Canonical Allele Identifier: CA377510066

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774098A>C (hg19) ; chr10:g.89014341A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014341A>C , CM000672.2:g.89014341A>C	GRCh38
NC_000010.10:g.90774098A>C , CM000672.1:g.90774098A>C	GRCh37
NC_000010.9:g.90764078A>C	NCBI36
NG_009089.2:g.28811A>C , LRG_134:g.28811A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1208A>C
ENST00000355740.8:c.*222A>C	ENSP00000347979.3:n.*222A>C
ENST00000357339.7:c.836A>C	ENSP00000349896.2:p.Lys279Thr
ENST00000371857.8:n.2444A>C
ENST00000460510.6:c.182A>C	ENSP00000512812.1:p.Lys61Thr
ENST00000466081.6:n.2548A>C
ENST00000477270.6:c.944A>C	ENSP00000512813.1:p.Lys315Thr
ENST00000479522.6:c.*328A>C	ENSP00000424113.1:n.*328A>C
ENST00000484444.6:c.*340A>C	ENSP00000420975.1:n.*340A>C
ENST00000488877.6:c.790A>C	ENSP00000425159.1:n.790A>C
ENST00000492756.7:c.*328A>C	ENSP00000422453.1:n.*328A>C
ENST00000494799.6:c.182A>C	ENSP00000512834.1:p.Lys61Thr
ENST00000562983.3:c.182A>C	ENSP00000512845.1:p.Lys61Thr
ENST00000612663.6:c.*301A>C	ENSP00000477997.3:n.*301A>C
ENST00000640140.2:n.1044A>C
ENST00000640250.2:n.398A>C
ENST00000640681.2:n.1003A>C
ENST00000696723.1:n.4532A>C
ENST00000696741.1:n.2537A>C
ENST00000696742.1:n.2264A>C
ENST00000696743.1:n.3667A>C
ENST00000696744.1:n.938A>C
ENST00000696767.1:n.1233A>C
ENST00000696768.1:c.*222A>C	ENSP00000512859.1:n.*222A>C
ENST00000696769.1:n.2588A>C
ENST00000696771.1:c.182A>C	ENSP00000512860.1:p.Lys61Thr
ENST00000696772.1:n.2502A>C
ENST00000696773.1:n.2241A>C
ENST00000696774.1:n.6009A>C
ENST00000696776.1:c.992A>C	ENSP00000512861.1:p.Lys331Thr
ENST00000696777.1:n.2307A>C
ENST00000696778.1:n.1335A>C
ENST00000696779.1:c.506A>C	ENSP00000512862.1:p.Lys169Thr
ENST00000696780.1:c.929A>C	ENSP00000512863.1:p.Lys310Thr
ENST00000696781.1:c.644A>C	ENSP00000512864.1:p.Lys215Thr
ENST00000696782.1:c.*301A>C	ENSP00000512865.1:n.*301A>C
ENST00000696783.1:n.2767A>C
ENST00000696992.1:n.2016A>C
ENST00000696995.1:n.4428A>C
ENST00000696996.1:n.2341A>C
ENST00000696997.1:c.*529A>C	ENSP00000513028.1:n.*529A>C
ENST00000696998.1:n.2153A>C
ENST00000696999.1:c.182A>C	ENSP00000513029.1:p.Lys61Thr
ENST00000697036.1:c.*315A>C	ENSP00000513060.1:n.*315A>C
ENST00000697037.1:n.934A>C
ENST00000697093.1:n.3135A>C
ENST00000697094.1:n.3482A>C
ENST00000697095.1:c.*2100A>C	ENSP00000513104.1:n.*2100A>C
ENST00000697096.1:n.2032A>C
ENST00000697097.1:c.182A>C	ENSP00000513105.1:p.Lys61Thr
ENST00000562983.2:n.1085A>C
ENST00000690268.1:c.980A>C	ENSP00000509810.1:p.Lys327Thr
ENST00000355740.7:c.*225A>C	ENSP00000347979.3:n.*225A>C
ENST00000612663.5:c.*301A>C	ENSP00000477997.3:n.*301A>C
ENST00000640140.1:n.1071A>C
ENST00000640250.1:n.398A>C
ENST00000640681.1:n.1020A>C
ENST00000652046.1:c.899A>C MANE Select	ENSP00000498466.1:p.Lys300Thr
ENST00000352159.8:c.*216A>C	ENSP00000345601.4:n.*216A>C
ENST00000355279.2:c.874A>C	ENSP00000347426.2:n.874A>C
ENST00000355740.6:c.899A>C	ENSP00000347979.2:p.Lys300Thr
ENST00000357339.6:c.836A>C	ENSP00000349896.2:p.Lys279Thr
ENST00000479522.5:c.*328A>C	ENSP00000424113.1:n.*328A>C
ENST00000484444.5:c.*340A>C	ENSP00000420975.1:n.*340A>C
ENST00000488877.5:c.*340A>C	ENSP00000425159.1:n.*340A>C
ENST00000492756.5:c.727A>C	ENSP00000422453.1:n.727A>C
ENST00000494410.5:c.*257A>C	ENSP00000423755.1:n.*257A>C
ENST00000612663.4:c.*246A>C	ENSP00000477997.2:n.*246A>C
NM_000043.4:c.899A>C , LRG_134t1:c.899A>C	NP_000034.1:p.Lys300Thr
NM_152871.2:c.836A>C	NP_690610.1:p.Lys279Thr
NM_152872.2:c.*211A>C	NP_690611.1:n.*211A>C
NR_028033.2:n.1073A>C
NR_028034.2:n.935A>C
NR_028035.2:n.998A>C
NR_028036.2:n.1136A>C
XM_006717819.2:c.980A>C	XP_006717882.1:p.Lys327Thr
XM_011539764.1:c.1061A>C	XP_011538066.1:p.Lys354Thr
XM_011539765.1:c.998A>C	XP_011538067.1:p.Lys333Thr
XM_011539766.1:c.980A>C	XP_011538068.1:p.Lys327Thr
XM_011539767.1:c.944A>C	XP_011538069.1:p.Lys315Thr
XR_945732.1:n.967A>C
XR_945733.1:n.904A>C
NM_000043.5:c.899A>C	NP_000034.1:p.Lys300Thr
NM_001320619.1:c.*222A>C	NP_001307548.1:n.*222A>C
NM_152871.3:c.836A>C	NP_690610.1:p.Lys279Thr
NM_152872.3:c.*211A>C	NP_690611.1:n.*211A>C
NR_028033.3:n.1045A>C
NR_028034.3:n.907A>C
NR_028035.3:n.970A>C
NR_028036.3:n.1108A>C
NR_135313.1:n.1025A>C
NR_135314.1:n.1208A>C
NR_135315.1:n.961A>C
XM_006717819.3:c.980A>C	XP_006717882.1:p.Lys327Thr
XM_011539764.2:c.1061A>C	XP_011538066.1:p.Lys354Thr
XM_011539765.2:c.998A>C	XP_011538067.1:p.Lys333Thr
XM_011539766.2:c.980A>C	XP_011538068.1:p.Lys327Thr
XM_011539767.3:c.944A>C	XP_011538069.1:p.Lys315Thr
XR_945732.3:n.967A>C
XR_945733.2:n.904A>C
NM_000043.6:c.899A>C MANE Select	NP_000034.1:p.Lys300Thr
NM_001320619.2:c.*222A>C	NP_001307548.1:n.*222A>C
NM_152871.4:c.836A>C	NP_690610.1:p.Lys279Thr
NM_152872.4:c.*211A>C	NP_690611.1:n.*211A>C
NR_028033.4:n.806A>C
NR_028034.4:n.668A>C
NR_028035.4:n.731A>C
NR_028036.4:n.869A>C
NR_135313.2:n.786A>C
NR_135314.2:n.1065A>C
NR_135315.2:n.818A>C