Canonical Allele Identifier: CA377509768

Gene: FAS

Linked Data

• COSMIC: COSM5699023
• MyVariant Identifiers: chr10:g.90773968G>T (hg19) ; chr10:g.89014211G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014211G>T , CM000672.2:g.89014211G>T	GRCh38
NC_000010.10:g.90773968G>T , CM000672.1:g.90773968G>T	GRCh37
NC_000010.9:g.90763948G>T	NCBI36
NG_009089.2:g.28681G>T , LRG_134:g.28681G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1078G>T
ENST00000355740.8:c.*92G>T	ENSP00000347979.3:n.*92G>T
ENST00000357339.7:c.706G>T	ENSP00000349896.2:p.Ala236Ser
ENST00000371857.8:n.2314G>T
ENST00000460510.6:c.52G>T	ENSP00000512812.1:p.Ala18Ser
ENST00000466081.6:n.2418G>T
ENST00000477270.6:c.814G>T	ENSP00000512813.1:p.Ala272Ser
ENST00000479522.6:c.*198G>T	ENSP00000424113.1:n.*198G>T
ENST00000484444.6:c.*210G>T	ENSP00000420975.1:n.*210G>T
ENST00000488877.6:c.660G>T	ENSP00000425159.1:n.660G>T
ENST00000492756.7:c.*198G>T	ENSP00000422453.1:n.*198G>T
ENST00000494799.6:c.52G>T	ENSP00000512834.1:p.Ala18Ser
ENST00000562983.3:c.52G>T	ENSP00000512845.1:p.Ala18Ser
ENST00000612663.6:c.*171G>T	ENSP00000477997.3:n.*171G>T
ENST00000640140.2:n.914G>T
ENST00000640250.2:n.268G>T
ENST00000640681.2:n.873G>T
ENST00000696723.1:n.4402G>T
ENST00000696741.1:n.2407G>T
ENST00000696742.1:n.2134G>T
ENST00000696743.1:n.3537G>T
ENST00000696744.1:n.808G>T
ENST00000696767.1:n.1103G>T
ENST00000696768.1:c.*92G>T	ENSP00000512859.1:n.*92G>T
ENST00000696769.1:n.2458G>T
ENST00000696771.1:c.52G>T	ENSP00000512860.1:p.Ala18Ser
ENST00000696772.1:n.2372G>T
ENST00000696773.1:n.2111G>T
ENST00000696774.1:n.5879G>T
ENST00000696776.1:c.862G>T	ENSP00000512861.1:p.Ala288Ser
ENST00000696777.1:n.2177G>T
ENST00000696778.1:n.1205G>T
ENST00000696779.1:c.376G>T	ENSP00000512862.1:p.Ala126Ser
ENST00000696780.1:c.799G>T	ENSP00000512863.1:p.Ala267Ser
ENST00000696781.1:c.514G>T	ENSP00000512864.1:p.Ala172Ser
ENST00000696782.1:c.*171G>T	ENSP00000512865.1:n.*171G>T
ENST00000696783.1:n.2637G>T
ENST00000696992.1:n.1886G>T
ENST00000696995.1:n.4298G>T
ENST00000696996.1:n.2211G>T
ENST00000696997.1:c.*399G>T	ENSP00000513028.1:n.*399G>T
ENST00000696998.1:n.2023G>T
ENST00000696999.1:c.52G>T	ENSP00000513029.1:p.Ala18Ser
ENST00000697035.1:c.*102G>T	ENSP00000513059.1:n.*102G>T
ENST00000697036.1:c.*185G>T	ENSP00000513060.1:n.*185G>T
ENST00000697037.1:n.804G>T
ENST00000697093.1:n.3005G>T
ENST00000697094.1:n.3352G>T
ENST00000697095.1:c.*1970G>T	ENSP00000513104.1:n.*1970G>T
ENST00000697096.1:n.1902G>T
ENST00000697097.1:c.52G>T	ENSP00000513105.1:p.Ala18Ser
ENST00000562983.2:n.955G>T
ENST00000690268.1:c.850G>T	ENSP00000509810.1:p.Ala284Ser
ENST00000355740.7:c.*95G>T	ENSP00000347979.3:n.*95G>T
ENST00000612663.5:c.*171G>T	ENSP00000477997.3:n.*171G>T
ENST00000640140.1:n.941G>T
ENST00000640250.1:n.268G>T
ENST00000640681.1:n.890G>T
ENST00000652046.1:c.769G>T MANE Select	ENSP00000498466.1:p.Ala257Ser
ENST00000352159.8:c.*86G>T	ENSP00000345601.4:n.*86G>T
ENST00000355279.2:c.744G>T	ENSP00000347426.2:n.744G>T
ENST00000355740.6:c.769G>T	ENSP00000347979.2:p.Ala257Ser
ENST00000357339.6:c.706G>T	ENSP00000349896.2:p.Ala236Ser
ENST00000479522.5:c.*198G>T	ENSP00000424113.1:n.*198G>T
ENST00000484444.5:c.*210G>T	ENSP00000420975.1:n.*210G>T
ENST00000488877.5:c.*210G>T	ENSP00000425159.1:n.*210G>T
ENST00000492756.5:c.597G>T	ENSP00000422453.1:n.597G>T
ENST00000494410.5:c.*127G>T	ENSP00000423755.1:n.*127G>T
ENST00000494799.5:n.676G>T
ENST00000612663.4:c.*116G>T	ENSP00000477997.2:n.*116G>T
NM_000043.4:c.769G>T , LRG_134t1:c.769G>T	NP_000034.1:p.Ala257Ser
NM_152871.2:c.706G>T	NP_690610.1:p.Ala236Ser
NM_152872.2:c.*81G>T	NP_690611.1:n.*81G>T
NR_028033.2:n.943G>T
NR_028034.2:n.805G>T
NR_028035.2:n.868G>T
NR_028036.2:n.1006G>T
XM_006717819.2:c.850G>T	XP_006717882.1:p.Ala284Ser
XM_011539764.1:c.931G>T	XP_011538066.1:p.Ala311Ser
XM_011539765.1:c.868G>T	XP_011538067.1:p.Ala290Ser
XM_011539766.1:c.850G>T	XP_011538068.1:p.Ala284Ser
XM_011539767.1:c.814G>T	XP_011538069.1:p.Ala272Ser
XR_945732.1:n.837G>T
XR_945733.1:n.774G>T
NM_000043.5:c.769G>T	NP_000034.1:p.Ala257Ser
NM_001320619.1:c.*92G>T	NP_001307548.1:n.*92G>T
NM_152871.3:c.706G>T	NP_690610.1:p.Ala236Ser
NM_152872.3:c.*81G>T	NP_690611.1:n.*81G>T
NR_028033.3:n.915G>T
NR_028034.3:n.777G>T
NR_028035.3:n.840G>T
NR_028036.3:n.978G>T
NR_135313.1:n.895G>T
NR_135314.1:n.1078G>T
NR_135315.1:n.831G>T
XM_006717819.3:c.850G>T	XP_006717882.1:p.Ala284Ser
XM_011539764.2:c.931G>T	XP_011538066.1:p.Ala311Ser
XM_011539765.2:c.868G>T	XP_011538067.1:p.Ala290Ser
XM_011539766.2:c.850G>T	XP_011538068.1:p.Ala284Ser
XM_011539767.3:c.814G>T	XP_011538069.1:p.Ala272Ser
XR_945732.3:n.837G>T
XR_945733.2:n.774G>T
NM_000043.6:c.769G>T MANE Select	NP_000034.1:p.Ala257Ser
NM_001320619.2:c.*92G>T	NP_001307548.1:n.*92G>T
NM_152871.4:c.706G>T	NP_690610.1:p.Ala236Ser
NM_152872.4:c.*81G>T	NP_690611.1:n.*81G>T
NR_028033.4:n.676G>T
NR_028034.4:n.538G>T
NR_028035.4:n.601G>T
NR_028036.4:n.739G>T
NR_135313.2:n.656G>T
NR_135314.2:n.935G>T
NR_135315.2:n.688G>T