Canonical Allele Identifier: CA2535970728

Gene: FAS

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014488T>C , CM000672.2:g.89014488T>C	GRCh38
NC_000010.10:g.90774245T>C , CM000672.1:g.90774245T>C	GRCh37
NC_000010.9:g.90764225T>C	NCBI36
NG_009089.2:g.28958T>C , LRG_134:g.28958T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1355T>C
ENST00000355740.8:c.*369T>C	ENSP00000347979.3:n.*369T>C
ENST00000357339.7:c.*38T>C	ENSP00000349896.2:n.*38T>C
ENST00000371857.8:n.2591T>C
ENST00000460510.6:c.*38T>C	ENSP00000512812.1:n.*38T>C
ENST00000466081.6:n.2695T>C
ENST00000477270.6:c.*38T>C	ENSP00000512813.1:n.*38T>C
ENST00000479522.6:c.*475T>C	ENSP00000424113.1:n.*475T>C
ENST00000484444.6:c.*487T>C	ENSP00000420975.1:n.*487T>C
ENST00000488877.6:c.937T>C	ENSP00000425159.1:n.937T>C
ENST00000492756.7:c.*475T>C	ENSP00000422453.1:n.*475T>C
ENST00000494799.6:c.*38T>C	ENSP00000512834.1:n.*38T>C
ENST00000562983.3:c.*38T>C	ENSP00000512845.1:n.*38T>C
ENST00000612663.6:c.*448T>C	ENSP00000477997.3:n.*448T>C
ENST00000640140.2:n.1191T>C
ENST00000640250.2:n.545T>C
ENST00000640681.2:n.1150T>C
ENST00000696723.1:n.4679T>C
ENST00000696741.1:n.2684T>C
ENST00000696742.1:n.2411T>C
ENST00000696743.1:n.3814T>C
ENST00000696744.1:n.1085T>C
ENST00000696767.1:n.1380T>C
ENST00000696768.1:c.*369T>C	ENSP00000512859.1:n.*369T>C
ENST00000696769.1:n.2735T>C
ENST00000696771.1:c.*38T>C	ENSP00000512860.1:n.*38T>C
ENST00000696772.1:n.2649T>C
ENST00000696773.1:n.2388T>C
ENST00000696774.1:n.6156T>C
ENST00000696776.1:c.*38T>C	ENSP00000512861.1:n.*38T>C
ENST00000696777.1:n.2454T>C
ENST00000696778.1:n.1482T>C
ENST00000696779.1:c.*38T>C	ENSP00000512862.1:n.*38T>C
ENST00000696780.1:c.*38T>C	ENSP00000512863.1:n.*38T>C
ENST00000696781.1:c.*38T>C	ENSP00000512864.1:n.*38T>C
ENST00000696782.1:c.*448T>C	ENSP00000512865.1:n.*448T>C
ENST00000696783.1:n.2914T>C
ENST00000696992.1:n.2163T>C
ENST00000696995.1:n.4575T>C
ENST00000696996.1:n.2488T>C
ENST00000696997.1:c.*676T>C	ENSP00000513028.1:n.*676T>C
ENST00000696998.1:n.2300T>C
ENST00000696999.1:c.*38T>C	ENSP00000513029.1:n.*38T>C
ENST00000697036.1:c.*462T>C	ENSP00000513060.1:n.*462T>C
ENST00000697037.1:n.1081T>C
ENST00000697093.1:n.3282T>C
ENST00000697094.1:n.3629T>C
ENST00000697095.1:c.*2247T>C	ENSP00000513104.1:n.*2247T>C
ENST00000697096.1:n.2179T>C
ENST00000697097.1:c.*38T>C	ENSP00000513105.1:n.*38T>C
ENST00000562983.2:n.1232T>C
ENST00000690268.1:c.*38T>C	ENSP00000509810.1:n.*38T>C
ENST00000355740.7:c.*372T>C	ENSP00000347979.3:n.*372T>C
ENST00000640140.1:n.1218T>C
ENST00000640250.1:n.545T>C
ENST00000640681.1:n.1167T>C
ENST00000652046.1:c.*38T>C MANE Select	ENSP00000498466.1:n.*38T>C
ENST00000352159.8:c.*363T>C	ENSP00000345601.4:n.*363T>C
ENST00000355740.6:c.*38T>C	ENSP00000347979.2:n.*38T>C
ENST00000479522.5:c.*475T>C	ENSP00000424113.1:n.*475T>C
ENST00000484444.5:c.*487T>C	ENSP00000420975.1:n.*487T>C
ENST00000494410.5:c.*404T>C	ENSP00000423755.1:n.*404T>C
NM_000043.4:c.*38T>C , LRG_134t1:c.*38T>C	NP_000034.1:n.*38T>C
NM_152871.2:c.*38T>C	NP_690610.1:n.*38T>C
NM_152872.2:c.*358T>C	NP_690611.1:n.*358T>C
NR_028033.2:n.1220T>C
NR_028034.2:n.1082T>C
NR_028035.2:n.1145T>C
NR_028036.2:n.1283T>C
XM_006717819.2:c.*38T>C	XP_006717882.1:n.*38T>C
XM_011539764.1:c.*38T>C	XP_011538066.1:n.*38T>C
XM_011539765.1:c.*38T>C	XP_011538067.1:n.*38T>C
XM_011539766.1:c.*38T>C	XP_011538068.1:n.*38T>C
XM_011539767.1:c.*38T>C	XP_011538069.1:n.*38T>C
XR_945733.1:n.1051T>C
NM_000043.5:c.*38T>C	NP_000034.1:n.*38T>C
NM_001320619.1:c.*369T>C	NP_001307548.1:n.*369T>C
NM_152871.3:c.*38T>C	NP_690610.1:n.*38T>C
NM_152872.3:c.*358T>C	NP_690611.1:n.*358T>C
NR_028033.3:n.1192T>C
NR_028034.3:n.1054T>C
NR_028035.3:n.1117T>C
NR_028036.3:n.1255T>C
NR_135313.1:n.1172T>C
NR_135314.1:n.1355T>C
NR_135315.1:n.1108T>C
XM_006717819.3:c.*38T>C	XP_006717882.1:n.*38T>C
XM_011539764.2:c.*38T>C	XP_011538066.1:n.*38T>C
XM_011539765.2:c.*38T>C	XP_011538067.1:n.*38T>C
XM_011539766.2:c.*38T>C	XP_011538068.1:n.*38T>C
XM_011539767.3:c.*38T>C	XP_011538069.1:n.*38T>C
XR_945732.3:n.1114T>C
XR_945733.2:n.1051T>C
NM_000043.6:c.*38T>C MANE Select	NP_000034.1:n.*38T>C
NM_001320619.2:c.*369T>C	NP_001307548.1:n.*369T>C
NM_152871.4:c.*38T>C	NP_690610.1:n.*38T>C
NM_152872.4:c.*358T>C	NP_690611.1:n.*358T>C
NR_028033.4:n.953T>C
NR_028034.4:n.815T>C
NR_028035.4:n.878T>C
NR_028036.4:n.1016T>C
NR_135313.2:n.933T>C
NR_135314.2:n.1212T>C
NR_135315.2:n.965T>C