Canonical Allele Identifier: CA377509984

Gene: FAS

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1172A>C
ENST00000355740.8:c.*186A>C	ENSP00000347979.3:n.*186A>C
ENST00000357339.7:c.800A>C	ENSP00000349896.2:p.Lys267Thr
ENST00000371857.8:n.2408A>C
ENST00000460510.6:c.146A>C	ENSP00000512812.1:p.Lys49Thr
ENST00000466081.6:n.2512A>C
ENST00000477270.6:c.908A>C	ENSP00000512813.1:p.Lys303Thr
ENST00000479522.6:c.*292A>C	ENSP00000424113.1:n.*292A>C
ENST00000484444.6:c.*304A>C	ENSP00000420975.1:n.*304A>C
ENST00000488877.6:c.754A>C	ENSP00000425159.1:n.754A>C
ENST00000492756.7:c.*292A>C	ENSP00000422453.1:n.*292A>C
ENST00000494799.6:c.146A>C	ENSP00000512834.1:p.Lys49Thr
ENST00000562983.3:c.146A>C	ENSP00000512845.1:p.Lys49Thr
ENST00000612663.6:c.*265A>C	ENSP00000477997.3:n.*265A>C
ENST00000640140.2:n.1008A>C
ENST00000640250.2:n.362A>C
ENST00000640681.2:n.967A>C
ENST00000696723.1:n.4496A>C
ENST00000696741.1:n.2501A>C
ENST00000696742.1:n.2228A>C
ENST00000696743.1:n.3631A>C
ENST00000696744.1:n.902A>C
ENST00000696767.1:n.1197A>C
ENST00000696768.1:c.*186A>C	ENSP00000512859.1:n.*186A>C
ENST00000696769.1:n.2552A>C
ENST00000696771.1:c.146A>C	ENSP00000512860.1:p.Lys49Thr
ENST00000696772.1:n.2466A>C
ENST00000696773.1:n.2205A>C
ENST00000696774.1:n.5973A>C
ENST00000696776.1:c.956A>C	ENSP00000512861.1:p.Lys319Thr
ENST00000696777.1:n.2271A>C
ENST00000696778.1:n.1299A>C
ENST00000696779.1:c.470A>C	ENSP00000512862.1:p.Lys157Thr
ENST00000696780.1:c.893A>C	ENSP00000512863.1:p.Lys298Thr
ENST00000696781.1:c.608A>C	ENSP00000512864.1:p.Lys203Thr
ENST00000696782.1:c.*265A>C	ENSP00000512865.1:n.*265A>C
ENST00000696783.1:n.2731A>C
ENST00000696992.1:n.1980A>C
ENST00000696995.1:n.4392A>C
ENST00000696996.1:n.2305A>C
ENST00000696997.1:c.*493A>C	ENSP00000513028.1:n.*493A>C
ENST00000696998.1:n.2117A>C
ENST00000696999.1:c.146A>C	ENSP00000513029.1:p.Lys49Thr
ENST00000697036.1:c.*279A>C	ENSP00000513060.1:n.*279A>C
ENST00000697037.1:n.898A>C
ENST00000697093.1:n.3099A>C
ENST00000697094.1:n.3446A>C
ENST00000697095.1:c.*2064A>C	ENSP00000513104.1:n.*2064A>C
ENST00000697096.1:n.1996A>C
ENST00000697097.1:c.146A>C	ENSP00000513105.1:p.Lys49Thr
ENST00000562983.2:n.1049A>C
ENST00000690268.1:c.944A>C	ENSP00000509810.1:p.Lys315Thr
ENST00000355740.7:c.*189A>C	ENSP00000347979.3:n.*189A>C
ENST00000612663.5:c.*265A>C	ENSP00000477997.3:n.*265A>C
ENST00000640140.1:n.1035A>C
ENST00000640250.1:n.362A>C
ENST00000640681.1:n.984A>C
ENST00000652046.1:c.863A>C MANE Select	ENSP00000498466.1:p.Lys288Thr
ENST00000352159.8:c.*180A>C	ENSP00000345601.4:n.*180A>C
ENST00000355279.2:c.838A>C	ENSP00000347426.2:n.838A>C
ENST00000355740.6:c.863A>C	ENSP00000347979.2:p.Lys288Thr
ENST00000357339.6:c.800A>C	ENSP00000349896.2:p.Lys267Thr
ENST00000479522.5:c.*292A>C	ENSP00000424113.1:n.*292A>C
ENST00000484444.5:c.*304A>C	ENSP00000420975.1:n.*304A>C
ENST00000488877.5:c.*304A>C	ENSP00000425159.1:n.*304A>C
ENST00000492756.5:c.691A>C	ENSP00000422453.1:n.691A>C
ENST00000494410.5:c.*221A>C	ENSP00000423755.1:n.*221A>C
ENST00000612663.4:c.*210A>C	ENSP00000477997.2:n.*210A>C
NM_000043.4:c.863A>C , LRG_134t1:c.863A>C	NP_000034.1:p.Lys288Thr
NM_152871.2:c.800A>C	NP_690610.1:p.Lys267Thr
NM_152872.2:c.*175A>C	NP_690611.1:n.*175A>C
NR_028033.2:n.1037A>C
NR_028034.2:n.899A>C
NR_028035.2:n.962A>C
NR_028036.2:n.1100A>C
XM_006717819.2:c.944A>C	XP_006717882.1:p.Lys315Thr
XM_011539764.1:c.1025A>C	XP_011538066.1:p.Lys342Thr
XM_011539765.1:c.962A>C	XP_011538067.1:p.Lys321Thr
XM_011539766.1:c.944A>C	XP_011538068.1:p.Lys315Thr
XM_011539767.1:c.908A>C	XP_011538069.1:p.Lys303Thr
XR_945732.1:n.931A>C
XR_945733.1:n.868A>C
NM_000043.5:c.863A>C	NP_000034.1:p.Lys288Thr
NM_001320619.1:c.*186A>C	NP_001307548.1:n.*186A>C
NM_152871.3:c.800A>C	NP_690610.1:p.Lys267Thr
NM_152872.3:c.*175A>C	NP_690611.1:n.*175A>C
NR_028033.3:n.1009A>C
NR_028034.3:n.871A>C
NR_028035.3:n.934A>C
NR_028036.3:n.1072A>C
NR_135313.1:n.989A>C
NR_135314.1:n.1172A>C
NR_135315.1:n.925A>C
XM_006717819.3:c.944A>C	XP_006717882.1:p.Lys315Thr
XM_011539764.2:c.1025A>C	XP_011538066.1:p.Lys342Thr
XM_011539765.2:c.962A>C	XP_011538067.1:p.Lys321Thr
XM_011539766.2:c.944A>C	XP_011538068.1:p.Lys315Thr
XM_011539767.3:c.908A>C	XP_011538069.1:p.Lys303Thr
XR_945732.3:n.931A>C
XR_945733.2:n.868A>C
NM_000043.6:c.863A>C MANE Select	NP_000034.1:p.Lys288Thr
NM_001320619.2:c.*186A>C	NP_001307548.1:n.*186A>C
NM_152871.4:c.800A>C	NP_690610.1:p.Lys267Thr
NM_152872.4:c.*175A>C	NP_690611.1:n.*175A>C
NR_028033.4:n.770A>C
NR_028034.4:n.632A>C
NR_028035.4:n.695A>C
NR_028036.4:n.833A>C
NR_135313.2:n.750A>C
NR_135314.2:n.1029A>C
NR_135315.2:n.782A>C