Canonical Allele Identifier: CA377509590

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773901C>T (hg19) ; chr10:g.89014144C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014144C>T , CM000672.2:g.89014144C>T	GRCh38
NC_000010.10:g.90773901C>T , CM000672.1:g.90773901C>T	GRCh37
NC_000010.9:g.90763881C>T	NCBI36
NG_009089.2:g.28614C>T , LRG_134:g.28614C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1011C>T
ENST00000355740.8:c.*25C>T	ENSP00000347979.3:n.*25C>T
ENST00000357339.7:c.639C>T	ENSP00000349896.2:p.Thr213=
ENST00000371857.8:n.2247C>T
ENST00000460510.6:c.-16C>T	ENSP00000512812.1:n.-16C>T
ENST00000466081.6:n.2351C>T
ENST00000477270.6:c.747C>T	ENSP00000512813.1:p.Thr249=
ENST00000479522.6:c.*131C>T	ENSP00000424113.1:n.*131C>T
ENST00000484444.6:c.*143C>T	ENSP00000420975.1:n.*143C>T
ENST00000488877.6:c.593C>T	ENSP00000425159.1:n.593C>T
ENST00000492756.7:c.*131C>T	ENSP00000422453.1:n.*131C>T
ENST00000494799.6:c.-16C>T	ENSP00000512834.1:n.-16C>T
ENST00000562983.3:c.-16C>T	ENSP00000512845.1:n.-16C>T
ENST00000612663.6:c.*104C>T	ENSP00000477997.3:n.*104C>T
ENST00000640140.2:n.847C>T
ENST00000640250.2:n.201C>T
ENST00000640681.2:n.806C>T
ENST00000696723.1:n.4335C>T
ENST00000696741.1:n.2340C>T
ENST00000696742.1:n.2067C>T
ENST00000696743.1:n.3470C>T
ENST00000696744.1:n.741C>T
ENST00000696767.1:n.1036C>T
ENST00000696768.1:c.*25C>T	ENSP00000512859.1:n.*25C>T
ENST00000696769.1:n.2391C>T
ENST00000696771.1:c.-16C>T	ENSP00000512860.1:n.-16C>T
ENST00000696772.1:n.2305C>T
ENST00000696773.1:n.2044C>T
ENST00000696774.1:n.5812C>T
ENST00000696776.1:c.795C>T	ENSP00000512861.1:p.Thr265=
ENST00000696777.1:n.2110C>T
ENST00000696778.1:n.1138C>T
ENST00000696779.1:c.309C>T	ENSP00000512862.1:p.Thr103=
ENST00000696780.1:c.732C>T	ENSP00000512863.1:p.Thr244=
ENST00000696781.1:c.447C>T	ENSP00000512864.1:p.Thr149=
ENST00000696782.1:c.*104C>T	ENSP00000512865.1:n.*104C>T
ENST00000696783.1:n.2570C>T
ENST00000696992.1:n.1819C>T
ENST00000696995.1:n.4231C>T
ENST00000696996.1:n.2144C>T
ENST00000696997.1:c.*332C>T	ENSP00000513028.1:n.*332C>T
ENST00000696998.1:n.1956C>T
ENST00000696999.1:c.-16C>T	ENSP00000513029.1:n.-16C>T
ENST00000697035.1:c.*35C>T	ENSP00000513059.1:n.*35C>T
ENST00000697036.1:c.*118C>T	ENSP00000513060.1:n.*118C>T
ENST00000697037.1:n.737C>T
ENST00000697093.1:n.2938C>T
ENST00000697094.1:n.3285C>T
ENST00000697095.1:c.*1903C>T	ENSP00000513104.1:n.*1903C>T
ENST00000697096.1:n.1835C>T
ENST00000697097.1:c.-16C>T	ENSP00000513105.1:n.-16C>T
ENST00000562983.2:n.888C>T
ENST00000690268.1:c.783C>T	ENSP00000509810.1:p.Thr261=
ENST00000355740.7:c.*28C>T	ENSP00000347979.3:n.*28C>T
ENST00000612663.5:c.*104C>T	ENSP00000477997.3:n.*104C>T
ENST00000640140.1:n.874C>T
ENST00000640250.1:n.201C>T
ENST00000640681.1:n.823C>T
ENST00000652046.1:c.702C>T MANE Select	ENSP00000498466.1:p.Thr234=
ENST00000313771.9:n.1011C>T
ENST00000352159.8:c.*19C>T	ENSP00000345601.4:n.*19C>T
ENST00000355279.2:c.677C>T	ENSP00000347426.2:n.677C>T
ENST00000355740.6:c.702C>T	ENSP00000347979.2:p.Thr234=
ENST00000357339.6:c.639C>T	ENSP00000349896.2:p.Thr213=
ENST00000479522.5:c.*131C>T	ENSP00000424113.1:n.*131C>T
ENST00000484444.5:c.*143C>T	ENSP00000420975.1:n.*143C>T
ENST00000488877.5:c.*143C>T	ENSP00000425159.1:n.*143C>T
ENST00000492756.5:c.530C>T	ENSP00000422453.1:n.530C>T
ENST00000494410.5:c.*60C>T	ENSP00000423755.1:n.*60C>T
ENST00000494799.5:n.609C>T
ENST00000612663.4:c.*49C>T	ENSP00000477997.2:n.*49C>T
ENST00000615406.4:c.702C>T	ENSP00000484575.1:p.Thr234=
ENST00000626542.2:c.700C>T	ENSP00000485876.1:p.His234Tyr
NM_000043.4:c.702C>T , LRG_134t1:c.702C>T	NP_000034.1:p.Thr234=
NM_152871.2:c.639C>T	NP_690610.1:p.Thr213=
NM_152872.2:c.*14C>T	NP_690611.1:n.*14C>T
NR_028033.2:n.876C>T
NR_028034.2:n.738C>T
NR_028035.2:n.801C>T
NR_028036.2:n.939C>T
XM_006717819.2:c.783C>T	XP_006717882.1:p.Thr261=
XM_011539764.1:c.864C>T	XP_011538066.1:p.Thr288=
XM_011539765.1:c.801C>T	XP_011538067.1:p.Thr267=
XM_011539766.1:c.783C>T	XP_011538068.1:p.Thr261=
XM_011539767.1:c.747C>T	XP_011538069.1:p.Thr249=
XR_945732.1:n.770C>T
XR_945733.1:n.707C>T
NM_000043.5:c.702C>T	NP_000034.1:p.Thr234=
NM_001320619.1:c.*25C>T	NP_001307548.1:n.*25C>T
NM_152871.3:c.639C>T	NP_690610.1:p.Thr213=
NM_152872.3:c.*14C>T	NP_690611.1:n.*14C>T
NR_028033.3:n.848C>T
NR_028034.3:n.710C>T
NR_028035.3:n.773C>T
NR_028036.3:n.911C>T
NR_135313.1:n.828C>T
NR_135314.1:n.1011C>T
NR_135315.1:n.764C>T
XM_006717819.3:c.783C>T	XP_006717882.1:p.Thr261=
XM_011539764.2:c.864C>T	XP_011538066.1:p.Thr288=
XM_011539765.2:c.801C>T	XP_011538067.1:p.Thr267=
XM_011539766.2:c.783C>T	XP_011538068.1:p.Thr261=
XM_011539767.3:c.747C>T	XP_011538069.1:p.Thr249=
XR_945732.3:n.770C>T
XR_945733.2:n.707C>T
NM_000043.6:c.702C>T MANE Select	NP_000034.1:p.Thr234=
NM_001320619.2:c.*25C>T	NP_001307548.1:n.*25C>T
NM_152871.4:c.639C>T	NP_690610.1:p.Thr213=
NM_152872.4:c.*14C>T	NP_690611.1:n.*14C>T
NR_028033.4:n.609C>T
NR_028034.4:n.471C>T
NR_028035.4:n.534C>T
NR_028036.4:n.672C>T
NR_135313.2:n.589C>T
NR_135314.2:n.868C>T
NR_135315.2:n.621C>T