Canonical Allele Identifier: CA470975021

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774030G>A (hg19)

Genomic Alleles

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

Transcript Alleles

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