Canonical Allele Identifier: CA2788920984

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014496T>C , CM000672.2:g.89014496T>C	GRCh38
NC_000010.10:g.90774253T>C , CM000672.1:g.90774253T>C	GRCh37
NC_000010.9:g.90764233T>C	NCBI36
NG_009089.2:g.28966T>C , LRG_134:g.28966T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1363T>C
ENST00000355740.8:c.*377T>C	ENSP00000347979.3:n.*377T>C
ENST00000357339.7:c.*46T>C	ENSP00000349896.2:n.*46T>C
ENST00000371857.8:n.2599T>C
ENST00000460510.6:c.*46T>C	ENSP00000512812.1:n.*46T>C
ENST00000466081.6:n.2703T>C
ENST00000477270.6:c.*46T>C	ENSP00000512813.1:n.*46T>C
ENST00000479522.6:c.*483T>C	ENSP00000424113.1:n.*483T>C
ENST00000484444.6:c.*495T>C	ENSP00000420975.1:n.*495T>C
ENST00000488877.6:c.945T>C	ENSP00000425159.1:n.945T>C
ENST00000492756.7:c.*483T>C	ENSP00000422453.1:n.*483T>C
ENST00000494799.6:c.*46T>C	ENSP00000512834.1:n.*46T>C
ENST00000562983.3:c.*46T>C	ENSP00000512845.1:n.*46T>C
ENST00000612663.6:c.*456T>C	ENSP00000477997.3:n.*456T>C
ENST00000640140.2:n.1199T>C
ENST00000640250.2:n.553T>C
ENST00000640681.2:n.1158T>C
ENST00000696723.1:n.4687T>C
ENST00000696741.1:n.2692T>C
ENST00000696742.1:n.2419T>C
ENST00000696743.1:n.3822T>C
ENST00000696744.1:n.1093T>C
ENST00000696767.1:n.1388T>C
ENST00000696768.1:c.*377T>C	ENSP00000512859.1:n.*377T>C
ENST00000696769.1:n.2743T>C
ENST00000696771.1:c.*46T>C	ENSP00000512860.1:n.*46T>C
ENST00000696772.1:n.2657T>C
ENST00000696773.1:n.2396T>C
ENST00000696774.1:n.6164T>C
ENST00000696776.1:c.*46T>C	ENSP00000512861.1:n.*46T>C
ENST00000696777.1:n.2462T>C
ENST00000696778.1:n.1490T>C
ENST00000696779.1:c.*46T>C	ENSP00000512862.1:n.*46T>C
ENST00000696780.1:c.*46T>C	ENSP00000512863.1:n.*46T>C
ENST00000696781.1:c.*46T>C	ENSP00000512864.1:n.*46T>C
ENST00000696782.1:c.*456T>C	ENSP00000512865.1:n.*456T>C
ENST00000696783.1:n.2922T>C
ENST00000696992.1:n.2171T>C
ENST00000696995.1:n.4583T>C
ENST00000696996.1:n.2496T>C
ENST00000696997.1:c.*684T>C	ENSP00000513028.1:n.*684T>C
ENST00000696998.1:n.2308T>C
ENST00000696999.1:c.*46T>C	ENSP00000513029.1:n.*46T>C
ENST00000697036.1:c.*470T>C	ENSP00000513060.1:n.*470T>C
ENST00000697037.1:n.1089T>C
ENST00000697093.1:n.3290T>C
ENST00000697094.1:n.3637T>C
ENST00000697095.1:c.*2255T>C	ENSP00000513104.1:n.*2255T>C
ENST00000697096.1:n.2187T>C
ENST00000697097.1:c.*46T>C	ENSP00000513105.1:n.*46T>C
ENST00000562983.2:n.1240T>C
ENST00000690268.1:c.*46T>C	ENSP00000509810.1:n.*46T>C
ENST00000355740.7:c.*380T>C	ENSP00000347979.3:n.*380T>C
ENST00000640140.1:n.1226T>C
ENST00000640250.1:n.553T>C
ENST00000640681.1:n.1175T>C
ENST00000652046.1:c.*46T>C MANE Select	ENSP00000498466.1:n.*46T>C
ENST00000352159.8:c.*371T>C	ENSP00000345601.4:n.*371T>C
ENST00000355740.6:c.*46T>C	ENSP00000347979.2:n.*46T>C
ENST00000479522.5:c.*483T>C	ENSP00000424113.1:n.*483T>C
ENST00000484444.5:c.*495T>C	ENSP00000420975.1:n.*495T>C
ENST00000494410.5:c.*412T>C	ENSP00000423755.1:n.*412T>C
NM_000043.4:c.*46T>C , LRG_134t1:c.*46T>C	NP_000034.1:n.*46T>C
NM_152871.2:c.*46T>C	NP_690610.1:n.*46T>C
NM_152872.2:c.*366T>C	NP_690611.1:n.*366T>C
NR_028033.2:n.1228T>C
NR_028034.2:n.1090T>C
NR_028035.2:n.1153T>C
NR_028036.2:n.1291T>C
XM_006717819.2:c.*46T>C	XP_006717882.1:n.*46T>C
XM_011539764.1:c.*46T>C	XP_011538066.1:n.*46T>C
XM_011539765.1:c.*46T>C	XP_011538067.1:n.*46T>C
XM_011539766.1:c.*46T>C	XP_011538068.1:n.*46T>C
XM_011539767.1:c.*46T>C	XP_011538069.1:n.*46T>C
XR_945733.1:n.1059T>C
NM_000043.5:c.*46T>C	NP_000034.1:n.*46T>C
NM_001320619.1:c.*377T>C	NP_001307548.1:n.*377T>C
NM_152871.3:c.*46T>C	NP_690610.1:n.*46T>C
NM_152872.3:c.*366T>C	NP_690611.1:n.*366T>C
NR_028033.3:n.1200T>C
NR_028034.3:n.1062T>C
NR_028035.3:n.1125T>C
NR_028036.3:n.1263T>C
NR_135313.1:n.1180T>C
NR_135314.1:n.1363T>C
NR_135315.1:n.1116T>C
XM_006717819.3:c.*46T>C	XP_006717882.1:n.*46T>C
XM_011539764.2:c.*46T>C	XP_011538066.1:n.*46T>C
XM_011539765.2:c.*46T>C	XP_011538067.1:n.*46T>C
XM_011539766.2:c.*46T>C	XP_011538068.1:n.*46T>C
XM_011539767.3:c.*46T>C	XP_011538069.1:n.*46T>C
XR_945732.3:n.1122T>C
XR_945733.2:n.1059T>C
NM_000043.6:c.*46T>C MANE Select	NP_000034.1:n.*46T>C
NM_001320619.2:c.*377T>C	NP_001307548.1:n.*377T>C
NM_152871.4:c.*46T>C	NP_690610.1:n.*46T>C
NM_152872.4:c.*366T>C	NP_690611.1:n.*366T>C
NR_028033.4:n.961T>C
NR_028034.4:n.823T>C
NR_028035.4:n.886T>C
NR_028036.4:n.1024T>C
NR_135313.2:n.941T>C
NR_135314.2:n.1220T>C
NR_135315.2:n.973T>C