Canonical Allele Identifier: CA377509609

Gene: FAS

Linked Data

• gnomAD v4: 10-89014151-G-T
• MyVariant Identifiers: chr10:g.90773908G>T (hg19) ; chr10:g.89014151G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014151G>T , CM000672.2:g.89014151G>T	GRCh38
NC_000010.10:g.90773908G>T , CM000672.1:g.90773908G>T	GRCh37
NC_000010.9:g.90763888G>T	NCBI36
NG_009089.2:g.28621G>T , LRG_134:g.28621G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1018G>T
ENST00000355740.8:c.*32G>T	ENSP00000347979.3:n.*32G>T
ENST00000357339.7:c.646G>T	ENSP00000349896.2:p.Ala216Ser
ENST00000371857.8:n.2254G>T
ENST00000460510.6:c.-9G>T	ENSP00000512812.1:n.-9G>T
ENST00000466081.6:n.2358G>T
ENST00000477270.6:c.754G>T	ENSP00000512813.1:p.Ala252Ser
ENST00000479522.6:c.*138G>T	ENSP00000424113.1:n.*138G>T
ENST00000484444.6:c.*150G>T	ENSP00000420975.1:n.*150G>T
ENST00000488877.6:c.600G>T	ENSP00000425159.1:n.600G>T
ENST00000492756.7:c.*138G>T	ENSP00000422453.1:n.*138G>T
ENST00000494799.6:c.-9G>T	ENSP00000512834.1:n.-9G>T
ENST00000562983.3:c.-9G>T	ENSP00000512845.1:n.-9G>T
ENST00000612663.6:c.*111G>T	ENSP00000477997.3:n.*111G>T
ENST00000640140.2:n.854G>T
ENST00000640250.2:n.208G>T
ENST00000640681.2:n.813G>T
ENST00000696723.1:n.4342G>T
ENST00000696741.1:n.2347G>T
ENST00000696742.1:n.2074G>T
ENST00000696743.1:n.3477G>T
ENST00000696744.1:n.748G>T
ENST00000696767.1:n.1043G>T
ENST00000696768.1:c.*32G>T	ENSP00000512859.1:n.*32G>T
ENST00000696769.1:n.2398G>T
ENST00000696771.1:c.-9G>T	ENSP00000512860.1:n.-9G>T
ENST00000696772.1:n.2312G>T
ENST00000696773.1:n.2051G>T
ENST00000696774.1:n.5819G>T
ENST00000696776.1:c.802G>T	ENSP00000512861.1:p.Ala268Ser
ENST00000696777.1:n.2117G>T
ENST00000696778.1:n.1145G>T
ENST00000696779.1:c.316G>T	ENSP00000512862.1:p.Ala106Ser
ENST00000696780.1:c.739G>T	ENSP00000512863.1:p.Ala247Ser
ENST00000696781.1:c.454G>T	ENSP00000512864.1:p.Ala152Ser
ENST00000696782.1:c.*111G>T	ENSP00000512865.1:n.*111G>T
ENST00000696783.1:n.2577G>T
ENST00000696992.1:n.1826G>T
ENST00000696995.1:n.4238G>T
ENST00000696996.1:n.2151G>T
ENST00000696997.1:c.*339G>T	ENSP00000513028.1:n.*339G>T
ENST00000696998.1:n.1963G>T
ENST00000696999.1:c.-9G>T	ENSP00000513029.1:n.-9G>T
ENST00000697035.1:c.*42G>T	ENSP00000513059.1:n.*42G>T
ENST00000697036.1:c.*125G>T	ENSP00000513060.1:n.*125G>T
ENST00000697037.1:n.744G>T
ENST00000697093.1:n.2945G>T
ENST00000697094.1:n.3292G>T
ENST00000697095.1:c.*1910G>T	ENSP00000513104.1:n.*1910G>T
ENST00000697096.1:n.1842G>T
ENST00000697097.1:c.-9G>T	ENSP00000513105.1:n.-9G>T
ENST00000562983.2:n.895G>T
ENST00000690268.1:c.790G>T	ENSP00000509810.1:p.Ala264Ser
ENST00000355740.7:c.*35G>T	ENSP00000347979.3:n.*35G>T
ENST00000612663.5:c.*111G>T	ENSP00000477997.3:n.*111G>T
ENST00000640140.1:n.881G>T
ENST00000640250.1:n.208G>T
ENST00000640681.1:n.830G>T
ENST00000652046.1:c.709G>T MANE Select	ENSP00000498466.1:p.Ala237Ser
ENST00000313771.9:n.1018G>T
ENST00000352159.8:c.*26G>T	ENSP00000345601.4:n.*26G>T
ENST00000355279.2:c.684G>T	ENSP00000347426.2:n.684G>T
ENST00000355740.6:c.709G>T	ENSP00000347979.2:p.Ala237Ser
ENST00000357339.6:c.646G>T	ENSP00000349896.2:p.Ala216Ser
ENST00000479522.5:c.*138G>T	ENSP00000424113.1:n.*138G>T
ENST00000484444.5:c.*150G>T	ENSP00000420975.1:n.*150G>T
ENST00000488877.5:c.*150G>T	ENSP00000425159.1:n.*150G>T
ENST00000492756.5:c.537G>T	ENSP00000422453.1:n.537G>T
ENST00000494410.5:c.*67G>T	ENSP00000423755.1:n.*67G>T
ENST00000494799.5:n.616G>T
ENST00000612663.4:c.*56G>T	ENSP00000477997.2:n.*56G>T
ENST00000615406.4:c.709G>T	ENSP00000484575.1:p.Ala237Ser
ENST00000626542.2:c.707G>T	ENSP00000485876.1:p.Cys236Phe
NM_000043.4:c.709G>T , LRG_134t1:c.709G>T	NP_000034.1:p.Ala237Ser
NM_152871.2:c.646G>T	NP_690610.1:p.Ala216Ser
NM_152872.2:c.*21G>T	NP_690611.1:n.*21G>T
NR_028033.2:n.883G>T
NR_028034.2:n.745G>T
NR_028035.2:n.808G>T
NR_028036.2:n.946G>T
XM_006717819.2:c.790G>T	XP_006717882.1:p.Ala264Ser
XM_011539764.1:c.871G>T	XP_011538066.1:p.Ala291Ser
XM_011539765.1:c.808G>T	XP_011538067.1:p.Ala270Ser
XM_011539766.1:c.790G>T	XP_011538068.1:p.Ala264Ser
XM_011539767.1:c.754G>T	XP_011538069.1:p.Ala252Ser
XR_945732.1:n.777G>T
XR_945733.1:n.714G>T
NM_000043.5:c.709G>T	NP_000034.1:p.Ala237Ser
NM_001320619.1:c.*32G>T	NP_001307548.1:n.*32G>T
NM_152871.3:c.646G>T	NP_690610.1:p.Ala216Ser
NM_152872.3:c.*21G>T	NP_690611.1:n.*21G>T
NR_028033.3:n.855G>T
NR_028034.3:n.717G>T
NR_028035.3:n.780G>T
NR_028036.3:n.918G>T
NR_135313.1:n.835G>T
NR_135314.1:n.1018G>T
NR_135315.1:n.771G>T
XM_006717819.3:c.790G>T	XP_006717882.1:p.Ala264Ser
XM_011539764.2:c.871G>T	XP_011538066.1:p.Ala291Ser
XM_011539765.2:c.808G>T	XP_011538067.1:p.Ala270Ser
XM_011539766.2:c.790G>T	XP_011538068.1:p.Ala264Ser
XM_011539767.3:c.754G>T	XP_011538069.1:p.Ala252Ser
XR_945732.3:n.777G>T
XR_945733.2:n.714G>T
NM_000043.6:c.709G>T MANE Select	NP_000034.1:p.Ala237Ser
NM_001320619.2:c.*32G>T	NP_001307548.1:n.*32G>T
NM_152871.4:c.646G>T	NP_690610.1:p.Ala216Ser
NM_152872.4:c.*21G>T	NP_690611.1:n.*21G>T
NR_028033.4:n.616G>T
NR_028034.4:n.478G>T
NR_028035.4:n.541G>T
NR_028036.4:n.679G>T
NR_135313.2:n.596G>T
NR_135314.2:n.875G>T
NR_135315.2:n.628G>T