Canonical Allele Identifier: CA377509934

Gene: FAS

Linked Data

• MyVariant Identifiers: chr10:g.90774041G>C (hg19) ; chr10:g.89014284G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014284G>C , CM000672.2:g.89014284G>C	GRCh38
NC_000010.10:g.90774041G>C , CM000672.1:g.90774041G>C	GRCh37
NC_000010.9:g.90764021G>C	NCBI36
NG_009089.2:g.28754G>C , LRG_134:g.28754G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1151G>C
ENST00000355740.8:c.*165G>C	ENSP00000347979.3:n.*165G>C
ENST00000357339.7:c.779G>C	ENSP00000349896.2:p.Trp260Ser
ENST00000371857.8:n.2387G>C
ENST00000460510.6:c.125G>C	ENSP00000512812.1:p.Trp42Ser
ENST00000466081.6:n.2491G>C
ENST00000477270.6:c.887G>C	ENSP00000512813.1:p.Trp296Ser
ENST00000479522.6:c.*271G>C	ENSP00000424113.1:n.*271G>C
ENST00000484444.6:c.*283G>C	ENSP00000420975.1:n.*283G>C
ENST00000488877.6:c.733G>C	ENSP00000425159.1:n.733G>C
ENST00000492756.7:c.*271G>C	ENSP00000422453.1:n.*271G>C
ENST00000494799.6:c.125G>C	ENSP00000512834.1:p.Trp42Ser
ENST00000562983.3:c.125G>C	ENSP00000512845.1:p.Trp42Ser
ENST00000612663.6:c.*244G>C	ENSP00000477997.3:n.*244G>C
ENST00000640140.2:n.987G>C
ENST00000640250.2:n.341G>C
ENST00000640681.2:n.946G>C
ENST00000696723.1:n.4475G>C
ENST00000696741.1:n.2480G>C
ENST00000696742.1:n.2207G>C
ENST00000696743.1:n.3610G>C
ENST00000696744.1:n.881G>C
ENST00000696767.1:n.1176G>C
ENST00000696768.1:c.*165G>C	ENSP00000512859.1:n.*165G>C
ENST00000696769.1:n.2531G>C
ENST00000696771.1:c.125G>C	ENSP00000512860.1:p.Trp42Ser
ENST00000696772.1:n.2445G>C
ENST00000696773.1:n.2184G>C
ENST00000696774.1:n.5952G>C
ENST00000696776.1:c.935G>C	ENSP00000512861.1:p.Trp312Ser
ENST00000696777.1:n.2250G>C
ENST00000696778.1:n.1278G>C
ENST00000696779.1:c.449G>C	ENSP00000512862.1:p.Trp150Ser
ENST00000696780.1:c.872G>C	ENSP00000512863.1:p.Trp291Ser
ENST00000696781.1:c.587G>C	ENSP00000512864.1:p.Trp196Ser
ENST00000696782.1:c.*244G>C	ENSP00000512865.1:n.*244G>C
ENST00000696783.1:n.2710G>C
ENST00000696992.1:n.1959G>C
ENST00000696995.1:n.4371G>C
ENST00000696996.1:n.2284G>C
ENST00000696997.1:c.*472G>C	ENSP00000513028.1:n.*472G>C
ENST00000696998.1:n.2096G>C
ENST00000696999.1:c.125G>C	ENSP00000513029.1:p.Trp42Ser
ENST00000697035.1:c.*175G>C	ENSP00000513059.1:n.*175G>C
ENST00000697036.1:c.*258G>C	ENSP00000513060.1:n.*258G>C
ENST00000697037.1:n.877G>C
ENST00000697093.1:n.3078G>C
ENST00000697094.1:n.3425G>C
ENST00000697095.1:c.*2043G>C	ENSP00000513104.1:n.*2043G>C
ENST00000697096.1:n.1975G>C
ENST00000697097.1:c.125G>C	ENSP00000513105.1:p.Trp42Ser
ENST00000562983.2:n.1028G>C
ENST00000690268.1:c.923G>C	ENSP00000509810.1:p.Trp308Ser
ENST00000355740.7:c.*168G>C	ENSP00000347979.3:n.*168G>C
ENST00000612663.5:c.*244G>C	ENSP00000477997.3:n.*244G>C
ENST00000640140.1:n.1014G>C
ENST00000640250.1:n.341G>C
ENST00000640681.1:n.963G>C
ENST00000652046.1:c.842G>C MANE Select	ENSP00000498466.1:p.Trp281Ser
ENST00000352159.8:c.*159G>C	ENSP00000345601.4:n.*159G>C
ENST00000355279.2:c.817G>C	ENSP00000347426.2:n.817G>C
ENST00000355740.6:c.842G>C	ENSP00000347979.2:p.Trp281Ser
ENST00000357339.6:c.779G>C	ENSP00000349896.2:p.Trp260Ser
ENST00000479522.5:c.*271G>C	ENSP00000424113.1:n.*271G>C
ENST00000484444.5:c.*283G>C	ENSP00000420975.1:n.*283G>C
ENST00000488877.5:c.*283G>C	ENSP00000425159.1:n.*283G>C
ENST00000492756.5:c.670G>C	ENSP00000422453.1:n.670G>C
ENST00000494410.5:c.*200G>C	ENSP00000423755.1:n.*200G>C
ENST00000612663.4:c.*189G>C	ENSP00000477997.2:n.*189G>C
NM_000043.4:c.842G>C , LRG_134t1:c.842G>C	NP_000034.1:p.Trp281Ser
NM_152871.2:c.779G>C	NP_690610.1:p.Trp260Ser
NM_152872.2:c.*154G>C	NP_690611.1:n.*154G>C
NR_028033.2:n.1016G>C
NR_028034.2:n.878G>C
NR_028035.2:n.941G>C
NR_028036.2:n.1079G>C
XM_006717819.2:c.923G>C	XP_006717882.1:p.Trp308Ser
XM_011539764.1:c.1004G>C	XP_011538066.1:p.Trp335Ser
XM_011539765.1:c.941G>C	XP_011538067.1:p.Trp314Ser
XM_011539766.1:c.923G>C	XP_011538068.1:p.Trp308Ser
XM_011539767.1:c.887G>C	XP_011538069.1:p.Trp296Ser
XR_945732.1:n.910G>C
XR_945733.1:n.847G>C
NM_000043.5:c.842G>C	NP_000034.1:p.Trp281Ser
NM_001320619.1:c.*165G>C	NP_001307548.1:n.*165G>C
NM_152871.3:c.779G>C	NP_690610.1:p.Trp260Ser
NM_152872.3:c.*154G>C	NP_690611.1:n.*154G>C
NR_028033.3:n.988G>C
NR_028034.3:n.850G>C
NR_028035.3:n.913G>C
NR_028036.3:n.1051G>C
NR_135313.1:n.968G>C
NR_135314.1:n.1151G>C
NR_135315.1:n.904G>C
XM_006717819.3:c.923G>C	XP_006717882.1:p.Trp308Ser
XM_011539764.2:c.1004G>C	XP_011538066.1:p.Trp335Ser
XM_011539765.2:c.941G>C	XP_011538067.1:p.Trp314Ser
XM_011539766.2:c.923G>C	XP_011538068.1:p.Trp308Ser
XM_011539767.3:c.887G>C	XP_011538069.1:p.Trp296Ser
XR_945732.3:n.910G>C
XR_945733.2:n.847G>C
NM_000043.6:c.842G>C MANE Select	NP_000034.1:p.Trp281Ser
NM_001320619.2:c.*165G>C	NP_001307548.1:n.*165G>C
NM_152871.4:c.779G>C	NP_690610.1:p.Trp260Ser
NM_152872.4:c.*154G>C	NP_690611.1:n.*154G>C
NR_028033.4:n.749G>C
NR_028034.4:n.611G>C
NR_028035.4:n.674G>C
NR_028036.4:n.812G>C
NR_135313.2:n.729G>C
NR_135314.2:n.1008G>C
NR_135315.2:n.761G>C