Canonical Allele Identifier: CA377509986

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774062A>T (hg19) ; chr10:g.89014305A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014305A>T , CM000672.2:g.89014305A>T	GRCh38
NC_000010.10:g.90774062A>T , CM000672.1:g.90774062A>T	GRCh37
NC_000010.9:g.90764042A>T	NCBI36
NG_009089.2:g.28775A>T , LRG_134:g.28775A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1172A>T
ENST00000355740.8:c.*186A>T	ENSP00000347979.3:n.*186A>T
ENST00000357339.7:c.800A>T	ENSP00000349896.2:p.Lys267Ile
ENST00000371857.8:n.2408A>T
ENST00000460510.6:c.146A>T	ENSP00000512812.1:p.Lys49Ile
ENST00000466081.6:n.2512A>T
ENST00000477270.6:c.908A>T	ENSP00000512813.1:p.Lys303Ile
ENST00000479522.6:c.*292A>T	ENSP00000424113.1:n.*292A>T
ENST00000484444.6:c.*304A>T	ENSP00000420975.1:n.*304A>T
ENST00000488877.6:c.754A>T	ENSP00000425159.1:n.754A>T
ENST00000492756.7:c.*292A>T	ENSP00000422453.1:n.*292A>T
ENST00000494799.6:c.146A>T	ENSP00000512834.1:p.Lys49Ile
ENST00000562983.3:c.146A>T	ENSP00000512845.1:p.Lys49Ile
ENST00000612663.6:c.*265A>T	ENSP00000477997.3:n.*265A>T
ENST00000640140.2:n.1008A>T
ENST00000640250.2:n.362A>T
ENST00000640681.2:n.967A>T
ENST00000696723.1:n.4496A>T
ENST00000696741.1:n.2501A>T
ENST00000696742.1:n.2228A>T
ENST00000696743.1:n.3631A>T
ENST00000696744.1:n.902A>T
ENST00000696767.1:n.1197A>T
ENST00000696768.1:c.*186A>T	ENSP00000512859.1:n.*186A>T
ENST00000696769.1:n.2552A>T
ENST00000696771.1:c.146A>T	ENSP00000512860.1:p.Lys49Ile
ENST00000696772.1:n.2466A>T
ENST00000696773.1:n.2205A>T
ENST00000696774.1:n.5973A>T
ENST00000696776.1:c.956A>T	ENSP00000512861.1:p.Lys319Ile
ENST00000696777.1:n.2271A>T
ENST00000696778.1:n.1299A>T
ENST00000696779.1:c.470A>T	ENSP00000512862.1:p.Lys157Ile
ENST00000696780.1:c.893A>T	ENSP00000512863.1:p.Lys298Ile
ENST00000696781.1:c.608A>T	ENSP00000512864.1:p.Lys203Ile
ENST00000696782.1:c.*265A>T	ENSP00000512865.1:n.*265A>T
ENST00000696783.1:n.2731A>T
ENST00000696992.1:n.1980A>T
ENST00000696995.1:n.4392A>T
ENST00000696996.1:n.2305A>T
ENST00000696997.1:c.*493A>T	ENSP00000513028.1:n.*493A>T
ENST00000696998.1:n.2117A>T
ENST00000696999.1:c.146A>T	ENSP00000513029.1:p.Lys49Ile
ENST00000697036.1:c.*279A>T	ENSP00000513060.1:n.*279A>T
ENST00000697037.1:n.898A>T
ENST00000697093.1:n.3099A>T
ENST00000697094.1:n.3446A>T
ENST00000697095.1:c.*2064A>T	ENSP00000513104.1:n.*2064A>T
ENST00000697096.1:n.1996A>T
ENST00000697097.1:c.146A>T	ENSP00000513105.1:p.Lys49Ile
ENST00000562983.2:n.1049A>T
ENST00000690268.1:c.944A>T	ENSP00000509810.1:p.Lys315Ile
ENST00000355740.7:c.*189A>T	ENSP00000347979.3:n.*189A>T
ENST00000612663.5:c.*265A>T	ENSP00000477997.3:n.*265A>T
ENST00000640140.1:n.1035A>T
ENST00000640250.1:n.362A>T
ENST00000640681.1:n.984A>T
ENST00000652046.1:c.863A>T MANE Select	ENSP00000498466.1:p.Lys288Ile
ENST00000352159.8:c.*180A>T	ENSP00000345601.4:n.*180A>T
ENST00000355279.2:c.838A>T	ENSP00000347426.2:n.838A>T
ENST00000355740.6:c.863A>T	ENSP00000347979.2:p.Lys288Ile
ENST00000357339.6:c.800A>T	ENSP00000349896.2:p.Lys267Ile
ENST00000479522.5:c.*292A>T	ENSP00000424113.1:n.*292A>T
ENST00000484444.5:c.*304A>T	ENSP00000420975.1:n.*304A>T
ENST00000488877.5:c.*304A>T	ENSP00000425159.1:n.*304A>T
ENST00000492756.5:c.691A>T	ENSP00000422453.1:n.691A>T
ENST00000494410.5:c.*221A>T	ENSP00000423755.1:n.*221A>T
ENST00000612663.4:c.*210A>T	ENSP00000477997.2:n.*210A>T
NM_000043.4:c.863A>T , LRG_134t1:c.863A>T	NP_000034.1:p.Lys288Ile
NM_152871.2:c.800A>T	NP_690610.1:p.Lys267Ile
NM_152872.2:c.*175A>T	NP_690611.1:n.*175A>T
NR_028033.2:n.1037A>T
NR_028034.2:n.899A>T
NR_028035.2:n.962A>T
NR_028036.2:n.1100A>T
XM_006717819.2:c.944A>T	XP_006717882.1:p.Lys315Ile
XM_011539764.1:c.1025A>T	XP_011538066.1:p.Lys342Ile
XM_011539765.1:c.962A>T	XP_011538067.1:p.Lys321Ile
XM_011539766.1:c.944A>T	XP_011538068.1:p.Lys315Ile
XM_011539767.1:c.908A>T	XP_011538069.1:p.Lys303Ile
XR_945732.1:n.931A>T
XR_945733.1:n.868A>T
NM_000043.5:c.863A>T	NP_000034.1:p.Lys288Ile
NM_001320619.1:c.*186A>T	NP_001307548.1:n.*186A>T
NM_152871.3:c.800A>T	NP_690610.1:p.Lys267Ile
NM_152872.3:c.*175A>T	NP_690611.1:n.*175A>T
NR_028033.3:n.1009A>T
NR_028034.3:n.871A>T
NR_028035.3:n.934A>T
NR_028036.3:n.1072A>T
NR_135313.1:n.989A>T
NR_135314.1:n.1172A>T
NR_135315.1:n.925A>T
XM_006717819.3:c.944A>T	XP_006717882.1:p.Lys315Ile
XM_011539764.2:c.1025A>T	XP_011538066.1:p.Lys342Ile
XM_011539765.2:c.962A>T	XP_011538067.1:p.Lys321Ile
XM_011539766.2:c.944A>T	XP_011538068.1:p.Lys315Ile
XM_011539767.3:c.908A>T	XP_011538069.1:p.Lys303Ile
XR_945732.3:n.931A>T
XR_945733.2:n.868A>T
NM_000043.6:c.863A>T MANE Select	NP_000034.1:p.Lys288Ile
NM_001320619.2:c.*186A>T	NP_001307548.1:n.*186A>T
NM_152871.4:c.800A>T	NP_690610.1:p.Lys267Ile
NM_152872.4:c.*175A>T	NP_690611.1:n.*175A>T
NR_028033.4:n.770A>T
NR_028034.4:n.632A>T
NR_028035.4:n.695A>T
NR_028036.4:n.833A>T
NR_135313.2:n.750A>T
NR_135314.2:n.1029A>T
NR_135315.2:n.782A>T