Canonical Allele Identifier: CA377510044

Gene: FAS

Linked Data

• gnomAD v4: 10-89014331-G-T
• MyVariant Identifiers: chr10:g.90774088G>T (hg19) ; chr10:g.89014331G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014331G>T , CM000672.2:g.89014331G>T	GRCh38
NC_000010.10:g.90774088G>T , CM000672.1:g.90774088G>T	GRCh37
NC_000010.9:g.90764068G>T	NCBI36
NG_009089.2:g.28801G>T , LRG_134:g.28801G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1198G>T
ENST00000355740.8:c.*212G>T	ENSP00000347979.3:n.*212G>T
ENST00000357339.7:c.826G>T	ENSP00000349896.2:p.Asp276Tyr
ENST00000371857.8:n.2434G>T
ENST00000460510.6:c.172G>T	ENSP00000512812.1:p.Asp58Tyr
ENST00000466081.6:n.2538G>T
ENST00000477270.6:c.934G>T	ENSP00000512813.1:p.Asp312Tyr
ENST00000479522.6:c.*318G>T	ENSP00000424113.1:n.*318G>T
ENST00000484444.6:c.*330G>T	ENSP00000420975.1:n.*330G>T
ENST00000488877.6:c.780G>T	ENSP00000425159.1:n.780G>T
ENST00000492756.7:c.*318G>T	ENSP00000422453.1:n.*318G>T
ENST00000494799.6:c.172G>T	ENSP00000512834.1:p.Asp58Tyr
ENST00000562983.3:c.172G>T	ENSP00000512845.1:p.Asp58Tyr
ENST00000612663.6:c.*291G>T	ENSP00000477997.3:n.*291G>T
ENST00000640140.2:n.1034G>T
ENST00000640250.2:n.388G>T
ENST00000640681.2:n.993G>T
ENST00000696723.1:n.4522G>T
ENST00000696741.1:n.2527G>T
ENST00000696742.1:n.2254G>T
ENST00000696743.1:n.3657G>T
ENST00000696744.1:n.928G>T
ENST00000696767.1:n.1223G>T
ENST00000696768.1:c.*212G>T	ENSP00000512859.1:n.*212G>T
ENST00000696769.1:n.2578G>T
ENST00000696771.1:c.172G>T	ENSP00000512860.1:p.Asp58Tyr
ENST00000696772.1:n.2492G>T
ENST00000696773.1:n.2231G>T
ENST00000696774.1:n.5999G>T
ENST00000696776.1:c.982G>T	ENSP00000512861.1:p.Asp328Tyr
ENST00000696777.1:n.2297G>T
ENST00000696778.1:n.1325G>T
ENST00000696779.1:c.496G>T	ENSP00000512862.1:p.Asp166Tyr
ENST00000696780.1:c.919G>T	ENSP00000512863.1:p.Asp307Tyr
ENST00000696781.1:c.634G>T	ENSP00000512864.1:p.Asp212Tyr
ENST00000696782.1:c.*291G>T	ENSP00000512865.1:n.*291G>T
ENST00000696783.1:n.2757G>T
ENST00000696992.1:n.2006G>T
ENST00000696995.1:n.4418G>T
ENST00000696996.1:n.2331G>T
ENST00000696997.1:c.*519G>T	ENSP00000513028.1:n.*519G>T
ENST00000696998.1:n.2143G>T
ENST00000696999.1:c.172G>T	ENSP00000513029.1:p.Asp58Tyr
ENST00000697036.1:c.*305G>T	ENSP00000513060.1:n.*305G>T
ENST00000697037.1:n.924G>T
ENST00000697093.1:n.3125G>T
ENST00000697094.1:n.3472G>T
ENST00000697095.1:c.*2090G>T	ENSP00000513104.1:n.*2090G>T
ENST00000697096.1:n.2022G>T
ENST00000697097.1:c.172G>T	ENSP00000513105.1:p.Asp58Tyr
ENST00000562983.2:n.1075G>T
ENST00000690268.1:c.970G>T	ENSP00000509810.1:p.Asp324Tyr
ENST00000355740.7:c.*215G>T	ENSP00000347979.3:n.*215G>T
ENST00000612663.5:c.*291G>T	ENSP00000477997.3:n.*291G>T
ENST00000640140.1:n.1061G>T
ENST00000640250.1:n.388G>T
ENST00000640681.1:n.1010G>T
ENST00000652046.1:c.889G>T MANE Select	ENSP00000498466.1:p.Asp297Tyr
ENST00000352159.8:c.*206G>T	ENSP00000345601.4:n.*206G>T
ENST00000355279.2:c.864G>T	ENSP00000347426.2:n.864G>T
ENST00000355740.6:c.889G>T	ENSP00000347979.2:p.Asp297Tyr
ENST00000357339.6:c.826G>T	ENSP00000349896.2:p.Asp276Tyr
ENST00000479522.5:c.*318G>T	ENSP00000424113.1:n.*318G>T
ENST00000484444.5:c.*330G>T	ENSP00000420975.1:n.*330G>T
ENST00000488877.5:c.*330G>T	ENSP00000425159.1:n.*330G>T
ENST00000492756.5:c.717G>T	ENSP00000422453.1:n.717G>T
ENST00000494410.5:c.*247G>T	ENSP00000423755.1:n.*247G>T
ENST00000612663.4:c.*236G>T	ENSP00000477997.2:n.*236G>T
NM_000043.4:c.889G>T , LRG_134t1:c.889G>T	NP_000034.1:p.Asp297Tyr
NM_152871.2:c.826G>T	NP_690610.1:p.Asp276Tyr
NM_152872.2:c.*201G>T	NP_690611.1:n.*201G>T
NR_028033.2:n.1063G>T
NR_028034.2:n.925G>T
NR_028035.2:n.988G>T
NR_028036.2:n.1126G>T
XM_006717819.2:c.970G>T	XP_006717882.1:p.Asp324Tyr
XM_011539764.1:c.1051G>T	XP_011538066.1:p.Asp351Tyr
XM_011539765.1:c.988G>T	XP_011538067.1:p.Asp330Tyr
XM_011539766.1:c.970G>T	XP_011538068.1:p.Asp324Tyr
XM_011539767.1:c.934G>T	XP_011538069.1:p.Asp312Tyr
XR_945732.1:n.957G>T
XR_945733.1:n.894G>T
NM_000043.5:c.889G>T	NP_000034.1:p.Asp297Tyr
NM_001320619.1:c.*212G>T	NP_001307548.1:n.*212G>T
NM_152871.3:c.826G>T	NP_690610.1:p.Asp276Tyr
NM_152872.3:c.*201G>T	NP_690611.1:n.*201G>T
NR_028033.3:n.1035G>T
NR_028034.3:n.897G>T
NR_028035.3:n.960G>T
NR_028036.3:n.1098G>T
NR_135313.1:n.1015G>T
NR_135314.1:n.1198G>T
NR_135315.1:n.951G>T
XM_006717819.3:c.970G>T	XP_006717882.1:p.Asp324Tyr
XM_011539764.2:c.1051G>T	XP_011538066.1:p.Asp351Tyr
XM_011539765.2:c.988G>T	XP_011538067.1:p.Asp330Tyr
XM_011539766.2:c.970G>T	XP_011538068.1:p.Asp324Tyr
XM_011539767.3:c.934G>T	XP_011538069.1:p.Asp312Tyr
XR_945732.3:n.957G>T
XR_945733.2:n.894G>T
NM_000043.6:c.889G>T MANE Select	NP_000034.1:p.Asp297Tyr
NM_001320619.2:c.*212G>T	NP_001307548.1:n.*212G>T
NM_152871.4:c.826G>T	NP_690610.1:p.Asp276Tyr
NM_152872.4:c.*201G>T	NP_690611.1:n.*201G>T
NR_028033.4:n.796G>T
NR_028034.4:n.658G>T
NR_028035.4:n.721G>T
NR_028036.4:n.859G>T
NR_135313.2:n.776G>T
NR_135314.2:n.1055G>T
NR_135315.2:n.808G>T