Canonical Allele Identifier: CA1926639345

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014220G= , CM000672.2:g.89014220G=	GRCh38
NC_000010.10:g.90773977G= , CM000672.1:g.90773977G=	GRCh37
NC_000010.9:g.90763957G=	NCBI36
NG_009089.2:g.28690G= , LRG_134:g.28690G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1087G=
ENST00000355740.8:c.*101G=	ENSP00000347979.3:n.*101G=
ENST00000357339.7:c.715G=	ENSP00000349896.2:p.Asp239=
ENST00000371857.8:n.2323G=
ENST00000460510.6:c.61G=	ENSP00000512812.1:p.Asp21=
ENST00000466081.6:n.2427G=
ENST00000477270.6:c.823G=	ENSP00000512813.1:p.Asp275=
ENST00000479522.6:c.*207G=	ENSP00000424113.1:n.*207G=
ENST00000484444.6:c.*219G=	ENSP00000420975.1:n.*219G=
ENST00000488877.6:c.669G=	ENSP00000425159.1:n.669G=
ENST00000492756.7:c.*207G=	ENSP00000422453.1:n.*207G=
ENST00000494799.6:c.61G=	ENSP00000512834.1:p.Asp21=
ENST00000562983.3:c.61G=	ENSP00000512845.1:p.Asp21=
ENST00000612663.6:c.*180G=	ENSP00000477997.3:n.*180G=
ENST00000640140.2:n.923G=
ENST00000640250.2:n.277G=
ENST00000640681.2:n.882G=
ENST00000696723.1:n.4411G=
ENST00000696741.1:n.2416G=
ENST00000696742.1:n.2143G=
ENST00000696743.1:n.3546G=
ENST00000696744.1:n.817G=
ENST00000696767.1:n.1112G=
ENST00000696768.1:c.*101G=	ENSP00000512859.1:n.*101G=
ENST00000696769.1:n.2467G=
ENST00000696771.1:c.61G=	ENSP00000512860.1:p.Asp21=
ENST00000696772.1:n.2381G=
ENST00000696773.1:n.2120G=
ENST00000696774.1:n.5888G=
ENST00000696776.1:c.871G=	ENSP00000512861.1:p.Asp291=
ENST00000696777.1:n.2186G=
ENST00000696778.1:n.1214G=
ENST00000696779.1:c.385G=	ENSP00000512862.1:p.Asp129=
ENST00000696780.1:c.808G=	ENSP00000512863.1:p.Asp270=
ENST00000696781.1:c.523G=	ENSP00000512864.1:p.Asp175=
ENST00000696782.1:c.*180G=	ENSP00000512865.1:n.*180G=
ENST00000696783.1:n.2646G=
ENST00000696992.1:n.1895G=
ENST00000696995.1:n.4307G=
ENST00000696996.1:n.2220G=
ENST00000696997.1:c.*408G=	ENSP00000513028.1:n.*408G=
ENST00000696998.1:n.2032G=
ENST00000696999.1:c.61G=	ENSP00000513029.1:p.Asp21=
ENST00000697035.1:c.*111G=	ENSP00000513059.1:n.*111G=
ENST00000697036.1:c.*194G=	ENSP00000513060.1:n.*194G=
ENST00000697037.1:n.813G=
ENST00000697093.1:n.3014G=
ENST00000697094.1:n.3361G=
ENST00000697095.1:c.*1979G=	ENSP00000513104.1:n.*1979G=
ENST00000697096.1:n.1911G=
ENST00000697097.1:c.61G=	ENSP00000513105.1:p.Asp21=
ENST00000562983.2:n.964G=
ENST00000690268.1:c.859G=	ENSP00000509810.1:p.Asp287=
ENST00000355740.7:c.*104G=	ENSP00000347979.3:n.*104G=
ENST00000612663.5:c.*180G=	ENSP00000477997.3:n.*180G=
ENST00000640140.1:n.950G=
ENST00000640250.1:n.277G=
ENST00000640681.1:n.899G=
ENST00000652046.1:c.778G= MANE Select	ENSP00000498466.1:p.Asp260=
ENST00000352159.8:c.*95G=	ENSP00000345601.4:n.*95G=
ENST00000355279.2:c.753G=	ENSP00000347426.2:n.753G=
ENST00000355740.6:c.778G=	ENSP00000347979.2:p.Asp260=
ENST00000357339.6:c.715G=	ENSP00000349896.2:p.Asp239=
ENST00000479522.5:c.*207G=	ENSP00000424113.1:n.*207G=
ENST00000484444.5:c.*219G=	ENSP00000420975.1:n.*219G=
ENST00000488877.5:c.*219G=	ENSP00000425159.1:n.*219G=
ENST00000492756.5:c.606G=	ENSP00000422453.1:n.606G=
ENST00000494410.5:c.*136G=	ENSP00000423755.1:n.*136G=
ENST00000612663.4:c.*125G=	ENSP00000477997.2:n.*125G=
NM_000043.4:c.778G= , LRG_134t1:c.778G=	NP_000034.1:p.Asp260=
NM_152871.2:c.715G=	NP_690610.1:p.Asp239=
NM_152872.2:c.*90G=	NP_690611.1:n.*90G=
NR_028033.2:n.952G=
NR_028034.2:n.814G=
NR_028035.2:n.877G=
NR_028036.2:n.1015G=
XM_006717819.2:c.859G=	XP_006717882.1:p.Asp287=
XM_011539764.1:c.940G=	XP_011538066.1:p.Asp314=
XM_011539765.1:c.877G=	XP_011538067.1:p.Asp293=
XM_011539766.1:c.859G=	XP_011538068.1:p.Asp287=
XM_011539767.1:c.823G=	XP_011538069.1:p.Asp275=
XR_945732.1:n.846G=
XR_945733.1:n.783G=
NM_000043.5:c.778G=	NP_000034.1:p.Asp260=
NM_001320619.1:c.*101G=	NP_001307548.1:n.*101G=
NM_152871.3:c.715G=	NP_690610.1:p.Asp239=
NM_152872.3:c.*90G=	NP_690611.1:n.*90G=
NR_028033.3:n.924G=
NR_028034.3:n.786G=
NR_028035.3:n.849G=
NR_028036.3:n.987G=
NR_135313.1:n.904G=
NR_135314.1:n.1087G=
NR_135315.1:n.840G=
XM_006717819.3:c.859G=	XP_006717882.1:p.Asp287=
XM_011539764.2:c.940G=	XP_011538066.1:p.Asp314=
XM_011539765.2:c.877G=	XP_011538067.1:p.Asp293=
XM_011539766.2:c.859G=	XP_011538068.1:p.Asp287=
XM_011539767.3:c.823G=	XP_011538069.1:p.Asp275=
XR_945732.3:n.846G=
XR_945733.2:n.783G=
NM_000043.6:c.778G= MANE Select	NP_000034.1:p.Asp260=
NM_001320619.2:c.*101G=	NP_001307548.1:n.*101G=
NM_152871.4:c.715G=	NP_690610.1:p.Asp239=
NM_152872.4:c.*90G=	NP_690611.1:n.*90G=
NR_028033.4:n.685G=
NR_028034.4:n.547G=
NR_028035.4:n.610G=
NR_028036.4:n.748G=
NR_135313.2:n.665G=
NR_135314.2:n.944G=
NR_135315.2:n.697G=