Canonical Allele Identifier: CA377509649

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773922A>T (hg19) ; chr10:g.89014165A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014165A>T , CM000672.2:g.89014165A>T	GRCh38
NC_000010.10:g.90773922A>T , CM000672.1:g.90773922A>T	GRCh37
NC_000010.9:g.90763902A>T	NCBI36
NG_009089.2:g.28635A>T , LRG_134:g.28635A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1032A>T
ENST00000355740.8:c.*46A>T	ENSP00000347979.3:n.*46A>T
ENST00000357339.7:c.660A>T	ENSP00000349896.2:p.Thr220=
ENST00000371857.8:n.2268A>T
ENST00000460510.6:c.6A>T	ENSP00000512812.1:p.Thr2=
ENST00000466081.6:n.2372A>T
ENST00000477270.6:c.768A>T	ENSP00000512813.1:p.Thr256=
ENST00000479522.6:c.*152A>T	ENSP00000424113.1:n.*152A>T
ENST00000484444.6:c.*164A>T	ENSP00000420975.1:n.*164A>T
ENST00000488877.6:c.614A>T	ENSP00000425159.1:n.614A>T
ENST00000492756.7:c.*152A>T	ENSP00000422453.1:n.*152A>T
ENST00000494799.6:c.6A>T	ENSP00000512834.1:p.Thr2=
ENST00000562983.3:c.6A>T	ENSP00000512845.1:p.Thr2=
ENST00000612663.6:c.*125A>T	ENSP00000477997.3:n.*125A>T
ENST00000640140.2:n.868A>T
ENST00000640250.2:n.222A>T
ENST00000640681.2:n.827A>T
ENST00000696723.1:n.4356A>T
ENST00000696741.1:n.2361A>T
ENST00000696742.1:n.2088A>T
ENST00000696743.1:n.3491A>T
ENST00000696744.1:n.762A>T
ENST00000696767.1:n.1057A>T
ENST00000696768.1:c.*46A>T	ENSP00000512859.1:n.*46A>T
ENST00000696769.1:n.2412A>T
ENST00000696771.1:c.6A>T	ENSP00000512860.1:p.Thr2=
ENST00000696772.1:n.2326A>T
ENST00000696773.1:n.2065A>T
ENST00000696774.1:n.5833A>T
ENST00000696776.1:c.816A>T	ENSP00000512861.1:p.Thr272=
ENST00000696777.1:n.2131A>T
ENST00000696778.1:n.1159A>T
ENST00000696779.1:c.330A>T	ENSP00000512862.1:p.Thr110=
ENST00000696780.1:c.753A>T	ENSP00000512863.1:p.Thr251=
ENST00000696781.1:c.468A>T	ENSP00000512864.1:p.Thr156=
ENST00000696782.1:c.*125A>T	ENSP00000512865.1:n.*125A>T
ENST00000696783.1:n.2591A>T
ENST00000696992.1:n.1840A>T
ENST00000696995.1:n.4252A>T
ENST00000696996.1:n.2165A>T
ENST00000696997.1:c.*353A>T	ENSP00000513028.1:n.*353A>T
ENST00000696998.1:n.1977A>T
ENST00000696999.1:c.6A>T	ENSP00000513029.1:p.Thr2=
ENST00000697035.1:c.*56A>T	ENSP00000513059.1:n.*56A>T
ENST00000697036.1:c.*139A>T	ENSP00000513060.1:n.*139A>T
ENST00000697037.1:n.758A>T
ENST00000697093.1:n.2959A>T
ENST00000697094.1:n.3306A>T
ENST00000697095.1:c.*1924A>T	ENSP00000513104.1:n.*1924A>T
ENST00000697096.1:n.1856A>T
ENST00000697097.1:c.6A>T	ENSP00000513105.1:p.Thr2=
ENST00000562983.2:n.909A>T
ENST00000690268.1:c.804A>T	ENSP00000509810.1:p.Thr268=
ENST00000355740.7:c.*49A>T	ENSP00000347979.3:n.*49A>T
ENST00000612663.5:c.*125A>T	ENSP00000477997.3:n.*125A>T
ENST00000640140.1:n.895A>T
ENST00000640250.1:n.222A>T
ENST00000640681.1:n.844A>T
ENST00000652046.1:c.723A>T MANE Select	ENSP00000498466.1:p.Thr241=
ENST00000313771.9:n.1032A>T
ENST00000352159.8:c.*40A>T	ENSP00000345601.4:n.*40A>T
ENST00000355279.2:c.698A>T	ENSP00000347426.2:n.698A>T
ENST00000355740.6:c.723A>T	ENSP00000347979.2:p.Thr241=
ENST00000357339.6:c.660A>T	ENSP00000349896.2:p.Thr220=
ENST00000479522.5:c.*152A>T	ENSP00000424113.1:n.*152A>T
ENST00000484444.5:c.*164A>T	ENSP00000420975.1:n.*164A>T
ENST00000488877.5:c.*164A>T	ENSP00000425159.1:n.*164A>T
ENST00000492756.5:c.551A>T	ENSP00000422453.1:n.551A>T
ENST00000494410.5:c.*81A>T	ENSP00000423755.1:n.*81A>T
ENST00000494799.5:n.630A>T
ENST00000612663.4:c.*70A>T	ENSP00000477997.2:n.*70A>T
ENST00000615406.4:c.723A>T	ENSP00000484575.1:p.Thr241=
ENST00000626542.2:c.721A>T	ENSP00000485876.1:p.Thr241Ser
NM_000043.4:c.723A>T , LRG_134t1:c.723A>T	NP_000034.1:p.Thr241=
NM_152871.2:c.660A>T	NP_690610.1:p.Thr220=
NM_152872.2:c.*35A>T	NP_690611.1:n.*35A>T
NR_028033.2:n.897A>T
NR_028034.2:n.759A>T
NR_028035.2:n.822A>T
NR_028036.2:n.960A>T
XM_006717819.2:c.804A>T	XP_006717882.1:p.Thr268=
XM_011539764.1:c.885A>T	XP_011538066.1:p.Thr295=
XM_011539765.1:c.822A>T	XP_011538067.1:p.Thr274=
XM_011539766.1:c.804A>T	XP_011538068.1:p.Thr268=
XM_011539767.1:c.768A>T	XP_011538069.1:p.Thr256=
XR_945732.1:n.791A>T
XR_945733.1:n.728A>T
NM_000043.5:c.723A>T	NP_000034.1:p.Thr241=
NM_001320619.1:c.*46A>T	NP_001307548.1:n.*46A>T
NM_152871.3:c.660A>T	NP_690610.1:p.Thr220=
NM_152872.3:c.*35A>T	NP_690611.1:n.*35A>T
NR_028033.3:n.869A>T
NR_028034.3:n.731A>T
NR_028035.3:n.794A>T
NR_028036.3:n.932A>T
NR_135313.1:n.849A>T
NR_135314.1:n.1032A>T
NR_135315.1:n.785A>T
XM_006717819.3:c.804A>T	XP_006717882.1:p.Thr268=
XM_011539764.2:c.885A>T	XP_011538066.1:p.Thr295=
XM_011539765.2:c.822A>T	XP_011538067.1:p.Thr274=
XM_011539766.2:c.804A>T	XP_011538068.1:p.Thr268=
XM_011539767.3:c.768A>T	XP_011538069.1:p.Thr256=
XR_945732.3:n.791A>T
XR_945733.2:n.728A>T
NM_000043.6:c.723A>T MANE Select	NP_000034.1:p.Thr241=
NM_001320619.2:c.*46A>T	NP_001307548.1:n.*46A>T
NM_152871.4:c.660A>T	NP_690610.1:p.Thr220=
NM_152872.4:c.*35A>T	NP_690611.1:n.*35A>T
NR_028033.4:n.630A>T
NR_028034.4:n.492A>T
NR_028035.4:n.555A>T
NR_028036.4:n.693A>T
NR_135313.2:n.610A>T
NR_135314.2:n.889A>T
NR_135315.2:n.642A>T