Canonical Allele Identifier: CA1926639532

Gene: FAS

Linked Data

• dbSNP Id: rs1848706386

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.89014668T>C , CM000672.2:g.89014668T>C	GRCh38
NC_000010.10:g.90774425T>C , CM000672.1:g.90774425T>C	GRCh37
NC_000010.9:g.90764405T>C	NCBI36
NG_009089.2:g.29138T>C , LRG_134:g.29138T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313771.10:n.1535T>C
ENST00000355740.8:c.*549T>C	ENSP00000347979.3:n.*549T>C
ENST00000357339.7:c.*218T>C	ENSP00000349896.2:n.*218T>C
ENST00000371857.8:n.2771T>C
ENST00000460510.6:c.*218T>C	ENSP00000512812.1:n.*218T>C
ENST00000466081.6:n.2875T>C
ENST00000477270.6:c.*218T>C	ENSP00000512813.1:n.*218T>C
ENST00000492756.7:c.*655T>C	ENSP00000422453.1:n.*655T>C
ENST00000494799.6:c.*218T>C	ENSP00000512834.1:n.*218T>C
ENST00000562983.3:c.*218T>C	ENSP00000512845.1:n.*218T>C
ENST00000612663.6:c.*628T>C	ENSP00000477997.3:n.*628T>C
ENST00000640140.2:n.1371T>C
ENST00000640250.2:n.725T>C
ENST00000640681.2:n.1330T>C
ENST00000696723.1:n.4859T>C
ENST00000696741.1:n.2864T>C
ENST00000696742.1:n.2591T>C
ENST00000696743.1:n.3994T>C
ENST00000696744.1:n.1265T>C
ENST00000696767.1:n.1560T>C
ENST00000696768.1:c.*549T>C	ENSP00000512859.1:n.*549T>C
ENST00000696771.1:c.*218T>C	ENSP00000512860.1:n.*218T>C
ENST00000696772.1:n.2829T>C
ENST00000696773.1:n.2568T>C
ENST00000696774.1:n.6336T>C
ENST00000696776.1:c.*218T>C	ENSP00000512861.1:n.*218T>C
ENST00000696777.1:n.2634T>C
ENST00000696778.1:n.1662T>C
ENST00000696779.1:c.*218T>C	ENSP00000512862.1:n.*218T>C
ENST00000696780.1:c.*218T>C	ENSP00000512863.1:n.*218T>C
ENST00000696781.1:c.*218T>C	ENSP00000512864.1:n.*218T>C
ENST00000696782.1:c.*628T>C	ENSP00000512865.1:n.*628T>C
ENST00000696783.1:n.3094T>C
ENST00000696992.1:n.2343T>C
ENST00000696995.1:n.4755T>C
ENST00000696996.1:n.2668T>C
ENST00000696997.1:c.*856T>C	ENSP00000513028.1:n.*856T>C
ENST00000696998.1:n.2480T>C
ENST00000696999.1:c.*218T>C	ENSP00000513029.1:n.*218T>C
ENST00000697036.1:c.*642T>C	ENSP00000513060.1:n.*642T>C
ENST00000697037.1:n.1261T>C
ENST00000697093.1:n.3462T>C
ENST00000697094.1:n.3809T>C
ENST00000697095.1:c.*2427T>C	ENSP00000513104.1:n.*2427T>C
ENST00000697096.1:n.2359T>C
ENST00000697097.1:c.*218T>C	ENSP00000513105.1:n.*218T>C
ENST00000562983.2:n.1412T>C
ENST00000690268.1:c.*218T>C	ENSP00000509810.1:n.*218T>C
ENST00000355740.7:c.*552T>C	ENSP00000347979.3:n.*552T>C
ENST00000640140.1:n.1398T>C
ENST00000640250.1:n.725T>C
ENST00000640681.1:n.1347T>C
ENST00000652046.1:c.*218T>C MANE Select	ENSP00000498466.1:n.*218T>C
ENST00000352159.8:c.*543T>C	ENSP00000345601.4:n.*543T>C
ENST00000355740.6:c.*218T>C	ENSP00000347979.2:n.*218T>C
NM_000043.4:c.*218T>C , LRG_134t1:c.*218T>C	NP_000034.1:n.*218T>C
NM_152871.2:c.*218T>C	NP_690610.1:n.*218T>C
NM_152872.2:c.*538T>C	NP_690611.1:n.*538T>C
NR_028033.2:n.1400T>C
NR_028034.2:n.1262T>C
NR_028035.2:n.1325T>C
NR_028036.2:n.1463T>C
XM_006717819.2:c.*218T>C	XP_006717882.1:n.*218T>C
XM_011539764.1:c.*218T>C	XP_011538066.1:n.*218T>C
XM_011539765.1:c.*218T>C	XP_011538067.1:n.*218T>C
XM_011539766.1:c.*218T>C	XP_011538068.1:n.*218T>C
XM_011539767.1:c.*218T>C	XP_011538069.1:n.*218T>C
NM_000043.5:c.*218T>C	NP_000034.1:n.*218T>C
NM_001320619.1:c.*549T>C	NP_001307548.1:n.*549T>C
NM_152871.3:c.*218T>C	NP_690610.1:n.*218T>C
NM_152872.3:c.*538T>C	NP_690611.1:n.*538T>C
NR_028033.3:n.1372T>C
NR_028034.3:n.1234T>C
NR_028035.3:n.1297T>C
NR_028036.3:n.1435T>C
NR_135313.1:n.1352T>C
NR_135314.1:n.1535T>C
NR_135315.1:n.1288T>C
XM_006717819.3:c.*218T>C	XP_006717882.1:n.*218T>C
XM_011539764.2:c.*218T>C	XP_011538066.1:n.*218T>C
XM_011539765.2:c.*218T>C	XP_011538067.1:n.*218T>C
XM_011539766.2:c.*218T>C	XP_011538068.1:n.*218T>C
XM_011539767.3:c.*218T>C	XP_011538069.1:n.*218T>C
XR_945732.3:n.1294T>C
XR_945733.2:n.1231T>C
NM_000043.6:c.*218T>C MANE Select	NP_000034.1:n.*218T>C
NM_001320619.2:c.*549T>C	NP_001307548.1:n.*549T>C
NM_152871.4:c.*218T>C	NP_690610.1:n.*218T>C
NM_152872.4:c.*538T>C	NP_690611.1:n.*538T>C
NR_028033.4:n.1133T>C
NR_028034.4:n.995T>C
NR_028035.4:n.1058T>C
NR_028036.4:n.1196T>C
NR_135313.2:n.1113T>C
NR_135314.2:n.1392T>C
NR_135315.2:n.1145T>C