Canonical Allele Identifier: CA1926639363

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014273G= , CM000672.2:g.89014273G=	GRCh38
NC_000010.10:g.90774030G= , CM000672.1:g.90774030G=	GRCh37
NC_000010.9:g.90764010G=	NCBI36
NG_009089.2:g.28743G= , LRG_134:g.28743G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1140G=
ENST00000355740.8:c.*154G=	ENSP00000347979.3:n.*154G=
ENST00000357339.7:c.768G=	ENSP00000349896.2:p.Leu256=
ENST00000371857.8:n.2376G=
ENST00000460510.6:c.114G=	ENSP00000512812.1:p.Leu38=
ENST00000466081.6:n.2480G=
ENST00000477270.6:c.876G=	ENSP00000512813.1:p.Leu292=
ENST00000479522.6:c.*260G=	ENSP00000424113.1:n.*260G=
ENST00000484444.6:c.*272G=	ENSP00000420975.1:n.*272G=
ENST00000488877.6:c.722G=	ENSP00000425159.1:n.722G=
ENST00000492756.7:c.*260G=	ENSP00000422453.1:n.*260G=
ENST00000494799.6:c.114G=	ENSP00000512834.1:p.Leu38=
ENST00000562983.3:c.114G=	ENSP00000512845.1:p.Leu38=
ENST00000612663.6:c.*233G=	ENSP00000477997.3:n.*233G=
ENST00000640140.2:n.976G=
ENST00000640250.2:n.330G=
ENST00000640681.2:n.935G=
ENST00000696723.1:n.4464G=
ENST00000696741.1:n.2469G=
ENST00000696742.1:n.2196G=
ENST00000696743.1:n.3599G=
ENST00000696744.1:n.870G=
ENST00000696767.1:n.1165G=
ENST00000696768.1:c.*154G=	ENSP00000512859.1:n.*154G=
ENST00000696769.1:n.2520G=
ENST00000696771.1:c.114G=	ENSP00000512860.1:p.Leu38=
ENST00000696772.1:n.2434G=
ENST00000696773.1:n.2173G=
ENST00000696774.1:n.5941G=
ENST00000696776.1:c.924G=	ENSP00000512861.1:p.Leu308=
ENST00000696777.1:n.2239G=
ENST00000696778.1:n.1267G=
ENST00000696779.1:c.438G=	ENSP00000512862.1:p.Leu146=
ENST00000696780.1:c.861G=	ENSP00000512863.1:p.Leu287=
ENST00000696781.1:c.576G=	ENSP00000512864.1:p.Leu192=
ENST00000696782.1:c.*233G=	ENSP00000512865.1:n.*233G=
ENST00000696783.1:n.2699G=
ENST00000696992.1:n.1948G=
ENST00000696995.1:n.4360G=
ENST00000696996.1:n.2273G=
ENST00000696997.1:c.*461G=	ENSP00000513028.1:n.*461G=
ENST00000696998.1:n.2085G=
ENST00000696999.1:c.114G=	ENSP00000513029.1:p.Leu38=
ENST00000697035.1:c.*164G=	ENSP00000513059.1:n.*164G=
ENST00000697036.1:c.*247G=	ENSP00000513060.1:n.*247G=
ENST00000697037.1:n.866G=
ENST00000697093.1:n.3067G=
ENST00000697094.1:n.3414G=
ENST00000697095.1:c.*2032G=	ENSP00000513104.1:n.*2032G=
ENST00000697096.1:n.1964G=
ENST00000697097.1:c.114G=	ENSP00000513105.1:p.Leu38=
ENST00000562983.2:n.1017G=
ENST00000690268.1:c.912G=	ENSP00000509810.1:p.Leu304=
ENST00000355740.7:c.*157G=	ENSP00000347979.3:n.*157G=
ENST00000612663.5:c.*233G=	ENSP00000477997.3:n.*233G=
ENST00000640140.1:n.1003G=
ENST00000640250.1:n.330G=
ENST00000640681.1:n.952G=
ENST00000652046.1:c.831G= MANE Select	ENSP00000498466.1:p.Leu277=
ENST00000352159.8:c.*148G=	ENSP00000345601.4:n.*148G=
ENST00000355279.2:c.806G=	ENSP00000347426.2:n.806G=
ENST00000355740.6:c.831G=	ENSP00000347979.2:p.Leu277=
ENST00000357339.6:c.768G=	ENSP00000349896.2:p.Leu256=
ENST00000479522.5:c.*260G=	ENSP00000424113.1:n.*260G=
ENST00000484444.5:c.*272G=	ENSP00000420975.1:n.*272G=
ENST00000488877.5:c.*272G=	ENSP00000425159.1:n.*272G=
ENST00000492756.5:c.659G=	ENSP00000422453.1:n.659G=
ENST00000494410.5:c.*189G=	ENSP00000423755.1:n.*189G=
ENST00000612663.4:c.*178G=	ENSP00000477997.2:n.*178G=
NM_000043.4:c.831G= , LRG_134t1:c.831G=	NP_000034.1:p.Leu277=
NM_152871.2:c.768G=	NP_690610.1:p.Leu256=
NM_152872.2:c.*143G=	NP_690611.1:n.*143G=
NR_028033.2:n.1005G=
NR_028034.2:n.867G=
NR_028035.2:n.930G=
NR_028036.2:n.1068G=
XM_006717819.2:c.912G=	XP_006717882.1:p.Leu304=
XM_011539764.1:c.993G=	XP_011538066.1:p.Leu331=
XM_011539765.1:c.930G=	XP_011538067.1:p.Leu310=
XM_011539766.1:c.912G=	XP_011538068.1:p.Leu304=
XM_011539767.1:c.876G=	XP_011538069.1:p.Leu292=
XR_945732.1:n.899G=
XR_945733.1:n.836G=
NM_000043.5:c.831G=	NP_000034.1:p.Leu277=
NM_001320619.1:c.*154G=	NP_001307548.1:n.*154G=
NM_152871.3:c.768G=	NP_690610.1:p.Leu256=
NM_152872.3:c.*143G=	NP_690611.1:n.*143G=
NR_028033.3:n.977G=
NR_028034.3:n.839G=
NR_028035.3:n.902G=
NR_028036.3:n.1040G=
NR_135313.1:n.957G=
NR_135314.1:n.1140G=
NR_135315.1:n.893G=
XM_006717819.3:c.912G=	XP_006717882.1:p.Leu304=
XM_011539764.2:c.993G=	XP_011538066.1:p.Leu331=
XM_011539765.2:c.930G=	XP_011538067.1:p.Leu310=
XM_011539766.2:c.912G=	XP_011538068.1:p.Leu304=
XM_011539767.3:c.876G=	XP_011538069.1:p.Leu292=
XR_945732.3:n.899G=
XR_945733.2:n.836G=
NM_000043.6:c.831G= MANE Select	NP_000034.1:p.Leu277=
NM_001320619.2:c.*154G=	NP_001307548.1:n.*154G=
NM_152871.4:c.768G=	NP_690610.1:p.Leu256=
NM_152872.4:c.*143G=	NP_690611.1:n.*143G=
NR_028033.4:n.738G=
NR_028034.4:n.600G=
NR_028035.4:n.663G=
NR_028036.4:n.801G=
NR_135313.2:n.718G=
NR_135314.2:n.997G=
NR_135315.2:n.750G=