Canonical Allele Identifier: CA377509733

Gene: FAS

Linked Data

• ClinVar Variation Id: 863735
• ClinVar RCV Id: RCV001070775
• dbSNP Id: rs1848671126
• MyVariant Identifiers: chr10:g.90773957G>T (hg19) ; chr10:g.89014200G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014200G>T , CM000672.2:g.89014200G>T	GRCh38
NC_000010.10:g.90773957G>T , CM000672.1:g.90773957G>T	GRCh37
NC_000010.9:g.90763937G>T	NCBI36
NG_009089.2:g.28670G>T , LRG_134:g.28670G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1067G>T
ENST00000355740.8:c.*81G>T	ENSP00000347979.3:n.*81G>T
ENST00000357339.7:c.695G>T	ENSP00000349896.2:p.Gly232Val
ENST00000371857.8:n.2303G>T
ENST00000460510.6:c.41G>T	ENSP00000512812.1:p.Gly14Val
ENST00000466081.6:n.2407G>T
ENST00000477270.6:c.803G>T	ENSP00000512813.1:p.Gly268Val
ENST00000479522.6:c.*187G>T	ENSP00000424113.1:n.*187G>T
ENST00000484444.6:c.*199G>T	ENSP00000420975.1:n.*199G>T
ENST00000488877.6:c.649G>T	ENSP00000425159.1:n.649G>T
ENST00000492756.7:c.*187G>T	ENSP00000422453.1:n.*187G>T
ENST00000494799.6:c.41G>T	ENSP00000512834.1:p.Gly14Val
ENST00000562983.3:c.41G>T	ENSP00000512845.1:p.Gly14Val
ENST00000612663.6:c.*160G>T	ENSP00000477997.3:n.*160G>T
ENST00000640140.2:n.903G>T
ENST00000640250.2:n.257G>T
ENST00000640681.2:n.862G>T
ENST00000696723.1:n.4391G>T
ENST00000696741.1:n.2396G>T
ENST00000696742.1:n.2123G>T
ENST00000696743.1:n.3526G>T
ENST00000696744.1:n.797G>T
ENST00000696767.1:n.1092G>T
ENST00000696768.1:c.*81G>T	ENSP00000512859.1:n.*81G>T
ENST00000696769.1:n.2447G>T
ENST00000696771.1:c.41G>T	ENSP00000512860.1:p.Gly14Val
ENST00000696772.1:n.2361G>T
ENST00000696773.1:n.2100G>T
ENST00000696774.1:n.5868G>T
ENST00000696776.1:c.851G>T	ENSP00000512861.1:p.Gly284Val
ENST00000696777.1:n.2166G>T
ENST00000696778.1:n.1194G>T
ENST00000696779.1:c.365G>T	ENSP00000512862.1:p.Gly122Val
ENST00000696780.1:c.788G>T	ENSP00000512863.1:p.Gly263Val
ENST00000696781.1:c.503G>T	ENSP00000512864.1:p.Gly168Val
ENST00000696782.1:c.*160G>T	ENSP00000512865.1:n.*160G>T
ENST00000696783.1:n.2626G>T
ENST00000696992.1:n.1875G>T
ENST00000696995.1:n.4287G>T
ENST00000696996.1:n.2200G>T
ENST00000696997.1:c.*388G>T	ENSP00000513028.1:n.*388G>T
ENST00000696998.1:n.2012G>T
ENST00000696999.1:c.41G>T	ENSP00000513029.1:p.Gly14Val
ENST00000697035.1:c.*91G>T	ENSP00000513059.1:n.*91G>T
ENST00000697036.1:c.*174G>T	ENSP00000513060.1:n.*174G>T
ENST00000697037.1:n.793G>T
ENST00000697093.1:n.2994G>T
ENST00000697094.1:n.3341G>T
ENST00000697095.1:c.*1959G>T	ENSP00000513104.1:n.*1959G>T
ENST00000697096.1:n.1891G>T
ENST00000697097.1:c.41G>T	ENSP00000513105.1:p.Gly14Val
ENST00000562983.2:n.944G>T
ENST00000690268.1:c.839G>T	ENSP00000509810.1:p.Gly280Val
ENST00000355740.7:c.*84G>T	ENSP00000347979.3:n.*84G>T
ENST00000612663.5:c.*160G>T	ENSP00000477997.3:n.*160G>T
ENST00000640140.1:n.930G>T
ENST00000640250.1:n.257G>T
ENST00000640681.1:n.879G>T
ENST00000652046.1:c.758G>T MANE Select	ENSP00000498466.1:p.Gly253Val
ENST00000352159.8:c.*75G>T	ENSP00000345601.4:n.*75G>T
ENST00000355279.2:c.733G>T	ENSP00000347426.2:n.733G>T
ENST00000355740.6:c.758G>T	ENSP00000347979.2:p.Gly253Val
ENST00000357339.6:c.695G>T	ENSP00000349896.2:p.Gly232Val
ENST00000479522.5:c.*187G>T	ENSP00000424113.1:n.*187G>T
ENST00000484444.5:c.*199G>T	ENSP00000420975.1:n.*199G>T
ENST00000488877.5:c.*199G>T	ENSP00000425159.1:n.*199G>T
ENST00000492756.5:c.586G>T	ENSP00000422453.1:n.586G>T
ENST00000494410.5:c.*116G>T	ENSP00000423755.1:n.*116G>T
ENST00000494799.5:n.665G>T
ENST00000612663.4:c.*105G>T	ENSP00000477997.2:n.*105G>T
ENST00000615406.4:c.756G>T	ENSP00000484575.1:p.Trp252Cys
NM_000043.4:c.758G>T , LRG_134t1:c.758G>T	NP_000034.1:p.Gly253Val
NM_152871.2:c.695G>T	NP_690610.1:p.Gly232Val
NM_152872.2:c.*70G>T	NP_690611.1:n.*70G>T
NR_028033.2:n.932G>T
NR_028034.2:n.794G>T
NR_028035.2:n.857G>T
NR_028036.2:n.995G>T
XM_006717819.2:c.839G>T	XP_006717882.1:p.Gly280Val
XM_011539764.1:c.920G>T	XP_011538066.1:p.Gly307Val
XM_011539765.1:c.857G>T	XP_011538067.1:p.Gly286Val
XM_011539766.1:c.839G>T	XP_011538068.1:p.Gly280Val
XM_011539767.1:c.803G>T	XP_011538069.1:p.Gly268Val
XR_945732.1:n.826G>T
XR_945733.1:n.763G>T
NM_000043.5:c.758G>T	NP_000034.1:p.Gly253Val
NM_001320619.1:c.*81G>T	NP_001307548.1:n.*81G>T
NM_152871.3:c.695G>T	NP_690610.1:p.Gly232Val
NM_152872.3:c.*70G>T	NP_690611.1:n.*70G>T
NR_028033.3:n.904G>T
NR_028034.3:n.766G>T
NR_028035.3:n.829G>T
NR_028036.3:n.967G>T
NR_135313.1:n.884G>T
NR_135314.1:n.1067G>T
NR_135315.1:n.820G>T
XM_006717819.3:c.839G>T	XP_006717882.1:p.Gly280Val
XM_011539764.2:c.920G>T	XP_011538066.1:p.Gly307Val
XM_011539765.2:c.857G>T	XP_011538067.1:p.Gly286Val
XM_011539766.2:c.839G>T	XP_011538068.1:p.Gly280Val
XM_011539767.3:c.803G>T	XP_011538069.1:p.Gly268Val
XR_945732.3:n.826G>T
XR_945733.2:n.763G>T
NM_000043.6:c.758G>T MANE Select	NP_000034.1:p.Gly253Val
NM_001320619.2:c.*81G>T	NP_001307548.1:n.*81G>T
NM_152871.4:c.695G>T	NP_690610.1:p.Gly232Val
NM_152872.4:c.*70G>T	NP_690611.1:n.*70G>T
NR_028033.4:n.665G>T
NR_028034.4:n.527G>T
NR_028035.4:n.590G>T
NR_028036.4:n.728G>T
NR_135313.2:n.645G>T
NR_135314.2:n.924G>T
NR_135315.2:n.677G>T