Canonical Allele Identifier: CA377509542

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773882A>T (hg19) ; chr10:g.89014125A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014125A>T , CM000672.2:g.89014125A>T	GRCh38
NC_000010.10:g.90773882A>T , CM000672.1:g.90773882A>T	GRCh37
NC_000010.9:g.90763862A>T	NCBI36
NG_009089.2:g.28595A>T , LRG_134:g.28595A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.992A>T
ENST00000355740.8:c.*6A>T	ENSP00000347979.3:n.*6A>T
ENST00000357339.7:c.620A>T	ENSP00000349896.2:p.Asp207Val
ENST00000371857.8:n.2228A>T
ENST00000460510.6:c.-35A>T	ENSP00000512812.1:n.-35A>T
ENST00000466081.6:n.2332A>T
ENST00000477270.6:c.728A>T	ENSP00000512813.1:p.Asp243Val
ENST00000479522.6:c.*112A>T	ENSP00000424113.1:n.*112A>T
ENST00000484444.6:c.*124A>T	ENSP00000420975.1:n.*124A>T
ENST00000488877.6:c.574A>T	ENSP00000425159.1:n.574A>T
ENST00000492756.7:c.*112A>T	ENSP00000422453.1:n.*112A>T
ENST00000494799.6:c.-35A>T	ENSP00000512834.1:n.-35A>T
ENST00000562983.3:c.-35A>T	ENSP00000512845.1:n.-35A>T
ENST00000612663.6:c.*85A>T	ENSP00000477997.3:n.*85A>T
ENST00000640140.2:n.828A>T
ENST00000640250.2:n.182A>T
ENST00000640681.2:n.787A>T
ENST00000696723.1:n.4316A>T
ENST00000696741.1:n.2321A>T
ENST00000696742.1:n.2048A>T
ENST00000696743.1:n.3451A>T
ENST00000696744.1:n.722A>T
ENST00000696767.1:n.1017A>T
ENST00000696768.1:c.*6A>T	ENSP00000512859.1:n.*6A>T
ENST00000696769.1:n.2372A>T
ENST00000696771.1:c.-35A>T	ENSP00000512860.1:n.-35A>T
ENST00000696772.1:n.2286A>T
ENST00000696773.1:n.2025A>T
ENST00000696774.1:n.5793A>T
ENST00000696776.1:c.776A>T	ENSP00000512861.1:p.Asp259Val
ENST00000696777.1:n.2091A>T
ENST00000696778.1:n.1119A>T
ENST00000696779.1:c.290A>T	ENSP00000512862.1:p.Asp97Val
ENST00000696780.1:c.713A>T	ENSP00000512863.1:p.Asp238Val
ENST00000696781.1:c.428A>T	ENSP00000512864.1:p.Asp143Val
ENST00000696782.1:c.*85A>T	ENSP00000512865.1:n.*85A>T
ENST00000696783.1:n.2551A>T
ENST00000696992.1:n.1800A>T
ENST00000696995.1:n.4212A>T
ENST00000696996.1:n.2125A>T
ENST00000696997.1:c.*313A>T	ENSP00000513028.1:n.*313A>T
ENST00000696998.1:n.1937A>T
ENST00000696999.1:c.-35A>T	ENSP00000513029.1:n.-35A>T
ENST00000697035.1:c.*16A>T	ENSP00000513059.1:n.*16A>T
ENST00000697036.1:c.*99A>T	ENSP00000513060.1:n.*99A>T
ENST00000697037.1:n.718A>T
ENST00000697093.1:n.2919A>T
ENST00000697094.1:n.3266A>T
ENST00000697095.1:c.*1884A>T	ENSP00000513104.1:n.*1884A>T
ENST00000697096.1:n.1816A>T
ENST00000697097.1:c.-35A>T	ENSP00000513105.1:n.-35A>T
ENST00000562983.2:n.869A>T
ENST00000690268.1:c.764A>T	ENSP00000509810.1:p.Asp255Val
ENST00000355740.7:c.*9A>T	ENSP00000347979.3:n.*9A>T
ENST00000612663.5:c.*85A>T	ENSP00000477997.3:n.*85A>T
ENST00000640140.1:n.855A>T
ENST00000640250.1:n.182A>T
ENST00000640681.1:n.804A>T
ENST00000652046.1:c.683A>T MANE Select	ENSP00000498466.1:p.Asp228Val
ENST00000313771.9:n.992A>T
ENST00000352159.8:c.702A>T	ENSP00000345601.4:p.Ter234Cys
ENST00000355279.2:c.658A>T	ENSP00000347426.2:p.Thr220Ser
ENST00000355740.6:c.683A>T	ENSP00000347979.2:p.Asp228Val
ENST00000357339.6:c.620A>T	ENSP00000349896.2:p.Asp207Val
ENST00000479522.5:c.*112A>T	ENSP00000424113.1:n.*112A>T
ENST00000484444.5:c.*124A>T	ENSP00000420975.1:n.*124A>T
ENST00000488877.5:c.*124A>T	ENSP00000425159.1:n.*124A>T
ENST00000492756.5:c.511A>T	ENSP00000422453.1:n.511A>T
ENST00000494410.5:c.*41A>T	ENSP00000423755.1:n.*41A>T
ENST00000494799.5:n.590A>T
ENST00000612663.4:c.*30A>T	ENSP00000477997.2:n.*30A>T
ENST00000615406.4:c.683A>T	ENSP00000484575.1:p.Asp228Val
ENST00000626542.2:c.683A>T	ENSP00000485876.1:p.Asp228Val
NM_000043.4:c.683A>T , LRG_134t1:c.683A>T	NP_000034.1:p.Asp228Val
NM_152871.2:c.620A>T	NP_690610.1:p.Asp207Val
NM_152872.2:c.658A>T	NP_690611.1:p.Thr220Ser
NR_028033.2:n.857A>T
NR_028034.2:n.719A>T
NR_028035.2:n.782A>T
NR_028036.2:n.920A>T
XM_006717819.2:c.764A>T	XP_006717882.1:p.Asp255Val
XM_011539764.1:c.845A>T	XP_011538066.1:p.Asp282Val
XM_011539765.1:c.782A>T	XP_011538067.1:p.Asp261Val
XM_011539766.1:c.764A>T	XP_011538068.1:p.Asp255Val
XM_011539767.1:c.728A>T	XP_011538069.1:p.Asp243Val
XR_945732.1:n.751A>T
XR_945733.1:n.688A>T
NM_000043.5:c.683A>T	NP_000034.1:p.Asp228Val
NM_001320619.1:c.*6A>T	NP_001307548.1:n.*6A>T
NM_152871.3:c.620A>T	NP_690610.1:p.Asp207Val
NM_152872.3:c.658A>T	NP_690611.1:p.Thr220Ser
NR_028033.3:n.829A>T
NR_028034.3:n.691A>T
NR_028035.3:n.754A>T
NR_028036.3:n.892A>T
NR_135313.1:n.809A>T
NR_135314.1:n.992A>T
NR_135315.1:n.745A>T
XM_006717819.3:c.764A>T	XP_006717882.1:p.Asp255Val
XM_011539764.2:c.845A>T	XP_011538066.1:p.Asp282Val
XM_011539765.2:c.782A>T	XP_011538067.1:p.Asp261Val
XM_011539766.2:c.764A>T	XP_011538068.1:p.Asp255Val
XM_011539767.3:c.728A>T	XP_011538069.1:p.Asp243Val
XR_945732.3:n.751A>T
XR_945733.2:n.688A>T
NM_000043.6:c.683A>T MANE Select	NP_000034.1:p.Asp228Val
NM_001320619.2:c.*6A>T	NP_001307548.1:n.*6A>T
NM_152871.4:c.620A>T	NP_690610.1:p.Asp207Val
NM_152872.4:c.658A>T	NP_690611.1:p.Thr220Ser
NR_028033.4:n.590A>T
NR_028034.4:n.452A>T
NR_028035.4:n.515A>T
NR_028036.4:n.653A>T
NR_135313.2:n.570A>T
NR_135314.2:n.849A>T
NR_135315.2:n.602A>T