Canonical Allele Identifier: CA377509614

Gene: FAS

Linked Data

• dbSNP Id: rs1307415458
• gnomAD v2: 10-90773909-C-T
• gnomAD v4: 10-89014152-C-T
• MyVariant Identifiers: chr10:g.90773909C>T (hg19) ; chr10:g.89014152C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014152C>T , CM000672.2:g.89014152C>T	GRCh38
NC_000010.10:g.90773909C>T , CM000672.1:g.90773909C>T	GRCh37
NC_000010.9:g.90763889C>T	NCBI36
NG_009089.2:g.28622C>T , LRG_134:g.28622C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000313771.10:n.1019C>T
ENST00000355740.8:c.*33C>T	ENSP00000347979.3:n.*33C>T
ENST00000357339.7:c.647C>T	ENSP00000349896.2:p.Ala216Val
ENST00000371857.8:n.2255C>T
ENST00000460510.6:c.-8C>T	ENSP00000512812.1:n.-8C>T
ENST00000466081.6:n.2359C>T
ENST00000477270.6:c.755C>T	ENSP00000512813.1:p.Ala252Val
ENST00000479522.6:c.*139C>T	ENSP00000424113.1:n.*139C>T
ENST00000484444.6:c.*151C>T	ENSP00000420975.1:n.*151C>T
ENST00000488877.6:c.601C>T	ENSP00000425159.1:n.601C>T
ENST00000492756.7:c.*139C>T	ENSP00000422453.1:n.*139C>T
ENST00000494799.6:c.-8C>T	ENSP00000512834.1:n.-8C>T
ENST00000562983.3:c.-8C>T	ENSP00000512845.1:n.-8C>T
ENST00000612663.6:c.*112C>T	ENSP00000477997.3:n.*112C>T
ENST00000640140.2:n.855C>T
ENST00000640250.2:n.209C>T
ENST00000640681.2:n.814C>T
ENST00000696723.1:n.4343C>T
ENST00000696741.1:n.2348C>T
ENST00000696742.1:n.2075C>T
ENST00000696743.1:n.3478C>T
ENST00000696744.1:n.749C>T
ENST00000696767.1:n.1044C>T
ENST00000696768.1:c.*33C>T	ENSP00000512859.1:n.*33C>T
ENST00000696769.1:n.2399C>T
ENST00000696771.1:c.-8C>T	ENSP00000512860.1:n.-8C>T
ENST00000696772.1:n.2313C>T
ENST00000696773.1:n.2052C>T
ENST00000696774.1:n.5820C>T
ENST00000696776.1:c.803C>T	ENSP00000512861.1:p.Ala268Val
ENST00000696777.1:n.2118C>T
ENST00000696778.1:n.1146C>T
ENST00000696779.1:c.317C>T	ENSP00000512862.1:p.Ala106Val
ENST00000696780.1:c.740C>T	ENSP00000512863.1:p.Ala247Val
ENST00000696781.1:c.455C>T	ENSP00000512864.1:p.Ala152Val
ENST00000696782.1:c.*112C>T	ENSP00000512865.1:n.*112C>T
ENST00000696783.1:n.2578C>T
ENST00000696992.1:n.1827C>T
ENST00000696995.1:n.4239C>T
ENST00000696996.1:n.2152C>T
ENST00000696997.1:c.*340C>T	ENSP00000513028.1:n.*340C>T
ENST00000696998.1:n.1964C>T
ENST00000696999.1:c.-8C>T	ENSP00000513029.1:n.-8C>T
ENST00000697035.1:c.*43C>T	ENSP00000513059.1:n.*43C>T
ENST00000697036.1:c.*126C>T	ENSP00000513060.1:n.*126C>T
ENST00000697037.1:n.745C>T
ENST00000697093.1:n.2946C>T
ENST00000697094.1:n.3293C>T
ENST00000697095.1:c.*1911C>T	ENSP00000513104.1:n.*1911C>T
ENST00000697096.1:n.1843C>T
ENST00000697097.1:c.-8C>T	ENSP00000513105.1:n.-8C>T
ENST00000562983.2:n.896C>T
ENST00000690268.1:c.791C>T	ENSP00000509810.1:p.Ala264Val
ENST00000355740.7:c.*36C>T	ENSP00000347979.3:n.*36C>T
ENST00000612663.5:c.*112C>T	ENSP00000477997.3:n.*112C>T
ENST00000640140.1:n.882C>T
ENST00000640250.1:n.209C>T
ENST00000640681.1:n.831C>T
ENST00000652046.1:c.710C>T MANE Select	ENSP00000498466.1:p.Ala237Val
ENST00000313771.9:n.1019C>T
ENST00000352159.8:c.*27C>T	ENSP00000345601.4:n.*27C>T
ENST00000355279.2:c.685C>T	ENSP00000347426.2:n.685C>T
ENST00000355740.6:c.710C>T	ENSP00000347979.2:p.Ala237Val
ENST00000357339.6:c.647C>T	ENSP00000349896.2:p.Ala216Val
ENST00000479522.5:c.*139C>T	ENSP00000424113.1:n.*139C>T
ENST00000484444.5:c.*151C>T	ENSP00000420975.1:n.*151C>T
ENST00000488877.5:c.*151C>T	ENSP00000425159.1:n.*151C>T
ENST00000492756.5:c.538C>T	ENSP00000422453.1:n.538C>T
ENST00000494410.5:c.*68C>T	ENSP00000423755.1:n.*68C>T
ENST00000494799.5:n.617C>T
ENST00000612663.4:c.*57C>T	ENSP00000477997.2:n.*57C>T
ENST00000615406.4:c.710C>T	ENSP00000484575.1:p.Ala237Val
ENST00000626542.2:c.708C>T	ENSP00000485876.1:p.Cys236=
NM_000043.4:c.710C>T , LRG_134t1:c.710C>T	NP_000034.1:p.Ala237Val
NM_152871.2:c.647C>T	NP_690610.1:p.Ala216Val
NM_152872.2:c.*22C>T	NP_690611.1:n.*22C>T
NR_028033.2:n.884C>T
NR_028034.2:n.746C>T
NR_028035.2:n.809C>T
NR_028036.2:n.947C>T
XM_006717819.2:c.791C>T	XP_006717882.1:p.Ala264Val
XM_011539764.1:c.872C>T	XP_011538066.1:p.Ala291Val
XM_011539765.1:c.809C>T	XP_011538067.1:p.Ala270Val
XM_011539766.1:c.791C>T	XP_011538068.1:p.Ala264Val
XM_011539767.1:c.755C>T	XP_011538069.1:p.Ala252Val
XR_945732.1:n.778C>T
XR_945733.1:n.715C>T
NM_000043.5:c.710C>T	NP_000034.1:p.Ala237Val
NM_001320619.1:c.*33C>T	NP_001307548.1:n.*33C>T
NM_152871.3:c.647C>T	NP_690610.1:p.Ala216Val
NM_152872.3:c.*22C>T	NP_690611.1:n.*22C>T
NR_028033.3:n.856C>T
NR_028034.3:n.718C>T
NR_028035.3:n.781C>T
NR_028036.3:n.919C>T
NR_135313.1:n.836C>T
NR_135314.1:n.1019C>T
NR_135315.1:n.772C>T
XM_006717819.3:c.791C>T	XP_006717882.1:p.Ala264Val
XM_011539764.2:c.872C>T	XP_011538066.1:p.Ala291Val
XM_011539765.2:c.809C>T	XP_011538067.1:p.Ala270Val
XM_011539766.2:c.791C>T	XP_011538068.1:p.Ala264Val
XM_011539767.3:c.755C>T	XP_011538069.1:p.Ala252Val
XR_945732.3:n.778C>T
XR_945733.2:n.715C>T
NM_000043.6:c.710C>T MANE Select	NP_000034.1:p.Ala237Val
NM_001320619.2:c.*33C>T	NP_001307548.1:n.*33C>T
NM_152871.4:c.647C>T	NP_690610.1:p.Ala216Val
NM_152872.4:c.*22C>T	NP_690611.1:n.*22C>T
NR_028033.4:n.617C>T
NR_028034.4:n.479C>T
NR_028035.4:n.542C>T
NR_028036.4:n.680C>T
NR_135313.2:n.597C>T
NR_135314.2:n.876C>T
NR_135315.2:n.629C>T