Canonical Allele Identifier: CA377509674

Gene: FAS

Linked Data

• gnomAD v4: 10-89014174-A-C
• MyVariant Identifiers: chr10:g.90773931A>C (hg19) ; chr10:g.89014174A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014174A>C , CM000672.2:g.89014174A>C	GRCh38
NC_000010.10:g.90773931A>C , CM000672.1:g.90773931A>C	GRCh37
NC_000010.9:g.90763911A>C	NCBI36
NG_009089.2:g.28644A>C , LRG_134:g.28644A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1041A>C
ENST00000355740.8:c.*55A>C	ENSP00000347979.3:n.*55A>C
ENST00000357339.7:c.669A>C	ENSP00000349896.2:p.Gln223His
ENST00000371857.8:n.2277A>C
ENST00000460510.6:c.15A>C	ENSP00000512812.1:p.Gln5His
ENST00000466081.6:n.2381A>C
ENST00000477270.6:c.777A>C	ENSP00000512813.1:p.Gln259His
ENST00000479522.6:c.*161A>C	ENSP00000424113.1:n.*161A>C
ENST00000484444.6:c.*173A>C	ENSP00000420975.1:n.*173A>C
ENST00000488877.6:c.623A>C	ENSP00000425159.1:n.623A>C
ENST00000492756.7:c.*161A>C	ENSP00000422453.1:n.*161A>C
ENST00000494799.6:c.15A>C	ENSP00000512834.1:p.Gln5His
ENST00000562983.3:c.15A>C	ENSP00000512845.1:p.Gln5His
ENST00000612663.6:c.*134A>C	ENSP00000477997.3:n.*134A>C
ENST00000640140.2:n.877A>C
ENST00000640250.2:n.231A>C
ENST00000640681.2:n.836A>C
ENST00000696723.1:n.4365A>C
ENST00000696741.1:n.2370A>C
ENST00000696742.1:n.2097A>C
ENST00000696743.1:n.3500A>C
ENST00000696744.1:n.771A>C
ENST00000696767.1:n.1066A>C
ENST00000696768.1:c.*55A>C	ENSP00000512859.1:n.*55A>C
ENST00000696769.1:n.2421A>C
ENST00000696771.1:c.15A>C	ENSP00000512860.1:p.Gln5His
ENST00000696772.1:n.2335A>C
ENST00000696773.1:n.2074A>C
ENST00000696774.1:n.5842A>C
ENST00000696776.1:c.825A>C	ENSP00000512861.1:p.Gln275His
ENST00000696777.1:n.2140A>C
ENST00000696778.1:n.1168A>C
ENST00000696779.1:c.339A>C	ENSP00000512862.1:p.Gln113His
ENST00000696780.1:c.762A>C	ENSP00000512863.1:p.Gln254His
ENST00000696781.1:c.477A>C	ENSP00000512864.1:p.Gln159His
ENST00000696782.1:c.*134A>C	ENSP00000512865.1:n.*134A>C
ENST00000696783.1:n.2600A>C
ENST00000696992.1:n.1849A>C
ENST00000696995.1:n.4261A>C
ENST00000696996.1:n.2174A>C
ENST00000696997.1:c.*362A>C	ENSP00000513028.1:n.*362A>C
ENST00000696998.1:n.1986A>C
ENST00000696999.1:c.15A>C	ENSP00000513029.1:p.Gln5His
ENST00000697035.1:c.*65A>C	ENSP00000513059.1:n.*65A>C
ENST00000697036.1:c.*148A>C	ENSP00000513060.1:n.*148A>C
ENST00000697037.1:n.767A>C
ENST00000697093.1:n.2968A>C
ENST00000697094.1:n.3315A>C
ENST00000697095.1:c.*1933A>C	ENSP00000513104.1:n.*1933A>C
ENST00000697096.1:n.1865A>C
ENST00000697097.1:c.15A>C	ENSP00000513105.1:p.Gln5His
ENST00000562983.2:n.918A>C
ENST00000690268.1:c.813A>C	ENSP00000509810.1:p.Gln271His
ENST00000355740.7:c.*58A>C	ENSP00000347979.3:n.*58A>C
ENST00000612663.5:c.*134A>C	ENSP00000477997.3:n.*134A>C
ENST00000640140.1:n.904A>C
ENST00000640250.1:n.231A>C
ENST00000640681.1:n.853A>C
ENST00000652046.1:c.732A>C MANE Select	ENSP00000498466.1:p.Gln244His
ENST00000313771.9:n.1041A>C
ENST00000352159.8:c.*49A>C	ENSP00000345601.4:n.*49A>C
ENST00000355279.2:c.707A>C	ENSP00000347426.2:n.707A>C
ENST00000355740.6:c.732A>C	ENSP00000347979.2:p.Gln244His
ENST00000357339.6:c.669A>C	ENSP00000349896.2:p.Gln223His
ENST00000479522.5:c.*161A>C	ENSP00000424113.1:n.*161A>C
ENST00000484444.5:c.*173A>C	ENSP00000420975.1:n.*173A>C
ENST00000488877.5:c.*173A>C	ENSP00000425159.1:n.*173A>C
ENST00000492756.5:c.560A>C	ENSP00000422453.1:n.560A>C
ENST00000494410.5:c.*90A>C	ENSP00000423755.1:n.*90A>C
ENST00000494799.5:n.639A>C
ENST00000612663.4:c.*79A>C	ENSP00000477997.2:n.*79A>C
ENST00000615406.4:c.732A>C	ENSP00000484575.1:p.Gln244His
ENST00000626542.2:c.730A>C	ENSP00000485876.1:p.Ser244Arg
NM_000043.4:c.732A>C , LRG_134t1:c.732A>C	NP_000034.1:p.Gln244His
NM_152871.2:c.669A>C	NP_690610.1:p.Gln223His
NM_152872.2:c.*44A>C	NP_690611.1:n.*44A>C
NR_028033.2:n.906A>C
NR_028034.2:n.768A>C
NR_028035.2:n.831A>C
NR_028036.2:n.969A>C
XM_006717819.2:c.813A>C	XP_006717882.1:p.Gln271His
XM_011539764.1:c.894A>C	XP_011538066.1:p.Gln298His
XM_011539765.1:c.831A>C	XP_011538067.1:p.Gln277His
XM_011539766.1:c.813A>C	XP_011538068.1:p.Gln271His
XM_011539767.1:c.777A>C	XP_011538069.1:p.Gln259His
XR_945732.1:n.800A>C
XR_945733.1:n.737A>C
NM_000043.5:c.732A>C	NP_000034.1:p.Gln244His
NM_001320619.1:c.*55A>C	NP_001307548.1:n.*55A>C
NM_152871.3:c.669A>C	NP_690610.1:p.Gln223His
NM_152872.3:c.*44A>C	NP_690611.1:n.*44A>C
NR_028033.3:n.878A>C
NR_028034.3:n.740A>C
NR_028035.3:n.803A>C
NR_028036.3:n.941A>C
NR_135313.1:n.858A>C
NR_135314.1:n.1041A>C
NR_135315.1:n.794A>C
XM_006717819.3:c.813A>C	XP_006717882.1:p.Gln271His
XM_011539764.2:c.894A>C	XP_011538066.1:p.Gln298His
XM_011539765.2:c.831A>C	XP_011538067.1:p.Gln277His
XM_011539766.2:c.813A>C	XP_011538068.1:p.Gln271His
XM_011539767.3:c.777A>C	XP_011538069.1:p.Gln259His
XR_945732.3:n.800A>C
XR_945733.2:n.737A>C
NM_000043.6:c.732A>C MANE Select	NP_000034.1:p.Gln244His
NM_001320619.2:c.*55A>C	NP_001307548.1:n.*55A>C
NM_152871.4:c.669A>C	NP_690610.1:p.Gln223His
NM_152872.4:c.*44A>C	NP_690611.1:n.*44A>C
NR_028033.4:n.639A>C
NR_028034.4:n.501A>C
NR_028035.4:n.564A>C
NR_028036.4:n.702A>C
NR_135313.2:n.619A>C
NR_135314.2:n.898A>C
NR_135315.2:n.651A>C