Canonical Allele Identifier: CA377509900

Gene: FAS

Linked Data

• gnomAD v4: 10-89014268-C-T
• COSMIC: COSM26157
• MyVariant Identifiers: chr10:g.90774025C>T (hg19) ; chr10:g.89014268C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014268C>T , CM000672.2:g.89014268C>T	GRCh38
NC_000010.10:g.90774025C>T , CM000672.1:g.90774025C>T	GRCh37
NC_000010.9:g.90764005C>T	NCBI36
NG_009089.2:g.28738C>T , LRG_134:g.28738C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1135C>T
ENST00000355740.8:c.*149C>T	ENSP00000347979.3:n.*149C>T
ENST00000357339.7:c.763C>T	ENSP00000349896.2:p.Gln255Ter
ENST00000371857.8:n.2371C>T
ENST00000460510.6:c.109C>T	ENSP00000512812.1:p.Gln37Ter
ENST00000466081.6:n.2475C>T
ENST00000477270.6:c.871C>T	ENSP00000512813.1:p.Gln291Ter
ENST00000479522.6:c.*255C>T	ENSP00000424113.1:n.*255C>T
ENST00000484444.6:c.*267C>T	ENSP00000420975.1:n.*267C>T
ENST00000488877.6:c.717C>T	ENSP00000425159.1:n.717C>T
ENST00000492756.7:c.*255C>T	ENSP00000422453.1:n.*255C>T
ENST00000494799.6:c.109C>T	ENSP00000512834.1:p.Gln37Ter
ENST00000562983.3:c.109C>T	ENSP00000512845.1:p.Gln37Ter
ENST00000612663.6:c.*228C>T	ENSP00000477997.3:n.*228C>T
ENST00000640140.2:n.971C>T
ENST00000640250.2:n.325C>T
ENST00000640681.2:n.930C>T
ENST00000696723.1:n.4459C>T
ENST00000696741.1:n.2464C>T
ENST00000696742.1:n.2191C>T
ENST00000696743.1:n.3594C>T
ENST00000696744.1:n.865C>T
ENST00000696767.1:n.1160C>T
ENST00000696768.1:c.*149C>T	ENSP00000512859.1:n.*149C>T
ENST00000696769.1:n.2515C>T
ENST00000696771.1:c.109C>T	ENSP00000512860.1:p.Gln37Ter
ENST00000696772.1:n.2429C>T
ENST00000696773.1:n.2168C>T
ENST00000696774.1:n.5936C>T
ENST00000696776.1:c.919C>T	ENSP00000512861.1:p.Gln307Ter
ENST00000696777.1:n.2234C>T
ENST00000696778.1:n.1262C>T
ENST00000696779.1:c.433C>T	ENSP00000512862.1:p.Gln145Ter
ENST00000696780.1:c.856C>T	ENSP00000512863.1:p.Gln286Ter
ENST00000696781.1:c.571C>T	ENSP00000512864.1:p.Gln191Ter
ENST00000696782.1:c.*228C>T	ENSP00000512865.1:n.*228C>T
ENST00000696783.1:n.2694C>T
ENST00000696992.1:n.1943C>T
ENST00000696995.1:n.4355C>T
ENST00000696996.1:n.2268C>T
ENST00000696997.1:c.*456C>T	ENSP00000513028.1:n.*456C>T
ENST00000696998.1:n.2080C>T
ENST00000696999.1:c.109C>T	ENSP00000513029.1:p.Gln37Ter
ENST00000697035.1:c.*159C>T	ENSP00000513059.1:n.*159C>T
ENST00000697036.1:c.*242C>T	ENSP00000513060.1:n.*242C>T
ENST00000697037.1:n.861C>T
ENST00000697093.1:n.3062C>T
ENST00000697094.1:n.3409C>T
ENST00000697095.1:c.*2027C>T	ENSP00000513104.1:n.*2027C>T
ENST00000697096.1:n.1959C>T
ENST00000697097.1:c.109C>T	ENSP00000513105.1:p.Gln37Ter
ENST00000562983.2:n.1012C>T
ENST00000690268.1:c.907C>T	ENSP00000509810.1:p.Gln303Ter
ENST00000355740.7:c.*152C>T	ENSP00000347979.3:n.*152C>T
ENST00000612663.5:c.*228C>T	ENSP00000477997.3:n.*228C>T
ENST00000640140.1:n.998C>T
ENST00000640250.1:n.325C>T
ENST00000640681.1:n.947C>T
ENST00000652046.1:c.826C>T MANE Select	ENSP00000498466.1:p.Gln276Ter
ENST00000352159.8:c.*143C>T	ENSP00000345601.4:n.*143C>T
ENST00000355279.2:c.801C>T	ENSP00000347426.2:n.801C>T
ENST00000355740.6:c.826C>T	ENSP00000347979.2:p.Gln276Ter
ENST00000357339.6:c.763C>T	ENSP00000349896.2:p.Gln255Ter
ENST00000479522.5:c.*255C>T	ENSP00000424113.1:n.*255C>T
ENST00000484444.5:c.*267C>T	ENSP00000420975.1:n.*267C>T
ENST00000488877.5:c.*267C>T	ENSP00000425159.1:n.*267C>T
ENST00000492756.5:c.654C>T	ENSP00000422453.1:n.654C>T
ENST00000494410.5:c.*184C>T	ENSP00000423755.1:n.*184C>T
ENST00000612663.4:c.*173C>T	ENSP00000477997.2:n.*173C>T
NM_000043.4:c.826C>T , LRG_134t1:c.826C>T	NP_000034.1:p.Gln276Ter
NM_152871.2:c.763C>T	NP_690610.1:p.Gln255Ter
NM_152872.2:c.*138C>T	NP_690611.1:n.*138C>T
NR_028033.2:n.1000C>T
NR_028034.2:n.862C>T
NR_028035.2:n.925C>T
NR_028036.2:n.1063C>T
XM_006717819.2:c.907C>T	XP_006717882.1:p.Gln303Ter
XM_011539764.1:c.988C>T	XP_011538066.1:p.Gln330Ter
XM_011539765.1:c.925C>T	XP_011538067.1:p.Gln309Ter
XM_011539766.1:c.907C>T	XP_011538068.1:p.Gln303Ter
XM_011539767.1:c.871C>T	XP_011538069.1:p.Gln291Ter
XR_945732.1:n.894C>T
XR_945733.1:n.831C>T
NM_000043.5:c.826C>T	NP_000034.1:p.Gln276Ter
NM_001320619.1:c.*149C>T	NP_001307548.1:n.*149C>T
NM_152871.3:c.763C>T	NP_690610.1:p.Gln255Ter
NM_152872.3:c.*138C>T	NP_690611.1:n.*138C>T
NR_028033.3:n.972C>T
NR_028034.3:n.834C>T
NR_028035.3:n.897C>T
NR_028036.3:n.1035C>T
NR_135313.1:n.952C>T
NR_135314.1:n.1135C>T
NR_135315.1:n.888C>T
XM_006717819.3:c.907C>T	XP_006717882.1:p.Gln303Ter
XM_011539764.2:c.988C>T	XP_011538066.1:p.Gln330Ter
XM_011539765.2:c.925C>T	XP_011538067.1:p.Gln309Ter
XM_011539766.2:c.907C>T	XP_011538068.1:p.Gln303Ter
XM_011539767.3:c.871C>T	XP_011538069.1:p.Gln291Ter
XR_945732.3:n.894C>T
XR_945733.2:n.831C>T
NM_000043.6:c.826C>T MANE Select	NP_000034.1:p.Gln276Ter
NM_001320619.2:c.*149C>T	NP_001307548.1:n.*149C>T
NM_152871.4:c.763C>T	NP_690610.1:p.Gln255Ter
NM_152872.4:c.*138C>T	NP_690611.1:n.*138C>T
NR_028033.4:n.733C>T
NR_028034.4:n.595C>T
NR_028035.4:n.658C>T
NR_028036.4:n.796C>T
NR_135313.2:n.713C>T
NR_135314.2:n.992C>T
NR_135315.2:n.745C>T