Canonical Allele Identifier: CA377509563

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90773891A>C (hg19) ; chr10:g.89014134A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014134A>C , CM000672.2:g.89014134A>C	GRCh38
NC_000010.10:g.90773891A>C , CM000672.1:g.90773891A>C	GRCh37
NC_000010.9:g.90763871A>C	NCBI36
NG_009089.2:g.28604A>C , LRG_134:g.28604A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1001A>C
ENST00000355740.8:c.*15A>C	ENSP00000347979.3:n.*15A>C
ENST00000357339.7:c.629A>C	ENSP00000349896.2:p.Lys210Thr
ENST00000371857.8:n.2237A>C
ENST00000460510.6:c.-26A>C	ENSP00000512812.1:n.-26A>C
ENST00000466081.6:n.2341A>C
ENST00000477270.6:c.737A>C	ENSP00000512813.1:p.Lys246Thr
ENST00000479522.6:c.*121A>C	ENSP00000424113.1:n.*121A>C
ENST00000484444.6:c.*133A>C	ENSP00000420975.1:n.*133A>C
ENST00000488877.6:c.583A>C	ENSP00000425159.1:n.583A>C
ENST00000492756.7:c.*121A>C	ENSP00000422453.1:n.*121A>C
ENST00000494799.6:c.-26A>C	ENSP00000512834.1:n.-26A>C
ENST00000562983.3:c.-26A>C	ENSP00000512845.1:n.-26A>C
ENST00000612663.6:c.*94A>C	ENSP00000477997.3:n.*94A>C
ENST00000640140.2:n.837A>C
ENST00000640250.2:n.191A>C
ENST00000640681.2:n.796A>C
ENST00000696723.1:n.4325A>C
ENST00000696741.1:n.2330A>C
ENST00000696742.1:n.2057A>C
ENST00000696743.1:n.3460A>C
ENST00000696744.1:n.731A>C
ENST00000696767.1:n.1026A>C
ENST00000696768.1:c.*15A>C	ENSP00000512859.1:n.*15A>C
ENST00000696769.1:n.2381A>C
ENST00000696771.1:c.-26A>C	ENSP00000512860.1:n.-26A>C
ENST00000696772.1:n.2295A>C
ENST00000696773.1:n.2034A>C
ENST00000696774.1:n.5802A>C
ENST00000696776.1:c.785A>C	ENSP00000512861.1:p.Lys262Thr
ENST00000696777.1:n.2100A>C
ENST00000696778.1:n.1128A>C
ENST00000696779.1:c.299A>C	ENSP00000512862.1:p.Lys100Thr
ENST00000696780.1:c.722A>C	ENSP00000512863.1:p.Lys241Thr
ENST00000696781.1:c.437A>C	ENSP00000512864.1:p.Lys146Thr
ENST00000696782.1:c.*94A>C	ENSP00000512865.1:n.*94A>C
ENST00000696783.1:n.2560A>C
ENST00000696992.1:n.1809A>C
ENST00000696995.1:n.4221A>C
ENST00000696996.1:n.2134A>C
ENST00000696997.1:c.*322A>C	ENSP00000513028.1:n.*322A>C
ENST00000696998.1:n.1946A>C
ENST00000696999.1:c.-26A>C	ENSP00000513029.1:n.-26A>C
ENST00000697035.1:c.*25A>C	ENSP00000513059.1:n.*25A>C
ENST00000697036.1:c.*108A>C	ENSP00000513060.1:n.*108A>C
ENST00000697037.1:n.727A>C
ENST00000697093.1:n.2928A>C
ENST00000697094.1:n.3275A>C
ENST00000697095.1:c.*1893A>C	ENSP00000513104.1:n.*1893A>C
ENST00000697096.1:n.1825A>C
ENST00000697097.1:c.-26A>C	ENSP00000513105.1:n.-26A>C
ENST00000562983.2:n.878A>C
ENST00000690268.1:c.773A>C	ENSP00000509810.1:p.Lys258Thr
ENST00000355740.7:c.*18A>C	ENSP00000347979.3:n.*18A>C
ENST00000612663.5:c.*94A>C	ENSP00000477997.3:n.*94A>C
ENST00000640140.1:n.864A>C
ENST00000640250.1:n.191A>C
ENST00000640681.1:n.813A>C
ENST00000652046.1:c.692A>C MANE Select	ENSP00000498466.1:p.Lys231Thr
ENST00000313771.9:n.1001A>C
ENST00000352159.8:c.*9A>C	ENSP00000345601.4:n.*9A>C
ENST00000355279.2:c.667A>C	ENSP00000347426.2:n.667A>C
ENST00000355740.6:c.692A>C	ENSP00000347979.2:p.Lys231Thr
ENST00000357339.6:c.629A>C	ENSP00000349896.2:p.Lys210Thr
ENST00000479522.5:c.*121A>C	ENSP00000424113.1:n.*121A>C
ENST00000484444.5:c.*133A>C	ENSP00000420975.1:n.*133A>C
ENST00000488877.5:c.*133A>C	ENSP00000425159.1:n.*133A>C
ENST00000492756.5:c.520A>C	ENSP00000422453.1:n.520A>C
ENST00000494410.5:c.*50A>C	ENSP00000423755.1:n.*50A>C
ENST00000494799.5:n.599A>C
ENST00000612663.4:c.*39A>C	ENSP00000477997.2:n.*39A>C
ENST00000615406.4:c.692A>C	ENSP00000484575.1:p.Lys231Thr
ENST00000626542.2:c.692A>C	ENSP00000485876.1:p.Lys231Thr
NM_000043.4:c.692A>C , LRG_134t1:c.692A>C	NP_000034.1:p.Lys231Thr
NM_152871.2:c.629A>C	NP_690610.1:p.Lys210Thr
NM_152872.2:c.*4A>C	NP_690611.1:n.*4A>C
NR_028033.2:n.866A>C
NR_028034.2:n.728A>C
NR_028035.2:n.791A>C
NR_028036.2:n.929A>C
XM_006717819.2:c.773A>C	XP_006717882.1:p.Lys258Thr
XM_011539764.1:c.854A>C	XP_011538066.1:p.Lys285Thr
XM_011539765.1:c.791A>C	XP_011538067.1:p.Lys264Thr
XM_011539766.1:c.773A>C	XP_011538068.1:p.Lys258Thr
XM_011539767.1:c.737A>C	XP_011538069.1:p.Lys246Thr
XR_945732.1:n.760A>C
XR_945733.1:n.697A>C
NM_000043.5:c.692A>C	NP_000034.1:p.Lys231Thr
NM_001320619.1:c.*15A>C	NP_001307548.1:n.*15A>C
NM_152871.3:c.629A>C	NP_690610.1:p.Lys210Thr
NM_152872.3:c.*4A>C	NP_690611.1:n.*4A>C
NR_028033.3:n.838A>C
NR_028034.3:n.700A>C
NR_028035.3:n.763A>C
NR_028036.3:n.901A>C
NR_135313.1:n.818A>C
NR_135314.1:n.1001A>C
NR_135315.1:n.754A>C
XM_006717819.3:c.773A>C	XP_006717882.1:p.Lys258Thr
XM_011539764.2:c.854A>C	XP_011538066.1:p.Lys285Thr
XM_011539765.2:c.791A>C	XP_011538067.1:p.Lys264Thr
XM_011539766.2:c.773A>C	XP_011538068.1:p.Lys258Thr
XM_011539767.3:c.737A>C	XP_011538069.1:p.Lys246Thr
XR_945732.3:n.760A>C
XR_945733.2:n.697A>C
NM_000043.6:c.692A>C MANE Select	NP_000034.1:p.Lys231Thr
NM_001320619.2:c.*15A>C	NP_001307548.1:n.*15A>C
NM_152871.4:c.629A>C	NP_690610.1:p.Lys210Thr
NM_152872.4:c.*4A>C	NP_690611.1:n.*4A>C
NR_028033.4:n.599A>C
NR_028034.4:n.461A>C
NR_028035.4:n.524A>C
NR_028036.4:n.662A>C
NR_135313.2:n.579A>C
NR_135314.2:n.858A>C
NR_135315.2:n.611A>C