000010.10:g.90774102C= , CM000672.1:g.90774102C=	GRCh37
NC_000010.9:g.90764082C=	NCBI36
NG_009089.2:g.28815C= , LRG_134:g.28815C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1212C=
ENST00000355740.8:c.*226C=	ENSP00000347979.3:n.*226C=
ENST00000357339.7:c.840C=	ENSP00000349896.2:p.Ala280=
ENST00000371857.8:n.2448C=
ENST00000460510.6:c.186C=	ENSP00000512812.1:p.Ala62=
ENST00000466081.6:n.2552C=
ENST00000477270.6:c.948C=	ENSP00000512813.1:p.Ala316=
ENST00000479522.6:c.*332C=	ENSP00000424113.1:n.*332C=
ENST00000484444.6:c.*344C=	ENSP00000420975.1:n.*344C=
ENST00000488877.6:c.794C=	ENSP00000425159.1:n.794C=
ENST00000492756.7:c.*332C=	ENSP00000422453.1:n.*332C=
ENST00000494799.6:c.186C=	ENSP00000512834.1:p.Ala62=
ENST00000562983.3:c.186C=	ENSP00000512845.1:p.Ala62=
ENST00000612663.6:c.*305C=	ENSP00000477997.3:n.*305C=
ENST00000640140.2:n.1048C=
ENST00000640250.2:n.402C=
ENST00000640681.2:n.1007C=
ENST00000696723.1:n.4536C=
ENST00000696741.1:n.2541C=
ENST00000696742.1:n.2268C=
ENST00000696743.1:n.3671C=
ENST00000696744.1:n.942C=
ENST00000696767.1:n.1237C=
ENST00000696768.1:c.*226C=	ENSP00000512859.1:n.*226C=
ENST00000696769.1:n.2592C=
ENST00000696771.1:c.186C=	ENSP00000512860.1:p.Ala62=
ENST00000696772.1:n.2506C=
ENST00000696773.1:n.2245C=
ENST00000696774.1:n.6013C=
ENST00000696776.1:c.996C=	ENSP00000512861.1:p.Ala332=
ENST00000696777.1:n.2311C=
ENST00000696778.1:n.1339C=
ENST00000696779.1:c.510C=	ENSP00000512862.1:p.Ala170=
ENST00000696780.1:c.933C=	ENSP00000512863.1:p.Ala311=
ENST00000696781.1:c.648C=	ENSP00000512864.1:p.Ala216=
ENST00000696782.1:c.*305C=	ENSP00000512865.1:n.*305C=
ENST00000696783.1:n.2771C=
ENST00000696992.1:n.2020C=
ENST00000696995.1:n.4432C=
ENST00000696996.1:n.2345C=
ENST00000696997.1:c.*533C=	ENSP00000513028.1:n.*533C=
ENST00000696998.1:n.2157C=
ENST00000696999.1:c.186C=	ENSP00000513029.1:p.Ala62=
ENST00000697036.1:c.*319C=	ENSP00000513060.1:n.*319C=
ENST00000697037.1:n.938C=
ENST00000697093.1:n.3139C=
ENST00000697094.1:n.3486C=
ENST00000697095.1:c.*2104C=	ENSP00000513104.1:n.*2104C=
ENST00000697096.1:n.2036C=
ENST00000697097.1:c.186C=	ENSP00000513105.1:p.Ala62=
ENST00000562983.2:n.1089C=
ENST00000690268.1:c.984C=	ENSP00000509810.1:p.Ala328=
ENST00000355740.7:c.*229C=	ENSP00000347979.3:n.*229C=
ENST00000612663.5:c.*305C=	ENSP00000477997.3:n.*305C=
ENST00000640140.1:n.1075C=
ENST00000640250.1:n.402C=
ENST00000640681.1:n.1024C=
ENST00000652046.1:c.903C= MANE Select	ENSP00000498466.1:p.Ala301=
ENST00000352159.8:c.*220C=	ENSP00000345601.4:n.*220C=
ENST00000355279.2:c.878C=	ENSP00000347426.2:n.878C=
ENST00000355740.6:c.903C=	ENSP00000347979.2:p.Ala301=
ENST00000357339.6:c.840C=	ENSP00000349896.2:p.Ala280=
ENST00000479522.5:c.*332C=	ENSP00000424113.1:n.*332C=
ENST00000484444.5:c.*344C=	ENSP00000420975.1:n.*344C=
ENST00000488877.5:c.*344C=	ENSP00000425159.1:n.*344C=
ENST00000492756.5:c.731C=	ENSP00000422453.1:n.731C=
ENST00000494410.5:c.*261C=	ENSP00000423755.1:n.*261C=
ENST00000612663.4:c.*250C=	ENSP00000477997.2:n.*250C=
NM_000043.4:c.903C= , LRG_134t1:c.903C=	NP_000034.1:p.Ala301=
NM_152871.2:c.840C=	NP_690610.1:p.Ala280=
NM_152872.2:c.*215C=	NP_690611.1:n.*215C=
NR_028033.2:n.1077C=
NR_028034.2:n.939C=
NR_028035.2:n.1002C=
NR_028036.2:n.1140C=
XM_006717819.2:c.984C=	XP_006717882.1:p.Ala328=
XM_011539764.1:c.1065C=	XP_011538066.1:p.Ala355=
XM_011539765.1:c.1002C=	XP_011538067.1:p.Ala334=
XM_011539766.1:c.984C=	XP_011538068.1:p.Ala328=
XM_011539767.1:c.948C=	XP_011538069.1:p.Ala316=
XR_945732.1:n.971C=
XR_945733.1:n.908C=
NM_000043.5:c.903C=	NP_000034.1:p.Ala301=
NM_001320619.1:c.*226C=	NP_001307548.1:n.*226C=
NM_152871.3:c.840C=	NP_690610.1:p.Ala280=
NM_152872.3:c.*215C=	NP_690611.1:n.*215C=
NR_028033.3:n.1049C=
NR_028034.3:n.911C=
NR_028035.3:n.974C=
NR_028036.3:n.1112C=
NR_135313.1:n.1029C=
NR_135314.1:n.1212C=
NR_135315.1:n.965C=
XM_006717819.3:c.984C=	XP_006717882.1:p.Ala328=
XM_011539764.2:c.1065C=	XP_011538066.1:p.Ala355=
XM_011539765.2:c.1002C=	XP_011538067.1:p.Ala334=
XM_011539766.2:c.984C=	XP_011538068.1:p.Ala328=
XM_011539767.3:c.948C=	XP_011538069.1:p.Ala316=
XR_945732.3:n.971C=
XR_945733.2:n.908C=
NM_000043.6:c.903C= MANE Select	NP_000034.1:p.Ala301=
NM_001320619.2:c.*226C=	NP_001307548.1:n.*226C=
NM_152871.4:c.840C=	NP_690610.1:p.Ala280=
NM_152872.4:c.*215C=	NP_690611.1:n.*215C=
NR_028033.4:n.810C=
NR_028034.4:n.672C=
NR_028035.4:n.735C=
NR_028036.4:n.873C=
NR_135313.2:n.790C=
NR_135314.2:n.1069C=
NR_135315.2:n.822C=