Canonical Allele Identifier: CA5593222

Gene: FAS

Linked Data

• dbSNP Id: rs781035943
• ExAC: 10:90774023 T / A
• MyVariant Identifiers: chr10:g.90774023T>A (hg19) ; chr10:g.89014266T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014266T>A , CM000672.2:g.89014266T>A	GRCh38
NC_000010.10:g.90774023T>A , CM000672.1:g.90774023T>A	GRCh37
NC_000010.9:g.90764003T>A	NCBI36
NG_009089.2:g.28736T>A , LRG_134:g.28736T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1133T>A
ENST00000355740.8:c.*147T>A	ENSP00000347979.3:n.*147T>A
ENST00000357339.7:c.761T>A	ENSP00000349896.2:p.Val254Asp
ENST00000371857.8:n.2369T>A
ENST00000460510.6:c.107T>A	ENSP00000512812.1:p.Val36Asp
ENST00000466081.6:n.2473T>A
ENST00000477270.6:c.869T>A	ENSP00000512813.1:p.Val290Asp
ENST00000479522.6:c.*253T>A	ENSP00000424113.1:n.*253T>A
ENST00000484444.6:c.*265T>A	ENSP00000420975.1:n.*265T>A
ENST00000488877.6:c.715T>A	ENSP00000425159.1:n.715T>A
ENST00000492756.7:c.*253T>A	ENSP00000422453.1:n.*253T>A
ENST00000494799.6:c.107T>A	ENSP00000512834.1:p.Val36Asp
ENST00000562983.3:c.107T>A	ENSP00000512845.1:p.Val36Asp
ENST00000612663.6:c.*226T>A	ENSP00000477997.3:n.*226T>A
ENST00000640140.2:n.969T>A
ENST00000640250.2:n.323T>A
ENST00000640681.2:n.928T>A
ENST00000696723.1:n.4457T>A
ENST00000696741.1:n.2462T>A
ENST00000696742.1:n.2189T>A
ENST00000696743.1:n.3592T>A
ENST00000696744.1:n.863T>A
ENST00000696767.1:n.1158T>A
ENST00000696768.1:c.*147T>A	ENSP00000512859.1:n.*147T>A
ENST00000696769.1:n.2513T>A
ENST00000696771.1:c.107T>A	ENSP00000512860.1:p.Val36Asp
ENST00000696772.1:n.2427T>A
ENST00000696773.1:n.2166T>A
ENST00000696774.1:n.5934T>A
ENST00000696776.1:c.917T>A	ENSP00000512861.1:p.Val306Asp
ENST00000696777.1:n.2232T>A
ENST00000696778.1:n.1260T>A
ENST00000696779.1:c.431T>A	ENSP00000512862.1:p.Val144Asp
ENST00000696780.1:c.854T>A	ENSP00000512863.1:p.Val285Asp
ENST00000696781.1:c.569T>A	ENSP00000512864.1:p.Val190Asp
ENST00000696782.1:c.*226T>A	ENSP00000512865.1:n.*226T>A
ENST00000696783.1:n.2692T>A
ENST00000696992.1:n.1941T>A
ENST00000696995.1:n.4353T>A
ENST00000696996.1:n.2266T>A
ENST00000696997.1:c.*454T>A	ENSP00000513028.1:n.*454T>A
ENST00000696998.1:n.2078T>A
ENST00000696999.1:c.107T>A	ENSP00000513029.1:p.Val36Asp
ENST00000697035.1:c.*157T>A	ENSP00000513059.1:n.*157T>A
ENST00000697036.1:c.*240T>A	ENSP00000513060.1:n.*240T>A
ENST00000697037.1:n.859T>A
ENST00000697093.1:n.3060T>A
ENST00000697094.1:n.3407T>A
ENST00000697095.1:c.*2025T>A	ENSP00000513104.1:n.*2025T>A
ENST00000697096.1:n.1957T>A
ENST00000697097.1:c.107T>A	ENSP00000513105.1:p.Val36Asp
ENST00000562983.2:n.1010T>A
ENST00000690268.1:c.905T>A	ENSP00000509810.1:p.Val302Asp
ENST00000355740.7:c.*150T>A	ENSP00000347979.3:n.*150T>A
ENST00000612663.5:c.*226T>A	ENSP00000477997.3:n.*226T>A
ENST00000640140.1:n.996T>A
ENST00000640250.1:n.323T>A
ENST00000640681.1:n.945T>A
ENST00000652046.1:c.824T>A MANE Select	ENSP00000498466.1:p.Val275Asp
ENST00000352159.8:c.*141T>A	ENSP00000345601.4:n.*141T>A
ENST00000355279.2:c.799T>A	ENSP00000347426.2:n.799T>A
ENST00000355740.6:c.824T>A	ENSP00000347979.2:p.Val275Asp
ENST00000357339.6:c.761T>A	ENSP00000349896.2:p.Val254Asp
ENST00000479522.5:c.*253T>A	ENSP00000424113.1:n.*253T>A
ENST00000484444.5:c.*265T>A	ENSP00000420975.1:n.*265T>A
ENST00000488877.5:c.*265T>A	ENSP00000425159.1:n.*265T>A
ENST00000492756.5:c.652T>A	ENSP00000422453.1:n.652T>A
ENST00000494410.5:c.*182T>A	ENSP00000423755.1:n.*182T>A
ENST00000612663.4:c.*171T>A	ENSP00000477997.2:n.*171T>A
NM_000043.4:c.824T>A , LRG_134t1:c.824T>A	NP_000034.1:p.Val275Asp
NM_152871.2:c.761T>A	NP_690610.1:p.Val254Asp
NM_152872.2:c.*136T>A	NP_690611.1:n.*136T>A
NR_028033.2:n.998T>A
NR_028034.2:n.860T>A
NR_028035.2:n.923T>A
NR_028036.2:n.1061T>A
XM_006717819.2:c.905T>A	XP_006717882.1:p.Val302Asp
XM_011539764.1:c.986T>A	XP_011538066.1:p.Val329Asp
XM_011539765.1:c.923T>A	XP_011538067.1:p.Val308Asp
XM_011539766.1:c.905T>A	XP_011538068.1:p.Val302Asp
XM_011539767.1:c.869T>A	XP_011538069.1:p.Val290Asp
XR_945732.1:n.892T>A
XR_945733.1:n.829T>A
NM_000043.5:c.824T>A	NP_000034.1:p.Val275Asp
NM_001320619.1:c.*147T>A	NP_001307548.1:n.*147T>A
NM_152871.3:c.761T>A	NP_690610.1:p.Val254Asp
NM_152872.3:c.*136T>A	NP_690611.1:n.*136T>A
NR_028033.3:n.970T>A
NR_028034.3:n.832T>A
NR_028035.3:n.895T>A
NR_028036.3:n.1033T>A
NR_135313.1:n.950T>A
NR_135314.1:n.1133T>A
NR_135315.1:n.886T>A
XM_006717819.3:c.905T>A	XP_006717882.1:p.Val302Asp
XM_011539764.2:c.986T>A	XP_011538066.1:p.Val329Asp
XM_011539765.2:c.923T>A	XP_011538067.1:p.Val308Asp
XM_011539766.2:c.905T>A	XP_011538068.1:p.Val302Asp
XM_011539767.3:c.869T>A	XP_011538069.1:p.Val290Asp
XR_945732.3:n.892T>A
XR_945733.2:n.829T>A
NM_000043.6:c.824T>A MANE Select	NP_000034.1:p.Val275Asp
NM_001320619.2:c.*147T>A	NP_001307548.1:n.*147T>A
NM_152871.4:c.761T>A	NP_690610.1:p.Val254Asp
NM_152872.4:c.*136T>A	NP_690611.1:n.*136T>A
NR_028033.4:n.731T>A
NR_028034.4:n.593T>A
NR_028035.4:n.656T>A
NR_028036.4:n.794T>A
NR_135313.2:n.711T>A
NR_135314.2:n.990T>A
NR_135315.2:n.743T>A