Canonical Allele Identifier: CA470975040

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774051T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014294T>A , CM000672.2:g.89014294T>A	GRCh38
NC_000010.10:g.90774051T>A , CM000672.1:g.90774051T>A	GRCh37
NC_000010.9:g.90764031T>A	NCBI36
NG_009089.2:g.28764T>A , LRG_134:g.28764T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1161T>A
ENST00000355740.8:c.*175T>A	ENSP00000347979.3:n.*175T>A
ENST00000357339.7:c.789T>A	ENSP00000349896.2:p.Leu263=
ENST00000371857.8:n.2397T>A
ENST00000460510.6:c.135T>A	ENSP00000512812.1:p.Leu45=
ENST00000466081.6:n.2501T>A
ENST00000477270.6:c.897T>A	ENSP00000512813.1:p.Leu299=
ENST00000479522.6:c.*281T>A	ENSP00000424113.1:n.*281T>A
ENST00000484444.6:c.*293T>A	ENSP00000420975.1:n.*293T>A
ENST00000488877.6:c.743T>A	ENSP00000425159.1:n.743T>A
ENST00000492756.7:c.*281T>A	ENSP00000422453.1:n.*281T>A
ENST00000494799.6:c.135T>A	ENSP00000512834.1:p.Leu45=
ENST00000562983.3:c.135T>A	ENSP00000512845.1:p.Leu45=
ENST00000612663.6:c.*254T>A	ENSP00000477997.3:n.*254T>A
ENST00000640140.2:n.997T>A
ENST00000640250.2:n.351T>A
ENST00000640681.2:n.956T>A
ENST00000696723.1:n.4485T>A
ENST00000696741.1:n.2490T>A
ENST00000696742.1:n.2217T>A
ENST00000696743.1:n.3620T>A
ENST00000696744.1:n.891T>A
ENST00000696767.1:n.1186T>A
ENST00000696768.1:c.*175T>A	ENSP00000512859.1:n.*175T>A
ENST00000696769.1:n.2541T>A
ENST00000696771.1:c.135T>A	ENSP00000512860.1:p.Leu45=
ENST00000696772.1:n.2455T>A
ENST00000696773.1:n.2194T>A
ENST00000696774.1:n.5962T>A
ENST00000696776.1:c.945T>A	ENSP00000512861.1:p.Leu315=
ENST00000696777.1:n.2260T>A
ENST00000696778.1:n.1288T>A
ENST00000696779.1:c.459T>A	ENSP00000512862.1:p.Leu153=
ENST00000696780.1:c.882T>A	ENSP00000512863.1:p.Leu294=
ENST00000696781.1:c.597T>A	ENSP00000512864.1:p.Leu199=
ENST00000696782.1:c.*254T>A	ENSP00000512865.1:n.*254T>A
ENST00000696783.1:n.2720T>A
ENST00000696992.1:n.1969T>A
ENST00000696995.1:n.4381T>A
ENST00000696996.1:n.2294T>A
ENST00000696997.1:c.*482T>A	ENSP00000513028.1:n.*482T>A
ENST00000696998.1:n.2106T>A
ENST00000696999.1:c.135T>A	ENSP00000513029.1:p.Leu45=
ENST00000697035.1:c.*185T>A	ENSP00000513059.1:n.*185T>A
ENST00000697036.1:c.*268T>A	ENSP00000513060.1:n.*268T>A
ENST00000697037.1:n.887T>A
ENST00000697093.1:n.3088T>A
ENST00000697094.1:n.3435T>A
ENST00000697095.1:c.*2053T>A	ENSP00000513104.1:n.*2053T>A
ENST00000697096.1:n.1985T>A
ENST00000697097.1:c.135T>A	ENSP00000513105.1:p.Leu45=
ENST00000562983.2:n.1038T>A
ENST00000690268.1:c.933T>A	ENSP00000509810.1:p.Leu311=
ENST00000355740.7:c.*178T>A	ENSP00000347979.3:n.*178T>A
ENST00000612663.5:c.*254T>A	ENSP00000477997.3:n.*254T>A
ENST00000640140.1:n.1024T>A
ENST00000640250.1:n.351T>A
ENST00000640681.1:n.973T>A
ENST00000652046.1:c.852T>A MANE Select	ENSP00000498466.1:p.Leu284=
ENST00000352159.8:c.*169T>A	ENSP00000345601.4:n.*169T>A
ENST00000355279.2:c.827T>A	ENSP00000347426.2:n.827T>A
ENST00000355740.6:c.852T>A	ENSP00000347979.2:p.Leu284=
ENST00000357339.6:c.789T>A	ENSP00000349896.2:p.Leu263=
ENST00000479522.5:c.*281T>A	ENSP00000424113.1:n.*281T>A
ENST00000484444.5:c.*293T>A	ENSP00000420975.1:n.*293T>A
ENST00000488877.5:c.*293T>A	ENSP00000425159.1:n.*293T>A
ENST00000492756.5:c.680T>A	ENSP00000422453.1:n.680T>A
ENST00000494410.5:c.*210T>A	ENSP00000423755.1:n.*210T>A
ENST00000612663.4:c.*199T>A	ENSP00000477997.2:n.*199T>A
NM_000043.4:c.852T>A , LRG_134t1:c.852T>A	NP_000034.1:p.Leu284=
NM_152871.2:c.789T>A	NP_690610.1:p.Leu263=
NM_152872.2:c.*164T>A	NP_690611.1:n.*164T>A
NR_028033.2:n.1026T>A
NR_028034.2:n.888T>A
NR_028035.2:n.951T>A
NR_028036.2:n.1089T>A
XM_006717819.2:c.933T>A	XP_006717882.1:p.Leu311=
XM_011539764.1:c.1014T>A	XP_011538066.1:p.Leu338=
XM_011539765.1:c.951T>A	XP_011538067.1:p.Leu317=
XM_011539766.1:c.933T>A	XP_011538068.1:p.Leu311=
XM_011539767.1:c.897T>A	XP_011538069.1:p.Leu299=
XR_945732.1:n.920T>A
XR_945733.1:n.857T>A
NM_000043.5:c.852T>A	NP_000034.1:p.Leu284=
NM_001320619.1:c.*175T>A	NP_001307548.1:n.*175T>A
NM_152871.3:c.789T>A	NP_690610.1:p.Leu263=
NM_152872.3:c.*164T>A	NP_690611.1:n.*164T>A
NR_028033.3:n.998T>A
NR_028034.3:n.860T>A
NR_028035.3:n.923T>A
NR_028036.3:n.1061T>A
NR_135313.1:n.978T>A
NR_135314.1:n.1161T>A
NR_135315.1:n.914T>A
XM_006717819.3:c.933T>A	XP_006717882.1:p.Leu311=
XM_011539764.2:c.1014T>A	XP_011538066.1:p.Leu338=
XM_011539765.2:c.951T>A	XP_011538067.1:p.Leu317=
XM_011539766.2:c.933T>A	XP_011538068.1:p.Leu311=
XM_011539767.3:c.897T>A	XP_011538069.1:p.Leu299=
XR_945732.3:n.920T>A
XR_945733.2:n.857T>A
NM_000043.6:c.852T>A MANE Select	NP_000034.1:p.Leu284=
NM_001320619.2:c.*175T>A	NP_001307548.1:n.*175T>A
NM_152871.4:c.789T>A	NP_690610.1:p.Leu263=
NM_152872.4:c.*164T>A	NP_690611.1:n.*164T>A
NR_028033.4:n.759T>A
NR_028034.4:n.621T>A
NR_028035.4:n.684T>A
NR_028036.4:n.822T>A
NR_135313.2:n.739T>A
NR_135314.2:n.1018T>A
NR_135315.2:n.771T>A